NAMPT INHIBITORS

- AbbVie Inc.

Disclosed are compounds which inhibit the activity of NAMPT, compositions containing the compounds and methods of treating diseases during which NAMPT is expressed.

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Description

This application claims priority to Patent Cooperation Treaty Patent Application Serial No. PCT/CN2012/075327, filed May 11, 2012, which is incorporated by reference in their entirety.

FIELD OF THE INVENTION

This invention pertains to compounds which inhibit the activity of NAMPT, compositions containing the compounds, and methods of treating diseases during which NAMPT is expressed.

BACKGROUND OF THE INVENTION

NAD+ (nicotinamide adenine dinucleotide) is a coenzyme that plays a critical role in many physiologically essential processes (Ziegkel, M. Eur. J. Biochem. 267, 1550-1564, 2000). NAD is necessary for several signaling pathways including among others poly ADP-ribosylation in DNA repair, mono-ADP-ribosylation in both the immune system and G-protein-coupled signaling, and NAD is also required by sirtuins for their deacetylase activity (Garten, A. et al Trends in Endocrinology and Metabolism, 20, 130-138, 2008).

NAMPT (also known as pre-B-cell-colony-enhancing factor (PBEF) and visfatin) is an enzyme that catalyzes the phosphoribosylation of nicotinamide and is the rate-limiting enzyme in one of two pathways that salvage NAD.

Increasing evidence suggests that NAMPT inhibitors have potential as anticancer agents. Cancer cells have a higher basal turnover of NAD and also display higher energy requirements compared with normal cells. Additionally, increased NAMPT expression has been reported in colorectal cancer (Van Beijnum, J. R. et allnt. J. Cancer 101, 118-127, 2002) and NAMPT is involved in angiogenesis (Kim, S. R. et al. Biochem. Biophys. Res. Commun. 357, 150-156, 2007). Small-molecule inhibitors of NAMPT have been shown to cause depletion of intracellular NAD+ levels and ultimately induce tumor cell death (Hansen, C M et al. Anticancer Res. 20, 42111-4220, 2000) as well as inhibit tumor growth in xenograft models (Olese, U. H. et al. Mol Cancer Ther. 9, 1609-1617, 2010).

NAMPT inhibitors also have potential as therapeutic agents in inflammatory and metabolic disorders (Galli, M. et al Cancer Res. 70, 8-11, 2010). For example, NAMPT is the predominant enzyme in T and B lymphocytes. Selective inhibition of NAMPT leads to NAD+ depletion in lymphocytes blocking the expansion that accompanies autoimmune disease progression whereas cell types expressing the other NAD+ generating pathways might be spared. A small molecule NAMPT inhibitor (FK866) has been shown to selectively block proliferation and induce apoptosis of activated T cells and was efficacious in animal models of arthritis (collagen-induced arthritis) (Busso, N. et al. Plos One 3, e2267, 2008). FK866 ameliorated the manifestations of experimental autoimmune encephalomyelitis (EAE), a model of T-cell mediated autoimmune disorders. (Bruzzone, S et al. Plos One 4, e7897, 2009). NaMPT activity increases NF-kB transcriptional activity in human vascular endothelial cell, resulting in MMP-2 and MMP-9 activation, suggesting a role for NAMPT inhibitors in the prevention of inflammatory mediated complications of obesity and type 2 diabetes (Adya, R. et. Al. Diabetes Care, 31, 758-760, 2008).

SUMMARY OF THE INVENTION

One embodiment of this invention, therefore, pertains to compounds or pharmaceutically acceptable salts thereof, which are useful as inhibitors of NAMPT, the compounds having Formula (I)

wherein

R1 and R2 are each independently selected from the group consisting of R6, C(O)R6, C(O)NHR6, and C(O)N(R6)2; wherein at least one of R1 and R2 is R6; or R1 and R2, together with the nitrogen to which they are attached form a heterocycloalkyl or heterocycloalkenyl ring; wherein the ring formed with R1 and R2 together with the nitrogen to which they are attached is optionally substituted with one or more substituents independently selected from the group consisting of R7, OR7, SR7, S(O)R7, SO2R7, C(O)R7, CO(O)R7, OC(O)R7, OC(O)OR7, NH2, NHR7, N(R7)2, NHC(O)R7, NR7C(O)R7, NHS(O)2R7, NR7S(O)2R7, NHC(O)OR7, NR7C(O)OR7, NHC(O)NH2, NHC(O)NHR7, NHC(O)N(R7)2, NR7C(O)NHR7, NR7C(O)N(R7)2, C(O)NH2, C(O)NHR7, C(O)N(R7)2, C(O)NHOH, C(O)NHOR7, C(O)NHSO2R7, C(O)NR7SO2R7, SO2NH2, SO2NHR7, SO2N(R7)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR7, C(N)N(R7)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R3, R4, and R5 are each independently selected from the group consisting of hydrogen, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6 haloalkyl, C1-6 hydroxyalkyl, F, Cl, Br and I;

R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, SR8, S(O)R8, SO2R8, C(O)R8, CO(O)R8, OC(O)R8, OC(O)OR8, NH2, NHR8, N(R8)2, NHC(O)R8, NR8C(O)R8, NHS(O)2R8, NR8S(O)2R8, NHC(O)OR8, NR8C(O)OR8, NHC(O)NH2, NHC(O)NHR8, NHC(O)N(R8)2, NR8C(O)NHR8, NR8C(O)N(R8)2, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)NHOH, C(O)NHOR8, C(O)NHSO2R8, C(O)NR8SO2R8, SO2NH2, SO2NHR8, SO2N(R8)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR8, C(N)N(R8)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, SR9, S(O)R9, SO2R9, C(O)R9, CO(O)R9, OC(O)R9, OC(O)OR9, NH2, NHR9, N(R9)2, NHC(O)R9, NR9C(O)R9, NHS(O)2R9, NR9S(O)2R9, NHC(O)OR9, NR9C(O)OR9, NHC(O)NH2, NHC(O)NHR9, NHC(O)N(R9)2, NR9C(O)NHR9, NR9C(O)N(R9)2, C(O)NH2, C(O)NHR9, C(O)N(R9)2, C(O)NHOH, C(O)NHOR9, C(O)NHSO2R9, C(O)NR9SO2R9, SO2NH2, SO2NHR9, SO2N(R9)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR9, C(N)N(R9)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R7, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R7 are each independently optionally substituted with one or more substituents independently selected from the group consisting of aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R7 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I;

R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R10, OR10, SR10, S(O)R10, SO2R10, C(O)R10, CO(O)R10, OC(O)R10, OC(O)OR10, NH2, NHR10, N(R10)2, NHC(O)R10, NR10C(O)R10, NHS(O)2R10, NR10S(O)2R10, NHC(O)OR10, NR10C(O)OR10, NHC(O)NH2, NHC(O)NHR10, NHC(O)N(R10)2, NR10C(O)NHR10, NR10C(O)N(R10)2, C(O)NH2, C(O)NHR10, C(O)N(R10)2, C(O)NHOH, C(O)NHOR10, C(O)NHSO2R10, C(O)NR10SO2R10, SO2NH2, SO2NHR10, SO2N(R10)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR10, C(N)N(R10)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, SR11, S(O)R11, SO2R11, C(O)R11, CO(O)R11, OC(O)R11, OC(O)OR11, NH2, NHR11, N(R11)2, NHC(O)R11, NR11C(O)R11, NHS(O)2R11, NR11S(O)2R11, NHC(O)OR11, NR11C(O)OR11, NHC(O)NH2, NHC(O)NHR11, NHC(O)N(R11)2, NR11C(O)NHR11, NR11C(O)N(R11)2, C(O)NH2, C(O)NHR11, C(O)N(R11)2, C(O)NHOH, C(O)NHOR11, C(O)NHSO2R11, C(O)NR11SO2R11, SO2NH2, SO2NHR11, SO2N(R11)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR11, C(N)N(R11)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R9, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R12, OR12, SR12, S(O)R12, SO2R12, C(O)R12, CO(O)R12, OC(O)R12, OC(O)OR12, NH2, NHR12, N(R12)2, NHC(O)R12, NR12C(O)R12, NHS(O)2R12, NR12S(O)2R12, NHC(O)OR12, NR12C(O)OR12, NHC(O)NH2, NHC(O)NHR12, NHC(O)N(R12)2, NR12C(O)NHR12, NR12C(O)N(R12)2, C(O)NH2, C(O)NHR12, C(O)N(R12)2, C(O)NHOH, C(O)NHOR12, C(O)NHSO2R12, C(O)NR12SO2R12, SO2NH2, SO2NHR12, SO2N(R12)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR12, C(N)N(R12)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R13, OR13, SR13, S(O)R13, SO2R13, C(O)R13, CO(O)R13, OC(O)R13, OC(O)OR13, NH2, NHR13, N(R13)2, NHC(O)R13, NR13C(O)R13, NHS(O)2R13, NR13S(O)2R13, NHC(O)OR13, NR13C(O)OR13, NHC(O)NH2, NHC(O)NHR13, NHC(O)N(R13)2, NR13C(O)NHR13, NR13C(O)N(R13)2, C(O)NH2, C(O)NHR13, C(O)N(R13)2, C(O)NHOH, C(O)NHOR13, C(O)NHSO2R13, C(O)NR13SO2R13, SO2NH2, SO2NHR13, SO2N(R13)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR13, C(N)N(R13)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R10, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6haloalkyl, and C1-6 hydroxyalkyl;

R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I;

R12, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; and

R13, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl; wherein the C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R13 are each independently optionally substituted with one or more substituents independently selected from the group consisting of alkoxy, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In one embodiment of Formula (I), R1 is C(O)R6; and R2 is R6. In another embodiment of Formula (I), R1 and R2 are each R6. In another embodiment of Formula (I), R1 is C(O)NHR6; and R2 is R6. In another embodiment of Formula (I), R1 is C(O)N(R6)2; and R2 is R6. In another embodiment of Formula (I), R3, R4 and R5 are hydrogen. In another embodiment of Formula (I), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, heterocycloalkyl, heteroaryl, and cycloalkyl; wherein the C1-6 alkyl, and C2-6 alkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, C(O)R8, CO(O)R8, OC(O)R8, N(R8)2, NHC(O)R8, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)OH, and OH; wherein the aryl, heterocycloalkyl, heteroaryl, and cycloalkyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, C(O)NH2, C(O)OH, OH, CN, F, Cl, Br and I.

Still another embodiment pertains to compounds, which are

  • 2-{(4-fluorobenzyl)[4-(pyridin-3-yl)benzyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{methyl[4-(pyridin-3-yl)benzyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(methyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(tetrahydro-2H-pyran-4-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(cyclohexylacetyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(3-methylbutanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[3-(morpholin-4-yl)propyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [3-(piperidin-1-yl)propyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [2-(pyrrolidin-1-yl)ethyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {2-[4-(propan-2-yl)piperazin-1-yl]ethyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzoyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(3-chlorobenzoyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzoyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(5-chloro-1,3-benzodioxol-4-yl)methyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-chlorobenzyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(2-chlorobenzyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(2,5-dichlorobenzyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[2-(methylamino)-2-oxoethyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[2-oxo-2-(propan-2-ylamino)ethyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(dimethylamino)-2-oxoethyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(diethylamino)-2-oxoethyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[2-(morpholin-4-yl)-2-oxoethyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(4-methylbenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(methoxyacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(N,N-dimethylglycyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(3,6-dihydropyridin-1(2H)-ylacetyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [(4-methylpiperidin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [(4-hydroxypiperidin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(4-methylpiperazin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[4-(propan-2-yl)piperazin-1-yl]acetyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(4-formylpiperazin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[4-(cyclopropylmethyl)piperazin-1-yl]acetyl}(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[4-(2-ethoxyethyl)piperazin-1-yl]acetyl}(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(cyclopropylcarbonyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[4-(prop-2-en-1-yl)piperazin-1-yl]acetyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[4-(3-methoxypropyl)piperazin-1-yl]acetyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[3-(dimethylamino)pyrrolidin-1-yl]acetyl}(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(morpholin-4-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [(3-hydroxypiperidin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[4-(2-hydroxyethyl)piperazin-1-yl]acetyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(1,4-dioxa-7-azaspiro[4.4]non-7-ylacetyl) (4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 1-{2-[(4-fluorobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)amino]-2-oxoethyl}pyridinium;
  • 2-{[2-(4-fluorophenyl)ethyl](3-methylbutanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(propan-2-ylcarbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(4-cyanophenyl)ethyl](3-methylbutanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(4-cyanophenyl)ethyl](tetrahydro-2H-pyran-4-ylacetyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(3-methylbutanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(tetrahydro-2H-pyran-4-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(4-cyanophenyl)ethyl](tetrahydrofuran-3-ylacetyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(3-methylbutanoyl)amino]-N-[3-(2-methyl-1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(3-methylbutanoyl)amino]-N-[3-(4-methyl-1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(2-fluorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(3-fluorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(2-chlorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(3-chlorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-chlorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(tetrahydrofuran-3-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(3-methylbutyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [(2-methylpropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N1-(4-fluorobenzyl)-N1-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)piperidine-1,3-dicarboxamide;
  • 2-{(4-fluorobenzyl) [(3-hydroxyazetidin-1-yl)carbonyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-(4-fluorobenzyl)-N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-1,4-dioxa-7-azaspiro[4.4]nonane-7-carboxamide;
  • 2-{(4-fluorobenzyl)[(3-methoxypyrrolidin-1-yl)carbonyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-methoxyethyl)(methyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-(4-fluorobenzyl)-N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-2,6-dimethylmorpholine-4-carboxamide;
  • 2-{[ethyl(2-methoxyethyl)carbamoyl](4-fluorobenzyl(4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-(4-fluorobenzyl)-N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-2,2-dimethylmorpholine-4-carboxamide;
  • N-(4-fluorobenzyl)-N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-1,4-oxazepane-4-carboxamide;
  • 2-[(4-fluorobenzoyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(4-methylbenzyl)amino]-1,3-thiazole-5-carboxamide;
  • N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-N-(3-methylbutyl)-1,2-oxazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(2-phenoxypropanoyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-propoxyethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [(tetrahydrofuran-2-ylmethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(1-methoxypropan-2-yl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(tetrahydro-2H-pyran-2-ylmethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-methoxyethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(2-ethoxyethyl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(1-methoxybutan-2-yl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(4-cyanophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(1,3-dioxolan-2-ylmethyl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[2-(propan-2-yloxy)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(1,4-dioxan-2-ylmethyl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(1,3-dimethoxypropan-2-yl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-methoxybutyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(tetrahydrofuran-3-ylcarbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(tetrahydro-2H-pyran-3-ylcarbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(pyrimidin-2-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(2-methoxypyridin-4-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(1,3-oxazol-4-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-{[(5-chloropyridin-2-yl)methyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(4-methylpyridin-3-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(6-methoxypyridin-3-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(4-methyl-1,3-thiazol-5-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[2-(3-hydroxyphenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-(pyridin-2-yl)ethyl]amino}-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(1,3-benzodioxol-5-yl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(4-chlorophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(3-fluorophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(4-hydroxyphenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(3-chlorophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{[2-(3-methoxyphenyl)ethyl](3-methoxypropanoyl)amino}-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(2-fluorophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-hydroxy-2-(4-methoxyphenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl)[1-(pyridin-2-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl)[(1-methyl-1H-pyrazol-4-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(2,6-difluorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(6-methylpyridin-3-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(4-chlorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(5-methylpyrazin-2-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(3-chlorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(5-methylpyridin-2-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(2,5-difluorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(2-methylbenzyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(3-methylbenzyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(pyridin-2-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(pyridin-3-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[2-(propan-2-yloxy)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(2-methoxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[2-(2-hydroxyethoxy)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(propan-2-yloxy)propyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(3-hydroxy-2,2-dimethylpropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(2-hydroxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(1-hydroxypropan-2-yl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(3-hydroxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[(2S)-1-hydroxybut-3-en-2-yl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(4-hydroxybutyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methylbutyl)[(2R)-2-phenoxypropanoyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methylbutyl)[(2S)-2-phenoxypropanoyl]amino}-1,3-thiazole-5-carboxamide;
  • N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-5-methyl-N-(3-methylbutyl)-1,2-oxazole-3-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(phenoxyacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(3-phenylpropanoyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(2-phenylpropanoyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-{[(4-fluorophenyl)acetyl](3-methylbutyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(3-amino-3-oxopropyl)carbamoyl](4-cyanobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[3-(acetylamino)-2-methylpropyl]carbamoyl}(4-cyanobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl){[3-(dimethylamino)-3-oxopropyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(3-ethoxy-2-hydroxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(diethylamino)propyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[2-(acetylamino)ethyl]carbamoyl}(4-cyanobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[2-(diethylamino)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)({2-[(2-methylpropanoyl)amino]ethyl}carbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[(2R)-1-hydroxybut-3-en-2-yl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(3-hydroxyazetidin-1-yl)propyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(3-methylbutyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(methoxyacetyl)(3-methylbutyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-[(cyclopropylcarbonyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • (2S)-1-[(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)(3-methylbutyl)amino]-1-oxopropan-2-yl acetate;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(tetrahydro-2H-pyran-4-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(tetrahydrofuran-3-ylcarbonyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-{[2-hydroxy-2-(3-methoxyphenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-(pyrazin-2-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[1-(3-hydroxyphenyl)propan-2-yl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • ethyl N-[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]-beta-alaninate;
  • ethyl 4-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoate;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoate;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-4-methylpentanoate;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2,2-dimethylpropanoate;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}cyclobutanecarboxylic acid;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2-methylpropanoate;
  • 2-{(4-cyanobenzyl)[(3-methoxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoic acid;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-4-methylpentanoic acid;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2,2-dimethylpropanoic acid;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2-methylpropanoic acid;
  • N-[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]-beta-alanine;
  • 4-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoic acid;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(tetrahydrofuran-2-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(tetrahydrofuran-3-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(2-methoxyethyl)(3-methoxypropanoyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(3-methoxypropyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(tetrahydro-2H-pyran-2-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(tetrahydrofuran-2-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-(propan-2-yloxy)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[2-(1,3-dioxolan-2-yl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(1,4-dioxan-2-ylmethyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[3-(4-fluorophenyl)propanoyl](2-methoxyethyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(2-methoxyethyl) [3-(pyridin-3-yl)propanoyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(2-methoxyethyl)(pyridin-3-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(2-methoxyethyl)(naphthalen-2-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(2-methoxyethyl)[(4-phenoxyphenyl)acetyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[(4-cyanophenyl)acetyl](2-methoxyethyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(4-aminophenyl)acetyl](2-methoxyethyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{2-[di(prop-2-en-1-yl)amino]ethyl}(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[3-(diethylamino)propyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(diethylamino)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [3-(pyrrolidin-1-yl)propyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[(1-ethyl-5-oxopyrrolidin-3-yl)methyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(5-oxopyrrolidin-2-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl)[3-oxo-3-(pyrrolidin-1-yl)propyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl)[2-oxo-2-(piperidin-1-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [3-(2-oxopyrrolidin-1-yl)propyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-(2-oxo-1,3-oxazolidin-3-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl) {2-[(2-methylpropanoyl)amino]ethyl}amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [3-(methylamino)-3-oxopropyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[3-(acetylamino)propyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-oxo-2-(pyrrolidin-1-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[3-(2-hydroxyethyl)-2-oxoimidazolidin-1-yl]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[3-(4-fluorophenyl)-2-oxoimidazolidin-1-yl]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(5-chloropyridin-2-yl)methyl](tetrahydro-2H-pyran-4-ylcarbonyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(5-chloropyridin-2-yl)methyl](tetrahydrofuran-3-ylcarbonyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(5-chloropyridin-2-yl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(5-chloropyridin-2-yl)ethyl](tetrahydrofuran-3-ylcarbonyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(5-chloropyridin-2-yl)ethyl][(2-methoxy ethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-([2-(5-chloropyridin-2-yl)ethyl]{[2-(propan-2-yloxy)ethyl]carbamoyl}amino)-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(1,3-benzodioxol-5-ylacetyl)(2-methoxyethyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(5S)-5-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-2-oxo-1,3-oxazolidin-3-yl}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(2-methoxyethyl)(pyridin-2-ylacetyl)amino]-1,3-thiazole-5-carboxamide; and pharmaceutically acceptable salts thereof.

Another embodiment pertains to a composition for treating inflammatory and tissue repair disorders; particularly rheumatoid arthritis, inflammatory bowel disease, asthma and COPD (chronic obstructive pulmonary disease), osteoarthritis, osteoporosis and fibrotic diseases; dermatosis, including psoriasis, atopic dermatitis and ultra-violet induced skin damage; autoimmune diseases including systemic upus erythematosis, multiple sclerosis, psoriatic arthritis, ankylosing spondylitis, tissue and organ rejection, Alzheimer's disease, stroke, athersclerosis, restenosis, diabetes, glomerulonephritis, cancer, particularly wherein the cancer is selected from breast, prostate, lung, colon, cervix, ovary, skin, CNS, bladder, pancreas, leukemia, lymphoma or Hodgkin's disease, cachexia, inflammation associated with infection and certain viral infections, including Acquired Immune Deficiency Syndrome (AIDS), adult respiratory distress syndrome, and ataxia telengiectasia, said composition comprising an excipient and a therapeutically effective amount of a compound of Formula (I), or pharmaceutically acceptable salts thereof.

Another embodiment pertains to a method of treating inflammatory and tissue repair disorders; particularly rheumatoid arthritis, inflammatory bowel disease, asthma and COPD (chronic obstructive pulmonary disease), osteoarthritis, osteoporosis and fibrotic diseases; dermatosis, including psoriasis, atopic dermatitis and ultra-violet induced skin damage; autoimmune diseases including systemic lupus erythematosis, multiple sclerosis, psoriatic arthritis, ankylosing spondylitis, tissue and organ rejection, Alzheimer's disease, stroke, athersclerosis, restenosis, diabetes, glomerulonephritis, cancer, particularly wherein the cancer is selected from breast, prostate, lung, colon, cervix, ovary, skin, CNS, bladder, pancreas, leukemia, lymphoma or Hodgkin's disease, cachexia, inflammation associated with infection and certain viral infections, including Acquired Immune Deficiency Syndrome (AIDS), adult respiratory distress syndrome, and ataxia telengiectasia in a patient, said method comprising administering to the patient a therapeutically effective amount of a compound of Formula (I), or pharmaceutically acceptable salts thereof.

Another embodiment pertains to a method of treating inflammatory and tissue repair disorders; particularly rheumatoid arthritis, inflammatory bowel disease, asthma and COPD (chronic obstructive pulmonary disease), osteoarthritis, osteoporosis and fibrotic diseases; dermatosis, including psoriasis, atopic dermatitis and ultra-violet induced skin damage; autoimmune diseases including systemic lupus erythematosis, multiple sclerosis, psoriatic arthritis, ankylosing spondylitis, tissue and organ rejection, Alzheimer's disease, stroke, athersclerosis, restenosis, diabetes, glomerulonephritis, cancer, particularly wherein the cancer is selected from breast, prostate, lung, colon, cervix, ovary, skin, CNS, bladder, pancreas, leukemia, lymphoma or Hodgkin's disease, cachexia, inflammation associated with infection and certain viral infections, including Acquired Immune Deficiency Syndrome (AIDS), adult respiratory distress syndrome, and ataxia telengiectasia or spleen cancer in a patient, said method comprising administering to the patient therapeutically effective amount of the compound of Formula (I), or pharmaceutically acceptable salts thereof; and a therapeutically effective amount of one additional therapeutic agent or more than one additional therapeutic agent.

DETAILED DESCRIPTION OF THE INVENTION

This detailed description is intended only to acquaint others skilled in the art with Applicants' invention, its principles, and its practical application so that others skilled in the art may adapt and apply the invention in its numerous forms, as they may be best suited to the requirements of a particular use. This description and its specific examples are intended for purposes of illustration only. This invention, therefore, is not limited to the embodiments described in this patent application, and may be variously modified.

ABBREVIATIONS AND DEFINITIONS

Unless otherwise defined herein, scientific and technical terms used in connection with the present invention shall have the meanings that are commonly understood by those of ordinary skill in the art. The meaning and scope of the terms should be clear, however, in the event of any latent ambiguity, definitions provided herein take precedent over any dictionary or extrinsic definition. In this application, the use of “or” means “and/or” unless stated otherwise. Furthermore, the use of the term “including”, as well as other forms, such as “includes” and “included”, is not limiting. With reference to the use of the words “comprise” or “comprises” or “comprising” in this patent application (including the claims), Applicants note that unless the context requires otherwise, those words are used on the basis and clear understanding that they are to be interpreted inclusively, rather than exclusively, and that Applicants intend each of those words to be so interpreted in construing this patent application, including the claims below. For a variable that occurs more than one time in any substituent or in the compound of the invention or any other formulae herein, its definition on each occurrence is independent of its definition at every other occurrence. Combinations of substituents are permissible only if such combinations result in stable compounds. Stable compounds are compounds which can be isolated in a useful degree of purity from a reaction mixture.

It is meant to be understood that proper valences are maintained for all combinations herein, that monovalent moieties having more than one atom are attached through their left ends, and that divalent moieties are drawn from left to right.

As used in the specification and the appended claims, unless specified to the contrary, the following terms have the meaning indicated:

The term “alkyl” (alone or in combination with another term(s)) means a straight- or branched-chain saturated hydrocarbyl substituent typically containing from 1 to about 10 carbon atoms; or in another embodiment, from 1 to about 8 carbon atoms; in another embodiment, from 1 to about 6 carbon atoms; and in another embodiment, from 1 to about 4 carbon atoms. Examples of such substituents include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, pentyl, iso-amyl, and hexyl and the like.

The term “alkenyl” (alone or in combination with another term(s)) means a straight- or branched-chain hydrocarbyl substituent containing one or more double bonds and typically from 2 to about 10 carbon atoms; or in another embodiment, from 2 to about 8 carbon atoms; in another embodiment, from 2 to about 6 carbon atoms; and in another embodiment, from 2 to about 4 carbon atoms. Examples of such substituents include ethenyl (vinyl), 2-propenyl, 3-propenyl, 1,4-pentadienyl, 1,4-butadienyl, 1-butenyl, 2-butenyl, and 3-butenyl and the like.

The term “alkynyl” (alone or in combination with another term(s)) means a straight- or branched-chain hydrocarbyl substituent containing one or more triple bonds and typically from 2 to about 10 carbon atoms; or in another embodiment, from 2 to about 8 carbon atoms; in another embodiment, from 2 to about 6 carbon atoms; and in another embodiment, from 2 to about 4 carbon atoms. Examples of such substituents include ethynyl, 2-propynyl, 3-propynyl, 2-butynyl, and 3-butynyl and the like.

The term “carbocyclyl” (alone or in combination with another term(s)) means a saturated cyclic (i.e., “cycloalkyl”), partially saturated cyclic (i.e., “cycloalkenyl”), or completely unsaturated (i.e., “aryl”) hydrocarbyl substituent containing from 3 to 14 carbon ring atoms (“ring atoms” are the atoms bound together to form the ring or rings of a cyclic substituent). A carbocyclyl may be a single-ring (monocyclic) or polycyclic ring structure.

A carbocyclyl may be a single ring structure, which typically contains from 3 to 8 ring atoms, more typically from 3 to 6 ring atoms, and even more typically 5 to 6 ring atoms. Examples of such single-ring carbocyclyls include cyclopropyl (cyclopropanyl), cyclobutyl (cyclobutanyl), cyclopentyl (cyclopentanyl), cyclopentenyl, cyclopentadienyl, cyclohexyl (cyclohexanyl), cyclohexenyl, cyclohexadienyl, and phenyl. A carbocyclyl may alternatively be polycyclic (i.e., may contain more than one ring). Examples of polycyclic carbocyclyls include bridged, fused, and spirocyclic carbocyclyls. In a spirocyclic carbocyclyl, one atom is common to two different rings. An example of a spirocyclic carbocyclyl is spiropentanyl. In a bridged carbocyclyl, the rings share at least two common non-adjacent atoms. Examples of bridged carbocyclyls include bicyclo[2.2.1]heptanyl, bicyclo[2.2.1]hept-2-enyl, and adamantanyl. In a fused-ring carbocyclyl system, two or more rings may be fused together, such that two rings share one common bond. Examples of two- or three-fused ring carbocyclyls include naphthalenyl, tetrahydronaphthalenyl (tetralinyl), indenyl, indanyl (dihydroindenyl), anthracenyl, phenanthrenyl, and decalinyl.

The term “cycloalkyl” (alone or in combination with another term(s)) means a saturated cyclic hydrocarbyl substituent containing from 3 to 14 carbon ring atoms. A cycloalkyl may be a single carbon ring, which typically contains from 3 to 8 carbon ring atoms and more typically from 3 to 6 ring atoms. Examples of single-ring cycloalkyls include cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl. A cycloalkyl may alternatively be polycyclic or contain more than one ring. Examples of polycyclic cycloalkyls include bridged, fused, and spirocyclic carbocyclyls.

The term “aryl” (alone or in combination with another term(s)) means an aromatic carbocyclyl containing from 6 to 14 carbon ring atoms. An aryl may be monocyclic or polycyclic (i.e., may contain more than one ring). In the case of polycyclic aromatic rings, only one ring the polycyclic system is required to be unsaturated while the remaining ring(s) may be saturated, partially saturated or unsaturated. Examples of aryls include phenyl, naphthalenyl, indenyl, indanyl, and tetrahydronapthyl.

In some instances, the number of carbon atoms in a hydrocarbyl substituent (e.g., alkyl, alkenyl, alkynyl, or cycloalkyl) is indicated by the prefix “Cx-Cy-”, wherein x is the minimum and y is the maximum number of carbon atoms in the substituent. Thus, for example, “C1-C6-alkyl” refers to an alkyl substituent containing from 1 to 6 carbon atoms.

Illustrating further, C3-C5-cycloalkyl means a saturated hydrocarbyl ring containing from 3 to 8 carbon ring atoms.

The term “hydrogen” (alone or in combination with another term(s)) means a hydrogen radical, and may be depicted as —H.

The term “hydroxy” (alone or in combination with another term(s)) means —OH.

The term “carboxy” (alone or in combination with another term(s)) means —C(O)—OH.

The term “amino” (alone or in combination with another term(s)) means —NH2.

The term “halogen” or “halo” (alone or in combination with another term(s)) means a fluorine radical (which may be depicted as —F), chlorine radical (which may be depicted as —Cl), bromine radical (which may be depicted as —Br), or iodine radical (which may be depicted as —I).

If a substituent is described as being “substituted”, a non-hydrogen radical is in the place of hydrogen radical on a carbon or nitrogen of the substituent. Thus, for example, a substituted alkyl substituent is an alkyl substituent in which at least one non-hydrogen radical is in the place of a hydrogen radical on the alkyl substituent. To illustrate, monofluoroalkyl is alkyl substituted with a fluoro radical, and difluoroalkyl is alkyl substituted with two fluoro radicals. It should be recognized that if there are more than one substitution on a substituent, each non-hydrogen radical may be identical or different (unless otherwise stated).

If a substituent is described as being “optionally substituted”, the substituent may be either (1) not substituted or (2) substituted. If a substituent is described as being optionally substituted with up to a particular number of non-hydrogen radicals, that substituent may be either (1) not substituted; or (2) substituted by up to that particular number of non-hydrogen radicals or by up to the maximum number of substitutable positions on the substituent, whichever is less. Thus, for example, if a substituent is described as a heteroaryl optionally substituted with up to 3 non-hydrogen radicals, then any heteroaryl with less than 3 substitutable positions would be optionally substituted by up to only as many non-hydrogen radicals as the heteroaryl has substitutable positions. To illustrate, tetrazolyl (which has only one substitutable position) would be optionally substituted with up to one non-hydrogen radical. To illustrate further, if an amino nitrogen is described as being optionally substituted with up to 2 non-hydrogen radicals, then a primary amino nitrogen will be optionally substituted with up to 2 non-hydrogen radicals, whereas a secondary amino nitrogen will be optionally substituted with up to only 1 non-hydrogen radical.

This patent application uses the terms “substituent” and “radical” interchangeably.

The prefix “halo” indicates that the substituent to which the prefix is attached is substituted with one or more independently selected halogen radicals. For example, haloalkyl means an alkyl substituent in which at least one hydrogen radical is replaced with a halogen radical. Examples of haloalkyls include chloromethyl, 1-bromoethyl, fluoromethyl, difluoromethyl, trifluoromethyl, and 1,1,1-trifluoroethyl. It should be recognized that if a substituent is substituted by more than one halogen radical, those halogen radicals may be identical or different (unless otherwise stated).

The prefix “perhalo” indicates that every hydrogen radical on the substituent to which the prefix is attached is replaced with independently selected halogen radicals, i.e., each hydrogen radical on the substituent is replaced with a halogen radical. If all the halogen radicals are identical, the prefix typically will identify the halogen radical. Thus, for example, the term “perfluoro” means that every hydrogen radical on the substituent to which the prefix is attached is substituted with a fluorine radical. To illustrate, the term “perfluoroalkyl” means an alkyl substituent wherein a fluorine radical is in the place of each hydrogen radical.

The term “carbonyl” (alone or in combination with another term(s)) means —C(O)—.

The term “aminocarbonyl” (alone or in combination with another term(s)) means —C(O)—NH2.

The term “oxo” (alone or in combination with another term(s)) means (═O).

The term “oxy” (alone or in combination with another term(s)) means an ether substituent, and may be depicted as —O—.

The term “alkylhydroxy” (alone or in combination with another term(s)) means -alkyl-OH.

The term “alkylamino” (alone or in combination with another term(s)) means -alkyl-NH2.

The term “alkyloxy” (alone or in combination with another term(s)) means an alkylether substituent, i.e., —O-alkyl. Examples of such a substituent include methoxy (—O—CH3), ethoxy, n-propoxy, isopropoxy, n-butoxy, iso-butoxy, sec-butoxy, and tert-butoxy.

The term “alkylcarbonyl” (alone or in combination with another term(s)) means —C(O)-alkyl.

The term “aminoalkylcarbonyl” (alone or in combination with another term(s)) means —C(O)-alkyl-NH2.

The term “alkyloxycarbonyl” (alone or in combination with another term(s)) means —C(O)—O-alkyl.

The term “carbocyclylcarbonyl” (alone or in combination with another term(s)) means —C(O)-carbocyclyl.

Similarly, the term “heterocyclylcarbonyl” (alone or in combination with another term(s)) means —C(O)-heterocyclyl.

The term “carbocyclylalkylcarbonyl” (alone or in combination with another term(s)) means —C(O)-alkyl-carbocyclyl.

Similarly, the term “heterocyclylalkylcarbonyl” (alone or in combination with another term(s)) means —C(O)-alkyl-heterocyclyl.

The term “carbocyclyloxycarbonyl” (alone or in combination with another term(s)) means —C(O)—O-carbocyclyl.

The term “carbocyclylalkyloxycarbonyl” (alone or in combination with another term(s)) means —C(O)—O-alkyl-carbocyclyl.

The term “thio” or “thia” (alone or in combination with another term(s)) means a thiaether substituent, i.e., an ether substituent wherein a divalent sulfur atom is in the place of the ether oxygen atom. Such a substituent may be depicted as —S—. This, for example, “alkyl-thio-alkyl” means alkyl-S-alkyl (alkyl-sulfanyl-alkyl).

The term “thiol” or “sulfhydryl” (alone or in combination with another term(s)) means a sulfhydryl substituent, and may be depicted as —SH.

The term “(thiocarbonyl)” (alone or in combination with another term(s)) means a carbonyl wherein the oxygen atom has been replaced with a sulfur. Such a substituent may be depicted as —C(S)—.

The term “sulfonyl” (alone or in combination with another term(s)) means —S(O)2—.

The term “aminosulfonyl” (alone or in combination with another term(s)) means —S(O)2—NH2.

The term “sulfinyl” or “sulfoxido” (alone or in combination with another term(s)) means —S(O)—.

The term “heterocyclyl” (alone or in combination with another term(s)) means a saturated (i.e., “heterocycloalkyl”), partially saturated (i.e., “heterocycloalkenyl”), or completely unsaturated (i.e., “heteroaryl”) ring structure containing a total of 3 to 14 ring atoms. At least one of the ring atoms is a heteroatom (i.e., oxygen, nitrogen, or sulfur), with the remaining ring atoms being independently selected from the group consisting of carbon, oxygen, nitrogen, and sulfur. A heterocyclyl may be a single-ring (monocyclic) or polycyclic ring structure.

A heterocyclyl may be a single ring, which typically contains from 3 to 7 ring atoms, more typically from 3 to 6 ring atoms, and even more typically 5 to 6 ring atoms. Examples of single-ring heterocyclyls include 1,2,3,6-tetrahydropyridine, thiomorpholinyl, tetrahydropyranyl, furanyl, dihydrofuranyl, tetrahydrofuranyl, thiophenyl (thiofuranyl), dihydrothiophenyl, tetrahydrothiophenyl, pyrrolyl, pyrrolinyl, pyrrolidinyl, imidazolyl, imidazolinyl, imidazolidinyl, pyrazolyl, pyrazolinyl, pyrazolidinyl, triazolyl, tetrazolyl, oxazolyl, oxazolidinyl, isoxazolidinyl, isoxazolyl, thiazolyl, isothiazolyl, thiazolinyl, isothiazolinyl, thiazolidinyl, isothiazolidinyl, thiodiazolyl, oxadiazolyl (including 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl (furazanyl), or 1,3,4-oxadiazolyl), oxatriazolyl (including 1,2,3,4-oxatriazolyl or 1,2,3,5-oxatriazolyl), dioxazolyl (including 1,2,3-dioxazolyl, 1,2,4-dioxazolyl, 1,3,2-dioxazolyl, or 1,3,4-dioxazolyl), oxathiazolyl, oxathiolyl, oxathiolanyl, pyranyl, dihydropyranyl, thiopyranyl, tetrahydrothiopyranyl, pyridinyl (azinyl), piperidinyl, diazinyl (including pyridazinyl (1,2-diazinyl), pyrimidinyl (1,3-diazinyl), or pyrazinyl (1,4-diazinyl)), piperazinyl, pyrrolidin-2-only, triazinyl (including 1,3,5-triazinyl, 1,2,4-triazinyl, and 1,2,3-triazinyl)), oxazinyl (including 1,2-oxazinyl, 1,3-oxazinyl, or 1,4-oxazinyl)), oxathiazinyl (including 1,2,3-oxathiazinyl, 1,2,4-oxathiazinyl, 1,2,5-oxathiazinyl, or 1,2,6-oxathiazinyl)), oxadiazinyl (including 1,2,3-oxadiazinyl, 1,2,4-oxadiazinyl, 1,4,2-oxadiazinyl, or 1,3,5-oxadiazinyl)), morpholinyl, azepinyl, oxepinyl, thiepinyl, and diazepinyl.

A heterocyclyl may alternatively be polycyclic (i.e., may contain more than one ring). Examples of polycyclic heterocyclyls include bridged, fused, and spirocyclic heterocyclyls. In a spirocyclic heterocyclyl, one atom is common to two different rings. In a bridged heterocyclyl, the rings share at least two common non-adjacent atoms. In a fused-ring heterocyclyl, two or more rings may be fused together, such that two rings share one common bond. Examples of fused-ring heterocyclyls include hexahydro-furo[3,4-c]pyrrole, hexahydro-furo[3,4-b]pyrrole, octahydro-pyrrolo[3,4-b]pyridine, octahydro-pyrrolo[3,4-c]pyridine, (3aR,6aR)-5-methyl-octahydro-pyrrolo[3,4-b]pyrrole, (3aR,6aR)-octahydro-pyrrolo[3,4-b]pyrrole, 6-methyl-2,6-diaza-bicyclo[3.2.0]heptane, (3aS,6aR)-2-methyl-octahydro-pyrrolo[3,4-c]pyrrole, decahydro-[1,5]naphthyridine, 2,3-dihydrobenzofuranyl, 2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indolyl, thieno[3,2-c]pyridinyl, furo[3,2-c]pyridinyl, phthalazin-1(2H)-onyl, isoquinolinyl, isoquinolin-1(2H)-onyl, 5,6,7,8-tetrahydrophthalazin-1(2H)-onyl, fluorophthalazin-1(2H)-onyl, (Z)-3H-benzo[d][1,2]diazepin-4(5H)-onyl, (trifluoromethyl)phthalazin-1(2H)-onyl, pyrrolo[1,2-d][1,2,4]triazin-1 (2H)-onyl, 1,2,3,4-tetrahydroisoquinolinyl, 2,3-dihydrobenzo[b][1,4]dioxinyl, 5,6,7,8-tetrahydrophthalazin-1(2H)-onyl, 5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazinyl, 5,6,7,8-tetrahydroimidazo[1,5-a]pyrazinyl, thieno[3,2-c]pyridinyl, furo[3,2-c]pyridinyl, indolizinyl, pyranopyrrolyl, 4H-quinolizinyl, purinyl, naphthyridinyl, pyridopyridinyl (including pyrido[3,4-b]-pyridinyl, pyrido[3,2-b]-pyridinyl, or pyrido[4,3-b]-pyridinyl), and pteridinyl. Other examples of fused-ring heterocyclyls include benzo-fused heterocyclyls, such as benzimidazolyl, benzo[d][1,3]dioxolyl, indolyl, isoindolyl (isobenzazolyl, pseudoisoindolyl), indoleninyl (pseudoindolyl), isoindazolyl (benzpyrazolyl), benzazinyl (including quinolinyl (1-benzazinyl) or isoquinolinyl (2-benzazinyl)), phthalazinyl, quinoxalinyl, quinazolinyl, benzodiazinyl (including cinnolinyl (1,2-benzodiazinyl) or quinazolinyl (1,3-benzodiazinyl)), benzopyranyl (including chromanyl or isochromanyl), benzoxazinyl (including 1,3,2-benzoxazinyl, 1,4,2-benzoxazinyl, 2,3,1-benzoxazinyl, or 3,1,4-benzoxazinyl), and benzisoxazinyl (including 1,2-benzisoxazinyl or 1,4-benzisoxazinyl). Examples of spirocyclic heterocyclyls include 1,4-dioxa-8-azaspiro[4.5]decanyl.

The term “heterocycloalkyl” (alone or in combination with another term(s)) means a saturated heterocyclyl.

The term “heteroaryl” (alone or in combination with another term(s)) means an aromatic heterocyclyl containing from 5 to 14 ring atoms. A heteroaryl may be a single ring or 2 or 3 fused rings. Examples of heteroaryl substituents include 6-membered ring substituents such as pyridyl, pyrazyl, pyrimidinyl, pyridazinyl, and 1,3,5-, 1,2,4- or 1,2,3-triazinyl; 5-membered ring substituents such as imidazyl, furanyl, thiophenyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, 1,2,3-, 1,2,4-, 1,2,5-, or 1,3,4-oxadiazolyl and isothiazolyl; 6/5-membered fused ring substituents such as benzothiofuranyl, benzisoxazolyl, benzoxazolyl, and purinyl; and 6/6-membered fused rings such as benzopyranyl, quinolinyl, isoquinolinyl, cinnolinyl, quinazolinyl, and benzoxazinyl.

A prefix attached to a multi-component substituent only applies to the first component. To illustrate, the term “alkylcycloalkyl” contains two components: alkyl and cycloalkyl. Thus, the C1-C6-prefix on C1-C6-alkylcycloalkyl means that the alkyl component of the alkylcycloalkyl contains from 1 to 6 carbon atoms; the C1-C6-prefix does not describe the cycloalkyl component. To illustrate further, the prefix “halo” on haloalkyloxyalkyl indicates that only the alkyloxy component of the alkyloxyalkyl substituent is substituted with one or more halogen radicals. If halogen substitution may alternatively or additionally occur on the alkyl component, the substituent would instead be described as “halogen-substituted alkyloxyalkyl” rather than “haloalkyloxyalkyl.” And finally, if the halogen substitution may only occur on the alkyl component, the substituent would instead be described as “alkyloxyhaloalkyl.”

The terms “treat”, “treating” and “treatment” refer to a method of alleviating or abrogating a disease and/or its attendant symptoms.

The terms “prevent”, “preventing” and “prevention” refer to a method of preventing the onset of a disease and/or its attendant symptoms or barring a subject from acquiring a disease. As used herein, “prevent”, “preventing” and “prevention” also include delaying the onset of a disease and/or its attendant symptoms and reducing a subject's risk of acquiring a disease.

The term “therapeutically effective amount” refers to that amount of the compound being administered sufficient to prevent development of or alleviate to some extent one or more of the symptoms of the condition or disorder being treated.

The term “modulate” refers to the ability of a compound to increase or decrease the function, or activity, of a kinase. “Modulation”, as used herein in its various forms, is intended to encompass antagonism, agonism, partial antagonism and/or partial agonism of the activity associated with kinase. Kinase inhibitors are compounds that, e.g., bind to, partially or totally block stimulation, decrease, prevent, delay activation, inactivate, desensitize, or down regulate signal transduction. Kinase activators are compounds that, e.g., bind to, stimulate, increase, open, activate, facilitate, enhance activation, sensitize or up regulate signal transduction.

The term “composition” as used herein is intended to encompass a product comprising the specified ingredients in the specified amounts, as well as any product which results, directly or indirectly, from combination of the specified ingredients in the specified amounts. By “pharmaceutically acceptable” it is meant the carrier, diluent or excipient must be compatible with the other ingredients of the formulation and not deleterious to the recipient thereof.

The “subject” is defined herein to include animals such as mammals, including, but not limited to, primates (e.g., humans), cows, sheep, goats, horses, dogs, cats, rabbits, rats, mice and the like. In preferred embodiments, the subject is a human.

Isotope Enriched or Labeled Compounds

Compounds of the invention can exist in isotope-labeled or -enriched form containing one or more atoms having an atomic mass or mass number different from the atomic mass or mass number most abundantly found in nature. Isotopes can be radioactive or non-radioactive isotopes. Isotopes of atoms such as hydrogen, carbon, phosphorous, sulfur, fluorine, chlorine, and iodine include, but are not limited to, 2H, 3H, 13C, 14C, 15N, 18O, 32P, 35S, 18F, 36Cl, and 125I. Compounds that contain other isotopes of these and/or other atoms are within the scope of this invention.

In another embodiment, the isotope-labeled compounds contain deuterium (2H), tritium (3H) or 14C isotopes. Isotope-labeled compounds of this invention can be prepared by the general methods well known to persons having ordinary skill in the art. Such isotope-labeled compounds can be conveniently prepared by carrying out the procedures disclosed in the Examples disclosed herein and Schemes by substituting a readily available isotope-labeled reagent for a non-labeled reagent. In some instances, compounds may be treated with isotope-labeled reagents to exchange a normal atom with its isotope, for example, hydrogen for deuterium can be exchanged by the action of a deuteric acid such as D2SO4/D2O. In addition to the above, relevant procedures and intermediates are disclosed, for instance, in Lizondo, J et al., Drugs Fut, 21(11), 1116 (1996); Brickner, S J et al., J Med Chem, 39(3), 673 (1996); Mallesham, B et al., Org Lett, 5(7), 963 (2003); PCT publications WO1997010223, WO2005099353, WO1995007271, WO2006008754; U.S. Pat. Nos. 7,538,189; 7,534,814; 7,531,685; 7,528,131; 7,521,421; 7,514,068; 7,511,013; and US Patent Application Publication Nos. 20090137457; 20090131485; 20090131363; 20090118238; 20090111840; 20090105338; 20090105307; 20090105147; 20090093422; 20090088416; and 20090082471, the methods are hereby incorporated by reference.

The isotope-labeled compounds of the invention may be used as standards to determine the effectiveness in binding assays. Isotope containing compounds have been used in pharmaceutical research to investigate the in vivo metabolic fate of the compounds by evaluation of the mechanism of action and metabolic pathway of the nonisotope-labeled parent compound (Blake et al. J. Pharm. Sci. 64, 3, 367-391 (1975)). Such metabolic studies are important in the design of safe, effective therapeutic drugs, either because the in vivo active compound administered to the patient or because the metabolites produced from the parent compound prove to be toxic or carcinogenic (Foster et al., Advances in Drug Research Vol. 14, pp. 2-36, Academic press, London, 1985; Kato et al., J. Labelled Comp. Radiopharmaceut., 36(10):927-932 (1995); Kushner et al., Can. J. Physiol. Pharmacol., 77, 79-88 (1999).

In addition, non-radio active isotope containing drugs, such as deuterated drugs called “heavy drugs,” can be used for the treatment of diseases and conditions related to NAMPT activity. Increasing the amount of an isotope present in a compound above its natural abundance is called enrichment. Examples of the amount of enrichment include from about 0.5, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, 16, 21, 25, 29, 33, 37, 42, 46, 50, 54, 58, 63, 67, 71, 75, 79, 84, 88, 92, 96, to about 100 mol %. Replacement of up to about 15% of normal atom with a heavy isotope has been effected and maintained for a period of days to weeks in mammals, including rodents and dogs, with minimal observed adverse effects (Czajka D M and Finkel A J, Ann. N.Y. Acad. Sci. 1960 84: 770; Thomson J F, Ann. New York Acad. Sci 1960 84: 736; Czakja D M et al., Am. J. Physiol. 1961 201: 357). Acute replacement of as high as 15%-23% in human fluids with deuterium was found not to cause toxicity (Blagojevic N et al. in “Dosimetry & Treatment Planning for Neutron Capture Therapy”, Zamenhof R, Solares G and Harling O Eds. 1994. Advanced Medical Publishing, Madison Wis. pp. 125-134; Diabetes Metab. 23: 251 (1997)).

Stable isotope labeling of a drug can alter its physico-chemical properties such as pKa and lipid solubility. These effects and alterations can affect the pharmacodynamic response of the drug molecule if the isotopic substitution affects a region involved in a ligand-receptor interaction. While some of the physical properties of a stable isotope-labeled molecule are different from those of the unlabeled one, the chemical and biological properties are the same, with one important exception: because of the increased mass of the heavy isotope, any bond involving the heavy isotope and another atom will be stronger than the same bond between the light isotope and that atom. Accordingly, the incorporation of an isotope at a site of metabolism or enzymatic transformation will slow said reactions potentially altering the pharmacokinetic profile or efficacy relative to the non-isotopic compound.

Compounds

Suitable groups for R1, R2, R3, R4, and R5 in compounds of Formula (I) are independently selected. The described embodiments of the present invention may be combined. Such combination is contemplated and within the scope of the present invention. For example, it is contemplated that embodiments for any of R1, R2, R3, R4, and R5 can be combined with embodiments defined for any other of R1, R2, R3, R4, and R5.

Embodiments of Formula (I)

One embodiment of this invention, therefore, pertains to compounds or pharmaceutically acceptable salts thereof, which are useful as inhibitors of NAMPT, the compounds having Formula (I)

wherein

R1 and R2 are each independently selected from the group consisting of R6, C(O)R6, C(O)NHR6, and C(O)N(R6)2; wherein at least one of R1 and R2 is R6; or

R1 and R2, together with the nitrogen to which they are attached form a heterocycloalkyl or heterocycloalkenyl ring; wherein the ring formed with R1 and R2 together with the nitrogen to which they are attached is optionally substituted with one or more substituents independently selected from the group consisting of R7, OR7, SR7, S(O)R7, SO2R7, C(O)R7, CO(O)R7, OC(O)R7, OC(O)OR7, NH2, NHR7, N(R7)2, NHC(O)R7, NR7C(O)R7, NHS(O)2R7, NR7S(O)2R7, NHC(O)OR7, NR7C(O)OR7, NHC(O)NH2, NHC(O)NHR7, NHC(O)N(R7)2, NR7C(O)NHR7, NR7C(O)N(R7)2, C(O)NH2, C(O)NHR7, C(O)N(R7)2, C(O)NHOH, C(O)NHOR7, C(O)NHSO2R7, C(O)NR7SO2R7, SO2NH2, SO2NHR7, SO2N(R7)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR7, C(N)N(R7)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R3, R4, and R5 are each independently selected from the group consisting of hydrogen, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6 haloalkyl, C1-6 hydroxyalkyl, F, Cl, Br and I;

R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, SR8, S(O)R8, SO2R8, C(O)R8, CO(O)R8, OC(O)R8, OC(O)OR8, NH2, NHR8, N(R8)2, NHC(O)R8, NR8C(O)R8, NHS(O)2R8, NR8S(O)2R8, NHC(O)OR8, NR8C(O)OR8, NHC(O)NH2, NHC(O)NHR8, NHC(O)N(R8)2, NR8C(O)NHR8, NR8C(O)N(R8)2, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)NHOH, C(O)NHOR8, C(O)NHSO2R8, C(O)NR8SO2R8, SO2NH2, SO2NHR8, SO2N(R8)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR8, C(N)N(R8)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, SR9, S(O)R9, SO2R9, C(O)R9, CO(O)R9, OC(O)R9, OC(O)OR9, NH2, NHR9, N(R9)2, NHC(O)R9, NR9C(O)R9, NHS(O)2R9, NR9S(O)2R9, NHC(O)OR9, NR9C(O)OR9, NHC(O)NH2, NHC(O)NHR9, NHC(O)N(R9)2, NR9C(O)NHR9, NR9C(O)N(R9)2, C(O)NH2, C(O)NHR9, C(O)N(R9)2, C(O)NHOH, C(O)NHOR9, C(O)NHSO2R9, C(O)NR9SO2R9, SO2NH2, SO2NHR9, SO2N(R9)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR9, C(N)N(R9)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R7, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R7 are each independently optionally substituted with one or more substituents independently selected from the group consisting of aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R7 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I;

R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R10, OR10, SR10, S(O)R10, SO2R10, C(O)R10, CO(O)R10, OC(O)R10, OC(O)OR10, NH2, NHR10, N(R10)2, NHC(O)R10, NR10C(O)R10, NHS(O)2R10, NR10S(O)2R10, NHC(O)OR10, NR10C(O)OR10, NHC(O)NH2, NHC(O)NHR10, NHC(O)N(R10)2, NR10C(O)NHR10, NR10C(O)N(R10)2, C(O)NH2, C(O)NHR10, C(O)N(R10)2, C(O)NHOH, C(O)NHOR10, C(O)NHSO2R10, C(O)NR10SO2R10, SO2NH2, SO2NHR10, SO2N(R10)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR10, C(N)N(R10)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, SR11, S(O)R11, SO2R11, C(O)R11, CO(O)R11, OC(O)R11, OC(O)OR11, NH2, NHR11, N(R11)2, NHC(O)R11, NR11C(O)R11, NHS(O)2R11, NR11S(O)2R11, NHC(O)OR11, NR11C(O)OR11, NHC(O)NH2, NHC(O)NHR11, NHC(O)N(R11)2, NR11C(O)NHR11, NR11C(O)N(R11)2, C(O)NH2, C(O)NHR11, C(O)N(R11)2, C(O)NHOH, C(O)NHOR11, C(O)NHSO2R11, C(O)NR11SO2R11, SO2NH2, SO2NHR11, SO2N(R11)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR11, C(N)N(R11)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R9, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R12, OR12, SR12, S(O)R12, SO2R12, C(O)R12, CO(O)R12, OC(O)R12, OC(O)OR12, NH2, NHR12, N(R12)2, NHC(O)R12, NR12C(O)R12, NHS(O)2R12, NR12S(O)2R12, NHC(O)OR12, NR12C(O)OR12, NHC(O)NH2, NHC(O)NHR12, NHC(O)N(R12)2, NR12C(O)NHR12, NR12C(O)N(R12)2, C(O)NH2, C(O)NHR12, C(O)N(R12)2, C(O)NHOH, C(O)NHOR12, C(O)NHSO2R12, C(O)NR12SO2R12, SO2NH2, SO2NHR12, SO2N(R12)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR12, C(N)N(R12)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R13, OR13, SR13, S(O)R13, SO2R13, C(O)R13, CO(O)R13, OC(O)R13, OC(O)OR13, NH2, NHR13, N(R13)2, NHC(O)R13, NR13C(O)R13, NHS(O)2R13, NR13S(O)2R13, NHC(O)OR13, NR13C(O)OR13, NHC(O)NH2, NHC(O)NHR13, NHC(O)N(R13)2, NR13C(O)NHR13, NR13C(O)N(R13)2, C(O)NH2, C(O)NHR13, C(O)N(R13)2, C(O)NHOH, C(O)NHOR13, C(O)NHSO2R13, C(O)NR13SO2R13, SO2NH2, SO2NHR13, SO2N(R13)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR13, C(N)N(R13)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R10, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6haloalkyl, and C1-6 hydroxyalkyl;

R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I;

R12, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; and

R13, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl; wherein the C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R13 are each independently optionally substituted with one or more substituents independently selected from the group consisting of alkoxy, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In one embodiment of Formula (I), R3, R4, and R5 are each independently selected from the group consisting of hydrogen, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6haloalkyl, C1-6 hydroxyalkyl, F, Cl, Br and I. In another embodiment of Formula (I), R3, R4, and R5 are are each independently selected from the group consisting of hydrogen and C1-6 alkyl. In another embodiment of Formula (I), one of R3, R4, and R5 is C1-6 alkyl, and the remainder are hydrogen. In another embodiment of Formula (I), R3 is C1-6 alkyl, and R4 and R5 are hydrogen. In another embodiment of Formula (I), R4 is C1-6 alkyl, and R3 and R5 are hydrogen. In another embodiment of Formula (I), R5 is C1-6 alkyl, and R3 and R4 are hydrogen. In another embodiment of Formula (I), R3, R4 and R5 are hydrogen.

In another embodiment of Formula (I), R3, R4, and R5 are each independently selected from the group consisting of hydrogen and methyl. In another embodiment of Formula (I), one of R3, R4, and R5 is methyl, and the remainder are hydrogen. In another embodiment of Formula (I), R3 is methyl, and R4 and R5 are hydrogen. In another embodiment of Formula (I), R4 is methyl, and R3 and R5 are hydrogen. In another embodiment of Formula (I), R5 is methyl, and R3 and R4 are hydrogen.

In one embodiment of Formula (I), R1 and R2 are each independently selected from the group consisting of R6, C(O)R6, C(O)NHR6, and C(O)N(R6)2; wherein at least one of R1 and R2 is R6. In another embodiment of Formula (I), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, SR8, S(O)R8, SO2R8, C(O)R8, CO(O)R8, OC(O)R8, OC(O)OR8, NH2, NHR8, N(R8)2, NHC(O)R8, NR8C(O)R8, NHS(O)2R8, NR8S(O)2R8, NHC(O)OR8, NR8C(O)OR8, NHC(O)NH2, NHC(O)NHR8, NHC(O)N(R8)2, NR8C(O)NHR8, NR8C(O)N(R8)2, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)NHOH, C(O)NHOR8, C(O)NHSO2R8, C(O)NR8SO2R8, SO2NH2, SO2NHR8, SO2N(R8)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR8, C(N)N(R8)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, SR9, S(O)R9, SO2R9, C(O)R9, CO(O)R9, OC(O)R9, OC(O)OR9, NH2, NHR9, N(R9)2, NHC(O)R9, NR9C(O)R9, NHS(O)2R9, NR9S(O)2R9, NHC(O)OR9, NR9C(O)OR9, NHC(O)NH2, NHC(O)NHR9, NHC(O)N(R9)2, NR9C(O)NHR9, NR9C(O)N(R9)2, C(O)NH2, C(O)NHR9, C(O)N(R9)2, C(O)NHOH, C(O)NHOR9, C(O)NHSO2R9, C(O)NR9SO2R9, SO2NH2, SO2NHR9, SO2N(R9)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR9, C(N)N(R9)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (I), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, heterocycloalkyl, heteroaryl, and cycloalkyl; wherein the C1-6 alkyl, and C2-6 alkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, C(O)R8, CO(O)R8, OC(O)R8, N(R8)2, NHC(O)R8, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)OH, and OH; wherein the aryl, heterocycloalkyl, heteroaryl, and cycloalkyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, C(O)NH2, C(O)OH, OH, CN, F, Cl, Br and I.

In one embodiment of Formula (I), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R10, OR10, SR10, S(O)R10, SO2R10, C(O)R10, CO(O)R10, OC(O)R10, OC(O)OR10, NH2, NHR10, N(R7)2, NHC(O)R10, NR10C(O)R10, NHS(O)2R10, NR10S(O)2R10, NHC(O)OR10, NR10C(O)OR10, NHC(O)NH2, NHC(O)NHR10, NHC(O)N(R10)2, NR10C(O)NHR10, NR10C(O)N(R10)2, C(O)NH2, C(O)NHR10, C(O)N(R10)2, C(O)NHOH, C(O)NHOR10, C(O)NHSO2R10, C(O)NR10SO2R10, SO2NH2, SO2NHR10, SO2N(R10)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR10, C(N)N(R10)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, SR11, S(O)R11, SO2R11, C(O)R11, CO(O)R11, OC(O)R11, OC(O)OR11, NH2, NHR11, N(R11)2, NHC(O)R11, NR11C(O)R11, NHS(O)2R11, NR11S(O)2R11, NHC(O)OR11, NR11C(O)OR11, NHC(O)NH2, NHC(O)NHR11, NHC(O)N(R11)2, NR11C(O)NHR11, NR11C(O)N(R11)2, C(O)NH2, C(O)NHR11, C(O)N(R11)2, C(O)NHOH, C(O)NHOR11, C(O)NHSO2R11, C(O)NR11SO2R11, SO2NH2, SO2NHR11, SO2N(R11)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR11, C(N)N(R11)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (I), R8, at each occurrence, is independently selected from the group consisting of C1-6alkyl, C2-6 alkenyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, and cycloalkyl; wherein the C1-6 alkyl and C2-6 alkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of OH, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, and heteroaryl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, NH2, N(R11)2, C(O)H, OH, CN, F, Cl, Br and I.

In one embodiment of Formula (I), R9, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R12, OR12, SR2, S(O)R12, SO2R12, C(O)R12, CO(O)R12, OC(O)R12, OC(O)OR12, NH2, NHR12, N(R12)2, NHC(O)R12, NR12C(O)R12, NHS(O)2R12, NR12S(O)2R12, NHC(O)OR12, NR12C(O)OR12, NHC(O)NH2, NHC(O)NHR12, NHC(O)N(R12)2, NR12C(O)NHR12, NR12C(O)N(R12)2, C(O)NH2, C(O)NHR12, C(O)N(R12)2, C(O)NHOH, C(O)NHOR12, C(O)NHSO2R12, C(O)NR12SO2R12, SO2NH2, SO2NHR12, SO2N(R12)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR12, C(N)N(R12)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R13, OR13, SR13, S(O)R13, SO2R13, C(O)R13, CO(O)R13, OC(O)R13, OC(O)OR13, NH2, NHR13, N(R13)2, NHC(O)R13, NR13C(O)R13, NHS(O)2R13, NR13S(O)2R13, NHC(O)OR13, NR13C(O)OR13, NHC(O)NH2, NHC(O)NHR13, NHC(O)N(R13)2, NR13C(O)NHR13, NR13C(O)N(R13)2, C(O)NH2, C(O)NHR13, C(O)N(R13)2, C(O)NHOH, C(O)NHOR13, C(O)NHSO2R13, C(O)NR13SO2R13, SO2NH2, SO2NHR13, SO2N(R13)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR13, C(N)N(R13)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (I), R9, at each occurrence, is C1-6 alkyl.

In one embodiment of Formula (I), R10, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6alkenyl, C2-6alkynyl, C1-6 haloalkyl, and C1-6 hydroxyalkyl.

In one embodiment of Formula (I), R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6alkenyl, C2-6alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6alkyl, C2-6 alkenyl, and C2-6alkynyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (I), R11, at each occurrence, is independently selected from the group consisting of C1-6alkyl, C2-6alkenyl, aryl, and heteroaryl; wherein the C1-6alkyl and C2-6alkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6alkoxy, cycloalkyl, OH, F, Cl, Br and I.

In one embodiment of Formula (I), R12, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6alkenyl, C2-6alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6alkyl, C2-6 alkenyl, and C2-6alkynyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In one embodiment of Formula (I), R13, at each occurrence, is independently selected from the group consisting of C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl; wherein the C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R13 are each independently optionally substituted with one or more substituents independently selected from the group consisting of alkoxy, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In another embodiment of Formula (I), R1 is C(O)R6; and R2 is R6. In another embodiment of Formula (I), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, aryl, heterocycloalkyl, heteroaryl, and cycloalkyl; wherein the C1-6 alkyl represented by R6 is independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, C(O)R8, OC(O)R8, N(R8)2, NHC(O)R8, C(O)NHR8, and OH; wherein the aryl, heterocycloalkyl, and heteroaryl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, C(O)NH2, OH, CN, F, Cl, Br and I. In another embodiment of Formula (I), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, and cycloalkyl; wherein the aryl, heterocycloalkyl, and heteroaryl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, NH2, N(R11)2, C(O)H, OH, CN, F, Cl, Br and I. In another embodiment of Formula (I), R9, at each occurrence, is C1-6 alkyl. In another embodiment of Formula (I), R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, and aryl; wherein the C1-6 alkyl and C2-6 alkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6alkoxy, cycloalkyl, OH, F, Cl, Br and I.

In another embodiment of Formula (I), R1 and R2 are each R6. In another embodiment of Formula (I), R6, at each occurrence, is C1-6alkyl; wherein the C1-6alkyl represented by R6 is independently optionally substituted with one or more substituents independently selected from the group consisting of R8, C(O)R8, C(O)NHR8, and C(O)N(R8)2.

In another embodiment of Formula (I), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, aryl, and heterocycloalkyl; wherein the aryl, and heterocycloalkyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, CN, F, Cl, Br and I. In another embodiment of Formula (I), R11, at each occurrence, is independently selected from the group consisting of C1-6alkyl and heteroaryl.

In another embodiment of Formula (I), R1 is C(O)NHR6; and R2 is R6. In another embodiment of Formula (I), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, heterocycloalkyl, and cycloalkyl; wherein the C1-6alkyl and C2-6 alkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, C(O)OR8, N(R8)2, NHC(O)R8, C(O)NH2, C(O)N(R8)2, C(O)OH, and OH; wherein the heterocycloalkyl, and cycloalkyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C(O)NH2, C(O)OH, F, Cl, Br and I. In another embodiment of Formula (I), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, aryl, heterocycloalkyl, and heteroaryl; wherein the C1-6alkyl represented by R8 is independently optionally substituted with one or more OH; wherein the aryl, heterocycloalkyl, and heteroaryl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of OH, CN, F, Cl, Br and I.

In another embodiment of Formula (I), R1 is C(O)N(R6)2; and R2 is R6. In another embodiment of Formula (I), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, heterocycloalkyl, and cycloalkyl; wherein the C1-6alkyl and C2-6 alkenyl represented by R6 are independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, C(O)OR8, N(R8)2, NHC(O)R8, C(O)NH2, C(O)N(R8)2, C(O)OH, and OH; wherein the heterocycloalkyl, and cycloalkyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of OH, F, Cl, Br and I. In another embodiment of Formula (I), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, aryl, and heterocycloalkyl; wherein the C1-6alkyl represented by R8 is independently optionally substituted with one or more OH; wherein the aryl and heterocycloalkyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of OH, CN, F, Cl, Br and I.

In another embodiment of Formula (I), R6, at each occurrence, is C1. alkyl; wherein the C1-6 alkyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, and OR8. In another embodiment of Formula (I), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, and aryl; wherein the aryl represented by R8 is independently optionally substituted with one or more substituents independently selected from the group consisting of F, Cl, Br and I.

In another embodiment of Formula (I), R1 and R2, together with the nitrogen to which they are attached form a heterocycloalkyl or heterocycloalkenyl ring. In another embodiment of Formula (I), R1 and R2, together with the nitrogen to which they are attached form a heterocycloalkyl ring. In another embodiment of Formula (I), R7, at each occurrence, is independently selected from the group consisting of C1. alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R7 are each independently optionally substituted with one or more substituents independently selected from the group consisting of aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R7 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (I), R1 and R2, together with the nitrogen to which they are attached form a heterocycloalkyl ring wherein the ring formed with R1 and R2 together with the nitrogen to which they are attached is optionally substituted with one or more R. In another embodiment of Formula (I), R7, at each occurrence, is independently selected from the group consisting of C1-6alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R7 are each independently optionally substituted with one or more substituents independently selected from the group consisting of aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R7 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (I), R7, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, and aryl; wherein the C1-6alkyl represented by R7 is independently optionally substituted with one or more substituents independently selected from the group consisting of aryl and OH; wherein the aryl represented by R7 is independently optionally substituted with one or more substituents independently selected from the group consisting of F, Cl, Br and I.

Still another embodiment pertains to compounds having Formula (I), which include

  • 2-{(4-fluorobenzyl)[4-(pyridin-3-yl)benzyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{methyl[4-(pyridin-3-yl)benzyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(methyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(tetrahydro-2H-pyran-4-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(cyclohexylacetyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(3-methylbutanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[3-(morpholin-4-yl)propyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[3-(piperidin-1-yl)propyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[2-(pyrrolidin-1-yl)ethyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {2-[4-(propan-2-yl)piperazin-1-yl]ethyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzoyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(3-chlorobenzoyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzoyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(5-chloro-1,3-benzodioxol-4-yl)methyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-chlorobenzyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(2-chlorobenzyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(2,5-dichlorobenzyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[2-(methylamino)-2-oxoethyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[2-oxo-2-(propan-2-ylamino)ethyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(dimethylamino)-2-oxoethyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(diethylamino)-2-oxoethyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[2-(morpholin-4-yl)-2-oxoethyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(4-methylbenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(methoxyacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(N,N-dimethylglycyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(3,6-dihydropyridin-1(2H)-ylacetyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [(4-methylpiperidin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [(4-hydroxypiperidin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(4-methylpiperazin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[4-(propan-2-yl)piperazin-1-yl]acetyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(4-formylpiperazin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[4-(cyclopropylmethyl)piperazin-1-yl]acetyl}(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[4-(2-ethoxyethyl)piperazin-1-yl]acetyl}(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(cyclopropylcarbonyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[4-(prop-2-en-1-yl)piperazin-1-yl]acetyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[4-(3-methoxypropyl)piperazin-1-yl]acetyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[3-(dimethylamino)pyrrolidin-1-yl]acetyl}(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(morpholin-4-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(3-hydroxypiperidin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[4-(2-hydroxyethyl)piperazin-1-yl]acetyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(1,4-dioxa-7-azaspiro[4.4]non-7-ylacetyl) (4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 1-{2-[(4-fluorobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)amino]-2-oxoethyl}pyridinium;
  • 2-{[2-(4-fluorophenyl)ethyl](3-methylbutanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(propan-2-ylcarbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(4-cyanophenyl)ethyl](3-methylbutanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(4-cyanophenyl)ethyl](tetrahydro-2H-pyran-4-ylacetyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(3-methylbutanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(tetrahydro-2H-pyran-4-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(4-cyanophenyl)ethyl](tetrahydrofuran-3-ylacetyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(3-methylbutanoyl)amino]-N-[3-(2-methyl-1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(3-methylbutanoyl)amino]-N-[3-(4-methyl-1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(2-fluorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(3-fluorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(2-chlorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(3-chlorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-chlorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(tetrahydrofuran-3-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(3-methylbutyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [(2-methylpropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N1-(4-fluorobenzyl)-N1-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)piperidine-1,3-dicarboxamide;
  • 2-{(4-fluorobenzyl) [(3-hydroxyazetidin-1-yl)carbonyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-(4-fluorobenzyl)-N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-1,4-dioxa-7-azaspiro[4.4]nonane-7-carboxamide;
  • 2-{(4-fluorobenzyl)[(3-methoxypyrrolidin-1-yl)carbonyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-methoxyethyl)(methyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-(4-fluorobenzyl)-N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-2,6-dimethylmorpholine-4-carboxamide;
  • 2-{[ethyl(2-methoxyethyl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-(4-fluorobenzyl)-N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-2,2-dimethylmorpholine-4-carboxamide;
  • N-(4-fluorobenzyl)-N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-1,4-oxazepane-4-carboxamide;
  • 2-[(4-fluorobenzoyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(4-methylbenzyl)amino]-1,3-thiazole-5-carboxamide;
  • N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-N-(3-methylbutyl)-1,2-oxazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(2-phenoxypropanoyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-propoxyethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [(tetrahydrofuran-2-ylmethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [(1-methoxypropan-2-yl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(tetrahydro-2H-pyran-2-ylmethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-methoxyethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(2-ethoxyethyl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(1-methoxybutan-2-yl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(4-cyanophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(1,3-dioxolan-2-ylmethyl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[2-(propan-2-yloxy)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(1,4-dioxan-2-ylmethyl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(1,3-dimethoxypropan-2-yl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-methoxybutyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(tetrahydrofuran-3-ylcarbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(tetrahydro-2H-pyran-3-ylcarbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(pyrimidin-2-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl)[(2-methoxypyridin-4-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(1,3-oxazol-4-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-{[(5-chloropyridin-2-yl)methyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(4-methylpyridin-3-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(6-methoxypyridin-3-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(4-methyl-1,3-thiazol-5-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[2-(3-hydroxyphenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-(pyridin-2-yl)ethyl]amino}-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(1,3-benzodioxol-5-yl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(4-chlorophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(3-fluorophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(4-hydroxyphenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(3-chlorophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{[2-(3-methoxyphenyl)ethyl](3-methoxypropanoyl)amino}-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(2-fluorophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-hydroxy-2-(4-methoxyphenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl)[1-(pyridin-2-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(1-methyl-1H-pyrazol-4-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(2,6-difluorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(6-methylpyridin-3-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(4-chlorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(5-methylpyrazin-2-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(3-chlorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(5-methylpyridin-2-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(2,5-difluorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(2-methylbenzyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(3-methylbenzyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(pyridin-2-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(pyridin-3-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[2-(propan-2-yloxy)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(2-methoxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[2-(2-hydroxyethoxy)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(propan-2-yloxy)propyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(3-hydroxy-2,2-dimethylpropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(2-hydroxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(1-hydroxypropan-2-yl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(3-hydroxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[(2S)-1-hydroxybut-3-en-2-yl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(4-hydroxybutyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methylbutyl)[(2R)-2-phenoxypropanoyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methylbutyl)[(2S)-2-phenoxypropanoyl]amino}-1,3-thiazole-5-carboxamide;
  • N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-5-methyl-N-(3-methylbutyl)-1,2-oxazole-3-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(phenoxyacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(3-phenylpropanoyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(2-phenylpropanoyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-{[(4-fluorophenyl)acetyl](3-methylbutyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(3-amino-3-oxopropyl)carbamoyl](4-cyanobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[3-(acetylamino)-2-methylpropyl]carbamoyl}(4-cyanobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(dimethylamino)-3-oxopropyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(3-ethoxy-2-hydroxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(diethylamino)propyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[2-(acetylamino)ethyl]carbamoyl}(4-cyanobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[2-(diethylamino)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)({2-[(2-methylpropanoyl)amino]ethyl}carbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl){[(2R)-1-hydroxybut-3-en-2-yl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(3-hydroxyazetidin-1-yl)propyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(3-methylbutyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(methoxyacetyl)(3-methylbutyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-[(cyclopropylcarbonyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • (2S)-1-[(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)(3-methylbutyl)amino]-1-oxopropan-2-yl acetate;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(tetrahydro-2H-pyran-4-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(tetrahydrofuran-3-ylcarbonyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-{[2-hydroxy-2-(3-methoxyphenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-(pyrazin-2-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[1-(3-hydroxyphenyl)propan-2-yl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • ethyl N-[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]-beta-alaninate;
  • ethyl 4-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoate;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoate;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-4-methylpentanoate;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2,2-dimethylpropanoate;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}cyclobutanecarboxylic acid;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2-methylpropanoate;
  • 2-{(4-cyanobenzyl)[(3-methoxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoic acid;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-4-methylpentanoic acid;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2,2-dimethylpropanoic acid;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2-methylpropanoic acid;
  • N-[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]-beta-alanine;
  • 4-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoic acid;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(tetrahydrofuran-2-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(tetrahydrofuran-3-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(2-methoxyethyl)(3-methoxypropanoyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(3-methoxypropyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(tetrahydro-2H-pyran-2-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(tetrahydrofuran-2-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-(propan-2-yloxy)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[2-(1,3-dioxolan-2-yl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(1,4-dioxan-2-ylmethyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[3-(4-fluorophenyl)propanoyl](2-methoxyethyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(2-methoxyethyl) [3-(pyridin-3-yl)propanoyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(2-methoxyethyl)(pyridin-3-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(2-methoxyethyl)(naphthalen-2-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(2-methoxyethyl)[(4-phenoxyphenyl)acetyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[(4-cyanophenyl)acetyl](2-methoxyethyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(4-aminophenyl)acetyl](2-methoxyethyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{2-[di(prop-2-en-1-yl)amino]ethyl}(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[3-(diethylamino)propyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(diethylamino)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [3-(pyrrolidin-1-yl)propyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[(1-ethyl-5-oxopyrrolidin-3-yl)methyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(5-oxopyrrolidin-2-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl)[3-oxo-3-(pyrrolidin-1-yl)propyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl)[2-oxo-2-(piperidin-1-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [3-(2-oxopyrrolidin-1-yl)propyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-(2-oxo-1,3-oxazolidin-3-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl) {2-[(2-methylpropanoyl)amino]ethyl}amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [3-(methylamino)-3-oxopropyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[3-(acetylamino)propyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl)[2-oxo-2-(pyrrolidin-1-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[3-(2-hydroxyethyl)-2-oxoimidazolidin-1-yl]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[3-(4-fluorophenyl)-2-oxoimidazolidin-1-yl]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(5-chloropyridin-2-yl)methyl](tetrahydro-2H-pyran-4-ylcarbonyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(5-chloropyridin-2-yl)methyl](tetrahydrofuran-3-ylcarbonyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(5-chloropyridin-2-yl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(5-chloropyridin-2-yl)ethyl](tetrahydrofuran-3-ylcarbonyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(5-chloropyridin-2-yl)ethyl][(2-methoxyethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-([2-(5-chloropyridin-2-yl)ethyl]{[2-(propan-2-yloxy)ethyl]carbamoyl}amino)-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(1,3-benzodioxol-5-ylacetyl)(2-methoxyethyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(5S)-5-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-2-oxo-1,3-oxazolidin-3-yl}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(2-methoxyethyl)(pyridin-2-ylacetyl)amino]-1,3-thiazole-5-carboxamide; and pharmaceutically acceptable salts thereof.

Embodiments of Formula (II)

In another aspect, the present invention provides compounds of Formula (II)

and pharmaceutically acceptable salts thereof; wherein R1 and R2 are as described herein for Formula (I).

One embodiment of this invention pertains to compounds of Formula (II) or pharmaceutically acceptable salts thereof;

wherein

R1 and R2 are each independently selected from the group consisting of R6, C(O)R6, C(O)NHR6, and C(O)N(R6)2; wherein at least one of R1 and R2 is R6; or

R1 and R2, together with the nitrogen to which they are attached form a heterocycloalkyl or heterocycloalkenyl ring; wherein the ring formed with R1 and R2 together with the nitrogen to which they are attached is optionally substituted with one or more substituents independently selected from the group consisting of R7, OR7, SR7, S(O)R7, SO2R7, C(O)R7, CO(O)R7, OC(O)R7, OC(O)OR7, NH2, NHR7, N(R7)2, NHC(O)R7, NR7C(O)R7, NHS(O)2R7, NR7S(O)2R7, NHC(O)OR7, NR7C(O)OR7, NHC(O)NH2, NHC(O)NHR7, NHC(O)N(R7)2, NR7C(O)NHR7, NR7C(O)N(R7)2, C(O)NH2, C(O)NHR7, C(O)N(R7)2, C(O)NHOH, C(O)NHOR7, C(O)NHSO2R7, C(O)NR7SO2R7, SO2NH2, SO2NHR7, SO2N(R7)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR7, C(N)N(R7)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, SR8, S(O)R8, SO2R8, C(O)R8, CO(O)R8, OC(O)R8, OC(O)OR8, NH2, NHR8, N(R8)2, NHC(O)R8, NR8C(O)R8, NHS(O)2R8, NR8S(O)2R8, NHC(O)OR8, NR8C(O)OR8, NHC(O)NH2, NHC(O)NHR8, NHC(O)N(R8)2, NR8C(O)NHR8, NR8C(O)N(R8)2, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)NHOH, C(O)NHOR8, C(O)NHSO2R8, C(O)NR8O2R8, SO2NH2, SO2NHR8, SO2N(R8)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR8, C(N)N(R8)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, SR9, S(O)R9, SO2R9, C(O)R9, CO(O)R9, OC(O)R9, OC(O)OR9, NH2, NHR9, N(R9)2, NHC(O)R9, NR9C(O)R9, NHS(O)2R9, NR9S(O)2R9, NHC(O)OR9, NR9C(O)OR9, NHC(O)NH2, NHC(O)NHR9, NHC(O)N(R9)2, NR9C(O)NHR9, NR9C(O)N(R9)2, C(O)NH2, C(O)NHR9, C(O)N(R9)2, C(O)NHOH, C(O)NHOR9, C(O)NHSO2R9, C(O)NR9SO2R9, SO2NH2, SO2NHR9, SO2N(R9)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR9, C(N)N(R9)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R7, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R7 are each independently optionally substituted with one or more substituents independently selected from the group consisting of aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R7 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I;

R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R10, OR10, SR10, S(O)R10, SO2R10, C(O)R10, CO(O)R10, OC(O)R10, OC(O)OR10, NH2, NHR10, N(R10)2, NHC(O)R10, NR10C(O)R10, NHS(O)2R10, NR10S(O)2R7, NHC(O)OR10, NR10C(O)OR10, NHC(O)NH2, NHC(O)NHR10, NHC(O)N(R10)2, NR10C(O)NHR10, NR10C(O)N(R10)2, C(O)NH2, C(O)NHR10, C(O)N(R10)2, C(O)NHOH, C(O)NHOR10, C(O)NHSO2R10, C(O)NR10SO2R10, SO2NH2, SO2NHR10, SO2N(R10)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR10, C(N)N(R10)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, SR11, S(O)R11, SO2R11, C(O)R11, CO(O)R11, OC(O)R11, OC(O)OR11, NH2, NHR11, N(R11)2, NHC(O)R11, NR11C(O)R11, NHS(O)2R11, NR11S(O)2R11, NHC(O)OR11, NR11C(O)OR11, NHC(O)NH2, NHC(O)NHR11, NHC(O)N(R11)2, NR11C(O)NHR11, NR11C(O)N(R11)2, C(O)NH2, C(O)NHR11, C(O)N(R11)2, C(O)NHOH, C(O)NHOR11, C(O)NHSO2R11, C(O)NR11SO2R11, SO2NH2, SO2NHR11, SO2N(R11)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR11, C(N)N(R11)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R9, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R12, OR12, SR12, S(O)R12, SO2R12, C(O)R12, CO(O)R12, OC(O)R12, OC(O)OR12, NH2, NHR12, N(R12)2, NHC(O)R12, NR12C(O)R12, NHS(O)2R12, NR12S(O)2R12, NHC(O)OR12, NR12C(O)OR12, NHC(O)NH2, NHC(O)NHR12, NHC(O)N(R12)2, NR12C(O)NHR12, NR12C(O)N(R12)2, C(O)NH2, C(O)NHR12, C(O)N(R12)2, C(O)NHOH, C(O)NHOR12, C(O)NHSO2R12, C(O)NR12SO2R12, SO2NH2, SO2NHR12, SO2N(R12)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR12, C(N)N(R12)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R13, OR13, SR13, S(O)R13, SO2R13, C(O)R13, CO(O)R13, OC(O)R13, OC(O)OR13, NH2, NHR13, N(R13)2, NHC(O)R13, NR13C(O)R13, NHS(O)2R13, NR13S(O)2R13, NHC(O)OR13, NR13C(O)OR13, NHC(O)NH2, NHC(O)NHR13, NHC(O)N(R13)2, NR13C(O)NHR13, NR13C(O)N(R13)2, C(O)NH2, C(O)NHR13, C(O)N(R13)2, C(O)NHOH, C(O)NHOR13, C(O)NHSO2R13, C(O)NR13SO2R13, SO2NH2, SO2NHR13, SO2N(R13)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR13, C(N)N(R13)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R10, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6 haloalkyl, and C1-6 hydroxyalkyl;

R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6alkenyl, and C2-6alkynyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I;

R12, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6alkenyl, C2-6alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6alkyl, C2-6alkenyl, and C2-6alkynyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; and

R13, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6alkenyl, and C2-6alkynyl; wherein the C1-6alkyl, C2-6alkenyl, and C2-6alkynyl represented by R13 are each independently optionally substituted with one or more substituents independently selected from the group consisting of alkoxy, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In one embodiment of Formula (II), R1 and R2 are each independently selected from the group consisting of R6, C(O)R6, C(O)NHR6, and C(O)N(R6)2; wherein at least one of R and R2 is R6. In another embodiment of Formula (II), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, SR8, S(O)R8, SO2R8, C(O)R8, CO(O)R8, OC(O)R8, OC(O)OR8, NH2, NHR8, N(R8)2, NHC(O)R8, NR8C(O)R8, NHS(O)2R8, NR8S(O)2R8, NHC(O)OR8, NR8C(O)OR8, NHC(O)NH2, NHC(O)NHR8, NHC(O)N(R8)2, NR8C(O)NHR8, NR8C(O)N(R8)2, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)NHOH, C(O)NHOR8, C(O)NHSO2R8, C(O)NR8O2R8, SO2NH2, SO2NHR8, SO2N(R8)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR8, C(N)N(R8)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, SR9, S(O)R9, SO2R9, C(O)R9, CO(O)R9, OC(O)R9, OC(O)OR9, NH2, NHR9, N(R9)2, NHC(O)R9, NR9C(O)R9, NHS(O)2R9, NR9S(O)2R9, NHC(O)OR9, NR9C(O)OR9, NHC(O)NH2, NHC(O)NHR9, NHC(O)N(R9)2, NR9C(O)NHR9, NR9C(O)N(R9)2, C(O)NH2, C(O)NHR9, C(O)N(R9)2, C(O)NHOH, C(O)NHOR9, C(O)NHSO2R9, C(O)NR9SO2R9, SO2NH2, SO2NHR9, SO2N(R9)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR9, C(N)N(R9)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (II), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, heterocycloalkyl, heteroaryl, and cycloalkyl; wherein the C1-6 alkyl, and C2-6 alkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, C(O)R8, CO(O)R8, OC(O)R8, N(R8)2, NHC(O)R8, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)OH, and OH; wherein the aryl, heterocycloalkyl, heteroaryl, and cycloalkyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, C(O)NH2, C(O)OH, OH, CN, F, Cl, Br and I.

In one embodiment of Formula (II), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R10, OR10, SR10, S(O)R10, SO2R10, C(O)R10, CO(O)R10, OC(O)R10, OC(O)OR10, NH2, NHR10, N(R10)2, NHC(O)R10, NR10C(O)R10, NHS(O)2R10, NR10S(O)2R10, NHC(O)OR10, NR10C(O)OR10, NHC(O)NH2, NHC(O)NHR10, NHC(O)N(R10)2, NR10C(O)NHR10, NR10C(O)N(R10)2, C(O)NH2, C(O)NHR10, C(O)N(R10)2, C(O)NHOH, C(O)NHOR10, C(O)NHSO2R10, C(O)NR10SO2R10, SO2NH2, SO2NHR10, SO2N(R10)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR10, C(N)N(R10)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, SR11, S(O)R11, SO2R11, C(O)R11, CO(O)R11, OC(O)R11, OC(O)OR11, NH2, NHR11, N(R11)2, NHC(O)R11, NR11C(O)R11, NHS(O)2R11, NR11S(O)2R11, NHC(O)OR11, NR11C(O)OR11, NHC(O)NH2, NHC(O)NHR11, NHC(O)N(R11)2, NR11C(O)NHR11, NR11C(O)N(R11)2, C(O)NH2, C(O)NHR11, C(O)N(R11)2, C(O)NHOH, C(O)NHOR11, C(O)NHSO2R11, C(O)NR11SO2R11, SO2NH2, SO2NHR11, SO2N(R11)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR11, C(N)N(R11)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (II), R8, at each occurrence, is independently selected from the group consisting of C1-6alkyl, C2-6 alkenyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, and cycloalkyl; wherein the C1-6 alkyl and C2-6 alkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of OH, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, and heteroaryl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, NH2, N(R11)2, C(O)H, OH, CN, F, Cl, Br and I.

In one embodiment of Formula (II), R9, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R12, OR12, SR12, S(O)R12, SO2R12, C(O)R12, CO(O)R12, OC(O)R12, OC(O)OR12, NH2, NHR12, N(R12)2, NHC(O)R12, NR12C(O)R12, NHS(O)2R12, NR12S(O)2R12, NHC(O)OR12, NR12C(O)OR12, NHC(O)NH2, NHC(O)NHR12, NHC(O)N(R12)2, NR12C(O)NHR12, NR12C(O)N(R12)2, C(O)NH2, C(O)NHR12, C(O)N(R12)2, C(O)NHOH, C(O)NHOR12, C(O)NHSO2R12, C(O)NR12SO2R12, SO2NH2, SO2NHR12, SO2N(R12)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR12, C(N)N(R12)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R13, OR13, SR13, S(O)R13, SO2R13, C(O)R13, CO(O)R13, OC(O)R13, OC(O)OR13, NH2, NHR13, N(R13)2, NHC(O)R13, NR13C(O)R13, NHS(O)2R13, NR13S(O)2R13, NHC(O)OR13, NR13C(O)OR13, NHC(O)NH2, NHC(O)NHR13, NHC(O)N(R13)2, NR13C(O)NHR13, NR13C(O)N(R13)2, C(O)NH2, C(O)NHR13, C(O)N(R13)2, C(O)NHOH, C(O)NHOR13, C(O)NHSO2R13, C(O)NR13SO2R13, SO2NH2, SO2NHR13, SO2N(R13)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR13, C(N)N(R13)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (II), R9, at each occurrence, is C1-6 alkyl.

In one embodiment of Formula (II), R10, at each occurrence, is independently selected from the group consisting of C1-6alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6haloalkyl, and C1-6 hydroxyalkyl.

In one embodiment of Formula (II), R11, at each occurrence, is independently selected from the group consisting of C1-6alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (II), R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, and heteroaryl; wherein the C1-6alkyl and C2-6 alkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6alkoxy, cycloalkyl, OH, F, Cl, Br and I.

In one embodiment of Formula (II), R12, at each occurrence, is independently selected from the group consisting of C1-6alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In one embodiment of Formula (II), R13, at each occurrence, is independently selected from the group consisting of C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R13 are each independently optionally substituted with one or more substituents independently selected from the group consisting of alkoxy, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In another embodiment of Formula (II), R1 is C(O)R6; and R2 is R6. In another embodiment of Formula (II), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, aryl, heterocycloalkyl, heteroaryl, and cycloalkyl; wherein the C1-6 alkyl represented by R6 is independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, C(O)R8, OC(O)R8, N(R8)2, NHC(O)R8, C(O)NHR8, and OH; wherein the aryl, heterocycloalkyl, and heteroaryl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, C(O)NH2, OH, CN, F, Cl, Br and I. In another embodiment of Formula (II), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, and cycloalkyl; wherein the aryl, heterocycloalkyl, and heteroaryl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, NH2, N(R11)2, C(O)H, OH, CN, F, Cl, Br and I. In another embodiment of Formula (II), R9, at each occurrence, is C1-6 alkyl. In another embodiment of Formula (II), R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, and aryl; wherein the C1-6 alkyl and C2-6 alkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6alkoxy, cycloalkyl, OH, F, Cl, Br and I.

In another embodiment of Formula (II), R1 and R2 are each R6. In another embodiment of Formula (II), R6, at each occurrence, is C1-6alkyl; wherein the C1-6alkyl represented by R6 is independently optionally substituted with one or more substituents independently selected from the group consisting of R8, C(O)R8, C(O)NHR8, and C(O)N(R8)2. In another embodiment of Formula (II), R8, at each occurrence, is independently selected from the group consisting of C1-6alkyl, aryl, and heterocycloalkyl; wherein the aryl, and heterocycloalkyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, CN, F, Cl, Br and I. In another embodiment of Formula (II), R11, at each occurrence, is independently selected from the group consisting of C1-6alkyl and heteroaryl.

In another embodiment of Formula (II), R1 is C(O)NHR6; and R2 is R6. In another embodiment of Formula (II), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, heterocycloalkyl, and cycloalkyl; wherein the C1-6alkyl and C2-6 alkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, C(O)OR8, N(R8)2, NHC(O)R8, C(O)NH2, C(O)N(R8)2, C(O)OH, and OH; wherein the heterocycloalkyl, and cycloalkyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C(O)NH2, C(O)OH, F, Cl, Br and I. In another embodiment of Formula (II), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, aryl, heterocycloalkyl, and heteroaryl; wherein the C1-6 alkyl is independently optionally substituted with one or more OH; wherein the aryl, heterocycloalkyl, and heteroaryl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of OH, CN, F, Cl, Br and I.

In another embodiment of Formula (II), R1 is C(O)N(R6)2; and R2 is R6. In another embodiment of Formula (II), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, heterocycloalkyl, and cycloalkyl; wherein the C1-6alkyl and C2-6 alkenyl represented by R6 are independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, C(O)OR8, N(R8)2, NHC(O)R8, C(O)NH2, C(O)N(R8)2, C(O)OH, and OH; wherein the heterocycloalkyl, and cycloalkyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of OH, F, Cl, Br and I. In another embodiment of Formula (II), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, aryl, and heterocycloalkyl; wherein the C1-6 alkyl is independently optionally substituted with one or more OH; wherein the aryl and heterocycloalkyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of OH, CN, F, Cl, Br and I.

In another embodiment of Formula (II), R1 and R2, together with the nitrogen to which they are attached form a heterocycloalkyl or heterocycloalkenyl ring. In another embodiment of Formula (II), R1 and R2, together with the nitrogen to which they are attached form a heterocycloalkyl ring. In another embodiment of Formula (II), R7, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R7 are each independently optionally substituted with one or more substituents independently selected from the group consisting of aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (II), R1 and R2, together with the nitrogen to which they are attached form a heterocycloalkyl ring wherein the ring formed with R1 and R2 together with the nitrogen to which they are attached is optionally substituted with one or more R. In another embodiment of Formula (II), R7, at each occurrence, is independently selected from the group consisting of C1-6alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R7 are each independently optionally substituted with one or more substituents independently selected from the group consisting of aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R7 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (II), R7, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, and aryl; wherein the C1-6alkyl is independently optionally substituted with one or more substituents independently selected from the group consisting of aryl and OH; wherein the aryl represented by R7 is independently optionally substituted with one or more substituents independently selected from the group consisting of F, Cl, Br and I.

Still another embodiment pertains to compounds having Formula (II), which include

  • 2-{(4-fluorobenzyl)[4-(pyridin-3-yl)benzyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{methyl[4-(pyridin-3-yl)benzyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(methyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(tetrahydro-2H-pyran-4-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(cyclohexylacetyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(3-methylbutanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[3-(morpholin-4-yl)propyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [3-(piperidin-1-yl)propyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [2-(pyrrolidin-1-yl)ethyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {2-[4-(propan-2-yl)piperazin-1-yl]ethyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzoyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(3-chlorobenzoyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzoyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(5-chloro-1,3-benzodioxol-4-yl)methyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-chlorobenzyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(2-chlorobenzyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(2,5-dichlorobenzyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[2-(methylamino)-2-oxoethyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[2-oxo-2-(propan-2-ylamino)ethyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(dimethylamino)-2-oxoethyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(diethylamino)-2-oxoethyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[2-(morpholin-4-yl)-2-oxoethyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(4-methylbenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(methoxyacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(N,N-dimethylglycyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(3,6-dihydropyridin-1(2H)-ylacetyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(4-methylpiperidin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [(4-hydroxypiperidin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(4-methylpiperazin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[4-(propan-2-yl)piperazin-1-yl]acetyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(4-formylpiperazin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[4-(cyclopropylmethyl)piperazin-1-yl]acetyl}(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[4-(2-ethoxyethyl)piperazin-1-yl]acetyl}(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(cyclopropylcarbonyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[4-(prop-2-en-1-yl)piperazin-1-yl]acetyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[4-(3-methoxypropyl)piperazin-1-yl]acetyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[3-(dimethylamino)pyrrolidin-1-yl]acetyl}(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(morpholin-4-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(3-hydroxypiperidin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[4-(2-hydroxyethyl)piperazin-1-yl]acetyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(1,4-dioxa-7-azaspiro[4.4]non-7-ylacetyl) (4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 1-{2-[(4-fluorobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)amino]-2-oxoethyl}pyridinium;
  • 2-{[2-(4-fluorophenyl)ethyl](3-methylbutanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(propan-2-ylcarbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(4-cyanophenyl)ethyl](3-methylbutanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(4-cyanophenyl)ethyl](tetrahydro-2H-pyran-4-ylacetyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(3-methylbutanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(tetrahydro-2H-pyran-4-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(4-cyanophenyl)ethyl](tetrahydrofuran-3-ylacetyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(2-fluorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(3-fluorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(2-chlorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(3-chlorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-chlorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(tetrahydrofuran-3-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(3-methylbutyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [(2-methylpropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N1-(4-fluorobenzyl)-N1-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)piperidine-1,3-dicarboxamide;
  • 2-{(4-fluorobenzyl)[(3-hydroxyazetidin-1-yl)carbonyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-(4-fluorobenzyl)-N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-1,4-dioxa-7-azaspiro[4.4]nonane-7-carboxamide;
  • 2-{(4-fluorobenzyl)[(3-methoxypyrrolidin-1-yl)carbonyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-methoxyethyl)(methyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-(4-fluorobenzyl)-N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-2,6-dimethylmorpholine-4-carboxamide;
  • 2-{[ethyl(2-methoxyethyl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-(4-fluorobenzyl)-N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-2,2-dimethylmorpholine-4-carboxamide;
  • N-(4-fluorobenzyl)-N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-1,4-oxazepane-4-carboxamide;
  • 2-[(4-fluorobenzoyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(4-methylbenzyl)amino]-1,3-thiazole-5-carboxamide;
  • N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-N-(3-methylbutyl)-1,2-oxazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(2-phenoxypropanoyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-propoxyethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(tetrahydrofuran-2-ylmethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [(1-methoxypropan-2-yl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(tetrahydro-2H-pyran-2-ylmethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-methoxyethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(2-ethoxyethyl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(1-methoxybutan-2-yl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(4-cyanophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(1,3-dioxolan-2-ylmethyl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl){[2-(propan-2-yloxy)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(1,4-dioxan-2-ylmethyl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(1,3-dimethoxypropan-2-yl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-methoxybutyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(tetrahydrofuran-3-ylcarbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(tetrahydro-2H-pyran-3-ylcarbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(pyrimidin-2-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(2-methoxypyridin-4-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(1,3-oxazol-4-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-{[(5-chloropyridin-2-yl)methyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl)[(4-methylpyridin-3-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(6-methoxypyridin-3-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(4-methyl-1,3-thiazol-5-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[2-(3-hydroxyphenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-(pyridin-2-yl)ethyl]amino}-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(1,3-benzodioxol-5-yl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(4-chlorophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(3-fluorophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(4-hydroxyphenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(3-chlorophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{[2-(3-methoxyphenyl)ethyl](3-methoxypropanoyl)amino}-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(2-fluorophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-hydroxy-2-(4-methoxyphenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl)[1-(pyridin-2-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(1-methyl-1H-pyrazol-4-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(2,6-difluorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(6-methylpyridin-3-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(4-chlorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(5-methylpyrazin-2-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(3-chlorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(5-methylpyridin-2-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(2,5-difluorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(2-methylbenzyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(3-methylbenzyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(pyridin-2-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(pyridin-3-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl){[2-(propan-2-yloxy)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(2-methoxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[2-(2-hydroxyethoxy)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(propan-2-yloxy)propyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(3-hydroxy-2,2-dimethylpropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(2-hydroxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(1-hydroxypropan-2-yl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(3-hydroxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[(2S)-1-hydroxybut-3-en-2-yl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(4-hydroxybutyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methylbutyl)[(2R)-2-phenoxypropanoyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methylbutyl)[(2S)-2-phenoxypropanoyl]amino}-1,3-thiazole-5-carboxamide;
  • N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-5-methyl-N-(3-methylbutyl)-1,2-oxazole-3-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(phenoxy acetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(3-phenylpropanoyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(2-phenylpropanoyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-{[(4-fluorophenyl)acetyl](3-methylbutyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(3-amino-3-oxopropyl)carbamoyl](4-cyanobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[3-(acetylamino)-2-methylpropyl]carbamoyl}(4-cyanobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(dimethylamino)-3-oxopropyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(3-ethoxy-2-hydroxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(diethylamino)propyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[2-(acetylamino)ethyl]carbamoyl}(4-cyanobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl){[2-(diethylamino)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)({2-[(2-methylpropanoyl)amino]ethyl}carbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[(2R)-1-hydroxybut-3-en-2-yl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(3-hydroxyazetidin-1-yl)propyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(3-methylbutyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(methoxyacetyl)(3-methylbutyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-[(cyclopropylcarbonyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • (2S)-1-[(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)(3-methylbutyl)amino]-1-oxopropan-2-yl acetate;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(tetrahydro-2H-pyran-4-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(tetrahydrofuran-3-ylcarbonyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-{[2-hydroxy-2-(3-methoxyphenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-(pyrazin-2-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[1-(3-hydroxyphenyl)propan-2-yl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • ethyl N-[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]-beta-alaninate;
  • ethyl 4-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoate;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoate;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-4-methylpentanoate;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2,2-dimethylpropanoate;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}cyclobutanecarboxylic acid;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2-methylpropanoate;
  • 2-{(4-cyanobenzyl)[(3-methoxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoic acid;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-4-methylpentanoic acid;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2,2-dimethylpropanoic acid;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2-methylpropanoic acid;
  • N-[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]-beta-alanine;
  • 4-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoic acid;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(tetrahydrofuran-2-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(tetrahydrofuran-3-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(2-methoxyethyl)(3-methoxypropanoyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(3-methoxypropyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(tetrahydro-2H-pyran-2-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(tetrahydrofuran-2-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-(propan-2-yloxy)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[2-(1,3-dioxolan-2-yl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(1,4-dioxan-2-ylmethyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[3-(4-fluorophenyl)propanoyl](2-methoxyethyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(2-methoxyethyl) [3-(pyridin-3-yl)propanoyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(2-methoxyethyl)(pyridin-3-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(2-methoxyethyl)(naphthalen-2-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(2-methoxyethyl)[(4-phenoxyphenyl)acetyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[(4-cyanophenyl)acetyl](2-methoxyethyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(4-aminophenyl)acetyl](2-methoxyethyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{2-[di(prop-2-en-1-yl)amino]ethyl}(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[3-(diethylamino)propyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(diethylamino)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [3-(pyrrolidin-1-yl)propyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[(1-ethyl-5-oxopyrrolidin-3-yl)methyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(5-oxopyrrolidin-2-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl)[3-oxo-3-(pyrrolidin-1-yl)propyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-oxo-2-(piperidin-1-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [3-(2-oxopyrrolidin-1-yl)propyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-(2-oxo-1,3-oxazolidin-3-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl) {2-[(2-methylpropanoyl)amino]ethyl}amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [3-(methylamino)-3-oxopropyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[3-(acetylamino)propyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-oxo-2-(pyrrolidin-1-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[3-(2-hydroxyethyl)-2-oxoimidazolidin-1-yl]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[3-(4-fluorophenyl)-2-oxoimidazolidin-1-yl]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(5-chloropyridin-2-yl)methyl](tetrahydro-2H-pyran-4-ylcarbonyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(5-chloropyridin-2-yl)methyl](tetrahydrofuran-3-ylcarbonyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(5-chloropyridin-2-yl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(5-chloropyridin-2-yl)ethyl](tetrahydrofuran-3-ylcarbonyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(5-chloropyridin-2-yl)ethyl][(2-methoxy ethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-([2-(5-chloropyridin-2-yl)ethyl]{[2-(propan-2-yloxy)ethyl]carbamoyl}amino)-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(1,3-benzodioxol-5-ylacetyl)(2-methoxyethyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(5S)-5-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-2-oxo-1,3-oxazolidin-3-yl}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(2-methoxyethyl)(pyridin-2-ylacetyl)amino]-1,3-thiazole-5-carboxamide; and pharmaceutically acceptable salts thereof.

Embodiments of Formula (III)

In another aspect, the present invention provides compounds of Formula (III)

and pharmaceutically acceptable salts thereof; wherein each R6 is as described herein for Formula (I).

One embodiment of this invention pertains to compounds of Formula (III) or pharmaceutically acceptable salts thereof;

wherein

R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, SR8, S(O)R8, SO2R8, C(O)R8, CO(O)R8, OC(O)R8, OC(O)OR8, NH2, NHR8, N(R8)2, NHC(O)R8, NR8C(O)R8, NHS(O)2R8, NR8S(O)2R8, NHC(O)OR8, NR8C(O)OR8, NHC(O)NH2, NHC(O)NHR8, NHC(O)N(R8)2, NR8C(O)NHR8, NR8C(O)N(R8)2, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)NHOH, C(O)NHOR8, C(O)NHSO2R8, C(O)NR8O2R8, SO2NH2, SO2NHR8, SO2N(R8)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR8, C(N)N(R8)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, SR9, S(O)R9, SO2R9, C(O)R9, CO(O)R9, OC(O)R9, OC(O)OR9, NH2, NHR9, N(R9)2, NHC(O)R9, NR9C(O)R9, NHS(O)2R9, NR9S(O)2R9, NHC(O)OR9, NR9C(O)OR9, NHC(O)NH2, NHC(O)NHR9, NHC(O)N(R9)2, NR9C(O)NHR9, NR9C(O)N(R9)2, C(O)NH2, C(O)NHR9, C(O)N(R9)2, C(O)NHOH, C(O)NHOR9, C(O)NHSO2R9, C(O)NR9SO2R9, SO2NH2, SO2NHR9, SO2N(R9)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR9, C(N)N(R9)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R10, OR10, SR10, S(O)R10, SO2R10, C(O)R10, CO(O)R10, OC(O)R10, OC(O)OR10, NH2, NHR10, N(R10)2, NHC(O)R10, NR10C(O)R10, NHS(O)2R10, NR10S(O)2R10, NHC(O)OR10, NR10C(O)OR10, NHC(O)NH2, NHC(O)NHR10, NHC(O)N(R10)2, NR10C(O)NHR10, NR10C(O)N(R7)2, C(O)NH2, C(O)NHR10, C(O)N(R10)2, C(O)NHOH, C(O)NHOR10, C(O)NHSO2R10, C(O)NR10SO2R10, SO2NH2, SO2NHR10, SO2N(R10)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR10, C(N)N(R10)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, SR11, S(O)R11, SO2R11, C(O)R11, CO(O)R11, OC(O)R11, OC(O)OR11, NH2, NHR11, N(R11)2, NHC(O)R11, NR11C(O)R11, NHS(O)2R11, NR11S(O)2R11, NHC(O)OR11, NR11C(O)OR11, NHC(O)NH2, NHC(O)NHR11, NHC(O)N(R11)2, NR11C(O)NHR11, NR11C(O)N(R11)2, C(O)NH2, C(O)NHR11, C(O)N(R11)2, C(O)NHOH, C(O)NHOR11, C(O)NHSO2R11, C(O)NR11SO2R11, SO2NH2, SO2NHR11, SO2N(R11)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR11, C(N)N(R11)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R9, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R12, OR12, SR12, S(O)R12, SO2R12, C(O)R12, CO(O)R12, OC(O)R12, OC(O)OR12, NH2, NHR12, N(R12)2, NHC(O)R12, NR12C(O)R12, NHS(O)2R12, NR12S(O)2R12, NHC(O)OR12, NR12C(O)OR12, NHC(O)NH2, NHC(O)NHR12, NHC(O)N(R12)2, NR12C(O)NHR12, NR12C(O)N(R12)2, C(O)NH2, C(O)NHR12, C(O)N(R12)2, C(O)NHOH, C(O)NHOR12, C(O)NHSO2R12, C(O)NR12SO2R12, SO2NH2, SO2NHR12, SO2N(R12)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR12, C(N)N(R12)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R13, OR13, SR13, S(O)R13, SO2R13, C(O)R13, CO(O)R13, OC(O)R13, OC(O)OR13, NH2, NHR13, N(R13)2, NHC(O)R13, NR13C(O)R13, NHS(O)2R13, NR13S(O)2R13, NHC(O)OR13, NR13C(O)OR13, NHC(O)NH2, NHC(O)NHR13, NHC(O)N(R13)2, NR13C(O)NHR13, NR13C(O)N(R13)2, C(O)NH2, C(O)NHR13, C(O)N(R13)2, C(O)NHOH, C(O)NHOR13, C(O)NHSO2R13, C(O)NR13SO2R13, SO2NH2, SO2NHR13, SO2N(R13)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR13, C(N)N(R13)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R10, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6haloalkyl, and C1-6 hydroxyalkyl;

R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I;

R12, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; and

R13, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl; wherein the C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R13 are each independently optionally substituted with one or more substituents independently selected from the group consisting of alkoxy, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In another embodiment of Formula (III), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, SR8, S(O)R8, SO2R8, C(O)R8, CO(O)R8, OC(O)R8, OC(O)OR8, NH2, NHR8, N(R8)2, NHC(O)R8, NR8C(O)R8, NHS(O)2R8, NR8S(O)2R8, NHC(O)OR8, NR8C(O)OR8, NHC(O)NH2, NHC(O)NHR8, NHC(O)N(R8)2, NR8C(O)NHR8, NR8C(O)N(R8)2, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)NHOH, C(O)NHOR8, C(O)NHSO2R8, C(O)NR8O2R8, SO2NH2, SO2NHR8, SO2N(R8)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR8, C(N)N(R8)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, SR9, S(O)R9, SO2R9, C(O)R9, CO(O)R9, OC(O)R9, OC(O)OR9, NH2, NHR9, N(R9)2, NHC(O)R9, NR9C(O)R9, NHS(O)2R9, NR9S(O)2R9, NHC(O)OR9, NR9C(O)OR9, NHC(O)NH2, NHC(O)NHR9, NHC(O)N(R9)2, NR9C(O)NHR9, NR9C(O)N(R9)2, C(O)NH2, C(O)NHR9, C(O)N(R9)2, C(O)NHOH, C(O)NHOR9, C(O)NHSO2R9, C(O)NR9SO2R9, SO2NH2, SO2NHR9, SO2N(R9)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR9, C(N)N(R9)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (III), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, heterocycloalkyl, heteroaryl, and cycloalkyl; wherein the C1-6 alkyl, and C2-6 alkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, C(O)R8, CO(O)R8, OC(O)R8, N(R8)2, NHC(O)R8, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)OH, and OH; wherein the aryl, heterocycloalkyl, heteroaryl, and cycloalkyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, C(O)NH2, C(O)OH, OH, CN, F, Cl, Br and I.

In one embodiment of Formula (III), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R10, OR10, SR10, S(O)R10, SO2R10, C(O)R10, CO(O)R10, OC(O)R10, OC(O)OR10, NH2, NHR10, N(R7)2, NHC(O)R10, NR10C(O)R10, NHS(O)2R10, NR10S(O)2R10, NHC(O)OR10, NR10C(O)OR10, NHC(O)NH2, NHC(O)NHR10, NHC(O)N(R7)2, NR10C(O)NHR10, NR10C(O)N(R10)2, C(O)NH2, C(O)NHR10, C(O)N(R10)2, C(O)NHOH, C(O)NHOR10, C(O)NHSO2R10, C(O)NR10SO2R10, SO2NH2, SO2NHR10, SO2N(R10)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR10, C(N)N(R10)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, SR11, S(O)R11, SO2R11, C(O)R11, CO(O)R11, OC(O)R11, OC(O)OR11, NH2, NHR11, N(R11)2, NHC(O)R11, NR11C(O)R11, NHS(O)2R11, NR11S(O)2R11, NHC(O)OR11, NR11C(O)OR11, NHC(O)NH2, NHC(O)NHR11, NHC(O)N(R11)2, NR11C(O)NHR11, NR11C(O)N(R11)2, C(O)NH2, C(O)NHR11, C(O)N(R11)2, C(O)NHOH, C(O)NHOR11, C(O)NHSO2R11, C(O)NR11SO2R11, SO2NH2, SO2NHR11, SO2N(R11)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR11, C(N)N(R11)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (III), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, and cycloalkyl; wherein the C1-6 alkyl and C2-6 alkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of OH, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, and heteroaryl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, NH2, N(R11)2, C(O)H, OH, CN, F, Cl, Br and I.

In one embodiment of Formula (III), R9, at each occurrence, is independently selected from the group consisting of C1-6alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R12, OR12, SR12, S(O)R12, SO2R12, C(O)R12, CO(O)R12, OC(O)R12, OC(O)OR12, NH2, NHR12, N(R12)2, NHC(O)R12, NR12C(O)R12, NHS(O)2R12, NR12S(O)2R12, NHC(O)OR12, NR12C(O)OR12, NHC(O)NH2, NHC(O)NHR12, NHC(O)N(R12)2, NR12C(O)NHR12, NR12C(O)N(R12)2, C(O)NH2, C(O)NHR12, C(O)N(R12)2, C(O)NHOH, C(O)NHOR12, C(O)NHSO2R12, C(O)NR12SO2R12, SO2NH2, SO2NHR12, SO2N(R12)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR12, C(N)N(R12)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R13, OR13, SR13, S(O)R13, SO2R13, C(O)R13, CO(O)R13, OC(O)R13, OC(O)OR13, NH2, NHR13, N(R13)2, NHC(O)R13, NR13C(O)R13, NHS(O)2R13, NR13S(O)2R13, NHC(O)OR13, NR13C(O)OR13, NHC(O)NH2, NHC(O)NHR13, NHC(O)N(R13)2, NR13C(O)NHR13, NR13C(O)N(R13)2, C(O)NH2, C(O)NHR13, C(O)N(R13)2, C(O)NHOH, C(O)NHOR13, C(O)NHSO2R13, C(O)NR13SO2R13, SO2NH2, SO2NHR13, SO2N(R13)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR13, C(N)N(R13)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (III), R9, at each occurrence, is C1-6 alkyl.

In one embodiment of Formula (III), R10, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6 haloalkyl, and C1-6 hydroxyalkyl.

In one embodiment of Formula (III), R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (III), R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, and heteroaryl; wherein the C1-6 alkyl and C2-6 alkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, cycloalkyl, OH, F, Cl, Br and I.

In one embodiment of Formula (III), R12, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In one embodiment of Formula (III), R13, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R13 are each independently optionally substituted with one or more substituents independently selected from the group consisting of alkoxy, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In another embodiment of Formula (III), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, aryl, heterocycloalkyl, heteroaryl, and cycloalkyl; wherein the C1-6 alkyl represented by R6 is independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, C(O)R8, OC(O)R8, N(R8)2, NHC(O)R8, C(O)NHR8, and OH; wherein the aryl, heterocycloalkyl, and heteroaryl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, C(O)NH2, OH, CN, F, Cl, Br and I. In another embodiment of Formula (III), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, and cycloalkyl; wherein the aryl, heterocycloalkyl, and heteroaryl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, NH2, N(R11)2, C(O)H, OH, CN, F, Cl, Br and I. In another embodiment of Formula (III), R9, at each occurrence, is C1-6 alkyl. In another embodiment of Formula (III), R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, and aryl; wherein the C1-6 alkyl and C2-6 alkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6alkoxy, cycloalkyl, OH, F, Cl, Br and I.

Still another embodiment pertains to compounds having Formula (III), which include

  • 2-[(4-fluorobenzyl)(tetrahydro-2H-pyran-4-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(cyclohexylacetyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(3-methylbutanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzoyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(3-chlorobenzoyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzoyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(methoxyacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(N,N-dimethylglycyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(3,6-dihydropyridin-1(2H)-ylacetyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(4-methylpiperidin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(4-hydroxypiperidin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(4-methylpiperazin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl){[4-(propan-2-yl)piperazin-1-yl]acetyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(4-formylpiperazin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[4-(cyclopropylmethyl)piperazin-1-yl]acetyl}(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[4-(2-ethoxyethyl)piperazin-1-yl]acetyl}(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(cyclopropylcarbonyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[4-(prop-2-en-1-yl)piperazin-1-yl]acetyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[4-(3-methoxypropyl)piperazin-1-yl]acetyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[3-(dimethylamino)pyrrolidin-1-yl]acetyl}(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(morpholin-4-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [(3-hydroxypiperidin-1-yl)acetyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[4-(2-hydroxyethyl)piperazin-1-yl]acetyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(1,4-dioxa-7-azaspiro[4.4]non-7-ylacetyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 1-{2-[(4-fluorobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)amino]-2-oxoethyl}pyridinium;
  • 2-{[2-(4-fluorophenyl)ethyl](3-methylbutanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(4-cyanophenyl)ethyl](3-methylbutanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(4-cyanophenyl)ethyl](tetrahydro-2H-pyran-4-ylacetyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(3-methylbutanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(tetrahydro-2H-pyran-4-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(4-cyanophenyl)ethyl](tetrahydrofuran-3-ylacetyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(tetrahydrofuran-3-ylacetyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N1-(4-fluorobenzyl)-N1-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)piperidine-1,3-dicarboxamide;
  • 2-{(4-fluorobenzyl) [(3-hydroxyazetidin-1-yl)carbonyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-(4-fluorobenzyl)-N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-1,4-dioxa-7-azaspiro[4.4]nonane-7-carboxamide;
  • 2-{(4-fluorobenzyl)[(3-methoxypyrrolidin-1-yl)carbonyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-(4-fluorobenzyl)-N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-2,6-dimethylmorpholine-4-carboxamide;
  • N-(4-fluorobenzyl)-N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-2,2-dimethylmorpholine-4-carboxamide;
  • N-(4-fluorobenzyl)-N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-1,4-oxazepane-4-carboxamide;
  • 2-[(4-fluorobenzoyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(4-methylbenzyl)amino]-1,3-thiazole-5-carboxamide;
  • N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-N-(3-methylbutyl)-1,2-oxazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(2-phenoxypropanoyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(4-cyanophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(pyrimidin-2-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl)[(2-methoxypyridin-4-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(1,3-oxazol-4-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-{[(5-chloropyridin-2-yl)methyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(4-methylpyridin-3-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(6-methoxypyridin-3-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(4-methyl-1,3-thiazol-5-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[2-(3-hydroxyphenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-(pyridin-2-yl)ethyl]amino}-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(1,3-benzodioxol-5-yl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(4-chlorophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(3-fluorophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(4-hydroxyphenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(3-chlorophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{[2-(3-methoxyphenyl)ethyl](3-methoxypropanoyl)amino}-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-(2-fluorophenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • 2-{[2-hydroxy-2-(4-methoxyphenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide acetate (1:1);
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl)[1-(pyridin-2-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(1-methyl-1H-pyrazol-4-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(2,6-difluorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(6-methylpyridin-3-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(4-chlorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(5-methylpyrazin-2-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(3-chlorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(5-methylpyridin-2-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(2,5-difluorobenzyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(2-methylbenzyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(3-methylbenzyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(pyridin-2-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(pyridin-3-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methylbutyl)[(2R)-2-phenoxypropanoyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methylbutyl)[(2S)-2-phenoxypropanoyl]amino}-1,3-thiazole-5-carboxamide;
  • N-(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)-5-methyl-N-(3-methylbutyl)-1,2-oxazole-3-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(phenoxyacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(3-phenylpropanoyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(2-phenylpropanoyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-{[(4-fluorophenyl)acetyl](3-methylbutyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(3-methylbutyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(methoxyacetyl)(3-methylbutyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-[(cyclopropylcarbonyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • (2S)-1-[(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)(3-methylbutyl)amino]-1-oxopropan-2-yl acetate;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(tetrahydro-2H-pyran-4-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(tetrahydrofuran-3-ylcarbonyl)amino]-1,3-thiazole-5-carboxamide;
  • 2-{[2-hydroxy-2-(3-methoxyphenyl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-(pyrazin-2-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[1-(3-hydroxyphenyl)propan-2-yl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(tetrahydrofuran-2-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methylbutyl)(tetrahydrofuran-3-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(2-methoxyethyl)(3-methoxypropanoyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(3-methoxypropyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(tetrahydro-2H-pyran-2-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl)(tetrahydrofuran-2-ylmethyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-(propan-2-yloxy)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[2-(1,3-dioxolan-2-yl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(1,4-dioxan-2-ylmethyl)(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[3-(4-fluorophenyl)propanoyl](2-methoxyethyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(2-methoxyethyl) [3-(pyridin-3-yl)propanoyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(2-methoxyethyl)(pyridin-3-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(2-methoxyethyl)(naphthalen-2-ylacetyl)amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(2-methoxyethyl) [(4-phenoxyphenyl)acetyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[(4-cyanophenyl)acetyl](2-methoxyethyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(4-aminophenyl)acetyl](2-methoxyethyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{2-[di(prop-2-en-1-yl)amino]ethyl}(3-methoxypropanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[3-(diethylamino)propyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(diethylamino)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [3-(pyrrolidin-1-yl)propyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[(1-ethyl-5-oxopyrrolidin-3-yl)methyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [(5-oxopyrrolidin-2-yl)methyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl)[3-oxo-3-(pyrrolidin-1-yl)propyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-oxo-2-(piperidin-1-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [3-(2-oxopyrrolidin-1-yl)propyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [2-(2-oxo-1,3-oxazolidin-3-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(3-methoxypropanoyl) {2-[(2-methylpropanoyl)amino]ethyl}amino]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl) [3-(methylamino)-3-oxopropyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[3-(acetylamino)propyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{(3-methoxypropanoyl)[2-oxo-2-(pyrrolidin-1-yl)ethyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-{[(5-chloropyridin-2-yl)methyl](tetrahydro-2H-pyran-4-ylcarbonyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(5-chloropyridin-2-yl)methyl](tetrahydrofuran-3-ylcarbonyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(5-chloropyridin-2-yl)ethyl](3-methoxypropanoyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(5-chloropyridin-2-yl)ethyl](tetrahydrofuran-3-ylcarbonyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(1,3-benzodioxol-5-ylacetyl)(2-methoxyethyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-[(2-methoxyethyl)(pyridin-2-ylacetyl)amino]-1,3-thiazole-5-carboxamide; and pharmaceutically acceptable salts thereof.

Embodiments of Formula (IV)

In another aspect, the present invention provides compounds of Formula (IV)

and pharmaceutically acceptable salts thereof; wherein each R6 is as described herein for Formula (I).

One embodiment of this invention pertains to compounds of Formula (IV) or pharmaceutically acceptable salts thereof;

wherein

R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, SR8, S(O)R8, SO2R8, C(O)R8, CO(O)R8, OC(O)R8, OC(O)OR8, NH2, NHR8, N(R8)2, NHC(O)R8, NR8C(O)R8, NHS(O)2R8, NR8S(O)2R8, NHC(O)OR8, NR8C(O)OR8, NHC(O)NH2, NHC(O)NHR8, NHC(O)N(R8)2, NR8C(O)NHR8, NR8C(O)N(R8)2, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)NHOH, C(O)NHOR8, C(O)NHSO2R8, C(O)NR8O2R8, SO2NH2, SO2NHR8, SO2N(R8)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR8, C(N)N(R8)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, SR9, S(O)R9, SO2R9, C(O)R9, CO(O)R9, OC(O)R9, OC(O)OR9, NH2, NHR9, N(R9)2, NHC(O)R9, NR9C(O)R9, NHS(O)2R9, NR9S(O)2R9, NHC(O)OR9, NR9C(O)OR9, NHC(O)NH2, NHC(O)NHR9, NHC(O)N(R9)2, NR9C(O)NHR9, NR9C(O)N(R9)2, C(O)NH2, C(O)NHR9, C(O)N(R9)2, C(O)NHOH, C(O)NHOR9, C(O)NHSO2R9, C(O)NR9SO2R9, SO2NH2, SO2NHR9, SO2N(R9)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR9, C(N)N(R9)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R10, OR10, SR10, S(O)R10, SO2R10, C(O)R10, CO(O)R10, OC(O)R10, OC(O)OR10, NH2, NHR10, N(R10)2, NHC(O)R10, NR10C(O)R10, NHS(O)2R10, NR10S(O)2R10, NHC(O)OR10, NR10C(O)OR10, NHC(O)NH2, NHC(O)NHR10, NHC(O)N(R10)2, NR10C(O)NHR10, NR10C(O)N(R10)2, C(O)NH2, C(O)NHR10, C(O)N(R10)2, C(O)NHOH, C(O)NHOR10, C(O)NHSO2R10, C(O)NR10SO2R10, SO2NH2, SO2NHR10, SO2N(R10)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR10, C(N)N(R10)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, SR11, S(O)R11, SO2R11, C(O)R11, CO(O)R11, OC(O)R11, OC(O)OR11, NH2, NHR11, N(R11)2, NHC(O)R11, NR11C(O)R11, NHS(O)2R11, NR11S(O)2R11, NHC(O)OR11, NR11C(O)OR11, NHC(O)NH2, NHC(O)NHR11, NHC(O)N(R11)2, NR11C(O)NHR11, NR11C(O)N(R11)2, C(O)NH2, C(O)NHR11, C(O)N(R11)2, C(O)NHOH, C(O)NHOR11, C(O)NHSO2R11, C(O)NR11SO2R11, SO2NH2, SO2NHR11, SO2N(R11)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR11, C(N)N(R11)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R9, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R12, OR12, SR12, S(O)R12, SO2R12, C(O)R12, CO(O)R12, OC(O)R12, OC(O)OR12, NH2, NHR12, N(R12)2, NHC(O)R12, NR12C(O)R12, NHS(O)2R12, NR12S(O)2R2, NHC(O)OR12, NR12C(O)OR12, NHC(O)NH2, NHC(O)NHR12, NHC(O)N(R12)2, NR12C(O)NHR12, NR12C(O)N(R12)2, C(O)NH2, C(O)NHR12, C(O)N(R12)2, C(O)NHOH, C(O)NHOR12, C(O)NHSO2R12, C(O)NR12SO2R12, SO2NH2, SO2NHR12, SO2N(R12)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR12, C(N)N(R12)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R13, OR13, SR13, S(O)R13, SO2R13, C(O)R13, CO(O)R13, OC(O)R13, OC(O)OR13, NH2, NHR13, N(R13)2, NHC(O)R13, NR13C(O)R13, NHS(O)2R13, NR13S(O)2R13, NHC(O)OR13, NR13C(O)OR13, NHC(O)NH2, NHC(O)NHR13, NHC(O)N(R13)2, NR13C(O)NHR13, NR13C(O)N(R13)2, C(O)NH2, C(O)NHR13, C(O)N(R13)2, C(O)NHOH, C(O)NHOR13, C(O)NHSO2R13, C(O)NR13SO2R13, SO2NH2, SO2NHR13, SO2N(R13)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR13, C(N)N(R13)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R10, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6haloalkyl, and C1-6 hydroxyalkyl;

R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6alkenyl, C2-6alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I;

R12, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6alkenyl, C2-6alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6alkyl, C2-6alkenyl, and C2-6alkynyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; and

R13, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6alkenyl, and C2-6alkynyl; wherein the C1-6alkyl, C2-6alkenyl, and C2-6alkynyl represented by R13 are each independently optionally substituted with one or more substituents independently selected from the group consisting of alkoxy, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In one embodiment of Formula (IV), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, SR8, S(O)R8, SO2R8, C(O)R8, CO(O)R8, OC(O)R8, OC(O)OR8, NH2, NHR8, N(R8)2, NHC(O)R8, NR8C(O)R8, NHS(O)2R8, NR8S(O)2R8, NHC(O)OR8, NR8C(O)OR8, NHC(O)NH2, NHC(O)NHR8, NHC(O)N(R8)2, NR8C(O)NHR8, NR8C(O)N(R8)2, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)NHOH, C(O)NHOR8, C(O)NHSO2R8, C(O)NR8O2R8, SO2NH2, SO2NHR8, SO2N(R8)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR8, C(N)N(R8)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, SR9, S(O)R9, SO2R9, C(O)R9, CO(O)R9, OC(O)R9, OC(O)OR9, NH2, NHR9, N(R9)2, NHC(O)R9, NR9C(O)R9, NHS(O)2R9, NR9S(O)2R9, NHC(O)OR9, NR9C(O)OR9, NHC(O)NH2, NHC(O)NHR9, NHC(O)N(R9)2, NR9C(O)NHR9, NR9C(O)N(R9)2, C(O)NH2, C(O)NHR9, C(O)N(R9)2, C(O)NHOH, C(O)NHOR9, C(O)NHSO2R9, C(O)NR9SO2R9, SO2NH2, SO2NHR9, SO2N(R9)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR9, C(N)N(R9)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (IV), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, heterocycloalkyl, heteroaryl, and cycloalkyl; wherein the C1-6 alkyl, and C2-6 alkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, C(O)R8, CO(O)R8, OC(O)R8, N(R8)2, NHC(O)R8, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)OH, and OH; wherein the aryl, heterocycloalkyl, heteroaryl, and cycloalkyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, C(O)NH2, C(O)OH, OH, CN, F, Cl, Br and I.

In one embodiment of Formula (IV), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R10, OR10, SR10, S(O)R10, SO2R10, C(O)R10, CO(O)R10, OC(O)R10, OC(O)OR10, NH2, NHR10, N(R10)2, NHC(O)R10, NR10C(O)R10, NHS(O)2R10, NR10S(O)2R10, NHC(O)OR10, NR10C(O)OR10, NHC(O)NH2, NHC(O)NHR10, NHC(O)N(R10)2, NR10C(O)NHR10, NR10C(O)N(R10)2, C(O)NH2, C(O)NHR10, C(O)N(R10)2, C(O)NHOH, C(O)NHOR10, C(O)NHSO2R10, C(O)NR10SO2R10, SO2NH2, SO2NHR10, SO2N(R10)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR10, C(N)N(R10)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, SR11, S(O)R11, SO2R11, C(O)R11, CO(O)R11, OC(O)R11, OC(O)OR11, NH2, NHR11, N(R11)2, NHC(O)R11, NR11C(O)R11, NHS(O)2R11, NR11S(O)2R11, NHC(O)OR11, NR11C(O)OR11, NHC(O)NH2, NHC(O)NHR11, NHC(O)N(R11)2, NR11C(O)NHR11, NR11C(O)N(R11)2, C(O)NH2, C(O)NHR11, C(O)N(R11)2, C(O)NHOH, C(O)NHOR11, C(O)NHSO2R11, C(O)NR11SO2R11, SO2NH2, SO2NHR11, SO2N(R11)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR11, C(N)N(R11)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (IV), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, and cycloalkyl; wherein the C1-6 alkyl and C2-6 alkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of OH, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, and heteroaryl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, NH2, N(R11)2, C(O)H, OH, CN, F, Cl, Br and I.

In one embodiment of Formula (IV), R9, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R12, OR12, SR2, S(O)R12, SO2R12, C(O)R12, CO(O)R12, OC(O)R12, OC(O)OR12, NH2, NHR12, N(R12)2, NHC(O)R12, NR12C(O)R12, NHS(O)2R12, NR12S(O)2R12, NHC(O)OR12, NR12C(O)OR12, NHC(O)NH2, NHC(O)NHR12, NHC(O)N(R12)2, NR12C(O)NHR12, NR12C(O)N(R12)2, C(O)NH2, C(O)NHR12, C(O)N(R12)2, C(O)NHOH, C(O)NHOR12, C(O)NHSO2R12, C(O)NR12SO2R12, SO2NH2, SO2NHR12, SO2N(R12)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR12, C(N)N(R12)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R13, OR13, SR13, S(O)R13, SO2R13, C(O)R13, CO(O)R13, OC(O)R13, OC(O)OR11, NH2, NHR7, N(R13)2, NHC(O)R13, NR13C(O)R13, NHS(O)2R13, NR13S(O)2R13, NHC(O)OR13, NR13C(O)OR13, NHC(O)NH2, NHC(O)NHR13, NHC(O)N(R13)2, NR13C(O)NHR13, NR13C(O)N(R13)2, C(O)NH2, C(O)NHR13, C(O)N(R13)2, C(O)NHOH, C(O)NHOR13, C(O)NHSO2R13, C(O)NR13SO2R13, SO2NH2, SO2NHR13, SO2N(R13)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR13, C(N)N(R13)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (IV), R9, at each occurrence, is C1-6 alkyl.

In one embodiment of Formula (IV), R10, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6 haloalkyl, and C1-6 hydroxyalkyl.

In one embodiment of Formula (IV), R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (IV), R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, and heteroaryl; wherein the C1-6 alkyl and C2-6 alkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, cycloalkyl, OH, F, Cl, Br and I.

In one embodiment of Formula (IV), R12, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In one embodiment of Formula (IV), R13, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R13 are each independently optionally substituted with one or more substituents independently selected from the group consisting of alkoxy, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In another embodiment of Formula (IV), R6, at each occurrence, is C1-6 alkyl; wherein the C1-6 alkyl represented by R6 is independently optionally substituted with one or more substituents independently selected from the group consisting of R8, C(O)R8, C(O)NHR8, and C(O)N(R8)2. In another embodiment of Formula (IV), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, aryl, and heterocycloalkyl; wherein the aryl, and heterocycloalkyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, CN, F, Cl, Br and I. In another embodiment of Formula (IV), R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl and heteroaryl.

Still another embodiment pertains to compounds having Formula (IV), which include

  • 2-{(4-fluorobenzyl)[4-(pyridin-3-yl)benzyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • N-[3-(1H-imidazol-1-yl)propyl]-2-{methyl[4-(pyridin-3-yl)benzyl]amino}-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(methyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [3-(morpholin-4-yl)propyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [3-(piperidin-1-yl)propyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [2-(pyrrolidin-1-yl)ethyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl){2-[4-(propan-2-yl)piperazin-1-yl]ethyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(5-chloro-1,3-benzodioxol-4-yl)methyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-chlorobenzyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(2-chlorobenzyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(2,5-dichlorobenzyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[2-(methylamino)-2-oxoethyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[2-oxo-2-(propan-2-ylamino)ethyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(dimethylamino)-2-oxoethyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[2-(diethylamino)-2-oxoethyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[2-(morpholin-4-yl)-2-oxoethyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(4-methylbenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(2-fluorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(3-fluorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(2-chlorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(3-chlorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-chlorobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)(3-methylbutyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide; and pharmaceutically acceptable salts thereof.

Embodiments of Formula (V)

In another aspect, the present invention provides compounds of Formula (V)

and pharmaceutically acceptable salts thereof; wherein each R6 is as described herein for Formula (I).

One embodiment of this invention pertains to compounds of Formula (V) or pharmaceutically acceptable salts thereof;

wherein

R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, SR8, S(O)R8, SO2R8, C(O)R8, CO(O)R8, OC(O)R8, OC(O)OR8, NH2, NHR8, N(R8)2, NHC(O)R8, NR8C(O)R8, NHS(O)2R8, NR8S(O)2R8, NHC(O)OR8, NR8C(O)OR8, NHC(O)NH2, NHC(O)NHR8, NHC(O)N(R8)2, NR8C(O)NHR8, NR8C(O)N(R8)2, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)NHOH, C(O)NHOR8, C(O)NHSO2R8, C(O)NR8O2R8, SO2NH2, SO2NHR8, SO2N(R8)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR8, C(N)N(R8)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, SR9, S(O)R9, SO2R9, C(O)R9, CO(O)R9, OC(O)R9, OC(O)OR9, NH2, NHR9, N(R9)2, NHC(O)R9, NR9C(O)R9, NHS(O)2R9, NR9S(O)2R9, NHC(O)OR9, NR9C(O)OR9, NHC(O)NH2, NHC(O)NHR9, NHC(O)N(R9)2, NR9C(O)NHR9, NR9C(O)N(R9)2, C(O)NH2, C(O)NHR9, C(O)N(R9)2, C(O)NHOH, C(O)NHOR9, C(O)NHSO2R9, C(O)NR9SO2R9, SO2NH2, SO2NHR9, SO2N(R9)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR9, C(N)N(R9)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R10, OR10, SR10, S(O)R10, SO2R10, C(O)R10, CO(O)R10, OC(O)R10, OC(O)OR10, NH2, NHR10, N(R10)2, NHC(O)R10, NR10C(O)R10, NHS(O)2R10, NR10S(O)2R10, NHC(O)OR10, NR10C(O)OR10, NHC(O)NH2, NHC(O)NHR10, NHC(O)N(R10)2, NR10C(O)NHR10, NR10C(O)N(R7)2, C(O)NH2, C(O)NHR10, C(O)N(R10)2, C(O)NHOH, C(O)NHOR10, C(O)NHSO2R10, C(O)NR10SO2R10, SO2NH2, SO2NHR10, SO2N(R10)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR10, C(N)N(R10)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, SR11, S(O)R11, SO2R11, C(O)R11, CO(O)R11, OC(O)R11, OC(O)OR11, NH2, NHR11, N(R11)2, NHC(O)R11, NR11C(O)R11, NHS(O)2R11, NR11S(O)2R11, NHC(O)OR11, NR11C(O)OR11, NHC(O)NH2, NHC(O)NHR11, NHC(O)N(R11)2, NR11C(O)NHR11, NR11C(O)N(R11)2, C(O)NH2, C(O)NHR11, C(O)N(R11)2, C(O)NHOH, C(O)NHOR11, C(O)NHSO2R11, C(O)NR11SO2R11, SO2NH2, SO2NHR11, SO2N(R11)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR11, C(N)N(R11)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R9, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R12, OR12, SR12, S(O)R12, SO2R12, C(O)R12, CO(O)R12, OC(O)R12, OC(O)OR12, NH2, NHR12, N(R12)2, NHC(O)R12, NR12C(O)R12, NHS(O)2R12, NR12S(O)2R12, NHC(O)OR12, NR12C(O)OR12, NHC(O)NH2, NHC(O)NHR12, NHC(O)N(R12)2, NR12C(O)NHR12, NR12C(O)N(R12)2, C(O)NH2, C(O)NHR12, C(O)N(R12)2, C(O)NHOH, C(O)NHOR12, C(O)NHSO2R12, C(O)NR12SO2R12, SO2NH2, SO2NHR12, SO2N(R12)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR12, C(N)N(R12)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R13, OR13, SR13, S(O)R13, SO2R13, C(O)R13, CO(O)R13, OC(O)R13, OC(O)OR13, NH2, NHR13, N(R13)2, NHC(O)R13, NR13C(O)R13, NHS(O)2R13, NR13S(O)2R13, NHC(O)OR13, NR13C(O)OR13, NHC(O)NH2, NHC(O)NHR13, NHC(O)N(R13)2, NR13C(O)NHR13, NR13C(O)N(R13)2, C(O)NH2, C(O)NHR13, C(O)N(R13)2, C(O)NHOH, C(O)NHOR13, C(O)NHSO2R13, C(O)NR13SO2R13, SO2NH2, SO2NHR13, SO2N(R13)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR13, C(N)N(R13)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R10, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6 haloalkyl, and C1-6 hydroxyalkyl;

R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I;

R12, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; and

R13, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl; wherein the C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R13 are each independently optionally substituted with one or more substituents independently selected from the group consisting of alkoxy, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In one embodiment of Formula (V), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, SR8, S(O)R8, SO2R8, C(O)R8, CO(O)R8, OC(O)R8, OC(O)OR8, NH2, NHR8, N(R8)2, NHC(O)R8, NR8C(O)R8, NHS(O)2R8, NR8S(O)2R8, NHC(O)OR8, NR8C(O)OR8, NHC(O)NH2, NHC(O)NHR8, NHC(O)N(R8)2, NR8C(O)NHR8, NR8C(O)N(R8)2, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)NHOH, C(O)NHOR8, C(O)NHSO2R8, C(O)NR8O2R8, SO2NH2, SO2NHR8, SO2N(R8)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR8, C(N)N(R8)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, SR9, S(O)R9, SO2R9, C(O)R9, CO(O)R9, OC(O)R9, OC(O)OR9, NH2, NHR9, N(R9)2, NHC(O)R9, NR9C(O)R9, NHS(O)2R9, NR9S(O)2R9, NHC(O)OR9, NR9C(O)OR9, NHC(O)NH2, NHC(O)NHR9, NHC(O)N(R9)2, NR9C(O)NHR9, NR9C(O)N(R9)2, C(O)NH2, C(O)NHR9, C(O)N(R9)2, C(O)NHOH, C(O)NHOR9, C(O)NHSO2R9, C(O)NR9SO2R9, SO2NH2, SO2NHR9, SO2N(R9)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR9, C(N)N(R9)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (V), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, heterocycloalkyl, heteroaryl, and cycloalkyl; wherein the C1-6 alkyl, and C2-6 alkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, C(O)R8, CO(O)R8, OC(O)R8, N(R8)2, NHC(O)R8, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)OH, and OH; wherein the aryl, heterocycloalkyl, heteroaryl, and cycloalkyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, C(O)NH2, C(O)OH, OH, CN, F, Cl, Br and I.

In one embodiment of Formula (V), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R10, OR10, SR10, S(O)R10, SO2R10, C(O)R10, CO(O)R10, OC(O)R10, OC(O)OR10, NH2, NHR10, N(R1)2, NHC(O)R10, NR10C(O)R10, NHS(O)2R10, NR10S(O)2R10, NHC(O)OR10, NR10C(O)OR10, NHC(O)NH2, NHC(O)NHR10, NHC(O)N(R10)2, NR10C(O)NHR10, NR10C(O)N(R10)2, C(O)NH2, C(O)NHR10, C(O)N(R10)2, C(O)NHOH, C(O)NHOR10, C(O)NHSO2R10, C(O)NR10SO2R10, SO2NH2, SO2NHR10, SO2N(R10)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR10, C(N)N(R10)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, SR11, S(O)R11, SO2R11, C(O)R11, CO(O)R11, OC(O)R11, OC(O)OR11, NH2, NHR11, N(R11)2, NHC(O)R11, NR11C(O)R11, NHS(O)2R11, NR11S(O)2R11, NHC(O)OR11, NR11C(O)OR11, NHC(O)NH2, NHC(O)NHR11, NHC(O)N(R11)2, NR11C(O)NHR11, NR11C(O)N(R11)2, C(O)NH2, C(O)NHR11, C(O)N(R11)2, C(O)NHOH, C(O)NHOR11, C(O)NHSO2R11, C(O)NR11SO2R11, SO2NH2, SO2NHR11, SO2N(R11)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR11, C(N)N(R11)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (V), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, and cycloalkyl; wherein the C1-6 alkyl and C2-6 alkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of OH, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, and heteroaryl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, NH2, N(R11)2, C(O)H, OH, CN, F, Cl, Br and I.

In one embodiment of Formula (V), R9, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R12, OR12, SR12, S(O)R12, SO2R12, C(O)R12, CO(O)R12, OC(O)R12, OC(O)OR12, NH2, NHR12, N(R12)2, NHC(O)R12, NR12C(O)R12, NHS(O)2R12, NR12S(O)2R12, NHC(O)OR12, NR12C(O)OR12, NHC(O)NH2, NHC(O)NHR12, NHC(O)N(R12)2, NR12C(O)NHR12, NR12C(O)N(R12)2, C(O)NH2, C(O)NHR12, C(O)N(R12)2, C(O)NHOH, C(O)NHOR12, C(O)NHSO2R12, C(O)NR12SO2R12, SO2NH2, SO2NHR12, SO2N(R12)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR12, C(N)N(R12)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R13, OR13, SR13, S(O)R13, SO2R13, C(O)R13, CO(O)R13, OC(O)R13, OC(O)OR13, NH2, NHR13, N(R13)2, NHC(O)R13, NR13C(O)R13, NHS(O)2R13, NR13S(O)2R13, NHC(O)OR13, NR13C(O)OR13, NHC(O)NH2, NHC(O)NHR13, NHC(O)N(R13)2, NR13C(O)NHR13, NR13C(O)N(R13)2, C(O)NH2, C(O)NHR13, C(O)N(R13)2, C(O)NHOH, C(O)NHOR13, C(O)NHSO2R13, C(O)NR13SO2R13, SO2NH2, SO2NHR13, SO2N(R13)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR13, C(N)N(R13)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (V), R9, at each occurrence, is C1-6 alkyl.

In one embodiment of Formula (V), R10, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6 haloalkyl, and C1-6 hydroxyalkyl.

In one embodiment of Formula (V), R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (V), R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, and heteroaryl; wherein the C1-6 alkyl and C2-6 alkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6alkoxy, cycloalkyl, OH, F, Cl, Br and I.

In one embodiment of Formula (V), R12, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In one embodiment of Formula (V), R13, at each occurrence, is independently selected from the group consisting of C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl; wherein the C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R13 are each independently optionally substituted with one or more substituents independently selected from the group consisting of alkoxy, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In another embodiment of Formula (V), R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, heterocycloalkyl, and cycloalkyl; wherein the C1-6 alkyl and C2-6 alkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, C(O)OR8, N(R8)2, NHC(O)R8, C(O)NH2, C(O)N(R8)2, C(O)OH, and OH; wherein the heterocycloalkyl, and cycloalkyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C(O)NH2, C(O)OH, F, Cl, Br and I. In another embodiment of Formula (V), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, aryl, heterocycloalkyl, and heteroaryl; wherein the C1-6 alkyl is independently optionally substituted with one or more OH; wherein the aryl, heterocycloalkyl, and heteroaryl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of OH, CN, F, Cl, Br and I.

Still another embodiment pertains to compounds having Formula (V), which include

  • 2-[(4-fluorobenzyl)(propan-2-ylcarbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(3-methylbutyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [(2-methylpropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-propoxyethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [(tetrahydrofuran-2-ylmethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [(1-methoxypropan-2-yl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(tetrahydro-2H-pyran-2-ylmethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-methoxyethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(2-ethoxyethyl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(1-methoxybutan-2-yl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(1,3-dioxolan-2-ylmethyl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[2-(propan-2-yloxy)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(1,4-dioxan-2-ylmethyl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(1,3-dimethoxypropan-2-yl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-methoxybutyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(tetrahydrofuran-3-ylcarbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(tetrahydro-2H-pyran-3-ylcarbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[2-(propan-2-yloxy)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(2-methoxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[2-(2-hydroxyethoxy)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(propan-2-yloxy)propyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(3-hydroxy-2,2-dimethylpropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(2-hydroxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(1-hydroxypropan-2-yl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(3-hydroxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[(2S)-1-hydroxybut-3-en-2-yl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(4-hydroxybutyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(3-amino-3-oxopropyl)carbamoyl](4-cyanobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[3-(acetylamino)-2-methylpropyl]carbamoyl}(4-cyanobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(dimethylamino)-3-oxopropyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(3-ethoxy-2-hydroxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(diethylamino)propyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[2-(acetylamino)ethyl]carbamoyl}(4-cyanobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[2-(diethylamino)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)({2-[(2-methylpropanoyl)amino]ethyl}carbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[(2R)-1-hydroxybut-3-en-2-yl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(3-hydroxyazetidin-1-yl)propyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • ethyl N-[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]-beta-alaninate;
  • ethyl 4-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoate;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoate;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-4-methylpentanoate;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2,2-dimethylpropanoate;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}cyclobutanecarboxylic acid;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2-methylpropanoate;
  • 2-{(4-cyanobenzyl)[(3-methoxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoic acid;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-4-methylpentanoic acid;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2,2-dimethylpropanoic acid;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2-methylpropanoic acid;
  • N-[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]-beta-alanine;
  • 4-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoic acid;
  • 2-{[2-(5-chloropyridin-2-yl)ethyl][(2-methoxyethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-([2-(5-chloropyridin-2-yl)ethyl]{[2-(propan-2-yloxy)ethyl]carbamoyl}amino)-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide; and pharmaceutically acceptable salts thereof.

Embodiments of Formula (VI)

In another aspect, the present invention provides compounds of Formula (VI)

and pharmaceutically acceptable salts thereof; wherein each R6 is as described herein for Formula (I), and RX is as described herein for substituents on R8 when R8 is aryl.

One embodiment of this invention pertains to compounds of Formula (VI) or pharmaceutically acceptable salts thereof;

wherein

R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, SR8, S(O)R8, SO2R8, C(O)R8, CO(O)R8, OC(O)R8, OC(O)OR8, NH2, NHR8, N(R8)2, NHC(O)R8, NR8C(O)R8, NHS(O)2R8, NR8S(O)2R8, NHC(O)OR8, NR8C(O)OR8, NHC(O)NH2, NHC(O)NHR8, NHC(O)N(R8)2, NR8C(O)NHR8, NR8C(O)N(R8)2, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)NHOH, C(O)NHOR8, C(O)NHSO2R8, C(O)NR8O2R8, SO2NH2, SO2NHR8, SO2N(R8)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR8, C(N)N(R8)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, SR9, S(O)R9, SO2R9, C(O)R9, CO(O)R9, OC(O)R9, OC(O)OR9, NH2, NHR9, N(R9)2, NHC(O)R9, NR9C(O)R9, NHS(O)2R9, NR9S(O)2R9, NHC(O)OR9, NR9C(O)OR9, NHC(O)NH2, NHC(O)NHR9, NHC(O)N(R9)2, NR9C(O)NHR9, NR9C(O)N(R9)2, C(O)NH2, C(O)NHR9, C(O)N(R9)2, C(O)NHOH, C(O)NHOR9, C(O)NHSO2R9, C(O)NR9SO2R9, SO2NH2, SO2NHR9, SO2N(R9)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR9, C(N)N(R9)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R10, OR10, SR10, S(O)R10, SO2R10, C(O)R10, CO(O)R10, OC(O)R10, OC(O)OR10, NH2, NHR10, N(R10)2, NHC(O)R10, NR10C(O)R10, NHS(O)2R10, NR10S(O)2R10, NHC(O)OR10, NR10C(O)OR10, NHC(O)NH2, NHC(O)NHR10, NHC(O)N(R10)2, NR10C(O)NHR10, NR10C(O)N(R7)2, C(O)NH2, C(O)NHR10, C(O)N(R10)2, C(O)NHOH, C(O)NHOR10, C(O)NHSO2R10, C(O)NR10SO2R10, SO2NH2, SO2NHR10, SO2N(R10)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR10, C(N)N(R10)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, SR11, S(O)R11, SO2R11, C(O)R11, CO(O)R11, OC(O)R11, OC(O)OR11, NH2, NHR11, N(R11)2, NHC(O)R11, NR11C(O)R11, NHS(O)2R11, NR11S(O)2R11, NHC(O)OR11, NR11C(O)OR11, NHC(O)NH2, NHC(O)NHR11, NHC(O)N(R11)2, NR11C(O)NHR11, NR11C(O)N(R11)2, C(O)NH2, C(O)NHR11, C(O)N(R11)2, C(O)NHOH, C(O)NHOR11, C(O)NHSO2R11, C(O)NR11SO2R11, SO2NH2, SO2NHR11, SO2N(R11)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR11, C(N)N(R11)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

Rx is independently selected from the group consisting of R11, OR11, SR11, S(O)R11, SO2R11, C(O)R11, CO(O)R11, OC(O)R11, OC(O)OR11, NH2, NHR11, N(R11)2, NHC(O)R11, NR11C(O)R11, NHS(O)2R11, NR11S(O)2R11, NHC(O)OR11, NR11C(O)OR11, NHC(O)NH2, NHC(O)NHR11, NHC(O)N(R11)2, NR11C(O)NHR11, NR11C(O)N(R11)2, C(O)NH2, C(O)NHR11, C(O)N(R11)2, C(O)NHOH, C(O)NHOR11, C(O)NHSO2R11, C(O)NR11SO2R11, SO2NH2, SO2NHR11, SO2N(R11)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR11, C(N)N(R11)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R9, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R12, OR12, SR12, S(O)R12, SO2R12, C(O)R12, CO(O)R12, OC(O)R12, OC(O)OR12, NH2, NHR12, N(R12)2, NHC(O)R12, NR12C(O)R12, NHS(O)2R12, NR12S(O)2R2, NHC(O)OR12, NR12C(O)OR12, NHC(O)NH2, NHC(O)NHR12, NHC(O)N(R12)2, NR12C(O)NHR12, NR12C(O)N(R12)2, C(O)NH2, C(O)NHR12, C(O)N(R12)2, C(O)NHOH, C(O)NHOR12, C(O)NHSO2R12, C(O)NR12SO2R12, SO2NH2, SO2NHR12, SO2N(R12)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR12, C(N)N(R12)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R13, OR13, SR13, S(O)R13, SO2R13, C(O)R13, CO(O)R13, OC(O)R13, OC(O)OR13, NH2, NHR13, N(R13)2, NHC(O)R13, NR13C(O)R13, NHS(O)2R13, NR13S(O)2R13, NHC(O)OR13, NR13C(O)OR13, NHC(O)NH2, NHC(O)NHR13, NHC(O)N(R13)2, NR13C(O)NHR13, NR13C(O)N(R13)2, C(O)NH2, C(O)NHR13, C(O)N(R13)2, C(O)NHOH, C(O)NHOR13, C(O)NHSO2R13, C(O)NR13SO2R13, SO2NH2, SO2NHR13, SO2N(R13)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR13, C(N)N(R13)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;

R10, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6 haloalkyl, and C1-6 hydroxyalkyl;

R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I;

R12, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; and

R13, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl; wherein the C1-6alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R13 are each independently optionally substituted with one or more substituents independently selected from the group consisting of alkoxy, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In one embodiment of Formula (IV), R6 is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, SR8, S(O)R8, SO2R8, C(O)R8, CO(O)R8, OC(O)R8, OC(O)OR8, NH2, NHR8, N(R8)2, NHC(O)R8, NR8C(O)R8, NHS(O)2R8, NR8S(O)2R8, NHC(O)OR8, NR8C(O)OR8, NHC(O)NH2, NHC(O)NHR8, NHC(O)N(R8)2, NR8C(O)NHR8, NR8C(O)N(R8)2, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)NHOH, C(O)NHOR8, C(O)NHSO2R8, C(O)NR8O2R8, SO2NH2, SO2NHR8, SO2N(R8)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR8, C(N)N(R8)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, SR9, S(O)R9, SO2R9, C(O)R9, CO(O)R9, OC(O)R9, OC(O)OR9, NH2, NHR9, N(R9)2, NHC(O)R9, NR9C(O)R9, NHS(O)2R9, NR9S(O)2R9, NHC(O)OR9, NR9C(O)OR9, NHC(O)NH2, NHC(O)NHR9, NHC(O)N(R9)2, NR9C(O)NHR9, NR9C(O)N(R9)2, C(O)NH2, C(O)NHR9, C(O)N(R9)2, C(O)NHOH, C(O)NHOR9, C(O)NHSO2R9, C(O)NR9SO2R9, SO2NH2, SO2NHR9, SO2N(R9)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR9, C(N)N(R9)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (IV), R6 is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, heterocycloalkyl, heteroaryl, and cycloalkyl; wherein the C1-6 alkyl, and C2-6 alkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, C(O)R8, CO(O)R8, OC(O)R8, N(R8)2, NHC(O)R8, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)OH, and OH; wherein the aryl, heterocycloalkyl, heteroaryl, and cycloalkyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, C(O)NH2, C(O)OH, OH, CN, F, Cl, Br and I.

In one embodiment of Formula (IV), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R10, OR10, SR10, S(O)R10, SO2R10, C(O)R10, CO(O)R10, OC(O)R10, OC(O)OR10, NH2, NHR10, N(R7)2, NHC(O)R10, NR10C(O)R10, NHS(O)2R10, NR10S(O)2R10, NHC(O)OR10, NR10C(O)OR10, NHC(O)NH2, NHC(O)NHR10, NHC(O)N(R7)2, NR10C(O)NHR10, NR10C(O)N(R10)2, C(O)NH2, C(O)NHR10, C(O)N(R10)2, C(O)NHOH, C(O)NHOR10, C(O)NHSO2R10, C(O)NR10SO2R10, SO2NH2, SO2NHR10, SO2N(R10)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR10, C(N)N(R10)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, SR11, S(O)R11, SO2R11, C(O)R11, CO(O)R11, OC(O)R11, OC(O)OR11, NH2, NHR11, N(R11)2, NHC(O)R11, NR11C(O)R11, NHS(O)2R11, NR11S(O)2R11, NHC(O)OR11, NR11C(O)OR11, NHC(O)NH2, NHC(O)NHR11, NHC(O)N(R11)2, NR11C(O)NHR11, NR11C(O)N(R11)2, C(O)NH2, C(O)NHR11, C(O)N(R11)2, C(O)NHOH, C(O)NHOR11, C(O)NHSO2R11, C(O)NR11SO2R11, SO2NH2, SO2NHR11, SO2N(R11)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR11, C(N)N(R11)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (IV), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, and cycloalkyl; wherein the C1-6 alkyl and C2-6 alkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of OH, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, and heteroaryl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, NH2, N(R11)2, C(O)H, OH, CN, F, Cl, Br and I.

In one embodiment of Formula (IV), R9, at each occurrence, is independently selected from the group consisting of C1-6alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R12, OR12, SR2, S(O)R12, SO2R12, C(O)R12, CO(O)R12, OC(O)R12, OC(O)OR12, NH2, NHR12, N(R12)2, NHC(O)R12, NR12C(O)R12, NHS(O)2R12, NR12S(O)2R12, NHC(O)OR12, NR12C(O)OR12, NHC(O)NH2, NHC(O)NHR12, NHC(O)N(R12)2, NR12C(O)NHR12, NR12C(O)N(R12)2, C(O)NH2, C(O)NHR12, C(O)N(R12)2, C(O)NHOH, C(O)NHOR12, C(O)NHSO2R12, C(O)NR12SO2R12, SO2NH2, SO2NHR12, SO2N(R12)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR12, C(N)N(R12)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R13, OR13, SR13, S(O)R13, SO2R13, C(O)R13, CO(O)R13, OC(O)R13, OC(O)OR13, NH2, NHR13, N(R13)2, NHC(O)R13, NR13C(O)R13, NHS(O)2R13, NR13S(O)2R13, NHC(O)OR13, NR13C(O)OR13, NHC(O)NH2, NHC(O)NHR13, NHC(O)N(R13)2, NR13C(O)NHR13, NR13C(O)N(R13)2, C(O)NH2, C(O)NHR13, C(O)N(R13)2, C(O)NHOH, C(O)NHOR13, C(O)NHSO2R13, C(O)NR13SO2R13, SO2NH2, SO2NHR13, SO2N(R13)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR13, C(N)N(R13)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (IV), R9, at each occurrence, is C1-6 alkyl.

In one embodiment of Formula (IV), R10, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6 haloalkyl, and C1-6 hydroxyalkyl.

In one embodiment of Formula (IV), R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I. In another embodiment of Formula (IV), R13, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, aryl, and heteroaryl; wherein the C1-6 alkyl and C2-6 alkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, cycloalkyl, OH, F, Cl, Br and I.

In one embodiment of Formula (IV), R12, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In one embodiment of Formula (IV), R13, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R13 are each independently optionally substituted with one or more substituents independently selected from the group consisting of alkoxy, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

In one embodiment of Formula (IV), R6 is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, heterocycloalkyl, and cycloalkyl; wherein the C1-6 alkyl and C2-6 alkenyl represented by R6 are independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, C(O)OR8, N(R8)2, NHC(O)R8, C(O)NH2, C(O)N(R8)2, C(O)OH, and OH; wherein the heterocycloalkyl, and cycloalkyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C(O)OH, F, Cl, Br and I. In another embodiment of Formula (IV), R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl and heterocycloalkyl; wherein the C1-6 alkyl is independently optionally substituted with one or more OH; wherein the heterocycloalkyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of OH, F, Cl, Br and I.

In one embodiment of Formula (IV), Rx is selected from the group consisting of CN, F, Cl, Br and I. In another embodiment of Formula (IV), Rx is selected from the group consisting of F, Cl, Br and I. In another embodiment of Formula (IV), Rx is CN. In another embodiment of Formula (IV), Rx is F.

Still another embodiment pertains to compounds having Formula (VI), which include

  • 2-[(4-fluorobenzyl)(propan-2-ylcarbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(3-methylbutyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-methylpropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-propoxyethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl) [(tetrahydrofuran-2-ylmethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(1-methoxypropan-2-yl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(tetrahydro-2H-pyran-2-ylmethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-methoxyethyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(2-ethoxyethyl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(1-methoxybutan-2-yl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(1,3-dioxolan-2-ylmethyl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl) {[2-(propan-2-yloxy)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(1,4-dioxan-2-ylmethyl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(1,3-dimethoxypropan-2-yl)carbamoyl](4-fluorobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-fluorobenzyl)[(2-methoxybutyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(tetrahydrofuran-3-ylcarbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-fluorobenzyl)(tetrahydro-2H-pyran-3-ylcarbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[2-(propan-2-yloxy)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(2-methoxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[2-(2-hydroxyethoxy)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(propan-2-yloxy)propyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(3-hydroxy-2,2-dimethylpropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(2-hydroxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(1-hydroxypropan-2-yl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(3-hydroxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[(2S)-1-hydroxybut-3-en-2-yl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(4-hydroxybutyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{[(3-amino-3-oxopropyl)carbamoyl](4-cyanobenzyl)amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[3-(acetylamino)-2-methylpropyl]carbamoyl}(4-cyanobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(dimethylamino)-3-oxopropyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-{(4-cyanobenzyl)[(3-ethoxy-2-hydroxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(diethylamino)propyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[{[2-(acetylamino)ethyl]carbamoyl}(4-cyanobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[2-(diethylamino)ethyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl)({2-[(2-methylpropanoyl)amino]ethyl}carbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[(2R)-1-hydroxybut-3-en-2-yl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 2-[(4-cyanobenzyl) {[3-(3-hydroxyazetidin-1-yl)propyl]carbamoyl}amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • ethyl N-[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]-beta-alaninate;
  • ethyl 4-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoate;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoate;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-4-methylpentanoate;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2,2-dimethylpropanoate;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}cyclobutanecarboxylic acid;
  • ethyl 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2-methylpropanoate;
  • 2-{(4-cyanobenzyl)[(3-methoxypropyl)carbamoyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoic acid;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-4-methylpentanoic acid;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2,2-dimethylpropanoic acid;
  • 3-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}-2-methylpropanoic acid;
  • N-[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]-beta-alanine;
  • 4-{[(4-cyanobenzyl)(5-{[3-(1H-imidazol-1-yl)propyl]carbamoyl}-1,3-thiazol-2-yl)carbamoyl]amino}butanoic acid; and pharmaceutically acceptable salts thereof.

Pharmaceutical Compositions, Combination Therapies, Methods of Treatment, and Administration

Another embodiment comprises pharmaceutical compositions comprising a compound having Formula (I) and an excipient.

Still another embodiment comprises methods of treating cancer in a mammal comprising administering thereto a therapeutically acceptable amount of a compound having Formula (I).

Still another embodiment pertains to compositions for treating diseases during which NAMPT is expressed, said compositions comprising an excipient and a therapeutically effective amount of the compound having Formula (I).

Still another embodiment pertains to methods of treating disease in a patient during which NAMPT is expressed, said methods comprising administering to the patient a therapeutically effective amount of a compound having Formula (I).

Still another embodiment pertains to compositions for treating inflammatory and tissue repair disorders; particularly rheumatoid arthritis, inflammatory bowel disease, asthma and COPD (chronic obstructive pulmonary disease), osteoarthritis, osteoporosis and fibrotic diseases; dermatosis, including psoriasis, atopic dermatitis and ultra-violet induced skin damage; autoimmune diseases including systemic lupus erythematosis, multiple sclerosis, psoriatic arthritis, ankylosing spondylitis, tissue and organ rejection, Alzheimer's disease, stroke, athersclerosis, restenosis, diabetes, glomerulonephritis, cancer, particularly wherein the cancer is selected from breast, prostate, lung, colon, cervix, ovary, skin, CNS, bladder, pancreas, leukemia, lymphoma or Hodgkin's disease, cachexia, inflammation associated with infection and certain viral infections, including Acquired Immune Deficiency Syndrome (AIDS), adult respiratory distress syndrome, and ataxia telengiectasia, said compositions comprising an excipient and a therapeutically effective amount of the compound having Formula (I).

Still another embodiment pertains to methods of treating inflammatory and tissue repair disorders; particularly rheumatoid arthritis, inflammatory bowel disease, asthma and COPD (chronic obstructive pulmonary disease), osteoarthritis, osteoporosis and fibrotic diseases; dermatosis, including psoriasis, atopic dermatitis and ultra-violet induced skin damage; autoimmune diseases including systemic lupus erythematosis, multiple sclerosis, psoriatic arthritis, ankylosing spondylitis, tissue and organ rejection, Alzheimer's disease, stroke, athersclerosis, restenosis, diabetes, glomerulonephritis, cancer, particularly wherein the cancer is selected from breast, prostate, lung, colon, cervix, ovary, skin, CNS, bladder, pancreas, leukemia, lymphoma or Hodgkin's disease, cachexia, inflammation associated with infection and certain viral infections, including Acquired Immune Deficiency Syndrome (AIDS), adult respiratory distress syndrome, and ataxia telengiectasia in a patient, said methods comprising administering to the patient a therapeutically effective amount of a compound having Formula (I).

Still another embodiment pertains to compositions for treating diseases during which NAMPT is expressed, said compositions comprising an excipient and a therapeutically effective amount of the compound having Formula (I) and a therapeutically effective amount of one additional therapeutic agent or more than one additional therapeutic agent.

Still another embodiment pertains to methods of treating disease in a patient during which NAMPT is expressed, said methods comprising administering to the patient a therapeutically effective amount of a compound having Formula (I) and a therapeutically effective amount of one additional therapeutic agent or more than one additional therapeutic agent.

Still another embodiment pertains to compositions for treating inflammatory and tissue repair disorders; particularly rheumatoid arthritis, inflammatory bowel disease, asthma and COPD (chronic obstructive pulmonary disease), osteoarthritis, osteoporosis and fibrotic diseases; dermatosis, including psoriasis, atopic dermatitis and ultra-violet induced skin damage; autoimmune diseases including systemic lupus erythematosis, multiple sclerosis, psoriatic arthritis, ankylosing spondylitis, tissue and organ rejection, Alzheimer's disease, stroke, athersclerosis, restenosis, diabetes, glomerulonephritis, cancer, particularly wherein the cancer is selected from breast, prostate, lung, colon, cervix, ovary, skin, CNS, bladder, pancreas, leukemia, lymphoma or Hodgkin's disease, cachexia, inflammation associated with infection and certain viral infections, including Acquired Immune Deficiency Syndrome (AIDS), adult respiratory distress syndrome, and ataxia telengiectasia, said compositions comprising an excipient and a therapeutically effective amount of the compound having Formula (I) and a therapeutically effective amount of one additional therapeutic agent or more than one additional therapeutic agent.

Still another embodiment pertains to methods of treating inflammatory and tissue repair disorders; particularly rheumatoid arthritis, inflammatory bowel disease, asthma and COPD (chronic obstructive pulmonary disease), osteoarthritis, osteoporosis and fibrotic diseases; dermatosis, including psoriasis, atopic dermatitis and ultra-violet induced skin damage; autoimmune diseases including systemic lupus erythematosis, multiple sclerosis, psoriatic arthritis, ankylosing spondylitis, tissue and organ rejection, Alzheimer's disease, stroke, athersclerosis, restenosis, diabetes, glomerulonephritis, cancer, particularly wherein the cancer is selected from breast, prostate, lung, colon, cervix, ovary, skin, CNS, bladder, pancreas, leukemia, lymphoma or Hodgkin's disease, cachexia, inflammation associated with infection and certain viral infections, including Acquired Immune Deficiency Syndrome (AIDS), adult respiratory distress syndrome, and ataxia telengiectasia in a patient, said methods comprising administering to the patient a therapeutically effective amount of the compound having Formula (I) and a therapeutically effective amount of one additional therapeutic agent or more than one additional therapeutic agent.

Metabolites of compounds having Formula (I), produced by in vitro or in vivo metabolic processes, may also have utility for treating diseases associated with NAMPT.

Certain precursor compounds which may be metabolized in vitro or in vivo to form compounds having Formula (I) may also have utility for treating diseases associated with NAMPT.

Compounds having Formula (I) may exist as acid addition salts, basic addition salts or zwitterions. Salts of the compounds are prepared during isolation or following purification of the compounds. Acid addition salts of the compounds are those derived from the reaction of the compounds with an acid. For example, the acetate, adipate, alginate, bicarbonate, citrate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, camphorate, camphorsufonate, digluconate, formate, fumarate, glycerophosphate, glutamate, hemisulfate, heptanoate, hexanoate, hydrochloride, hydrobromide, hydroiodide, lactobionate, lactate, maleate, mesitylenesulfonate, methanesulfonate, naphthylenesulfonate, nicotinate, oxalate, pamoate, pectinate, persulfate, phosphate, picrate, propionate, succinate, tartrate, thiocyanate, trichloroacetic, trifluoroacetic, para-toluenesulfonate, and undecanoate salts of the compounds are contemplated as being embraced by this invention. Basic addition salts of the compounds are those derived from the reaction of the compounds with the hydroxide, carbonate or bicarbonate of cations such as lithium, sodium, potassium, calcium, and magnesium.

The compounds having Formula (I) may be administered, for example, bucally, ophthalmically, orally, osmotically, parenterally (intramuscularly, intraperitoneally intrasternally, intravenously, subcutaneously), rectally, topically, transdermally or vaginally.

Therapeutically effective amounts of compounds having Formula (I) depend on the recipient of the treatment, the disorder being treated and the severity thereof, the composition containing the compound, the time of administration, the route of administration, the duration of treatment, the compound potency, its rate of clearance and whether or not another drug is co-administered. The amount of a compound of this invention having Formula (I) used to make a composition to be administered daily to a patient in a single dose or in divided doses is from about 0.03 to about 200 mg/kg body weight. Single dose compositions contain these amounts or a combination of submultiples thereof.

Compounds having Formula (I) may be administered with or without an excipient. Excipients include, for example, encapsulating materials or additives such as absorption accelerators, antioxidants, binders, buffers, coating agents, coloring agents, diluents, disintegrating agents, emulsifiers, extenders, fillers, flavoring agents, humectants, lubricants, perfumes, preservatives, propellants, releasing agents, sterilizing agents, sweeteners, solubilizers, wetting agents and mixtures thereof.

Excipients for preparation of compositions comprising a compound having Formula (I) to be administered orally in solid dosage form include, for example, agar, alginic acid, aluminum hydroxide, benzyl alcohol, benzyl benzoate, 1,3-butylene glycol, carbomers, castor oil, cellulose, cellulose acetate, cocoa butter, corn starch, corn oil, cottonseed oil, cross-povidone, diglycerides, ethanol, ethyl cellulose, ethyl laureate, ethyl oleate, fatty acid esters, gelatin, germ oil, glucose, glycerol, groundnut oil, hydroxypropylmethyl cellulose, isopropanol, isotonic saline, lactose, magnesium hydroxide, magnesium stearate, malt, mannitol, monoglycerides, olive oil, peanut oil, potassium phosphate salts, potato starch, povidone, propylene glycol, Ringer's solution, safflower oil, sesame oil, sodium carboxymethyl cellulose, sodium phosphate salts, sodium lauryl sulfate, sodium sorbitol, soybean oil, stearic acids, stearyl fumarate, sucrose, surfactants, talc, tragacanth, tetrahydrofurfuryl alcohol, triglycerides, water, and mixtures thereof. Excipients for preparation of compositions comprising a compound of this invention having Formula (I) to be administered ophthalmically or orally in liquid dosage forms include, for example, 1,3-butylene glycol, castor oil, corn oil, cottonseed oil, ethanol, fatty acid esters of sorbitan, germ oil, groundnut oil, glycerol, isopropanol, olive oil, polyethylene glycols, propylene glycol, sesame oil, water and mixtures thereof. Excipients for preparation of compositions comprising a compound of this invention having Formula (I) to be administered osmotically include, for example, chlorofluorohydrocarbons, ethanol, water and mixtures thereof. Excipients for preparation of compositions comprising a compound of this invention having Formula (I) to be administered parenterally include, for example, 1,3-butanediol, castor oil, corn oil, cottonseed oil, dextrose, germ oil, groundnut oil, liposomes, oleic acid, olive oil, peanut oil, Ringer's solution, safflower oil, sesame oil, soybean oil, U.S.P. or isotonic sodium chloride solution, water and mixtures thereof. Excipients for preparation of compositions comprising a compound of this invention having Formula (I) to be administered rectally or vaginally include, for example, cocoa butter, polyethylene glycol, wax and mixtures thereof.

Compounds having Formula (I) are expected to be useful when used with alkylating agents, angiogenesis inhibitors, antibodies, antimetabolites, antimitotics, antiproliferatives, antivirals, aurora kinase inhibitors, apoptosis promoters (for example, Bcl-xL, Bcl-w and Bfl-1) inhibitors, activators of death receptor pathway, Bcr-Abl kinase inhibitors, BiTE (Bi-Specific T cell Engager) antibodies, antibody drug conjugates, biologic response modifiers, cyclin-dependent kinase inhibitors, cell cycle inhibitors, cyclooxygenase-2 inhibitors, DVDs, leukemia viral oncogene homolog (ErbB2) receptor inhibitors, growth factor inhibitors, heat shock protein (HSP)-90 inhibitors, histone deacetylase (HDAC) inhibitors, hormonal therapies, immunologicals, inhibitors of inhibitors of apoptosis proteins (IAPs), intercalating antibiotics, kinase inhibitors, kinesin inhibitors, Jak2 inhibitors, mammalian target of rapamycin inhibitors, microRNA's, mitogen-activated extracellular signal-regulated kinase inhibitors, multivalent binding proteins, non-steroidal anti-inflammatory drugs (NSAIDs), poly ADP (adenosine diphosphate)-ribose polymerase (PARP) inhibitors, platinum chemotherapeutics, polo-like kinase (Plk) inhibitors, phosphoinositide-3 kinase (PI3K) inhibitors, proteosome inhibitors, purine analogs, pyrimidine analogs, receptor tyrosine kinase inhibitors, retinoids/deltoids plant alkaloids, small inhibitory ribonucleic acids (siRNAs), topoisomerase inhibitors, ubiquitin ligase inhibitors, and the like, and in combination with one or more of these agents.

BiTE antibodies are bi-specific antibodies that direct T-cells to attack cancer cells by simultaneously binding the two cells. The T-cell then attacks the target cancer cell. Examples of BiTE antibodies include adecatumumab (Micromet MT201), blinatumomab (Micromet MT103) and the like. Without being limited by theory, one of the mechanisms by which T-cells elicit apoptosis of the target cancer cell is by exocytosis of cytolytic granule components, which include perforin and granzyme B.

SiRNAs are molecules having endogenous RNA bases or chemically modified nucleotides. The modifications do not abolish cellular activity, but rather impart increased stability and/or increased cellular potency. Examples of chemical modifications include phosphorothioate groups, 2′-deoxynucleotide, 2′-OCH3-containing ribonucleotides, 2′-F-ribonucleotides, 2′-methoxyethyl ribonucleotides, combinations thereof and the like. The siRNA can have varying lengths (e.g., 10-200 bps) and structures (e.g., hairpins, single/double strands, bulges, nicks/gaps, mismatches) and are processed in cells to provide active gene silencing. A double-stranded siRNA (dsRNA) can have the same number of nucleotides on each strand (blunt ends) or asymmetric ends (overhangs). The overhang of 1-2 nucleotides can be present on the sense and/or the antisense strand, as well as present on the 5′- and/or the 3′-ends of a given strand.

Multivalent binding proteins are binding proteins comprising two or more antigen binding sites. Multivalent binding proteins are engineered to have the three or more antigen binding sites and are generally not naturally occurring antibodies. The term “multispecific binding protein” means a binding protein capable of binding two or more related or unrelated targets. Dual variable domain (DVD) binding proteins are tetravalent or multivalent binding proteins binding proteins comprising two or more antigen binding sites. Such DVDs may be monospecific (i.e., capable of binding one antigen) or multispecific (i.e., capable of binding two or more antigens). DVD binding proteins comprising two heavy chain DVD polypeptides and two light chain DVD polypeptides are referred to as DVD Ig's. Each half of a DVD Ig comprises a heavy chain DVD polypeptide, a light chain DVD polypeptide, and two antigen binding sites. Each binding site comprises a heavy chain variable domain and a light chain variable domain with a total of 6 CDRs involved in antigen binding per antigen binding site.

Alkylating agents include altretamine, AMD-473, AP-5280, apaziquone, bendamustine, brostallicin, busulfan, carboquone, carmustine (BCNU), chlorambucil, CLORETAZINE® (laromustine, VNP 40101M), cyclophosphamide, decarbazine, estramustine, fotemustine, glufosfamide, ifosfamide, KW-2170, lomustine (CCNU), mafosfamide, melphalan, mitobronitol, mitolactol, nimustine, nitrogen mustard N-oxide, ranimustine, temozolomide, thiotepa, TREANDA® (bendamustine), treosulfan, trofosfamide and the like.

Angiogenesis inhibitors include endothelial-specific receptor tyrosine kinase (Tie-2) inhibitors, epidermal growth factor receptor (EGFR) inhibitors, insulin growth factor-2 receptor (IGFR-2) inhibitors, matrix metalloproteinase-2 (MMP-2) inhibitors, matrix metalloproteinase-9 (MMP-9) inhibitors, platelet-derived growth factor receptor (PDGFR) inhibitors, thrombospondin analogs, vascular endothelial growth factor receptor tyrosine kinase (VEGFR) inhibitors and the like.

Antimetabolites include ALIMTA® (pemetrexed disodium, LY231514, MTA), 5-azacitidine, XELODA® (capecitabine), carmofur, LEUSTAT® (cladribine), clofarabine, cytarabine, cytarabine ocfosfate, cytosine arabinoside, decitabine, deferoxamine, doxifluridine, eflornithine, EICAR (5-ethynyl-1-β-D-ribofuranosylimidazole-4-carboxamide), enocitabine, ethnylcytidine, fludarabine, 5-fluorouracil alone or in combination with leucovorin, GEMZAR® (gemcitabine), hydroxyurea, ALKERAN®(melphalan), mercaptopurine, 6-mercaptopurine riboside, methotrexate, mycophenolic acid, nelarabine, nolatrexed, ocfosfate, pelitrexol, pentostatin, raltitrexed, Ribavirin, triapine, trimetrexate, S-1, tiazofurin, tegafur, TS-1, vidarabine, UFT and the like.

Antivirals include ritonavir, hydroxychloroquine and the like.

Aurora kinase inhibitors include ABT-348, AZD-1152, MLN-8054, VX-680, Aurora A-specific kinase inhibitors, Aurora B-specific kinase inhibitors and pan-Aurora kinase inhibitors and the like.

Bcl-2 protein inhibitors include AT-101 ((−)gossypol), GENASENSE® (G3139 or oblimersen (Bcl-2-targeting antisense oligonucleotide)), IPI-194, IPI-565, N-(4-(4-((4′-chloro(1,1′-biphenyl)-2-yl)methyl)piperazin-1-yl)benzoyl)-4-(((1R)-3-(dimethylamino)-1-((phenylsulfanyl)methyl)propyl)amino)-3-nitrobenzenesulfonamide) (ABT-737), N-(4-(4-((2-(4-chlorophenyl)-5,5-dimethyl-1-cyclohex-1-en-1-yl)methyl)piperazin-1-yl)benzoyl)-4-(((1R)-3-(morpholin-4-yl)-1-((phenylsulfanyl)methyl)propyl)amino)-3-((trifluoromethyl)sulfonyl)benzenesulfonamide (ABT-263), GX-070 (obatoclax) and the like.

Bcr-Abl kinase inhibitors include DASATINIB® (BMS-354825), GLEEVEC® (imatinib) and the like.

CDK inhibitors include AZD-5438, BMI-1040, BMS-032, BMS-387, CVT-2584, flavopyridol, GPC-286199, MCS-5A, PD0332991, PHA-690509, seliciclib (CYC-202, R-roscovitine), ZK-304709 and the like.

COX-2 inhibitors include ABT-963, ARCOXIA® (etoricoxib), BEXTRA® (valdecoxib), BMS347070, CELEBREX® (celecoxib), COX-189 (lumiracoxib), CT-3, DERAMAXX® (deracoxib), JTE-522, 4-methyl-2-(3,4-dimethylphenyl)-1-(4-sulfamoylphenyl-1H-pyrrole), MK-663 (etoricoxib), NS-398, parecoxib, RS-57067, SC-58125, SD-8381, SVT-2016, S-2474, T-614, VIOXX® (rofecoxib) and the like.

EGFR inhibitors include ABX-EGF, anti-EGFR immunoliposomes, EGF-vaccine, EMD-7200, ERBITUX® (cetuximab), HR3, IgA antibodies, IRESSA® (gefitinib), TARCEVA® (erlotinib or OSI-774), TP-38, EGFR fusion protein, TYKERB® (lapatinib) and the like.

ErbB2 receptor inhibitors include CP-724-714, CI-1033 (canertinib), HERCEPTIN® (trastuzumab), TYKERB® (lapatinib), OMNITARG® (2C4, petuzumab), TAK-165, GW-572016 (ionafarnib), GW-282974, EKB-569, PI-166, dHER2 (HER2 vaccine), APC-8024 (HER-2 vaccine), anti-HER/2neu bispecific antibody, B7.her2IgG3, AS HER2 trifunctional bispecfic antibodies, mAB AR-209, mAB 2B-1 and the like.

Histone deacetylase inhibitors include depsipeptide, LAQ-824, MS-275, trapoxin, suberoylanilide hydroxamic acid (SAHA), TSA, valproic acid and the like.

HSP-90 inhibitors include 17-AAG-nab, 17-AAG, CNF-101, CNF-1010, CNF-2024, 17-DMAG, geldanamycin, IPI-504, KOS-953, MYCOGRAB® (human recombinant antibody to HSP-90), NCS-683664, PU24FC1, PU-3, radicicol, SNX-2112, STA-9090 VER49009 and the like.

Inhibitors of inhibitors of apoptosis proteins include HGS 1029, GDC-0145, GDC-0152, LCL-161, LBW-242 and the like.

Antibody drug conjugates include anti-CD22-MC-MMAF, anti-CD22-MC-MMAE, anti-CD22-MCC-DM1, CR-011-vcMMAE, PSMA-ADC, MEDI-547, SGN-19Am SGN-35, SGN-75 and the like

Activators of death receptor pathway include TRAIL, antibodies or other agents that target TRAIL or death receptors (e.g., DR4 and DR5) such as Apomab, conatumumab, ETR2-ST01, GDC0145 (lexatumumab), HGS-1029, LBY-135, PRO-1762 and trastuzumab.

Kinesin inhibitors include Eg5 inhibitors such as AZD4877, ARRY-520; CENPE inhibitors such as GSK923295A and the like.

JAK-2 inhibitors include CEP-701 (lesaurtinib), XL019 and INCB018424 and the like.

MEK inhibitors include ARRY-142886, ARRY-438162 PD-325901, PD-98059 and the like. mTOR inhibitors include AP-23573, CCI-779, everolimus, RAD-001, rapamycin, temsirolimus, ATP-competitive TORC1/TORC2 inhibitors, including PI-103, PP242, PP30, Torin 1 and the like.

Non-steroidal anti-inflammatory drugs include AMIGESIC® (salsalate), DOLOBID® (diflunisal), MOTRIN® (ibuprofen), ORUDIS® (ketoprofen), RELAFEN® (nabumetone), FELDENE® (piroxicam), ibuprofen cream, ALEVE® (naproxen) and NAPROSYN® (naproxen), VOLTAREN® (diclofenac), INDOCIN® (indomethacin), CLINORIL® (sulindac), TOLECTIN® (tolmetin), LODINE® (etodolac), TORADOL® (ketorolac), DAYPRO® (oxaprozin) and the like.

PDGFR inhibitors include C-451, CP-673, CP-868596 and the like.

Platinum chemotherapeutics include cisplatin, ELOXATIN® (oxaliplatin) eptaplatin, lobaplatin, nedaplatin, PARAPLATIN® (carboplatin), satraplatin, picoplatin and the like.

Polo-like kinase inhibitors include BI-2536 and the like.

Phosphoinositide-3 kinase (PI3K) inhibitors include wortmannin, LY294002, XL-147, CAL-120, ONC-21, AEZS-127, ETP-45658, PX-866, GDC-0941, BGT226, BEZ235, XL765 and the like.

Thrombospondin analogs include ABT-510, ABT-567, ABT-898, TSP-1 and the like.

VEGFR inhibitors include AVASTIN® (bevacizumab), ABT-869, AEE-788, ANGIOZYME™ (a ribozyme that inhibits angiogenesis (Ribozyme Pharmaceuticals (Boulder, Colo.) and Chiron, (Emeryville, Calif.)), axitinib (AG-13736), AZD-2171, CP-547,632, IM-862, MACUGEN (pegaptamib), NEXAVAR® (sorafenib, BAY43-9006), pazopanib (GW-786034), vatalanib (PTK-787, ZK-222584), SUTENT® (sunitinib, SU-11248), VEGF trap, ZACTIMA™ (vandetanib, ZD-6474) and the like.

Antibiotics include intercalating antibiotics aclarubicin, actinomycin D, amrubicin, annamycin, adriamycin, BLENOXANE® (bleomycin), daunorubicin, CAELYX® or MYOCET® (liposomal doxorubicin), elsamitrucin, epirbucin, glarbuicin, ZAVEDOS® (idarubicin), mitomycin C, nemorubicin, neocarzinostatin, peplomycin, pirarubicin, rebeccamycin, stimalamer, streptozocin, VALSTAR® (valrubicin), zinostatin and the like.

Topoisomerase inhibitors include aclarubicin, 9-aminocamptothecin, amonafide, amsacrine, becatecarin, belotecan, BN-80915, CAMPTOSAR® (irinotecan hydrochloride), camptothecin, CARDIOXANE® (dexrazoxine), diflomotecan, edotecarin, ELLENCE® or PHARMORUBICIN® (epirubicin), etoposide, exatecan, 10-hydroxycamptothecin, gimatecan, lurtotecan, mitoxantrone, orathecin, pirarbucin, pixantrone, rubitecan, sobuzoxane, SN-38, tafluposide, topotecan and the like.

Antibodies include AVASTIN® (bevacizumab), CD40-specific antibodies, chTNT-1/B, denosumab, ERBITUX® (cetuximab), HUMAX-CD4® (zanolimumab), IGF1R-specific antibodies, lintuzumab, PANOREX® (edrecolomab), RENCAREX® (WX G250), RITUXAN® (rituximab), ticilimumab, trastuzimab, CD20 antibodies types I and II and the like.

Hormonal therapies include ARIMIDEX® (anastrozole), AROMASIN® (exemestane), arzoxifene, CASODEX® (bicalutamide), CETROTIDE® (cetrorelix), degarelix, deslorelin, DESOPAN® (trilostane), dexamethasone, DROGENIL® (flutamide), EVISTA® (raloxifene), AFEMA™ (fadrozole), FARESTON® (toremifene), FASLODEX® (fulvestrant), FEMARA® (letrozole), formestane, glucocorticoids, HECTOROL® (doxercalciferol), RENAGEL® (sevelamer carbonate), lasofoxifene, leuprolide acetate, MEGACE® (megesterol), MIFEPREX® (mifepristone), NILANDRON™ (nilutamide), NOLVADEX® (tamoxifen citrate), PLENAXIS™ (abarelix), prednisone, PROPECIA® (finasteride), rilostane, SUPREFACT® (buserelin), TRELSTAR® (luteinizing hormone releasing hormone (LHRH)), VANTAS® (Histrelin implant), VETORYL® (trilostane or modrastane), ZOLADEX® (fosrelin, goserelin) and the like.

Deltoids and retinoids include seocalcitol (EB1089, CB1093), lexacalcitrol (KH1060), fenretinide, PANRETIN® (aliretinoin), ATRAGEN® (liposomal tretinoin), TARGRETIN® (bexarotene), LGD-1550 and the like.

PARP inhibitors include ABT-888 (veliparib), olaparib, KU-59436, AZD-2281, AG-014699, BSI-201, BGP-15, INO-1001, ONO-2231 and the like.

Plant alkaloids include, but are not limited to, vincristine, vinblastine, vindesine, vinorelbine and the like.

Proteasome inhibitors include VELCADE® (bortezomib), MG132, NPI-0052, PR-171 and the like.

Examples of immunologicals include interferons and other immune-enhancing agents. Interferons include interferon alpha, interferon alpha-2a, interferon alpha-2b, interferon beta, interferon gamma-1a, ACTIMMUNE® (interferon gamma-1b) or interferon gamma-n1, combinations thereof and the like. Other agents include ALFAFERONE®, (IFN-α), BAM-002 (oxidized glutathione), BEROMUN® (tasonermin), BEXXAR® (tositumomab), CAMPATH® (alemtuzumab), CTLA4 (cytotoxic lymphocyte antigen 4), decarbazine, denileukin, epratuzumab, GRANOCYTE® (lenograstim), lentinan, leukocyte alpha interferon, imiquimod, MDX-010 (anti-CTLA-4), melanoma vaccine, mitumomab, molgramostim, MYLOTARG™ (gemtuzumab ozogamicin), NEUPOGEN® (filgrastim), OncoVAC-CL, OVAREX® (oregovomab), pemtumomab (Y-muHMFG1), PROVENGE® (sipuleucel-T), sargaramostim, sizofilan, teceleukin, THERACYS® (Bacillus Calmette-Guerin), ubenimex, VIRULIZIN® (immunotherapeutic, Lorus Pharmaceuticals), Z-100 (Specific Substance of Maruyama (SSM)), WF-10 (Tetrachlorodecaoxide (TCDO)), PROLEUKIN® (aldesleukin), ZADAXIN® (thymalfasin), ZENAPAX® (daclizumab), ZEVALIN® (90Y-Ibritumomab tiuxetan) and the like.

Biological response modifiers are agents that modify defense mechanisms of living organisms or biological responses, such as survival, growth or differentiation of tissue cells to direct them to have anti-tumor activity and include krestin, lentinan, sizofiran, picibanil PF-3512676 (CpG-8954), ubenimex and the like.

Pyrimidine analogs include cytarabine (ara C or Arabinoside C), cytosine arabinoside, doxifluridine, FLUDARA® (fludarabine), 5-FU (5-fluorouracil), floxuridine, GEMZAR® (gemcitabine), TOMUDEX® (ratitrexed), TROXATYL™ (triacetyluridine troxacitabine) and the like.

Purine analogs include LANVIS® (thioguanine) and PURI-NETHOL® (mercaptopurine).

Antimitotic agents include batabulin, epothilone D (KOS-862), N-(2-((4-hydroxyphenyl)amino)pyridin-3-yl)-4-methoxybenzenesulfonamide, ixabepilone (BMS 247550), paclitaxel, TAXOTERE® (docetaxel), PNU100940 (109881), patupilone, XRP-9881 (larotaxel), vinflunine, ZK-EPO (synthetic epothilone) and the like.

Ubiquitin ligase inhibitors include MDM2 inhibitors, such as nutlins, NEDD8 inhibitors such as MLN4924 and the like.

Compounds of this invention can also be used as radiosensitizers that enhance the efficacy of radiotherapy. Examples of radiotherapy include external beam radiotherapy, teletherapy, brachytherapy and sealed, unsealed source radiotherapy and the like.

Additionally, compounds having Formula (I) may be combined with other chemotherapeutic agents such as ABRAXANE™ (ABI-007), ABT-100 (farnesyl transferase inhibitor), ADVEXIN® (Ad5CMV-p53 vaccine), ALTOCOR® or MEVACOR® (lovastatin), AMPLIGEN® (poly I:poly C12U, a synthetic RNA), APTOSYN® (exisulind), AREDIA® (pamidronic acid), arglabin, L-asparaginase, atamestane (1-methyl-3,17-dione-androsta-1,4-diene), AVAGE® (tazarotene), AVE-8062 (combreastatin derivative) BEC2 (mitumomab), cachectin or cachexin (tumor necrosis factor), canvaxin (vaccine), CEAVAC® (cancer vaccine), CELEUK® (celmoleukin), CEPLENE® (histamine dihydrochloride), CERVARIX® (human papillomavirus vaccine), CHOP® (C: CYTOXAN® (cyclophosphamide); H: ADRIAMYCIN® (hydroxydoxorubicin); O: Vincristine (ONCOVIN®); P: prednisone), CYPAT™ (cyproterone acetate), combrestatin A4P, DAB(389)EGF (catalytic and translocation domains of diphtheria toxin fused via a His-Ala linker to human epidermal growth factor) or TransMID-107R™ (diphtheria toxins), dacarbazine, dactinomycin, 5,6-dimethylxanthenone-4-acetic acid (DMXAA), eniluracil, EVIZON™ (squalamine lactate), DIMERICINE® (T4N5 liposome lotion), discodermolide, DX-8951f (exatecan mesylate), enzastaurin, EP0906 (epithilone B), GARDASIL® (quadrivalent human papillomavirus (Types 6, 11, 16, 18) recombinant vaccine), GASTRIMMUNE®, GENASENSE®, GMK (ganglioside conjugate vaccine), GVAX® (prostate cancer vaccine), halofuginone, histerelin, hydroxycarbamide, ibandronic acid, IGN-101, IL-13-PE38, IL-13-PE38QQR (cintredekin besudotox), IL-13-pseudomonas exotoxin, interferon-α, interferon-γ, JUNOVAN™ or MEPACT™ (mifamurtide), lonafarnib, 5,10-methylenetetrahydrofolate, miltefosine (hexadecylphosphocholine), NEOVASTAT®(AE-941), NEUTREXIN® (trimetrexate glucuronate), NIPENT® (pentostatin), ONCONASE® (a ribonuclease enzyme), ONCOPHAGE® (melanoma vaccine treatment), ONCOVAX® (IL-2 Vaccine), ORATHECIN™ (rubitecan), OSIDEM® (antibody-based cell drug), OVAREX® MAb (murine monoclonal antibody), paclitaxel, PANDIMEX™ (aglycone saponins from ginseng comprising 20(S)protopanaxadiol (aPPD) and 20(S)protopanaxatriol (aPPT)), panitumumab, PANVAC®-VF (investigational cancer vaccine), pegaspargase, PEG Interferon A, phenoxodiol, procarbazine, rebimastat, REMOVAB® (catumaxomab), REVLIMID® (lenalidomide), RSR13 (efaproxiral), SOMATULINE® LA (lanreotide), SORIATANE®(acitretin), staurosporine (Streptomyces staurospores), talabostat (PT100), TARGRETIN® (bexarotene), TAXOPREXIN® (DHA-paclitaxel), TELCYTA® (canfosfamide, TLK286), temilifene, TEMODAR® (temozolomide), tesmilifene, thalidomide, THERATOPE® (STn-KLH), thymitaq (2-amino-3,4-dihydro-6-methyl-4-oxo-5-(4-pyridylthio)quinazoline dihydrochloride), TNFERADE™ (adenovector: DNA carrier containing the gene for tumor necrosis factor-α), TRACLEER® or ZAVESCA® (bosentan), tretinoin (Retin-A), tetrandrine, TRISENOX® (arsenic trioxide), VIRULIZIN®, ukrain (derivative of alkaloids from the greater celandine plant), vitaxin (anti-alphavbeta3 antibody), XCYTRIN® (motexafin gadolinium), XINLAY™ (atrasentan), XYOTAX™ (paclitaxel poliglumex), YONDELIS® (trabectedin), ZD-6126, ZINECARD® (dexrazoxane), ZOMETA® (zolendronic acid), zorubicin and the like.

Data

Determination of the utility of compounds having Formula (I) as binders to and inhibitors of NAMPT was performed using Time-Resolved Fluorescence Resonance Energy Transfer (TR-FRET) binding assays.

Time-Resolved Fluorescence Resonance Energy Transfer (TR-FRET) Binding Assay of NAMPT

Test compounds were serially diluted (typically 11 half log dilutions) in neat DMSO to 50× final concentrations prior to dilution with assay buffer (50 mM HEPES (NaOH), pH 7.5, 100 mM NaCl, 10 mM MgCl2, 1 mM DTT, 1% Glycerol) to 3× and 6% DMSO. Six L were transferred to 384-well low-volume plates (Owens Corning #3673). To this, 12 L of a 1.5× solution containing enzyme, probe and antibody were added. Final concentrations in the 18 L reactions were 1× assay buffer, 2% DMSO, 6.8 nM NAMPT (human, recombinant, C-terminally His-tagged), 200 nM probe (a potent nicotinamide-competitive inhibitor conjugated to Oregon Green 488) and 1 nM Tb-anti-His antibody (Invitrogen #PV5895). Reactions were equilibrated at room temperature for 3 hours prior to reading on an Envision multi-label plate reader (Perkin Elmer; Ex=337 nm, Em=520 and 495 nm). Time-resolved FRET ratios (Em520/Em495) were normalized to controls, plotted as a function of compound concentration and fit with the four-parameter logistic equation to determine IC50s.

Time-Resolved Fluorescence Resonance Energy Transfer (TR-FRET) Binding Assay of NAMPT with PRPP

Compound handling and data processing were identical to the assay in the absence of substrates (above). Final concentrations were 1× assay buffer, 2% DMSO, 2 nM NAMPT, 2 nM probe, 1 nM Tb-anti-His antibody (Invitrogen #PV5895), 200 M PRPP and 2.5 mM ATP. Reactions were equilibrated for 16 hours prior to measurement to allow for potential enzymatic modification of test compounds.

Table 1 shows the utility of compounds having Formula I to functionally inhibit NAMPT.

TABLE 1 TR-FRET Binding - TR-FRET IC50 (with Binding - PRPP) Example IC50 (μM) (μM) 1 0.0638 nd 2 7.56 0.00429 3 12.5 0.0715 4 1.22 0.000548 5 0.72 0.000461 6 nd nd 7 1.61 0.486 8 3.16 0.29 9 12.5 0.641 10 0.281 0.0196 11 0.476 0.00047 12 0.303 0.000241 13 1.75 0.000403 14 12.5 0.338 15 3.82 0.0921 16 4.72 0.217 17 12.5 1.22 18 4.82 0.814 19 12.5 12.5 20 12.5 12.5 21 0.996 0.505 22 0.384 0.0602 23 nd nd 24 4.14 0.000682 25 1.63 0.0014 26 12.5 0.00121 27 >10 0.000632 28 7.02 0.000833 29 >10 0.00216 30 >10 0.00229 31 3.6 0.000893 32 >10 0.00133 33 8.95 0.00122 34 7.57 0.000502 35 >10 0.00318 36 2.42 0.000725 37 4.81 0.000531 38 2.69 0.00135 39 2.39 0.000938 40 2.2 0.00199 41 8.5 0.0297 42 >10 0.0246 43 8.11 0.000709 44 >10 0.00777 45 0.611 0.000206 46 9.52 0.0022 47 nd nd 48 0.807 0.000701 49 1.69 0.00107 50 1.18 0.00252 51 >10 0.00494 52 1.01 0.000881 53 2.53 0.32 54 2.11 0.0056 55 >10 3.18 56 6.07 0.000719 57 >10 1.16 58 1.72 0.807 59 >10 0.266 60 >10 0.00497 61 1.9 0.00178 62 0.81 0.00108 63 2.25 0.000693 64 1.85 0.00297 65 >10 0.00537 66 >10 0.00242 67 >10 0.00353 68 >10 0.00468 69 >10 0.00398 70 >10 0.00508 71 0.533 0.0007 72 >10 0.00399 73 >10 0.00704 74 nd nd 75 nd nd 76 nd nd 77 0.0956 0.000774 78 2.9 0.000969 79 6.58 0.00277 80 8.02 0.00137 81 5.28 0.00178 82 7.54 0.00172 83 2.89 0.000998 84 3.2 0.00172 85 nd nd 86 >10 0.00266 87 2.26 0.00126 88 >10 0.000602 89 5.83 0.00198 90 >10 0.00225 91 8.69 0.000543 92 >10 0.000868 93 >10 0.0166 94 2.87 0.00122 95 3.89 0.0151 96 4.19 0.00335 97 >10 0.00589 98 1.5 0.00147 99 3.56 0.0015 100 nd nd 101 5.62 0.00284 102 0.306 0.00216 103 0.709 0.00306 104 0.445 0.00131 105 nd nd 106 1.93 0.0018 107 0.814 0.00224 108 1.45 0.00161 109 >10 0.00374 110 >10 0.0232 111 >10 0.00587 112 3.68 0.00208 113 4.99 0.00676 114 1.99 0.00231 115 1.42 0.0036 116 nd nd 117 1.25 0.00302 118 nd nd 119 4.57 0.00189 120 3.78 0.00229 121 >10 0.00925 122 >10 0.00431 123 3.82 0.000631 124 3.52 0.000624 125 >10 0.000712 126 4.18 0.0013 127 3.18 0.000533 128 >10 0.000727 129 >10 0.00116 130 >10 0.00111 131 4.78 0.000743 132 4.85 0.00102 133 0.0589 0.000527 134 0.2 0.000617 135 0.0937 0.000169 136 0.0244 0.000174 137 0.0402 0.000236 138 0.0555 0.000541 139 0.0561 0.000251 140 >10 0.0223 141 >10 0.0231 142 6.04 0.0169 143 >10 0.0137 144 >10 0.0332 145 >10 0.107 146 >10 0.098 147 >10 0.0719 148 >10 0.0606 149 >10 0.0942 150 0.252 0.00021 151 0.219 0.000412 152 0.768 0.000232 153 1.43 0.000286 154 0.23 0.000518 155 0.669 0.000254 156 nd nd 157 nd nd 158 nd nd 159 8.23 0.291 160 >10 0.195 161 >10 0.215 162 3.33 0.187 163 6.8 0.171 164 >10 0.583 165 0.34 0.0991 166 >10 0.63 167 nd nd 168 >10 1.39 169 8.45 0.266 170 nd nd 171 8.79 0.0321 172 >10 0.153 173 0.707 0.00233 174 0.334 0.000714 175 1.15 0.0006 176 7.36 0.000365 177 4.62 0.000653 178 6.97 0.000813 179 9.8 0.000492 180 7.71 0.000333 181 >10 0.000556 182 2.59 0.000264 183 2.94 0.000281 184 0.763 0.000285 185 0.633 0.000476 186 1.1 0.00123 187 3.21 0.000216 188 0.356 0.000195 189 4.7 0.000586 190 2.61 0.000606 191 >10 0.000265 192 >10 0.000262 193 6.06 0.000755 194 7.25 0.00112 195 >10 0.000338 196 7.01 0.000538 197 9.21 0.000251 198 2.61 0.000633 199 >10 0.000493 200 >10 0.000747 201 >10 0.000457 202 4.99 0.000405 203 >10 0.0136 204 3.73 0.00146 205 0.739 0.000177 206 5.63 0.000633 207 3.86 0.000331 208 2.89 0.00025 209 6.7 0.000245 210 2.74 0.000192 211 nd nd 212 5.71 0.00103 213 9.86 0.000411 nd = no data

Compounds which inhibit NAMPT are useful for treating diseases in which activation of NF-KB is implicated. Such methods are useful in the treatment of a variety of diseases including inflammatory and tissue repair disorders; particularly rheumatoid arthritis, inflammatory bowel disease, asthma and COPD (chronic obstructive pulmonary disease), osteoarthritis, osteoporosis and fibrotic diseases; dermatosis, including psoriasis, atopic dermatitis and ultra-violet induced skin damage; autoimmune diseases including systemic lupus erythematosis, multiple sclerosis, psoriatic arthritis, ankylosing spondylitis, tissue and organ rejection, Alzheimer's disease, stroke, athersclerosis, restenosis, diabetes, glomerulonephritis, cancer, particularly wherein the cancer is selected from breast, prostate, lung, colon, cervix, ovary, skin, CNS, bladder, pancreas, leukaemia, lymphoma or Hodgkin's disease, cachexia, inflammation associated with infection and certain viral infections, including Acquired Immune Deficiency Syndrome (AIDS), adult respiratory distress syndrome, and ataxia telengiectasia.

Involvement of NAMPT in the treatment of cancer is described in WO 97/48696. Involvement of NAMPT in immuno-supression is described in WO 97/48397. Involvement of NAMPT for the treatment of diseases involving angiogenesis is described in WO 2003/80054. Involvement of NAMPT for the treatment of rheumatoid arthritis and septic shock is described in WO 2008/025857. Involvement of NAMPT for the prophlaxis and treatment of ischaemia is described in WO 2009/109610.

Cancers include, but are not limited to, hematologic and solid tumor types such as acoustic neuroma, acute leukemia, acute lymphoblastic leukemia, acute myelogenous leukemia (monocytic, myeloblastic, adenocarcinoma, angiosarcoma, astrocytoma, myelomonocytic and promyelocytic), acute t-cell leukemia, basal cell carcinoma, bile duct carcinoma, bladder cancer, brain cancer, breast cancer (including estrogen-receptor positive breast cancer), bronchogenic carcinoma, Burkitt's lymphoma, cervical cancer, chondrosarcoma, chordoma, choriocarcinoma, chronic leukemia, chronic lymphocytic leukemia, chronic myelocytic (granulocytic) leukemia, chronic myelogenous leukemia, colon cancer, colorectal cancer, craniopharyngioma, cystadenocarcinoma, dysproliferative changes (dysplasias and metaplasias), embryonal carcinoma, endometrial cancer, endotheliosarcoma, ependymoma, epithelial carcinoma, erythroleukemia, esophageal cancer, estrogen-receptor positive breast cancer, essential thrombocythemia, Ewing's tumor, fibrosarcoma, gastric carcinoma, germ cell testicular cancer, gestational trophobalstic disease, glioblastoma, head and neck cancer, heavy chain disease, hemangioblastoma, hepatoma, hepatocellular cancer, hormone insensitive prostate cancer, leiomyosarcoma, liposarcoma, lung cancer (including small cell lung cancer and non-small cell lung cancer), lymphangioendothelio-sarcoma, lymphangiosarcoma, lymphoblastic leukemia, lymphoma (lymphoma, including diffuse large B-cell lymphoma, follicular lymphoma, Hodgkin's lymphoma and non-Hodgkin's lymphoma), malignancies and hyperproliferative disorders of the bladder, breast, colon, lung, ovaries, pancreas, prostate, skin and uterus, lymphoid malignancies of T-cell or B-cell origin, leukemia, medullary carcinoma, medulloblastoma, melanoma, meningioma, mesothelioma, multiple myeloma, myelogenous leukemia, myeloma, myxosarcoma, neuroblastoma, oligodendroglioma, oral cancer, osteogenic sarcoma, ovarian cancer, pancreatic cancer, papillary adenocarcinomas, papillary carcinoma, peripheral T-cell lymphoma, pinealoma, polycythemia vera, prostate cancer (including hormone-insensitive (refractory) prostate cancer), rectal cancer, renal cell carcinoma, retinoblastoma, rhabdomyosarcoma, sarcoma, sebaceous gland carcinoma, seminoma, skin cancer, small cell lung carcinoma, solid tumors (carcinomas and sarcomas), stomach cancer, squamous cell carcinoma, synovioma, sweat gland carcinoma, testicular cancer (including germ cell testicular cancer), thyroid cancer, Waldenstrom's macroglobulinemia, testicular tumors, uterine cancer, Wilms' tumor and the like.

Schemes and Experimentals

The following abbreviations have the meanings indicated. ADDP means 1,1′-(azodicarbonyl)dipiperidine; AD-mix-β means a mixture of (DHQD)2PHAL, K3Fe(CN)6, K2CO3, and K2SO4; 9-BBN means 9-borabicyclo(3.3.1)nonane; Boc means tert-butoxycarbonyl; (DHQD)2PHAL means hydroquinidine 1,4-phthalazinediyl diethyl ether; DBU means 1,8-diazabicyclo[5.4.0]undec-7-ene; DIBAL means diisobutylaluminum hydride; DIEA means diisopropylethylamine; DMAP means N,N-dimethylaminopyridine; DMF means N,N-dimethylformamide; dmpe means 1,2-bis(dimethylphosphino)ethane; DMSO means dimethylsulfoxide; dppb means 1,4-bis(diphenylphosphino)-butane; dppe means 1,2-bis(diphenylphosphino)ethane; dppf means 1,1′-bis(diphenylphosphino)ferrocene; dppm means 1,1-bis(diphenylphosphino)methane; EDAC HCl means 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; Fmoc means fluorenylmethoxycarbonyl; HATU means O-(7-azabenzotriazol-1-yl)-N,N′N′N′-tetramethyluronium hexafluorophosphate; HMPA means hexamethylphosphoramide; IPA means isopropyl alcohol; MP-BH3 means macroporous triethylammonium methylpolystyrene cyanoborohydride; TEA means triethylamine; TFA means trifluoroacetic acid; THF means tetrahydrofuran; NCS means N-chlorosuccinimide; NMM means N-methylmorpholine; NMP means N-methylpyrrolidine; PPh3 means triphenylphosphine.

The following schemes are presented to provide what is believed to be the most useful and readily understood description of procedures and conceptual aspects of this invention. Compounds of this invention may be made by synthetic chemical processes, examples of which are shown herein. It is meant to be understood that the order of the steps in the processes may be varied, that reagents, solvents and reaction conditions may be substituted for those specifically mentioned, and that vulnerable moieties may be protected and deprotected, as necessary.

Schemes

As shown in Scheme 1, 2-bromothiazole-5-carboxylic acid can be coupled with a suitable amine of formula (1), wherein R3, R4, and R5 are as described herein, under reaction conditions known to those skilled in the art and readily available in the literature, to provide compounds of formula (2). Compounds of formula (2) can be reacted with suitable amines of formula (3), wherein R6 is as described herein, to provide compounds of formula (4). The reaction is typically performed at an elevated temperature in a solvent such as but not limited to acetonitrile. Compounds of formula (6), which are representative of compounds of Formula (I), can be prepared by reacting compounds of formula (4) with a suitable compound of formula (5), wherein R6 as described herein. The reaction is typically performed in a suitable solvent such as but not limited to dichloromethane at ambient temperature in the presence of a base such as but not limited to pyridine.

Compounds of formula (4), which can be prepared as described in Scheme 1, can be reacted with bis(2,5-dioxopyrrolidin-1-yl)carbonate at an elevated temperature in the presence of a base such as but not limited to pyridine, followed by the addition of a base such as but not limited to N,N-diisopropylethylamine, and an amine of formula (3) to provide compounds of formula (6) which are representative of the compounds of Formula (I).

As shown in Scheme 3, compounds of formula (4), which can be prepared as described in Scheme 1, can be reacted with a suitable alkyl halide of formula (7), wherein X is an appropriate halide and R6 is as described herein, to provide compounds of formula (8), which are representative of the compounds of Formula (I). The reaction is typically performed at an elevated temperature in a suitable solvent such as but not limited to acetonitrile, and may involve the use of microwave heating.

Compounds of formula (4), which can be prepared as described in Scheme 1, can be reacted with compounds of formula (9), wherein R6 is as described herein, in the presence of a base such as but not limited to N, N-diisopropylethylamine, to provide compounds of formula (10), which are representative of the compounds of Formula (I). The reaction is typically performed at an elevated temperature in a suitable solvent such as but not limited to dimethylsulfoxide, methanol, or mixtures thereof.

As shown in Scheme 5, chloroacetyl bromide can be reacted with compounds of formula (4), which can be prepared as described in Scheme 5, in the presence of a base such as but not limited to pyridine, at a reduced temperature followed by reaction with a suitable amine of formula (11), wherein each R8 is as described herein, at an elevated temperature, to provide compounds of formula (12). The reaction is typically performed in a solvent such as but not limited to dichloromethane.

As shown in Scheme 6, compounds of formula (2), which can be prepared as described in Scheme 1, can be coupled with a suitable amine of formula (13), wherein R1 and R2 taken together with the N to which they are attached form a heterocycloalkyl or heterocycloalkenyl ring, to provide compounds of formula (14). The reaction is typically performed at an elevated temperature in the presence of potassium phosphate, a catalyst such as but not limited to tris(dibenzylideneacetone)dipalladium(0), and a ligand such as but not limited to 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (XantPhos). The reaction is typically performed in a suitable solvent such as but not limited to dioxane.

EXAMPLES

The following examples are presented to provide what is believed to be the most useful and readily understood description of procedures and conceptual aspects of this invention. Each exemplified compound and intermediate was named using ACD/ChemSketch Version 12.5 (13 May 2009), Advanced Chemistry Development Inc., Toronto, Ontario), or ChemDraw R Ver. 9.0.5 (CambridgeSoft, Cambridge, Mass.).

Experimentals Example 1 2-{(4-fluorobenzyl)[4-(pyridin-3-yl)benzyl]amino}-N-[3-(1H-imidazazol-1-yl)propyl]-1,3-thiazole-5-carboxamide

The title compound was prepared as described in Example 9, substituting 3-(4-(chloromethyl)phenyl)pyridine for 1-(2-chloroethyl)pyrrolidine.

Example 2 N-[3-(1H-imidazol-1-yl)propyl]-2-{methyl[4-(pyridin-3-yl)benzyl]amino}-1,3-thiazole-5-carboxamide Example 2A methyl 2-(4-(pyridin-3-yl)benzylamino)thiazole-5-carboxylate

To a 250 mL round-bottomed flask was added 4-(pyridin-3-yl)benzaldehyde (4 g, 21.8 mmol), methyl 2-aminothiazole-5-carboxylate (3.45 g, 21.83 mmol) and acetic acid (0.375 ml, 6.55 mmol) in toluene (109 ml). The reaction mixture was heated at reflux under Dean-Stark conditions for 3 hours, cooled to room temperature, and the volatiles were removed by rotary evaporation. Methanol was added, the solution was cooled to 0° C., and sodium borohydride (1.322 g, 34.9 mmol) was carefully added. The reaction was stirred at 0° C. for 15 minutes and allowed to warm to room temperature while stirring for an additional 2 hour. The solids were filtered off, washed with water and dried under high vaccuum to give the title compound which was used in the next step without further purification.

Example 2B 2-(methyl(4-(pyridin-3-yl)benzyl)amino)thiazole-5-carboxylic acid

Example 2A (500 mg, 1.537 mmol) was dissolved in tetrahydrofuran (7683 μl) and sodium hydride (92 mg, 2.305 mmol) was added carefully. The suspension was allowed to stir for about 20 minutes at room temperature. Iodomethane (106 μl, 1.690 mmol) was then added and the reaction was stirred for an additional 30 minutes. To the mixture was added excess 1N aqueous NaOH followed by additional methanol and stirred at 55° C. for 1.5 hours. The reaction mixture was concentrated by rotary evaporation and the residue was taken up in water. The pH was adjusted to around 5-6 by addition of 2 N aqueous HCl, upon which time white solids precipitated out and were collected by vacuum filtration. The solids were washed with water, diethyl ether, and dried under high vacuum overnight to provide the title compound.

Example 2C N-[3-(1H-imidazol-1-yl)propyl]-2-{methyl[4-(pyridin-3-yl)benzyl]amino}-1,3-thiazole-5-carboxamide

To a 20 mL vial was added Example 2B (100 mg, 0.307 mmol) and 3-(1H-imidazol-1-yl)propan-1-amine (40.3 μl, 0.338 mmol) in DMF (1229 μl). 1-Ethyl-3-[3-(dimethylamino)propyl]-carbodiimide hydrochloride (103 mg, 0.538 mmol) and 1-hydroxybenzotriazole hydrate (82 mg, 0.538 mmol) were added and the reaction mixture was stirred over the weekend at room temperature. The reaction mixture was purified directly by HPLC (0-70% water acetonitrile) to give the title compound. 1H NMR (300 MHz, DMSO-d6) δ 8.88 (d, J=1.8 Hz, 1H), 8.56 (dd, J=4.8, 1.5 Hz, 1H), 8.22 (t, J=5.6 Hz, 1H), 8.10-8.00 (m, 1H), 7.80 (s, 1H), 7.72 (d, J=8.2 Hz, 2H), 7.64 (s, 1H), 7.52-7.44 (m, 1H), 7.40 (d, J 8.2 Hz, 2H), 7.19 (s, 1H), 6.88 (s, 1H), 4.79 (s, 2H), 3.99 (t, J=6.9 Hz, 2H), 3.20-3.11 (m, 2H), 3.11 (s, 3H), 1.90 (p, J=6.9 Hz, 2H); MS (ESI(+)) m/e 433.13 (M+H)+.

Example 3 2-[(4-fluorobenzyl)(methyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide Example 3A methyl 2-(4-fluorobenzylamino)thiazole-5-carboxylate

The title compound was prepared as described in Example 2A, substituting 4-fluorobenzaldehyde for 4-(pyridin-3-yl)benzaldehyde.

Example 3B 2-((4-fluorobenzyl)(methyl)amino)thiazole-5-carboxylic acid

The title compound was prepared as described in Example 2B, substituting Example 3A for Example 2A.

Example 3C 2-[(4-fluorobenzyl)(methyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide

The title compound was prepared as described in Example 2C, substituting Example 3B for Example 2B. 1H NMR (300 MHz, DMSO-d6) δ 8.20 (t, J=5.6 Hz, 1H), 7.78 (s, 1H), 7.63 (s, 1H), 7.37-7.28 (m, 2H), 7.22-7.13 (m, 3H), 6.88 (t, J=1.1 Hz, 1H), 4.71 (bs, 2H), 3.99 (t, J=6.9 Hz, 2H), 3.20-3.09 (m, 2H), 3.05 (s, 3H), 1.90 (p, J=6.9 Hz, 2H); MS (ESI(+)) m/e 374.1 (M+H)+.

Example 6 2-[(4-fluorobenzyl)(3-methylbutanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide Example 6A N-(3-(1H-imidazol-1-yl)propyl)-2-bromothiazole-5-carboxamide

2-Bromothiazole-5-carboxylic acid (0.4 g, 1.923 mmol), 3-(1H-imidazole-1-yl)propan-1-amine (0.265 g, 2.115 mmol), and benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (BOP) (0.935 g, 2.115 mmol) were mixed in dichloromethane (7 ml), treated with Hunig's base (0.705 ml, 4.04 mmol) and stirred at 25° C. for 2 hours. The reaction mixture was diluted with dichloromethane and washed with water and brine. The organic layer was dried (MgSO4), filtered and concentrated. Purification by flash chromatography (silica gel, 2-20% methanol/dichloromethane) afforded the title compound.

Example 6B N-(3-(1H-imidazol-1-yl)propyl)-2-((4-fluorobenzyl)amino)thiazole-5-carboxamide

Example 6A (2 g, 6.35 mmol) and (4-fluorophenyl)methanamine (0.794 g, 6.35 mmol) in acetonitrile (10 ml) were stirred at 120° C. overnight. The reaction mixture was cooled, concentrated, taken into ethyl acetate and washed with saturated aqueous NaHCO3 and brine. The combined aqueous layers were extracted twice with ethyl acetate. The combined organic extracts were dried (MgSO4) and filtered. The filtrate was concentrated until solid material precipitated. The mixture was filtered to provide the title compound.

Example 6C 2-[(4-fluorobenzyl)(3-methylbutanoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide

Example 6B (0.2 g, 0.556 mmol) was dissolved in dichloromethane (2.7 ml) and pyridine (0.3 ml) and was treated dropwise with a solution of 3-methylbutanoyl chloride (0.102 ml, 0.835 mmol) in dichloromethane (0.5 ml). The reaction mixture was stirred at 25° C. for 2 hours, concentrated, and purified using reverse phase HPLC (Phenomenex Luna C8(2) 5 um 100A AXIA column (30 mm×75 mm) run with a gradient of acetonitrile (A) and 0.1% trifluoroacetic acid in water (B), at a flow rate of 50 mL/min (0-0.5 min 10% A, 0.5-7.0 min linear gradient 10-95% A, 7.0-10.0 min 95% A, 10.0-12.0 min linear gradient 95-10% A) to afford the title compound. 1H NMR (400 MHz, CDCl3) δ 7.87 (s, 1H), 7.60 (s, 1H), 7.19-7.07 (m, 3H), 7.07-6.97 (m, 3H), 5.89 (s, 1H), 5.47 (s, 2H), 4.07 (t, J=6.9 Hz, 2H), 3.46 (q, J=6.6 Hz, 2H), 2.43 (d, J=6.8 Hz, 2H), 2.36-2.19 (m, 1H), 2.19-2.04 (m, 2H), 0.93 (d, J 6.6 Hz, 6H); MS (ESI(+)) m/e 443.5 (M+H)+.

The following examples were prepared as described in Example 6, substituting the appropriate amine in Example 6B and the appropriate acyl chloride in Example 6C. Title compounds were purified by either flash chromatography (silica gel column eluting with a gradient of 0-10% methanol in dichloromethane) or reverse-phase HPLC (as described in Example 6C). Accordingly, some examples were isolated as trifluoroacetic acid salts.

MS EX NAME 1H NMR DATA DATA 4 2-[(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) fluorobenzyl)(tetrahydro- 9.08 (s, 1H), 7.93 (s, 1H), 7.36 (d, J = 14.1 Hz, m/e 486 2H-pyran-4- 2H), 7.17-7.08 (m, 2H), (M + H)+ ylacetyl)amino]-N-[3-(1H- 7.03 (t, J = 8.5 Hz, 2H), 6.76 (ddd, imidazol-1-yl)propyl]-1,3- J = 47.8, 25.3, 16.1 Hz, 1H), thiazole-5-carboxamide 5.47 (s, 2H), 4.31 (d, J = 2.8 Hz, 2H), 3.93 (d, J = 11.0 Hz, 2H), 3.50 (dd, J = 11.4, 5.8 Hz, 2H), 3.42 (t, J = 11.8 Hz, 2H), 2.48 (d, J = 6.7 Hz, 2H), 2.27-2.20 (m, 2H), 1.65 (d, J = 11.2 Hz, 2H), 1.30-1.14 (m, 2H). 5 2-[(cyclohexylacetyl)(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) fluorobenzyl)amino]-N-[3- 9.00 (s, 1H), 7.95 (s, 1H), 7.32 (d, J = 17.1 Hz, m/e 484 (1H-imidazol-1-yl)propyl]- 2H), 7.19-7.08 (m, 2H), (M + H)+ 1,3-thiazole-5-carboxamide 7.02 (t, J = 8.6 Hz, 2H), 6.77 (s, 1H), 5.46 (s, 2H), 4.29 (t, J = 6.5 Hz, 2H), 3.55-3.40 (m, 2H), 2.42 (d, J = 6.7 Hz, 2H), 2.23 (d, J = 6.8 Hz, 2H), 2.19 (d, J = 6.4 Hz, 1H), 1.71 (dd, J = 35.7, 15.8 Hz, 2H), 1.35-1.19 (m, 2H), 1.15 (d, J = 12.4 Hz, 2H), 1.00 (t, J = 12.6 Hz, 2H), 0.87 (dd, J = 22.6, 10.6 Hz, 2H). 11 2-[(4-cyanobenzoyl)(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) fluorobenzyl)amino]-N-[3- 9.33 (s, 1H), 8.05 (d, J = 6.3 Hz, 1H), m/e 489 (1H-imidazol-1-yl)propyl]- 7.69 (d, J = 8.4 Hz, 2H), 7.47 (d, J = 8.3 Hz, (M + H)+ 1,3-thiazole-5-carboxamide 2H), 7.31 (s, 2H), 6.97-6.89 (m, 4H), 6.82-6.71 (m, 1H), 5.31 (s, 2H), 4.35 (d, J = 4.9 Hz, 2H), 3.49 (d, J = 5.9 Hz, 2H), 2.23 (dd, J = 7.9, 2.8 Hz, 2H). 12 2-[(3-chlorobenzoyl)(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) fluorobenzyl)amino]-N-[3- 9.16 (s, 1H), 8.00 (s, 1H), m/e 498 (1H-imidazol-1-yl)propyl]- 7.51-7.44 (m, 1H), 7.38-7.32 (m, 4H), (M + H)+ 1,3-thiazole-5-carboxamide 7.01-6.88 (m, 5H), 5.37 (s, 2H), 4.34 (t, J = 6.4 Hz, 2H), 3.53-3.47 (m, 2H), 2.30-2.19 (m, 2H). 13 2-[(4-fluorobenzoyl)(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) fluorobenzyl)amino]-N-[3- 9.20 (s, 1H), 7.99 (s, 1H), m/e 482 (1H-imidazol-1-yl)propyl]- 7.48-7.39 (m, 2H), 7.35 (d, J = 15.2 Hz, 2H), (M + H)+ 1,3-thiazole-5-carboxamide 7.12 (dt, J = 19.0, 8.6 Hz, 2H), 6.96 (qd, J = 8.7, 6.0 Hz, 4H), 5.39 (s, 2H), 4.34 (t, J = 6.5 Hz, 2H), 3.51 (dd, J = 11.6, 6.0 Hz, 2H), 2.31-2.19 (m, 2H). 24 2-[(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) fluorobenzyl)(methoxyacetyl)amino]- 7.88 (s, 1H), 7.61 (s, 1H), 7.15 (dd, J = 8.6, m/e 432 N-[3-(1H- 5.2 Hz, 2H), 7.10 (s, 1H), (M + H)+ imidazol-1-yl)propyl]-1,3- 7.03 (d, J = 8.6 Hz, 2H), 6.99 (d, J = 8.1 Hz, thiazole-5-carboxamide 2H), 5.45 (s, 2H), 4.30-4.24 (m, 2H), 4.07 (t, J = 6.9 Hz, 2H), 3.48-3.43 (m, 5H), 2.18-2.10 (m, 2H). 25 2-[(4-fluorobenzyl)(3- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) methoxypropanoyl)amino]- 7.88 (s, 1H), 7.60 (s, 1H), 7.16 (dd, J = 8.6, m/e 446 N-[3-(1H-imidazol-1- 5.2 Hz, 2H), 7.10 (s, 1H), (M + H)+ yl)propyl]-1,3-thiazole-5- 7.04-6.99 (m, 2H), 6.98 (s, 1H), carboxamide 5.92 (s, 1H), 5.51 (s, 2H), 4.06 (t, J = 6.9 Hz, 2H), 3.75 (t, J = 6.2 Hz, 2H), 3.48-3.41 (m, 2H), 3.33 (s, 3H), 2.81 (t, J = 6.2 Hz, 2H), 2.12 (dd, J = 6.9, 3.9 Hz, 2H). 44 1-{2-[(4-fluorobenzyl)(5- (ESI(+)) {[3-(1H-imidazol-1- m/e 480 yl)propyl]carbamoyl}-1,3- (M + H)+ thiazol-2-yl)amino]-2- oxoethyl}pyridinium 45 2-{[2-(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) fluorophenyl)ethyl](3- 7.98 (s, 1H), 7.58 (s, 1H), m/e 458 methylbutanoyl)amino}-N- 7.20-7.07 (m, 3H), 7.07-6.95 (m, 3H), (M + H)+ [3-(1H-imidazol-1- 5.87 (dd, J = 8.9, 3.5 Hz, 1H), 4.35 (t, J = 7.3 Hz, yl)propyl]-1,3-thiazole-5- 2H), 4.07 (t, J = 6.9 Hz, carboxamide 2H), 3.46 (dd, J = 8.0, 4.8 Hz, 2H), 3.04 (t, J = 7.3 Hz, 2H), 2.21 (d, J = 6.7 Hz, 2H), 2.19-2.16 (m, 1H), 2.16-2.08 (m, 2H), 0.92 (d, J = 6.2 Hz, 6H). 48 2-{[2-(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) cyanophenyl)ethyl](3- 9.09 (s, 1H), 8.01 (s, 1H), 7.63 (d, J = 8.1 Hz, m/e 465 methylbutanoyl)amino}-N- 2H), 7.37 (s, 1H), 7.33 (d, J = 7.9 Hz, (M + H)+ [3-(1H-imidazol-1- 3H), 6.74 (s, 1H), 4.39 (t, yl)propyl]-1,3-thiazole-5- J = 7.4 Hz, 2H), 4.33 (t, J = 6.3 Hz, carboxamide 2H), 3.51 (d, J = 5.4 Hz, 2H), 3.20-3.07 (m, 2H), 2.31-2.21 (m, 5H), 0.95 (d, J = 6.4 Hz, 6H). 49 2-{[2-(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) cyanophenyl)ethyl](tetrahydro- 9.12 (s, 1H), 8.00 (s, 1H), 7.63 (d, J = 8.0 Hz, m/e 507 2H-pyran-4- 2H), 7.39 (s, 1H), 7.33 (d, J = 8.2 Hz, (M + H)+ ylacetyl)amino}-N-[3-(1H- 3H), 6.72 (s, 1H), imidazol-1-yl)propyl]-1,3- 4.45-4.25 (m, 4H), 3.97 (d, J = 8.2 Hz, thiazole-5-carboxamide 2H), 3.60-3.33 (m, 4H), 3.14 (t, J = 7.3 Hz, 2H), 2.33 (d, J = 6.5 Hz, 4H), 1.65 (d, J = 12.9 Hz, 2H), 1.36-1.19 (m, 2H). 50 2-[(4-cyanobenzyl)(3- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) methylbutanoyl)amino]-N- 9.21 (dd, J = 17.5, 1.7 Hz, 1H), 7.91 (d, m/e 451 [3-(1H-imidazol-1- J = 4.2 Hz, 1H), 7.64 (d, J = 8.3 Hz, (M + H)+ yl)propyl]-1,3-thiazole-5- 2H), 7.35 (d, J = 18.5 Hz, 2H), carboxamide 7.24 (s, 1H), 7.04-6.89 (m, 1H), 5.53 (s, 2H), 4.34 (dd, J = 9.6, 3.6 Hz, 2H), 3.57-3.43 (m, 2H), 2.38 (d, J = 6.7 Hz, 2H), 2.29-2.19 (m, 3H), 0.93 (d, J = 6.6 Hz, 6H). 51 2-[(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) cyanobenzyl)(tetrahydro- 9.12 (s, 1H), 8.00 (s, 1H), 7.63 (d, J = 8.0 Hz, m/e 493 2H-pyran-4- 2H), 7.39 (s, 1H), 7.33 (d, J = 8.2 Hz, (M + H)+ ylacetyl)amino]-N-[3-(1H- 3H), 6.72 (s, 1H), imidazol-1-yl)propyl]-1,3- 5.53 (s, 2H), 4.45-4.25 (m, 2H), thiazole-5-carboxamide 3.97 (d, J = 8.2 Hz, 2H), 3.60-3.33 (m, 2H), 3.14 (t, J = 7.3 Hz, 2H), 2.33 (d, J = 6.5 Hz, 4H), 1.65 (d, J = 12.9 Hz, 2H), 1.36-1.19 (m, 3H). 52 2-{[2-(4- 1H NMR (400 MHz, methanol-d4) (ESI(+)) cyanophenyl)ethyl](tetrahydrofuran- δ 9.00 (s, 1H), 8.06 (s, 1H), 7.73 (s, m/e 493 3-ylacetyl)amino}- 1H), 7.68 (d, J = 8.1 Hz, 2H), (M + H)+ N-[3-(1H-imidazol-1- 7.59 (s, 1H), 7.41 (d, J = 8.1 Hz, 2H), yl)propyl]-1,3-thiazole-5- 4.47 (t, J = 7.2 Hz, 2H), 4.34 (t, J = 6.9 Hz, carboxamide 2H), 4.02-3.88 (m, 1H), 3.79 (dt, J = 8.1, 4.0 Hz, 1H), 3.73 (dd, J = 15.5, 7.6 Hz, 1H), 3.41 (t, J = 6.4 Hz, 2H), 3.27-3.23 (m, 1H), 3.19 (t, J = 7.2 Hz, 2H), 2.64 (d, J = 9.4 Hz, 2H), 2.62-2.57 (m, 1H), 2.24-2.16 (m, 2H), 2.16-2.08 (m, 1H), 1.47 (dd, J = 12.6, 6.3 Hz, 1H). 53 2-[(4-fluorobenzyl)(3- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) methylbutanoyl)amino]-N- 7.94 (s, 1H), 7.31 (s, 1H), 7.25 (s, 1H), m/e 458 [3-(2-methyl-1H-imidazol- 7.18-7.08 (m, 2H), 7.02 (t, J = 8.5 Hz, (M + H)+ 1-yl)propyl]-1,3-thiazole-5- 2H), 6.66 (s, 1H), 5.47 (s, carboxamide 2H), 4.13 (t, J = 6.9 Hz, 2H), 3.52 (d, J = 5.9 Hz, 2H), 2.68 (s, 3H), 2.44 (d, J = 6.8 Hz, 2H), 2.31-2.22 (m, 1H), 2.14 (d, J = 6.4 Hz, 2H), 0.93 (d, J = 6.6 Hz, 6H). 54 2-[(4-fluorobenzyl)(3- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) methylbutanoyl)amino]-N- 8.85 (s, 1H), 7.95 (d, J = 7.1 Hz, 1H), m/e 458 [3-(4-methyl-1H-imidazol- 7.11 (dd, J = 8.5, 5.3 Hz, 2H), (M + H)+ 1-yl)propyl]-1,3-thiazole-5- 7.00 (dd, J = 20.2, 11.7 Hz, 4H), carboxamide 5.45 (s, 2H), 4.21 (t, J = 6.6 Hz, 2H), 3.55-3.40 (m, 2H), 2.45-2.38 (m, 2H), 2.32 (d, J = 5.6 Hz, 3H), 2.29-2.23 (m, 1H), 2.21-2.15 (m, 2H), 0.92 (d, J = 6.6 Hz, 6H). 61 2-[(4- 1H NMR (400 MHz, methanol-d4) (ESI(+)) cyanobenzyl)(tetrahydrofuran- δ 8.99 (s, 1H), 7.94 (s, 1H), m/e 479 3-ylacetyl)amino]-N-[3- 7.74-7.70 (m, 3H), 7.58 (s, 1H), 7.36 (d, (M + H)+ (1H-imidazol-1-yl)propyl]- J = 8.1 Hz, 2H), 5.63 (d, J = 4.1 Hz, 1,3-thiazole-5-carboxamide 2H), 4.32 (t, J = 6.9 Hz, 2H), 4.03-3.91 (m, 1H), 3.81-3.67 (m, 2H), 3.42-3.32 (m, 3H), 2.84-2.77 (m, 1H), 2.76-2.69 (m, 2H), 2.26-2.09 (m, 3H), 1.61-1.46 (m, 1H). 62 2-[(4-cyanobenzyl)(3- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) methoxypropanoyl)amino]- 9.18 (s, 1H), 7.91 (s, 1H), 7.63 (d, J = 8.3 Hz, m/e 453 N-[3-(1H-imidazol-1- 2H), 7.36 (d, J = 18.0 Hz, (M + H)+ yl)propyl]-1,3-thiazole-5- 2H), 7.28 (d, J = 8.3 Hz, 2H), carboxamide 6.92 (s, 1H), 5.58 (s, 2H), 4.34 (t, J = 6.5 Hz, 2H), 3.76 (t, J = 6.0 Hz, 2H), 3.50 (d, J = 5.8 Hz, 2H), 3.33 (s, 3H), 2.77 (t, J = 6.0 Hz, 2H), 2.32-2.18 (m, 2H). 74 2-[(4-fluorobenzoyl)(3- 1H NMR (400 MHz, DMSO-d6) δ (ESI(+)) methylbutyl)amino]-N-[3- 8.56 (t, J = 5.5 Hz, 1H), 8.15 (s, m/e 444 (1H-imidazol-1-yl)propyl]- 1H), 7.72 (dd, J = 8.7, 5.3 Hz, 3H), (M + H)+ 1,3-thiazole-5-carboxamide 7.39 (t, J = 8.9 Hz, 2H), 7.23 (s, 1H), 6.92 (s, 1H), 4.04 (dd, J = 15.5, 8.6 Hz, 4H), 3.21 (dd, J = 12.8, 6.7 Hz, 2H), 1.97 (dd, J = 13.9, 6.9 Hz, 2H), 1.49 (dd, J = 15.2, 7.1 Hz, 2H), 1.38 (dt, J = 13.2, 6.4 Hz, 1H), 0.67 (d, J = 6.5 Hz, 6H). 75 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-[(3- d6/D2O) δ ppm 8.80 (s, 1 H) m/e 442 methoxypropanoyl)(4- 7.98 (s, 1 H) 7.62 (s, 1 H) 7.49 (s, 1 H) (M + H)+ methylbenzyl)amino]-1,3- 7.11-7.17 (m, 3 H) 7.04-7.07 (m, thiazole-5-carboxamide 2 H) 5.46 (s, 2 H) 4.24 (t, J = 7.02 Hz, 3 H) 3.65 (t, J = 5.95 Hz, 2 H) 3.28-3.31 (m, 3 H) 2.86 (t, J = 5.95 Hz, 2 H) 2.27 (s, 4 H) 2.06-2.13 (m, 2 H). 76 N-(5-{[3-(1H-imidazol-1- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) yl)propyl]carbamoyl}-1,3- 9.16 (s, 1H), 8.42 (s, 1H), 8.08 (s, 1H), m/e 417 thiazol-2-yl)-N-(3- 7.35 (d, J = 13.4 Hz, 2H), (M + H)+ methylbutyl)-1,2-oxazole-5- 7.24-7.08 (m, 1H), 7.05 (s, 1H), 4.45 (d, carboxamide J = 6.7 Hz, 2H), 4.36 (t, J = 6.4 Hz, 2H), 3.55-3.49 (m, 2H), 2.28-2.23 (m, 3H), 1.75-1.69 (m, 2H), 1.52 (dd, J = 14.7, 7.1 Hz, 1H), 0.95 (d, J = 3.8 Hz, 6H). 77 N-[3-(1H-imidazol-1- 1H NMR (500 MHz, DMSO- (ESI(+)) yl)propyl]-2-[(3- d6/D2O) δ 8.12 (s, 1H), 7.68 (s, m/e 470 methylbutyl)(2- 1H), 7.33 (t, J = 8.0 Hz, 2H), (M + H)+ phenoxypropanoyl)amino]- 7.21 (s, 1H), 7.01 (t, J = 7.4 Hz, 1H), 1,3-thiazole-5-carboxamide 6.97 (d, J = 8.3 Hz, 2H), 6.91 (s, 1H), 5.58 (q, J = 6.3 Hz, 1H), 4.24 (t, J = 9.8 Hz, 1H), 4.07 (d, J = 10.8 Hz, 1H), 4.02 (t, J = 6.9 Hz, 2H), 3.20 (t, J = 6.9 Hz, 2H), 1.95 (p, J = 6.9 Hz, 2H), 1.60 (dd, J = 11.9, 7.6 Hz, 1H), 1.56 (d, J = 6.3 Hz, 3H), 1.51 (dd, J = 12.9, 6.5 Hz, 1H), 0.81 (dd, J = 28.5, 6.3 Hz, 6H). 85 2-{[2-(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) cyanophenyl)ethyl](3- 9.06 (s, 1H), 7.99 (s, 1H), 7.62 (d, J = 8.2 Hz, m/e 467 methoxypropanoyl)amino}- 2H), 7.39-7.33 (m, 4H), (M + H)+ N-[3-(1H-imidazol-1- 4.42 (s, 2H), 4.32 (s, 2H), 3.75 (t, J = 6.1 Hz, yl)propyl]-1,3-thiazole-5- 2H), 3.51 (d, J = 5.6 Hz, carboxamide 2H), 3.36 (s, 3H), 3.12-3.16 (m, 2H), 2.74 (t, J = 6.1 Hz, 2H), 2.20-2.25 (m, 2H). 93 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-[(3- d6/D2O) δ ppm 8.72 (d, J = 4.88 Hz, m/e 430 methoxypropanoyl)(pyrimidin- 2 H) 7.87 (s, 1 H) 7.59 (s, 1 H) (M + H)+ 2-ylmethyl)amino]-1,3- 7.38 (t, J = 4.88 Hz, 1 H) 7.13 (s, 1 thiazole-5-carboxamide H) 6.88 (s, 1 H) 5.65 (s, 2 H) 4.01 (t, J = 7.02 Hz, 2 H) 3.69 (t, J = 6.26 Hz, 2 H) 3.21-3.25 (m, 5 H) 2.89 (t, J = 6.26 Hz, 2 H) 1.93-2.02 (m, 2 H). 94 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 8.09 (d, J = 5.19 Hz, m/e 459 methoxypropanoyl)[(2- 1 H) 7.96 (s, 1 H) 7.60 (s, 1 H) (M + H)+ methoxypyridin-4- 7.13 (s, 1 H) 6.89 (s, 1 H) 6.79 (s, 1 yl)methyl]amino}-1,3- H) 6.51 (s, 1 H) 5.47 (s, 2 H) thiazole-5-carboxamide 4.02 (t, J = 6.87 Hz, 2 H) 3.82-3.86 (m, 3 H) 3.66 (t, J = 5.95 Hz, 2 H) 3.22-3.25 (m, 2 H) 3.21 (s, 3 H) 2.84 (t, J = 6.10 Hz, 2 H) 1.98 (t, J = 7.02 Hz, 2 H). 95 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-[(3- d6/D2O) δ ppm 8.00 (s, 1 H), m/e 419 methoxypropanoyl)(1,3- 7.60 (s, 1 H), 7.13 (s, 1 H), 6.89 (s, 1 H), (M + H)+ oxazol-4-ylmethyl)amino]- 5.36 (s, 1 H), 4.02 (t, 2 H), 1,3-thiazole-5-carboxamide 3.50-3.75 (m, 3 H), 3.22-3.25 (m, 4 H), 3.13 (t, J = 6.26 Hz, 2 H), 2.29-2.40 (m, 1 H), 1.94-2.03 (m, 2 H). 96 2-{[(5-chloropyridin-2- 1H NMR (400 MHz, methanol-d4) (ESI(+)) yl)methyl](3- δ 8.97 (s, 1H), 8.46 (d, J = 2.4 Hz, m/e 463 methoxypropanoyl)amino}- 1H), 7.90 (s, 1H), 7.80 (dd, J = 8.4, (M + H)+ N-[3-(1H-imidazol-1- 2.5 Hz, 1H), 7.70 (d, J = 1.6 Hz, yl)propyl]-1,3-thiazole-5- 1H), 7.57 (s, 1H), 7.39 (d, J = 8.4 Hz, carboxamide 1H), 5.60 (s, 2H), 4.31 (t, J = 6.9 Hz, 2H), 3.77 (t, J = 6.0 Hz, 2H), 3.38 (t, J = 6.3 Hz, 2H), 3.33 (s, 3H), 3.03 (t, J = 6.0 Hz, 2H), 2.25-2.08 (m, 2H). 97 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 8.31 (d, J = 4.88 Hz, m/e 443 methoxypropanoyl)[(4- 1 H), 7.93-7.95 (m, 1 H), (M + H)+ methylpyridin-3- 7.89 (s, 1 H), 7.60 (s, 1 H), 7.24 (d, J = 4.88 Hz, yl)methyl]amino}-1,3- 1 H), 7.13 (s, 1 H), thiazole-5-carboxamide 6.88 (s, 1 H), 5.48 (s, 1 H), 4.02 (t, J = 6.87 Hz, 2 H), 3.67 (q, J = 6.31 Hz, 2 H), 3.22-3.24 (m, 2 H), 3.20 (s, 3 H), 2.85 (t, J = 5.95 Hz, 2 H), 2.39 (s, 3 H), 1.94-2.02 (m, 2 H). 98 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 8.04 (d, J = 2.44 Hz, m/e 459 methoxypropanoyl)[(6- 1 H), 8.00 (s, 1 H), 7.60 (s, 1 (M + H)+ methoxypyridin-3- H), 7.55 (dd, J = 8.54, 2.44 Hz, 1 yl)methyl]amino}-1,3- H), 7.13 (s, 1 H), 6.89 (s, 1 H), thiazole-5-carboxamide 6.76 (d, J = 8.54 Hz, 1 H), 5.43 (s, 2 H), 4.02 (t, J = 6.87 Hz, 2 H), 3.82-3.86 (m, 3 H), 3.68 (t, J = 6.10 Hz, 3 H), 3.24 (d, J = 2.44 Hz, 2 H), 3.22 (s, 3 H), 2.90-2.95 (m, 2 H), 1.95-2.03 (m, 2 H), 1.22 (s, 1 H). 99 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 8.80 (s, 1 H), m/e 449 methoxypropanoyl)[(4- 8.05 (s, 1 H), 7.60 (s, 1 H), 7.14 (s, 1 H), (M + H)+ methyl-1,3-thiazol-5- 6.89 (s, 1 H), 5.58 (s, 2 H), 4.02 (t, yl)methyl]amino}-1,3- J = 7.02 Hz, 2 H), 3.69 (t, J = 6.10 Hz, thiazole-5-carboxamide 2 H), 3.22-3.25 (m, 5 H), 2.95 (t, J = 6.10 Hz, 2 H), 2.46 (s, 3 H), 1.95-2.03 (m, 2 H). 100 2-{[2-(3- 1H NMR (400 MHz, DMSO- (ESI(+)) hydroxyphenyl)ethyl](3- d6/D2O) δ ppm 7.63 (s, 1 H), m/e 458 methoxypropanoyl)amino}- 7.58-7.61 (m, 1 H), 7.33 (s, 1 H) 7.13 (s, (M + H)+ N-[3-(1H-imidazol-1- 2 H), 6.94-6.99 (m, 1 H), 6.89 (s, yl)propyl]-1,3-thiazole-5- 1 H), 3.98-4.02 (m, 2 H), 3.69 (t, carboxamide J = 6.26 Hz, 2 H), 3.50 (s, 2 H), 3.30 (s, 3 H), 3.19 (t, J = 6.87 Hz, 2 H), 2.88-2.93 (m, 2 H), 2.76-2.80 (m, 3 H), 1.93-1.97 (m, J = 6.41 Hz, 3 H). 101 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 8.49 (d, J = 4.88 Hz, m/e 443 methoxypropanoyl)[2- 1 H), 8.03 (s, 1 H), 7.62-7.71 (m, (M + H)+ (pyridin-2-yl)ethyl]amino}- 2 H), 7.21-7.25 (m, 2 H), 7.16 (s, 1,3-thiazole-5-carboxamide 1 H), 6.91 (s, 1 H), 4.52-4.57 (m, acetate (1:1) 2 H), 4.04 (t, J = 6.87 Hz, 2 H), 3.64 (t, J = 6.26 Hz, 2 H), 3.58-3.62 (m, 1 H), 3.24 (s, 3 H), 3.17-3.21 (m, 3 H), 2.84 (t, J = 6.26 Hz, 2 H), 1.96-2.04 (m, 2 H), 1.92 (s, 1 H). 102 2-{[2-(1,3-benzodioxol-5- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)ethyl](3- d6/D2O) δ ppm 8.06 (s, 1 H), m/e 486 methoxypropanoyl)amino}- 7.61 (s, 1 H), 7.14 (s, 1 H), 6.89 (s, 1 H), (M + H)+ N-[3-(1H-imidazol-1- 6.79 (d, J = 7.93 Hz, 1 H), 6.76 (d, yl)propyl]-1,3-thiazole-5- J = 1.53 Hz, 1 H), 6.65 (dd, J = 7.93, carboxamide acetate (1:1) 1.53 Hz, 1 H), 5.93 (s, 2 H), 4.34-4.38 (m, 2 H), 4.03 (t, J = 7.02 Hz, 2 H), 3.62 (t, J = 6.26 Hz, 2 H), 3.26-3.27 (m, 2 H), 3.24 (s, 3 H), 2.94 (t, J = 7.32 Hz, 2 H), 2.77 (t, J = 6.26 Hz, 2 H), 1.96-2.06 (m, 1 H), 1.88 (s, 1 H). 103 2-{[2-(4- 1H NMR (400 MHz, DMSO- (ESI(+)) chlorophenyl)ethyl](3- d6/D2O) δ ppm 8.05 (s, 1 H), m/e 476 methoxypropanoyl)amino}- 7.61 (s, 1 H), 7.31-7.34 (m, 2 H), (M + H)+ N-[3-(1H-imidazol-1- 7.23 (d, 2 H), 7.14 (s, 1 H), 6.89 (s, 1 yl)propyl]-1,3-thiazole-5- H), 4.37-4.42 (m, 2 H), 4.03 (t, J = 7.02 Hz, carboxamide acetate (1:1) 2 H), 3.63 (t, J = 6.26 Hz, 2 H), 3.25 (s, 2 H), 3.24 (s, 3 H), 3.02 (t, J = 7.32 Hz, 2 H), 2.79 (t, J = 6.26 Hz, 2 H), 1.96-2.04 (m, 2 H), 1.88 (s, 1 H). 104 2-{[2-(3- 1H NMR (400 MHz, DMSO- (ESI(+)) fluorophenyl)ethyl](3- d6/D2O) δ ppm 8.06 (s, 1 H), m/e 460 methoxypropanoyl)amino}- 7.61 (s, 1 H), 7.30-7.37 (m, 1 H), (M + H)+ N-[3-(1H-imidazol-1- 7.14 (s, 1 H), 6.99-7.08 (m, 3 H), yl)propyl]-1,3-thiazole-5- 6.90 (s, 1 H), 4.40-4.44 (m, 2 H), carboxamide acetate (1:1) 4.03 (t, J = 7.02 Hz, 2 H), 3.63 (t, J = 6.26 Hz, 2 H), 3.25 (s, 2 H), 3.24 (s, 3 H), 3.05 (t, J = 7.48 Hz, 2 H), 2.80 (t, J = 6.10 Hz, 2 H), 1.96-2.04 (m, 2 H), 1.90 (s, 1 H). 105 2-{[2-(4- 1H NMR (400 MHz, DMSO- (ESI(+)) hydroxyphenyl)ethyl](3- d6/D2O) δ ppm 7.59-7.63 (m, 2 m/e 458 methoxypropanoyl)amino}- H), 7.27 (d, J = 8.24 Hz, 2 H), (M + H)+ N-[3-(1H-imidazol-1- 7.13 (s, 1 H), 7.00-7.04 (m, 2 H), yl)propyl]-1,3-thiazole-5- 6.89 (s, 1 H), 4.00 (t, J = 7.02 Hz, 2 H), carboxamide acetate (1:1) 3.69 (t, J = 6.10 Hz, 2 H), 3.50 (t, J = 7.17 Hz, 2 H), 3.30 (s, 2 H), 3.17-3.24 (m, 3 H), 2.89 (t, J = 7.17 Hz, 2 H), 2.77 (t, J = 6.26 Hz, 2 H), 1.96 (q, J = 7.12 Hz, 2 H), 1.85 (s, 2 H). 106 2-{[2-(3- 1H NMR (400 MHz, DMSO- (ESI(+)) chlorophenyl)ethyl](3- d6/D2O) δ ppm 8.06 (s, 1 H), m/e 476 methoxypropanoyl)amino}- 7.62 (s, 1 H), 7.23-7.34 (m, 3 H), (M + H)+ N-[3-(1H-imidazol-1- 7.14-7.19 (m, 2 H), 6.90 (s, 1 H), yl)propyl]-1,3-thiazole-5- 4.39-4.44 (m, 2 H), 4.03 (t, J = 6.87 Hz, carboxamide acetate (1:1) 2 H), 3.63 (t, J = 6.26 Hz, 2 H), 3.22-3.26 (m, 5 H), 3.04 (t, J = 7.32 Hz, 2 H), 2.81 (t, J = 6.26 Hz, 2 H), 1.96-2.04 (m, 2 H), 1.92 (s, 1 H). 107 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{[2-(3- d6/D2O) δ ppm 8.07 (s, 1 H), m/e 472 methoxyphenyl)ethyl](3- 7.61 (s, 1 H), 7.21 (t, J = 7.78 Hz, 1 H), (M + H)+ methoxypropanoyl)amino}- 7.14 (s, 1 H), 6.90 (s, 1 H), 1,3-thiazole-5-carboxamide 6.75-6.82 (m, 3 H), 4.40 (t, J = 7.32 Hz, acetate (1:1) 2 H), 4.03 (t, J = 7.02 Hz, 2 H), 3.73 (s, 3 H), 3.60 (t, J = 6.10 Hz, 2 H), 3.24 (s, 2 H), 3.23 (s, 3 H), 2.99 (t, J = 7.32 Hz, 2 H), 2.74 (t, J = 6.26 Hz, 2 H), 1.96-2.05 (m, 2 H), 1.91 (s, 1 H). 108 2-{[2-(2- 1H NMR (400 MHz, DMSO- (ESI(+)) fluorophenyl)ethyl](3- d6/D2O) δ ppm 8.03 (s, 1 H), m/e 460 methoxypropanoyl)amino}- 7.61 (s, 1 H), 7.25-7.31 (m, 2 H), (M + H)+ N-[3-(1H-imidazol-1- 7.08-7.15 (m, 3 H), 6.90 (s, 1 H), yl)propyl]-1,3-thiazole-5- 4.43 (t, J = 7.32 Hz, 2 H), 4.03 (t, J = 6.87 Hz, carboxamide acetate (1:1) 2 H), 3.62 (t, J = 6.26 Hz, 2 H), 3.25 (s, 2 H), 3.23 (s, 3 H), 3.08 (t, J = 7.17 Hz, 2 H), 2.78 (t, J = 6.26 Hz, 2 H), 1.96-2.03 (m, 2 H), 1.90 (s, 1 H). 109 2-{[2-hydroxy-2-(4- 1H NMR (400 MHz, DMSO- (ESI(+)) methoxyphenyl)ethyl](3- d6/D2O) δ ppm 7.63 (s, 1 H), m/e 488 methoxypropanoyl)amino}- 7.59 (s, 1 H), 7.29 (d, J = 8.85 Hz, 2 H), (M + H)+ N-[3-(1H-imidazol-1- 7.13 (s, 1 H), 6.88-6.94 (m, 3 H), yl)propyl]-1,3-thiazole-5- 5.89 (t, J = 6.41 Hz, 1 H), 4.00 (t, J = 7.02 Hz, carboxamide acetate (1:1) 2 H), 3.76 (s, 3 H), 3.63 (d, J = 6.41 Hz, 2 H), 3.56 (t, J = 6.41 Hz, 2 H), 3.22 (s, 1 H), 3.20 (s, 3 H), 3.17-3.19 (m, 1 H), 2.54-2.57 (m, 2 H), 1.91-1.99 (m, 2 H), 1.86 (s, 1 H). 110 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 8.95 (s, 1 H), m/e 443 methoxypropanoyl)[1- 8.47 (s, 1 H), 7.94 (d, J = 14.04 Hz, 1 (M + H)+ (pyridin-2-yl)ethyl]amino}- H), 7.73-7.81 (m, 1 H), 7.68 (d, J = 4.88 Hz, 1,3-thiazole-5-carboxamide 1 H), 7.56 (d, J = 1.83 Hz, 1 H), 7.40 (d, J = 7.93 Hz, 1 H), 7.28 (d, J = 5.19 Hz, 1 H), 6.07-6.14 (m, 1 H), 4.26 (q, J = 7.02 Hz, 3 H), 3.60-3.69 (m, 3 H), 3.20 (s, 3 H), 2.71 (t, J = 6.26 Hz, 2 H), 2.05-2.15 (m, 3 H), 1.82 (d, J = 7.32 Hz, 3 H). 111 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 8.96 (d, J = 6.10 Hz, m/e 432 methoxypropanoyl)[(1- 1 H), 8.08 (d, J = 27.77 Hz, 1 H), (M + H)+ methyl-1H-pyrazol-4- 7.69 (d, J = 4.88 Hz, 1 H), yl)methyl]amino}-1,3- 7.56-7.59 (m, 1 H), 7.49 (s, 1 H), thiazole-5-carboxamide 7.27 (s, 1 H), 5.28 (s, 1 H), 4.24-4.32 (m, 4 H), 4.24-4.31 (m, 4 H), 3.75-3.79 (m, 4 H), 3.70 (t, J = 6.10 Hz, 1 H), 3.61 (t, J = 6.41 Hz, 1 H), 3.25 (s, 2 H), 3.23 (s, 2 H), 3.00 (t, J = 6.10 Hz, 1 H), 2.61 (t, 1 H), 2.11 (m, 1 H). 112 2-[(2,6-difluorobenzyl)(3- 1H NMR (400 MHz, DMSO- (ESI(+)) methoxypropanoyl)amino]- d6/D2O) δ ppm 8.70 (s, 1 H), m/e 461 N-[3-(1H-imidazol-1- 7.93 (s, 1 H), 7.58 (s, 1 H), 7.43 (s, 1 H), (M + H)+ yl)propyl]-1,3-thiazole-5- 7.36 (s, 1 H), 7.01 (t, J = 8.54 Hz, 2 carboxamide H), 5.53 (s, 2 H), 4.21 (t, J = 7.02 Hz, 2 H), 3.70 (t, J = 6.10 Hz, 2 H), 3.24 (s, 3 H), 2.99 (t, J = 6.26 Hz, 2 H), 2.03-2.10 (m, 2 H), 1.10 (td, 3 H). 113 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 8.95 (s, 1 H), m/e 443 methoxypropanoyl)[(6- 8.35 (s, 1 H), 7.98 (s, 1 H), 7.68 (d, J = 1.83 Hz, (M + H)+ methylpyridin-3- 1 H), 7.62 (dd, J = 8.24, yl)methyl]amino}-1,3- 2.14 Hz, 1 H), 7.56 (s, 1 H), thiazole-5-carboxamide 7.32 (d, J = 8.24 Hz, 1 H), 5.50 (s, 2 H), 4.26 (t, J = 7.17 Hz, 2 H), 3.65-3.70 (m, 3 H), 3.22 (s, 3 H), 2.92 (t, J = 5.95 Hz, 2 H), 2.48 (s, 3 H), 2.10 (q, J = 6.92 Hz, 3 H). 114 2-[(4-chlorobenzyl)(3- 1H NMR (400 MHz, DMSO- (ESI(+)) methoxypropanoyl)amino]- d6/D2O) δ ppm 8.85 (s, 1 H), m/e 462 N-[3-(1H-imidazol-1- 7.97 (s, 1 H), 7.64 (s, 1 H), 7.51 (s, 1 H), (M + H)+ yl)propyl]-1,3-thiazole-5- 7.37 (d, J = 8.24 Hz, 2 H), 7.20 (d, carboxamide J = 8.54 Hz, 2 H), 5.49 (s, 2 H), 4.24 (t, J = 7.17 Hz, 2 H), 3.66 (t, J = 5.95 Hz, 2 H), 3.28-3.30 (m, 2 H), 3.20 (s, 3 H), 2.86 (t, J = 6.10 Hz, 2 H), 2.06-2.14 (m, 2 H). 115 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 8.96 (s, 1 H), m/e 444 methoxypropanoyl)[(5- 8.52 (s, 1 H), 8.40 (s, 1 H), 7.92 (s, 1 H), (M + H)+ methylpyrazin-2- 7.68 (s, 1 H), 7.56 (s, 1 H), 5.56 (s, yl)methyl]amino}-1,3- 2 H), 4.25 (t, J = 7.02 Hz, 2 H), thiazole-5-carboxamide 3.70 (t, J = 6.26 Hz, 2 H), 3.18-3.25 (m, 5 H), 3.02 (t, J = 6.10 Hz, 2 H), 2.46 (s, 3 H), 2.06-2.13 (m, 2 H). 116 2-[(3-chlorobenzyl)(3- 1H NMR (400 MHz, DMSO- (ESI(+)) methoxypropanoyl)amino]- d6/D2O) δ ppm 8.72 (s, 1 H), m/e 462 N-[3-(1H-imidazol-1- 7.98 (s, 1 H), 7.59 (s, 1 H), 7.45 (s, 1 H), (M + H)+ yl)propyl]-1,3-thiazole-5- 7.37 (t, J = 7.78 Hz, 2 H), 7.22 (s, 1 carboxamide H), 7.12-7.16 (m, 1 H), 5.50 (s, 2 H), 4.22 (t, J = 7.02 Hz, 2 H), 3.66 (t, J = 6.10 Hz, 2 H), 3.28-3.30 (m, 2 H), 3.20 (s, 3 H), 2.87 (t, J = 5.95 Hz, 2 H), 2.08 (q, J = 6.92 Hz, 2 H). 117 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 8.97 (s, 1 H), m/e 443 methoxypropanoyl)[(5- 8.30 (s, 1 H), 7.92 (s, 1 H), 7.69 (s, 1 H), (M + H)+ methylpyridin-2- 7.56-7.61 (m, 2 H), 7.22 (d, J = 7.93 Hz, yl)methyl]amino}-1,3- 1 H), 5.52 (s, 1 H), thiazole-5-carboxamide 4.26 (t, J = 6.87 Hz, 2 H), 3.68 (t, J = 6.26 Hz, 2 H), 3.26 (s, 2 H), 3.23 (s, 3 H), 2.95 (t, J = 6.26 Hz, 2 H), 2.27 (s, 3 H), 2.05-2.15 (m, 2 H). 118 2-[(2,5-difluorobenzyl)(3- 1H NMR (400 MHz, DMSO- (ESI(+)) methoxypropanoyl)amino]- d6/D2O) δ ppm 8.73 (s, 1 H), m/e 464 N-[3-(1H-imidazol-1- 7.59 (s, 1 H), 7.45 (s, 1 H) (M + H)+ yl)propyl]-1,3-thiazole-5- 7.21-7.28 (m, J = 4.88 Hz, 1 H), carboxamide 7.05-7.17 (m, 2 H), 6.83 (s, 1 H), 5.50 (s, 2 H), 4.22 (t, J = 6.87 Hz, 2 H), 3.69 (t, J = 5.95 Hz, 2 H), 3.29 (t, 1 H), 3.24 (s, 1 H), 3.22 (s, 3 H), 2.91 (t, J = 6.10 Hz, 2 H), 2.05-2.12 (m, 2 H). 119 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-[(3- d6/D2O) δ ppm 8.92 (s, 1 H), m/e 442 methoxypropanoyl)(2- 7.67 (s, 1 H), 7.54 (s, 1 H), (M + H)+ methylbenzyl)amino]-1,3- 7.21-7.25 (m, 1 H), 7.14-7.19 (m, 2 H), thiazole-5-carboxamide 7.05-7.11 (m, 1 H), 6.68 (d, J = 7.63 Hz, 1 H), 5.45 (s, 2 H), 4.26 (t, J = 6.87 Hz, 2 H), 3.65 (t, J = 6.10 Hz, 2 H), 3.19 (s, 3 H), 2.80 (t, J = 6.10 Hz, 2 H), 2.37 (s, 3 H), 2.28 (d, J = 5.49 Hz, 2 H), 2.03-2.14 (m, 2 H). 120 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-[(3- d6/D2O) δ ppm 8.94 (s, 1 H), m/e 442 methoxypropanoyl)(3- 7.68 (s, 1 H), 7.56 (s, 1 H), 7.21 (t, J = 7.63 Hz, (M + H)+ methylbenzyl)amino]-1,3- 1 H), 7.02-7.10 (m, 2 thiazole-5-carboxamide H), 7.00 (s, 1 H), 6.93 (d, J = 7.63 Hz, 1 H), 5.48 (s, 2 H), 4.21-4.29 (m, 2 H), 3.65 (t, J = 6.10 Hz, 2 H), 3.29-3.31 (m, 2 H), 3.20 (s, 3 H), 2.86 (t, J = 6.10 Hz, 2 H), 2.26 (s, 3 H), 2.06-2.15 (m, 2 H). 121 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-[(3- d6/D2O) δ ppm 8.96 (s, 1 H), m/e 429 methoxypropanoyl)(pyridin- 8.47 (d, 1 H), 7.92 (s, 1 H), (M + H)+ 2-ylmethyl)amino]-1,3- 7.72-7.79 (m, 1 H), 7.69 (d, J = 1.53 Hz, 1 H), thiazole-5-carboxamide 7.57 (d, J = 1.83 Hz, 1 H), 7.26-7.34 (m, 2 H), 5.57 (s, 2 H), 4.26 (t, J = 6.87 Hz, 2 H), 3.68 (t, J = 5.95 Hz, 2 H), 3.26 (s, 2 H), 3.22 (s, 3 H), 2.95 (t, J = 6.26 Hz, 2 H), 2.06-2.14 (m, J = 13.35, 6.60, 6.60 Hz, 2 H). 122 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-[(3- d6/D2O) δ ppm 8.95 (s, 1 H), m/e 429 methoxypropanoyl)(pyridin- 8.45-8.51 (m, 2 H), 7.98 (s, 1 H), (M + H)+ 3-ylmethyl)amino]-1,3- 7.68 (s, 1 H), 7.64 (d, 1 H), 7.56 (s, 1 thiazole-5-carboxamide H), 7.40 (d, J = 4.88 Hz, 1 H), 5.53 (s, 2 H), 4.26 (t, J = 7.17 Hz, 2 H), 3.68 (t, J = 6.10 Hz, 2 H), 3.29-3.31 (m, 2 H), 3.21 (s, 3 H), 2.91 (t, J = 5.95 Hz, 2 H), 2.07-2.14 (m, 2 H). 133 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) yl)propyl]-2-{(3- 9.07 (s, 1H), 8.00 (s, 1H), 7.35 (d, J = 8.9 Hz, m/e 470 methylbutyl)[(2R)-2- 2H), 7.30 (t, J = 8.0 Hz, (M + H)+ phenoxypropanoyl]amino}- 2H), 7.01 (t, J = 7.4 Hz, 1H), 1,3-thiazole-5-carboxamide 6.89 (d, J = 8.0 Hz, 3H), 5.23 (d, J = 6.4 Hz, 1H), 4.31 (t, J = 6.5 Hz, 3H), 4.14 (t, J = 11.2 Hz, 1H), 3.48 (dd, J = 10.8, 5.2 Hz, 2H), 2.25-2.16 (m, 3H), 1.70 (d, J = 6.5 Hz, 3H), 1.63 (m, 2H), 0.90 (dd, J = 5.8, 3.4 Hz, 6H). 134 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) yl)propyl]-2-{(3- 9.06 (s, 1H), 8.00 (s, 1H), 7.35 (d, J = 9.8 Hz, m/e 470 methylbutyl)[(2S)-2- 2H), 7.30 (t, J = 8.0 Hz, (M + H)+ phenoxypropanoyl]amino}- 2H), 7.01 (t, J = 7.3 Hz, 1H), 1,3-thiazole-5-carboxamide 6.90 (d, J = 8.1 Hz, 2H), 6.77 (s, 1H), 5.23 (d, J = 6.3 Hz, 1H), 4.30 (t, J = 6.5 Hz, 3H), 4.16 (s, 1H), 3.49 (dd, J = 10.8, 5.2 Hz, 2H), 2.24-2.17 (m, 3H), 1.70 (d, J = 6.5 Hz, 3H), 1.63 (m, 2H), 0.90 (dd, J = 5.9, 3.2 Hz, 6H). 135 N-(5-{[3-(1H-imidazol-1- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) yl)propyl]carbamoyl}-1,3- 9.13 (s, 1H), 8.08 (s, 1H), 7.35 (d, J = 9.6 Hz, m/e 431 thiazol-2-yl)-5-methyl-N-(3- 2H), 7.12 (s, 1H), 6.44 (s, (M + H)+ methylbutyl)-1,2-oxazole-3- 1H), 4.61-4.49 (m, 2H), 4.35 (t, J = 6.5 Hz, carboxamide 2H), 3.51 (d, J = 5.6 Hz, 2H), 2.54 (s, 3H), 2.29-2.20 (m, 2H), 1.70-1.61 (m, 3H), 0.90 (d, J = 6.0 Hz, 6H). 136 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) yl)propyl]-2-[(3- 9.06 (s, 1H), 7.99 (s, 1H), m/e 456 methylbutyl)(phenoxyacetyl)amino]- 7.36-7.28 (m, 4H), 7.03 (t, J = 7.3 Hz, 2H), (M + H)+ 1,3-thiazole-5- 6.94 (d, J = 8.3 Hz, 2H), 4.99 (s, carboxamide 2H), 4.30 (t, J = 6.5 Hz, 2H), 4.24-4.08 (m, 2H), 3.47 (d, J = 5.6 Hz, 2H), 2.23-2.18 (m, 2H), 1.76-1.63 (m, 3H), 0.99 (d, J = 6.2 Hz, 6H). 137 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) yl)propyl]-2-[(3- 9.07 (s, 1H), 7.98 (s, 1H), 7.36 (d, J = 3.5 Hz, m/e 454 methylbutyl)(3- 2H), 7.34-7.29 (m, 2H), (M + H)+ phenylpropanoyl)amino]- 7.26-7.17 (m, 3H), 6.90 (s, 1H), 1,3-thiazole-5-carboxamide 4.32 (t, J = 6.5 Hz, 2H), 4.18-4.05 (m, 2H), 3.50 (d, J = 5.8 Hz, 2H), 3.10 (t, J = 7.5 Hz, 2H), 2.97-2.92 (m, 2H), 2.27-2.19 (m, 2H), 1.66 (dt, J = 12.9, 6.4 Hz, 1H), 1.53 (dd, J = 16.0, 7.1 Hz, 2H), 0.95 (d, J = 6.6 Hz, 6H). 138 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) yl)propyl]-2-[(3- 9.06 (s, 1H), 7.96 (s, 1H), 7.36 (dd, J = 11.5, m/e 454 methylbutyl)(2- 7.2 Hz, 4H), 7.29 (d, J = 7.2 Hz, (M + H)+ phenylpropanoyl)amino]- 1H), 7.24 (s, 2H), 6.62 (s, 1H), 1,3-thiazole-5-carboxamide 4.31 (t, J = 6.5 Hz, 2H), 4.20 (dt, J = 15.7, 8.4 Hz, 1H), 4.10 (q, J = 6.9 Hz, 1H), 3.94 (dt, J = 10.3, 7.4 Hz, 1H), 3.50 (d, J = 5.9 Hz, 2H), 2.25-2.18 (m, 2H), 1.63-1.58 (m, 1H), 1.57 (d, J = 6.8 Hz, 3H), 1.45 (dd, J = 15.8, 7.3 Hz, 2H), 0.93 (dd, J = 19.8, 6.6 Hz, 6H). 139 2-{[(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) fluorophenyl)acetyl](3- 9.04 (s, 1H), 7.97 (s, 1H), 7.33 (d, J = 9.4 Hz, m/e 458 methylbutyl)amino}-N-[3- 2H), 7.24 (dd, J = 8.4, 5.3 Hz, (M + H)+ (1H-imidazol-1-yl)propyl]- 2H), 7.06 (t, J = 8.6 Hz, 2H), 1,3-thiazole-5-carboxamide 6.78 (s, 1H), 4.29 (t, J = 6.2 Hz, 2H), 4.24-4.12 (m, 2H), 3.97 (s, 2H), 3.48 (d, J = 5.4 Hz, 2H), 2.23-2.18 (m, 2H), 1.71 (dt, J = 13.1, 6.6 Hz, 1H), 1.65-1.58 (m, 2H), 0.99 (d, J = 6.5 Hz, 6H). 150 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, methanol-d4) (ESI(+)) yl)propyl]-2-[(3- δ 8.98 (s, 1H), 8.01 (s, 1H), 7.71 (s, m/e 408 methoxypropanoyl)(3- 1H), 7.57 (s, 1H), 4.33 (t, J = 6.9 Hz, (M + H)+ methylbutyl)amino]-1,3- 2H), 4.30-4.23 (m, 2H), thiazole-5-carboxamide 3.79 (t, J = 5.9 Hz, 2H), 3.39 (t, J = 6.4 Hz, 2H), 3.36 (s, 3H), 2.97 (t, J = 5.9 Hz, 2H), 2.18 (p, J = 6.7 Hz, 2H), 1.72 (dt, J = 13.1, 6.7 Hz, 1H), 1.68-1.59 (m, 2H), 1.00 (d, J = 6.5 Hz, 6H). 151 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, methanol-d4) (ESI(+)) yl)propyl]-2- δ 8.98 (s, 1H), 8.03 (s, 1H), 7.71 (s, m/e 394 [(methoxyacetyl)(3- 1H), 7.57 (s, 1H), 4.49 (s, 2H), (M + H)+ methylbutyl)amino]-1,3- 4.33 (t, J = 6.8 Hz, 2H), thiazole-5-carboxamide 4.19-4.07 (m, 2H), 3.49 (s, 3H), 3.40 (t, J = 6.4 Hz, 2H), 2.19 (p, J = 6.6 Hz, 2H), 1.71 (dt, J = 12.8, 6.5 Hz, 1H), 1.67-1.56 (m, 2H), 1.00 (d, J = 6.4 Hz, 6H). 152 2-[(cyclopropylcarbonyl)(3- 1H NMR (400 MHz, methanol-d4) (ESI(+)) methylbutyl)amino]-N-[3- δ 8.97 (s, 1H), 8.00 (s, 1H), 7.70 (t, m/e 390 (1H-imidazol-1-yl)propyl]- J = 1.6 Hz, 1H), 7.56 (t, J = 1.6 Hz, (M + H)+ 1,3-thiazole-5-carboxamide 1H), 4.53-4.41 (m, 2H), 4.32 (t, J = 6.8 Hz, 2H), 3.39 (t, J = 6.4 Hz, 2H), 2.28-2.10 (m, 3H), 1.81-1.63 (m, 3H), 1.16-1.04 (m, 4H), 1.01 (d, J = 6.2 Hz, 6H). 153 (2S)-1-[(5-{[3-(1H- 1H NMR (400 MHz, methanol-d4) (ESI(+)) imidazol-1- δ 8.97 (s, 1H), 8.03 (s, 1H), 7.71 (s, m/e 436 yl)propyl]carbamoyl}-1,3- 1H), 7.57 (s, 1H), 5.50 (q, J = 6.8 Hz, (M + H)+ thiazol-2-yl)(3- 1H), 4.53 (s, 1H), 4.33 (t, J = 6.8 Hz, methylbutyl)amino]-1- 2H), 4.04-3.91 (m, 1H), oxopropan-2-yl acetate 3.39 (dd, J = 6.9, 5.6 Hz, 2H), 2.19 (p, J = 6.6 Hz, 2H), 2.12 (s, 3H), 1.80 (d, J = 5.4 Hz, 1H), 1.72 (dt, J = 11.2, 6.2 Hz, 2H), 1.54 (d, J = 6.8 Hz, 3H), 1.00 (dd, J = 6.1, 2.0 Hz, 6H). 154 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, methanol-d4) (ESI(+)) yl)propyl]-2-[(3- δ 10.13 (d, J = 1.5 Hz, 1H), m/e 448 methylbutyl)(tetrahydro-2H- 8.98 (s, 1H), 8.01 (s, 1H), 7.71 (s, 1H), (M + H)+ pyran-4-ylacetyl)amino]- 7.57 (s, 1H), 4.32 (t, J = 6.9 Hz, 1,3-thiazole-5-carboxamide 2H), 4.28-4.19 (m, 2H), 3.94 (dd, J = 11.4, 3.5 Hz, 2H), 3.47 (t, J = 11.0 Hz, 2H), 3.39 (t, J = 6.5 Hz, 2H), 2.67 (d, J = 6.7 Hz, 2H), 2.19 (dd, J = 13.3, 6.7 Hz, 3H), 1.73 (dd, J = 13.3, 6.4 Hz, 3H), 1.61 (dd, J = 15.7, 7.1 Hz, 2H), 1.39 (dd, J = 12.9, 4.3 Hz, 2H), 1.01 (d, J = 6.5 Hz, 6H). 155 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, methanol-d4) (ESI(+)) yl)propyl]-2-[(3- δ 8.98 (s, 1H), 8.02 (s, 1H), 7.71 (s, m/e 420 methylbutyl)(tetrahydrofuran- 1H), 7.57 (s, 1H), 4.31 (dt, J = 15.2, (M + H)+ 3-ylcarbonyl)amino]-1,3- 7.8 Hz, 4H), 4.07 (t, J = 8.2 Hz, thiazole-5-carboxamide 1H), 4.02-3.91 (m, 2H), 3.87 (dd, J = 14.7, 7.5 Hz, 1H), 3.74-3.59 (m, 1H), 3.39 (t, J = 6.5 Hz, 2H), 2.31 (dt, J = 15.2, 7.1 Hz, 1H), 2.19 (dq, J = 13.2, 6.6 Hz, 3H), 1.73 (td, J = 13.0, 6.4 Hz, 1H), 1.64 (dd, J = 14.5, 7.3 Hz, 2H), 1.01 (d, J = 6.5 Hz, 6H). 156 2-{[2-hydroxy-2-(3- 1H NMR (400 MHz, DMSO- (ESI(+)) methoxyphenyl)ethyl](3- d6/D2O) δ ppm 9.03 (s, 1 H), m/e 488 methoxypropanoyl)amino}- 7.74 (s, 1 H), 7.66 (s, 1 H), 7.63 (s, 1 H), (M + H)+ N-[3-(1H-imidazol-1- 7.29-7.34 (m, 1 H), yl)propyl]-1,3-thiazole-5- 6.89-6.96 (m, 3 H), 5.86-5.90 (m, 1 H), carboxamide 4.23 (t, J = 6.71 Hz, 2 H), 3.53-3.66 (m, 4 H), 3.22 (d, J = 2.44 Hz, 2 H), 3.20 (s, 3 H), 2.57-2.62 (m, 2 H), 2.02-2.06 (m, 2 H), 1.01-1.14 (m, 3 H). 157 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 9.04 (s, 1 H), m/e 444 methoxypropanoyl)[2- 8.55-8.57 (m, 2 H), 8.50 (d, J = 2.14 Hz, (M + H)+ (pyrazin-2-yl)ethyl]amino}- 1 H), 8.03 (s, 1 H), 7.75 (t, J = 1.68 Hz, 1,3-thiazole-5-carboxamide 1 H), 7.62-7.65 (m, 1 H), 4.55-4.59 (m, 2 H), 4.25 (t, J = 6.87 Hz, 3 H), 3.65 (t, J = 5.95 Hz, 2 H), 3.24-3.28 (m, 7 H), 2.92 (t, J = 6.10 Hz, 2 H), 2.06-2.11 (m, 2 H). 158 2-{[1-(3- 1H NMR (400 MHz, DMSO- (ESI(+)) hydroxyphenyl)propan-2- d6/D2O) δ ppm 9.02 (s, 1 H), m/e 472 yl](3- 7.74 (t, J = 1.83 Hz, 1 H), 7.63 (s, 2 H), (M + H)+ methoxypropanoyl)amino}- 7.34 (t, J = 7.63 Hz, 1 H), 7.14 (s, 1 N-[3-(1H-imidazol-1- H), 6.94-6.98 (m, 1 H), yl)propyl]-1,3-thiazole-5- 6.59-6.63 (m, 1 H), 4.22 (t, J = 6.87 Hz, carboxamide 2 H), 3.66 (t, J = 6.10 Hz, 3 H), 3.29 (s, 3 H), 3.17-3.24 (m, 4 H), 2.80 (t, J = 5.95 Hz, 3 H), 2.00-2.08 (m, 2 H), 1.15 (d, J = 6.41 Hz, 3 H). 173 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) yl)propyl]-2-[(3- 9.10 (s, 1H), 7.98 (s, 1H), 7.38 (d, J = 4.8 Hz, m/e 434 methylbutyl)(tetrahydrofuran- 2H), 6.83 (dd, J = 5.1, 2.6 Hz, (M + H)+ 2-ylacetyl)amino]-1,3- 1H), 4.42 (dd, J = 12.9, 6.7 Hz, thiazole-5-carboxamide 1H), 4.34 (t, J = 6.5 Hz, 2H), 4.20 (t, J = 8.3 Hz, 2H), 3.92 (dd, J = 15.0, 6.9 Hz, 1H), 3.80 (dd, J = 15.1, 6.9 Hz, 1H), 3.51 (ddd, J = 5.9, 4.6, 2.9 Hz, 2H), 3.04-2.96 (m, 2H), 2.78 (dd, J = 15.9, 5.4 Hz, 2H), 2.25 (dt, J = 15.8, 6.1 Hz, 3H), 1.97 (dt, J = 13.9, 6.9 Hz, 2H), 1.79-1.69 (m, 1H), 1.67-1.52 (m, 3H), 0.99 (d, J = 6.5 Hz, 6H). 174 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) yl)propyl]-2-[(3- 9.15 (s, 1H), 8.00 (s, 1H), 7.37 (d, J = 9.6 Hz, m/e 434 methylbutyl)(tetrahydrofuran- 2H), 6.81 (dd, J = 7.5, 3.3 Hz, (M + H)+ 3-ylacetyl)amino]-1,3- 1H), 4.34 (t, J = 6.5 Hz, 2H), thiazole-5-carboxamide 4.15 (dd, J = 9.7, 6.7 Hz, 2H), 4.04 (dd, J = 8.7, 6.9 Hz, 1H), 3.94 (td, J = 8.3, 5.1 Hz, 1H), 3.81 (dd, J = 15.9, 7.6 Hz, 1H), 3.51 (dt, J = 10.0, 5.1 Hz, 3H), 2.84 (dt, J = 10.4, 4.2 Hz, 1H), 2.79-2.66 (m, 2H), 2.36-2.18 (m, 3H), 1.72 (dt, J = 13.2, 6.6 Hz, 1H), 1.66-1.55 (m, 3H), 1.05-0.89 (m, 6H). 175 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) yl)propyl]-2-[(2- 9.21-9.10 (m, 1H), 7.99 (s, 1H), m/e 396 methoxyethyl)(3- 7.42-7.33 (m, 2H), 7.04-6.85 (m, 1H), (M + H)+ methoxypropanoyl)amino]- 4.40 (t, J = 4.9 Hz, 2H), 4.34 (dd, J = 9.2, 1,3-thiazole-5-carboxamide 3.5 Hz, 2H), 3.79 (t, J = 6.2 Hz, 2H), 3.68 (t, J = 4.9 Hz, 2H), 3.53-3.46 (m, 2H), 3.39 (s, 3H), 3.30 (s, 3H), 3.09 (t, J = 6.2 Hz, 2H), 2.26-2.21 (m, 2H). 176 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) yl)propyl]-2-[(3- 9.26-9.13 (m, 1H), 8.05-7.97 (m, m/e 410 methoxypropanoyl)(3- 1H), 7.36 (d, J = 8.6 Hz, 2H), (M + H)+ methoxypropypamino]-1,3- 7.04-6.87 (m, 1H), 4.40-4.32 (m, thiazole-5-carboxamide 2H), 4.32-4.23 (m, 2H), 3.81 (t, J = 6.1 Hz, 2H), 3.50 (d, J = 5.5 Hz, 2H), 3.44 (t, J = 5.6 Hz, 2H), 3.39 (s, 3H), 3.34 (s, 3H), 2.98 (t, J = 6.1 Hz, 2H), 2.26-2.20 (m, 2H), 2.08-1.99 (m, 2H). 177 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) yl)propyl]-2-[(3- 9.17 (s, 1H), 8.00 (s, 1H), 7.37 (dd, J = 8.1, m/e 436 methoxypropanoyl)(tetrahydro- 3.9 Hz, 2H), 6.88-6.77 (m, (M + H)+ 2H-pyran-2- 1H), 4.46-4.36 (m, 1H), ylmethyl)amino]-1,3- 4.37-4.30 (m, 2H), 4.03-3.84 (m, 2H), thiazole-5-carboxamide 3.84-3.73 (m, 2H), 3.74-3.61 (m, 2H), 3.55-3.46 (m, 2H), 3.39 (s, 3H), 3.33-3.19 (m, 3H), 2.99 (dt, J = 16.8, 6.8 Hz, 1H), 2.28-2.21 (m, 2H), 1.89-1.85 (m, 1H), 1.73 (ddd, J = 3.0, 1.3, 0.6 Hz, 1H), 1.52-1.48 (m, 2H), 1.23-1.13 (m, 2H). 178 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) yl)propyl]-2-[(3- 9.16 (d, J = 4.8 Hz, 1H), 8.00 (d, J = 4.2 Hz, m/e 422 methoxypropanoyl)(tetrahydrofuran- 1H), 7.36 (d, J = 7.9 Hz, (M + H)+ 2-ylmethyl)amino]- 2H), 6.89-6.78 (m, 1H), 4.54 (dd, 1,3-thiazole-5-carboxamide J = 14.5, 1.6 Hz, 1H), 4.37-4.30 (m, 2H), 4.30-4.23 (m, 1H), 4.10-3.95 (m, 1H), 3.87 (dd, J = 14.7, 6.5 Hz, 1H), 3.82-3.76 (m, 2H), 3.71 (dd, J = 8.2, 6.6 Hz, 1H), 3.55-3.45 (m, 2H), 3.39 (s, 3H), 3.26-3.12 (m, 1H), 3.03 (dt, J = 16.7, 6.8 Hz, 1H), 2.24-2.20 (m, 2H), 1.93 (d, J = 7.2 Hz, 2H), 1.66-1.50 (m, 2H). 179 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) yl)propyl]-2-{(3- 9.25-9.09 (m, 1H), 8.07-7.96 (m, m/e 424 methoxypropanoyl)[2- 1H), 7.35 (d, J = 11.4 Hz, 2H), (M + H)+ (propan-2- 6.98-6.78 (m, 1H), 4.38 (t, J = 4.9 Hz, yloxy)ethyl]amino}-1,3- 2H), 4.36-4.30 (m, 2H), thiazole-5-carboxamide 3.79 (dd, J = 8.1, 4.5 Hz, 2H), 3.75-3.68 (m, 3H), 3.49 (dd, J = 10.9, 4.8 Hz, 2H), 3.38 (s, 3H), 3.27 (dd, J = 7.0, 3.4 Hz, 1H), 3.13 (dd, J = 8.1, 4.4 Hz, 2H), 2.24-2.20 (m, 2H), 1.06 (d, J = 6.1 Hz, 6H). 180 2-{[2-(1,3-dioxolan-2- 1H NMR (400 MHz, methanol-d4) (ESI(+)) yl)ethyl](3- δ 8.98 (s, 1H), 8.59-8.49 (m, 1H), m/e 438 methoxypropanoyl)amino}- 8.02 (s, 1H), 7.71 (d, J = 1.5 Hz, (M + H)+ N-[3-(1H-imidazol-1- 1H), 7.57 (s, 1H), 4.95 (t, J = 4.3 Hz, yl)propyl]-1,3-thiazole-5- 1H), 4.37 (dd, J = 12.7, 5.0 Hz, carboxamide 2H), 4.34-4.29 (m, 2H), 3.99-3.91 (m, 2H), 3.85 (dd, J = 8.8, 5.1 Hz, 2H), 3.79 (t, J = 6.0 Hz, 2H), 3.43-3.37 (m, 2H), 3.36 (s, 3H), 3.03 (t, J = 6.0 Hz, 2H), 2.26-2.17 (m, 2H), 2.17-2.11 (m, 2H). 181 2-[(1,4-dioxan-2- (ESI(+)) ylmethyl)(3- m/e 438 methoxypropanoyl)amino]- (M + H)+ N-[3-(1H-imidazol-1- yl)propyl]-1,3-thiazole-5- carboxamide 182 2-{[3-(4- 1H NMR (400 MHz, methanol-d4) (ESI(+)) fluorophenyl)propanoyl](2- δ 8.96 (s, 1H), 7.99 (s, 1H), 7.70 (t, m/e methoxyethyl)amino}-N-[3- J = 1.7 Hz, 1H), 7.57 (t, J = 1.6 Hz, 55460 (1H-imidazol-1-yl)propyl]- 1H), 7.27 (dd, J = 8.6, 5.5 Hz, (M + H)+ 1,3-thiazole-5-carboxamide 2H), 6.99 (t, J = 8.8 Hz, 2H), 4.41 (t, J = 5.1 Hz, 2H), 4.33 (t, J = 6.9 Hz, 2H), 3.66 (t, J = 5.0 Hz, 2H), 3.40 (t, J = 6.4 Hz, 2H), 3.26 (s, 3H), 3.17 (t, J = 7.3 Hz, 2H), 3.01 (t, J = 7.2 Hz, 2H), 2.24-2.09 (m, 2H). 183 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, methanol-d4) (ESI(+)) yl)propyl]-2-{(2- δ 8.98 (s, 1H), 8.84 (s, 1H), m/e 443 methoxyethyl)[3-(pyridin-3- 8.70 (d, J = 5.5 Hz, 1H), 8.59 (d, J = 8.2 Hz, (M + H)+ yl)propanoyl]amino}-1,3- 1H), 8.01 (dd, J = 8.1, 5.7 Hz, thiazole-5-carboxamide 1H), 7.99 (s, 1H), 7.70 (t, J = 1.7 Hz, 1H), 7.57 (t,, J = 1.7 Hz, 1H), 4.45 (t, J = 5.0 Hz, 2H), 4.32 (t, J = 6.9 Hz, 2H), 3.69 (t, J = 4.9 Hz, 2H), 3.40 (dt, J = 9.9, 6.9 Hz, 4H), 3.27 (s, 3H), 2.18 (m, 2H). 184 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, methanol-d4) (ESI(+)) yl)propyl]-2-[(2- δ 8.97 (s, 1H), 8.81 (d, J = 9.1 Hz, m/e 429 methoxyethyl)(pyridin-3- 2H), 8.52 (d, J = 8.1 Hz, 1H), (M + H)+ ylacetyl)amino]-1,3- 8.06 (dd, J = 7.9, 5.9 Hz, 1H), 8.04 (s, thiazole-5-carboxamide 1H), 7.70 (t, J = 1.7 Hz, 1H), 7.56 (t, J = 1.7 Hz, 1H), 4.61 (t, J = 5.0 Hz, 2H), 4.58 (s, 2H), 4.32 (t, J = 6.9 Hz, 2H), 3.80 (t, J = 4.9 Hz, 2H), 3.39 (t, J = 6.4 Hz, 2H), 3.38 (s, 3H), 2.18 (m, 2H). 185 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, methanol-d4) (ESI(+)) yl)propyl]-2-[(2- δ 8.98 (s, 1H), 8.04 (s, 1H), m/e 478 methoxyethyl)(naphthalen- 7.92-7.79 (m, 0033H), 7.74 (d, J = 15.9 Hz, (M + H)+ 2-ylacetyl)amino]-1,3- 2H), 7.59 (s, 1H), 7.51 (dd, J = 6.8, thiazole-5-carboxamide 2.8 Hz, 2H), 7.42 (dd, J = 8.5, 1.7 Hz, 1H), 4.57 (t, J = 5.1 Hz, 2H), 4.44 (s, 2H), 4.35 (t, J = 6.8 Hz, 2H), 3.78 (t, J = 5.0 Hz, 2H), 3.42 (t, J = 6.2 Hz, 2H), 3.40 (s, 3H), 2.29-2.11 (m, 2H). 186 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, methanol-d4) (ESI(+)) yl)propyl]-2-{(2- δ 8.95 (s, 1H), 8.03 (t, J = 1.3 Hz, m/e 520 methoxyethyl)[(4- 1H), 7.70 (s, 1H), 7.58 (s, 1H), (M + H)+ phenoxyphenyl)acetyl]amino}- 7.40-7.33 (m, 2H), 7.27 (d, J = 8.5 Hz, 1,3-thiazole-5- 2H), 7.12 (dd, J = 11.3, 3.9 Hz, carboxamide 2H), 7.03-6.95 (m, 4H), 4.52 (t, J = 5.1 Hz, 2H), 4.35 (t, J = 6.9 Hz, 2H), 4.24 (s, 2 H), 3.76 (t, J = 5.1 Hz, 2H), 3.43 (t, J = 6.5 Hz, 2H), 3.38 (s, 3H), 2.34-2.12 (m, 2H). 187 2-{[(4- 1H NMR (400 MHz, methanol-d4) (ESI(+)) cyanophenyl)acetyl](2- δ ppm 8.94 (s, 1 H), 8.01 (s, 1H), m/e 453 methoxyethyl)amino}-N-[3- 7.70 (m, 3 H), 7.55 (s, 1 H), (M + H)+ (1H-imidazol-1-yl)propyl]- 7.44 (d, J = 8.1 Hz, 2H), 4.53 (t, J = 4.9 Hz, 1,3-thiazole-5-carboxamide 2H), 4.35 (s, 2H), 4.32 (t, J = 6.9 Hz, 2H), 3.75 (t, J = 4.9 Hz, 2H), 3.39 (t, J = 6.5 Hz, 2H), 3.36 (s, 3H), 2.19 (m, 2H). 188 2-{[(4- 1H NMR (400 MHz, methanol-d4) (ESI(+)) aminophenyl)acetyl](2- δ 9.02 (s, 1H), 8.07 (s, 1H), 7.74 (s, m/e 443 methoxyethyl)amino}-N-[3- 1H), 7.59 (s, 1H), 7.47 (d, J = 8.4 Hz, (M + H)+ (1H-imidazol-1-yl)propyl]- 2H), 7.40 (d, J = 8.4 Hz, 2H), 1,3-thiazole-5-carboxamide 4.57 (t, J = 4.9 Hz, 2H), 4.40-4.28 (m, 4H), 3.79 (t, J = 5.0 Hz, 2H), 3.42 (t, J = 6.5 Hz, 2H), 3.39 (s, 3H), 2.21 (m, 2H). 189 2-[{2-[di(prop-2-en-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)amino]ethyl}(3- d6/D2O) δ ppm 8.98 (s, 1 H), m/e 461 methoxypropanoyl)amino]- 8.05 (s, 1 H), 7.70 (s, 1 H), 7.59 (s, 1 H), (M + H)+ N-[3-(1H-imidazol-1- 5.89-6.01 (m, 2 H), yl)propyl]-1,3-thiazole-5- 5.49-5.59 (m, 4 H), 4.51 (t, 2 H), 4.27 (t, J = 7.02 Hz, carboxamide 2 H), 3.77 (d, J = 7.02 Hz, 4 H), 3.72 (t, J = 6.26 Hz, 2 H), 3.31-3.37 (m, 3 H), 3.29 (s, 4 H), 2.98 (t, J = 6.26 Hz, 2 H). 190 2-{[3- 1H NMR (400 MHz, DMSO- (ESI(+)) (diethylamino)propyl](3- d6/D2O) δ ppm 8.96 (s, 1 H), m/e 451 methoxypropanoyl)amino}- 8.04 (s, 1 H), 7.69 (s, 1 H), 7.57 (s, 1 H), (M + H)+ N-[3-(1H-imidazol-1- 4.21-4.30 (m, 4 H), 3.74 (t, J = 6.10 Hz, yl)propyl]-1,3-thiazole-5- 2 H), 3.31 (s, 2 H), carboxamide 3.29 (s, 3 H), 3.12-3.20 (m, 6 H), 2.98 (t, J = 6.10 Hz, 2 H), 2.07-2.15 (m, 4 H), 1.23 (t, J = 7.17 Hz, 6 H). 191 2-{[2- 1H NMR (400 MHz, DMSO- (ESI(+)) (diethylamino)ethyl](3- d6/D2O) δ ppm 8.97 (s, 1 H), m/e 437 methoxypropanoyl)amino}- 8.07 (s, 1 H), 7.69 (s, 1 H), 7.58 (s, 1 H), (M + H)+ N-[3-(1H-imidazol-1- 4.52 (t, 2 H), 4.27 (t, J = 7.02 Hz, 2 yl)propyl]-1,3-thiazole-5- H), 3.74 (t, J = 6.10 Hz, 2 H), carboxamide 3.44 (t, 2 H), 3.30 (s, 4 H), 3.29-3.29 (m, 3 H), 3.27 (s, 2 H), 3.01 (t, J = 6.10 Hz, 2 H), 2.07-2.16 (m, 2 H), 1.29 (t, J = 7.32 Hz, 6 H). 192 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 8.97 (s, 1 H), m/e 449 methoxypropanoyl)[3- 8.04 (s, 1 H), 7.69 (s, 1 H), 7.57 (s, 1 H), (M + H)+ (pyrrolidin-1- 4.21-4.31 (m, 4 H), 3.74 (t, J = 5.95 Hz, yl)propyl]amino}-1,3- 2 H), 3.29-3.31 (m, 6 thiazole-5-carboxamide H), 3.22-3.27 (m, 5 H), 2.98 (t, J = 6.10 Hz, 2 H), 2.07-2.16 (m, 4 H), 1.94-2.03 (m, 4 H). 193 2-{[(1-ethyl-5- 1H NMR (400 MHz, DMSO- (ESI(+)) oxopyrrolidin-3- d6/D2O) δ ppm 8.97 (s, 1 H), m/e 463 yl)methyl](3- 8.02 (s, 1 H), 7.69 (s, 1 H), 7.57 (s, 1 H), (M + H)+ methoxypropanoyl)amino}- 4.24-4.33 (m, 4 H), 3.72 (t, J = 6.10 Hz, N-[3-(1H-imidazol-1- 2 H), 3.41 (dd, J = 9.77, yl)propyl]-1,3-thiazole-5- 7.63 Hz, 1 H), 3.29-3.31 (m, 2 H), carboxamide 3.27 (s, 4 H), 3.14-3.21 (m, 3 H), 2.96 (t, J = 5.95 Hz, 2 H), 2.35 (dd, J = 16.63, 8.70 Hz, 1 H), 2.08-2.15 (m, 3 H), 1.00-1.04 (m, 3 H). 194 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 8.94 (s, 1 H), m/e 435 methoxypropanoyl)[(5- 8.01 (s, 1 H), 7.68 (s, 1 H), 7.56 (s, 1 H), (M + H)+ oxopyrrolidin-2- 4.21-4.31 (m, 4 H), 3.72 (t, J = 6.26 Hz, yl)methyl]amino}-1,3- 2 H), 3.29-3.31 (m, 2 thiazole-5-carboxamide H), 3.28 (s, 3 H), 2.89-3.04 (m, 3 H), 2.24-2.31 (m, 1 H), 2.07-2.19 (m, 4 H), 1.77-1.84 (m, 1 H). 195 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 8.97 (s, 1 H), m/e 463 methoxypropanoyl)[3-oxo- 8.02 (s, 1 H), 7.69 (s, 1 H), 7.57 (s, 1 H), (M + H)+ 3-(pyrrolidin-1- 4.39-4.43 (m, 2 H), 4.27 (t, J = 7.02 Hz, yl)propyl]amino}-1,3- 2 H), 3.71 (t, J = 6.10 Hz, thiazole-5-carboxamide 2 H), 3.29-3.43 (m, 8 H), 3.03 (t, J = 6.26 Hz, 2 H), 2.71-2.76 (m, 2 H), 2.08-2.15 (m, 2 H), 1.73-1.89 (m, 4 H). 196 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 8.97 (s, 1 H), m/e 463 methoxypropanoyl)[2-oxo- 7.95 (s, 1 H), 7.69 (s, 1 H), 7.57 (s, 1 H), (M + H)+ 2-(piperidin-1- 5.13 (s, 2 H), 4.27 (t, J = 7.02 Hz, 2 yl)ethyl]amino}-1,3- H), 3.68 (t, J = 6.26 Hz, 2 H), thiazole-5-carboxamide 3.42-3.54 (m, 4 H), 3.29-3.31 (m, 2 H), 3.27-3.27 (m, 3 H), 2.80 (t, J = 6.26 Hz, 2 H), 2.07-2.15 (m, 2 H), 1.47-1.68 (m, 6 H). 197 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 8.98 (s, 1 H), m/e 463 methoxypropanoyl)[3-(2- 8.03 (s, 1 H), 7.67-7.72 (m, 1 H), (M + H)+ oxopyrrolidin-1- 7.57 (s, 1 H), 4.27 (t, J = 7.02 Hz, 2 H), yl)propyl]amino}-1,3- 4.15-4.19 (m, 2 H), 3.72 (t, J = 6.10 Hz, thiazole-5-carboxamide 2 H), 3.38 (t, J = 7.02 Hz, 2 H), 3.31 (s, 1 H), 3.28 (s, 5 H), 3.26 (s, 1 H), 2.95 (t, J = 6.10 Hz, 2 H), 2.24 (t, J = 8.09 Hz, 2 H), 2.07-2.15 (m, 2 H), 1.88-2.00 (m, 4 H). 198 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 8.97 (s, 1 H), m/e 451 methoxypropanoyl)[2-(2- 8.03 (s, 1 H), 7.69 (s, 1 H), 7.57 (s, 1 H), (M + H)+ oxo-1,3-oxazolidin-3- 4.39 (t, J = 6.26 Hz, 2 H), 4.27 (t, J = 7.02 Hz, yl)ethyl]amino}-1,3- 2 H), 4.16-4.20 (m, 2 thiazole-5-carboxamide H), 3.73 (t, J = 6.10 Hz, 2 H), 3.57-3.62 (m, 2 H), 3.53 (t, J = 6.26 Hz, 2 H), 3.28-3.32 (m, 5 H), 2.98 (t, J = 6.26 Hz, 2 H), 2.08-2.15 (m, 2 H). 199 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-[(3- d6/D2O) δ ppm 8.97 (s, 1 H), m/e 451 methoxypropanoyl){2-[(2- 8.02 (s, 1 H), 7.66-7.71 (m, 1 H), (M + H)+ methylpropanoyl)amino]ethyl}amino]- 7.57-7.58 (m, 1 H), 4.26 (q, J = 6.92 Hz, 1,3-thiazole-5- 4 H), 3.71 (t, J = 6.10 Hz, 2 H), carboxamide 3.43 (t, J = 6.41 Hz, 2 H), 3.29-3.32 (m, 2 H), 3.28 (s, 3 H), 3.00 (t, J = 6.26 Hz, 2 H), 2.27-2.35 (m, 1 H), 2.08-2.15 (m, 2 H), 0.98 (d, J = 7.02 Hz, 6 H). 200 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 8.97 (s, 1 H), m/e 423 methoxypropanoyl)[3- 8.02 (s, 1 H), 7.69 (s, 1 H), 7.57 (s, 1 H), (M + H)+ (methylamino)-3- 4.37-4.41 (m, 2 H), 4.27 (t, J = 7.02 Hz, oxopropyl]amino}-1,3- 2 H), 3.71 (t, J = 6.10 Hz, thiazole-5-carboxamide 2 H), 3.31 (s, 2 H), 3.28 (s, 3 H), 3.01 (t, J = 6.26 Hz, 2 H), 2.58 (s, 3 H), 2.07-2.15 (m, 2 H). 201 2-{[3- 1H NMR (400 MHz, DMSO- (ESI(+)) (acetylamino)propyl](3- d6/D2O) δ ppm 8.98 (s, 1 H), m/e 437 methoxypropanoyl)amino}- 8.02 (s, 1 H), 7.68-7.70 (m, 1 H), (M + H)+ N-[3-(1H-imidazol-1- 7.57 (s, 1 H), 4.27 (t, J = 7.02 Hz, 2 H), yl)propyl]-1,3-thiazole-5- 4.17-4.22 (m, 2 H), 3.72 (t, J = 6.10 Hz, carboxamide 2 H), 3.31 (s, 2 H), 3.28 (s, 3 H), 3.13 (t, J = 6.87 Hz, 2 H), 2.94 (t, J = 6.10 Hz, 2 H), 2.08-2.15 (m, 2 H), 1.85-1.90 (m, 2 H), 1.84 (s, 3 H). 202 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO- (ESI(+)) yl)propyl]-2-{(3- d6/D2O) δ ppm 8.96-8.98 (m, 1 m/e 449 methoxypropanoyl)[2-oxo- H), 8.02 (s, 1 H), 7.68-7.70 (m, 1 (M + H)+ 2-(pyrrolidin-1- H), 7.58 (s, 1 H), 4.25-4.32 (m, 4 yl)ethyl]amino}-1,3- H), 3.72 (t, J = 5.95 Hz, 2 H), thiazole-5-carboxamide 3.40 (dd, J = 10.07, 7.63 Hz, 1 H), 3.29-3.31 (m, 2 H), 3.28-3.29 (m, 3 H), 3.15 (dd, J = 10.07, 5.49 Hz, 1 H), 2.95 (t, J = 6.10 Hz, 2 H), 2.85-2.92 (m, 1 H), 2.71 (s, 3 H), 2.34 (dd, J = 16.63, 8.70 Hz, 1 H), 2.08-2.15 (m, 3 H). 205 2-{[(5-chloropyridin-2- 1H NMR (500 MHz, methanol-d4) (ESI(+)) yl)methyl](tetrahydro-2H- δ 8.97 (s, 1H), 8.45 (d, J = 2.3 Hz, m/e 489 pyran-4-ylcarbonyl)amino}- 1H), 7.91 (s, 1H), 7.81 (dd, J = 8.4, (M + H)+ N-[3-(1H-imidazol-1- 2.4 Hz, 1H), 7.70 (s, 1H), 7.56 (s, yl)propyl]-1,3-thiazole-5- 1H), 7.42 (d, J = 8.4 Hz, 1H), carboxamide 5.66 (s, 2H), 4.32 (t, J = 6.9 Hz, 2H), 3.96 (dd, J = 11.6, 2.0 Hz, 2H), 3.44 (t, J = 11.2 Hz, 2H), 3.38 (t, J = 6.4 Hz, 2H), 3.26 (dt, J = 7.0, 5.2 Hz, 1H), 2.18 (p, J = 6.7 Hz, 2H), 1.90 (qd, J = 12.3, 4.4 Hz, 2H), 1.73 (d, J = 13.1 Hz, 2H). 206 2-{[(5-chloropyridin-2- 1H NMR (500 MHz, methanol-d4) (ESI(+)) yl)methyl](tetrahydrofuran- δ 8.97 (s, 1H), 8.45 (d, J = 2.4 Hz, m/e 475 3-ylcarbonyl)amino}-N-[3- 1H), 7.95-7.76 (m, 2H), 7.70 (t, J = 1.6 Hz, (M + H)+ (1H-imidazol-1-yl)propyl]- 1H), 7.56 (t, J = 1.6 Hz, 1,3-thiazole-5-carboxamide 1H), 7.42 (d, J = 8.5 Hz, 1H), 5.66 (s, 2H), 4.32 (t, J = 6.9 Hz, 2H), 3.97 (dq, J = 14.5, 6.0 Hz, 3H), 3.80 (dt, J = 14.3, 7.3 Hz, 2H), 3.38 (t, J = 6.4 Hz, 2H), 2.19 (tt, J = 13.2, 6.8 Hz, 4H). 207 2-{[2-(5-chloropyridin-2- 1H NMR (400 MHz, methanol-d4) (ESI(+)) yl)ethyl](3- δ 9.00 (s, 1H), 8.52 (d, J = 2.5 Hz, m/e 477 methoxypropanoyl)amino}- 1H), 8.01 (s, 1H), 7.81 (dd, J = 8.4, (M + H)+ N-[3-(1H-imidazol-1- 2.5 Hz, 1H), 7.72 (t, J = 1.6 Hz, yl)propyl]-1,3-thiazole-5- 1H), 7.58 (t, J = 1.6 Hz, 1H), carboxamide 7.32 (d, J = 8.4 Hz, 1H), 4.69-4.54 (m, 2H), 4.34 (t, J = 6.8 Hz, 2H), 3.73 (t, J = 5.9 Hz, 2H), 3.40 (t, J = 6.4 Hz, 2H), 3.34 (s, 3H), 3.27 (d, J = 7.3 Hz, 2H), 2.90 (t, J = 5.9 Hz, 2H), 2.27-2.08 (m, 2H). 208 2-{[2-(5-chloropyridin-2- 1H NMR (400 MHz, methanol-d4) (ESI(+)) yl)ethyl](tetrahydrofuran-3- δ 9.00 (s, 1H), 8.51 (d, J = 2.5 Hz, m/e 489 ylcarbonyl)amino}-N-[3- 1H), 8.03 (s, 1H), 7.79 (dd, J = 8.3, (M + H)+ (1H-imidazol-1-yl)propyl]- 2.5 Hz, 1H), 7.72 (t, J = 1.6 Hz, 1,3-thiazole-5-carboxamide 1H), 7.58 (t, J = 1.5 Hz, 1H), 7.32 (d, J = 8.4 Hz, 1H), 4.64 (dd, J = 8.2, 6.1 Hz, 2H), 4.34 (t, J = 6.8 Hz, 2H), 4.01-3.94 (m, 1H), 3.91 (dd, J = 8.5, 5.9 Hz, 2H), 3.86-3.79 (m, 1H), 3.71-3.56 (m, 1H), 3.40 (t, J = 6.5 Hz, 2H), 3.28 (d, J = 7.1 Hz, 2H), 2.27-2.18 (m, 2H), 2.17-1.98 (m, 2H). 209 2-{[2-(5-chloropyridin-2- 1H NMR (400 MHz, methanol-d4) (ESI(+)) yl)ethyl][(2- δ 8.99 (s, 1H), 8.54 (d, J = 2.4 Hz, m/e 493 methoxyethyl)carbamoyl]amino}- 1H), 8.01-7.77 (m, 2H), 7.71 (t, J = 1.6 Hz, (M + H)+ N-[3-(1H-imidazol- 1H), 7.58 (t, J = 1.5 Hz, 1-yl)propyl]-1,3-thiazole-5- 1H), 7.35 (d, J = 8.4 Hz, 1H), carboxamide 4.46 (t, J = 7.1 Hz, 2H), 4.33 (t, J = 6.9 Hz, 2H), 3.51 (dd, J = 8.2, 3.0 Hz, 2H), 3.45 (t, J = 5.1 Hz, 2H), 3.40 (t, J = 6.7 Hz, 2H), 3.38 (s, 3H), 3.24 (t, J = 7.1 Hz, 2H), 2.18 (p, J = 6.7 Hz, 2H). 210 2-([2-(5-chloropyridin-2- 1H NMR (400 MHz, methanol-d4) (ESI(+)) yl)ethyl]{[2-(propan-2- δ 8.99 (s, 1H), 8.54 (d, J = 2.5 Hz, m/e 521 yloxy)ethyl]carbamoyl}amino)- 1H), 7.89 (s, 1H), 7.80 (dd, J = 8.4, (M + H)+ N-[3-(1H-imidazol-1- 2.5 Hz, 1H), 7.71 (s, 1H), 7.58 (d, J = 1.5 Hz, yl)propyl]-1,3-thiazole-5- 1H), 7.34 (d, J = 8.4 Hz, carboxamide 1H), 4.46 (t, J = 7.1 Hz, 2H), 4.33 (t, J = 6.8 Hz, 2H), 3.65 (dt, J = 12.2, 6.1 Hz, 1H), 3.56 (t, J = 5.7 Hz, 2H), 3.43 (t, J = 5.6 Hz, 2H), 3.38 (t, J = 6.4 Hz, 2H), 3.22 (dt, J = 7.8, 4.0 Hz, 2H), 2.18 (p, J = 6.7 Hz, 2H), 1.16 (d, J = 6.1 Hz, 6H). 211 2-[(1,3-benzodioxol-5- 1H NMR (400 MHz, methanol-d4) (ESI(+)) ylacetyl)(2- δ 8.01 (s, 1H), 7.71 (s, 1H), 7.19 (s, m/e 472 methoxyethyl)amino]-N-[3- 1H), 6.98 (s, 1H), 6.87-6.69 (m, (M + H)+ (1H-imidazol-1-yl)propyl]- 3H), 5.95 (s, 2H), 4.49 (t, J = 5.0 Hz, 1,3-thiazole-5-carboxamide 2H), 4.15 (s, 3H), 4.12 (t, J = 7.0 Hz, 2H), 3.73 (t, J = 5.1 Hz, 2H), 3.40-3.35 (m, 5H), 2.17-1.88 (m, 2H). 213 N-[3-(1H-imidazol-1- 1H NMR (400 MHz, DMSO-d6) δ (ESI(+)) yl)propyl]-2-[(2- 8.55-8.31 (m, 1H), 8.09 (s, 1H), m/e 429 methoxyethyl)(pyridin-2- 7.79 (td, J = 7.7, 1.8 Hz, 1H), (M + H)+ ylacetyl)amino]-1,3- 7.64 (s, 1H), 7.64 (s, 1H), 7.37 (d, J = 7.8 Hz, thiazole-5-carboxamide 1H), 7.31 (dd, J = 7.5, 4.9 Hz, 1H), 7.19 (s, 1H), 6.88 (s, 1H), 4.45 (t, J = 5.2 Hz, 2H), 4.00 (t, J = 6.9 Hz, 2H), 3.66 (t, J = 5.3 Hz, 2H), 3.26 (s, 3H), 3.23-3.11 (m, 2H), 2.16-1.83 (m, 2H).

Example 46 2-[(4-fluorobenzyl)(propan-2-ylcarbamoyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide

Example 6B (0.072 g, 0.2 mmol) was dissolved in acetonitrile (1 ml) and pyridine (0.1 ml) and treated with bis(2,5-dioxopyrrolidin-1-yl)carbonate (0.064 g, 0.25 mmol). The reaction mixture was stirred at 50° C. for 3 hours, cooled, and treated with Hunig's base (0.105 ml, 0.6 mmol) and propan-2-amine (0.02 ml, 0.23 mmol). The reaction mixture was stirred further at 25° C. for 3 hours, concentrated purified by reverse-phase HPLC (as described in Example 6C) to provide the title compound. 1H NMR (400 MHz, DMSO-d6) δ 9.12 (s, 1H), 8.45 (t, J=5.6 Hz, 1H), 7.90 (s, 1H), 7.82 (d, J=1.5 Hz, 1H), 7.70 (d, J=1.5 Hz, 1H), 7.48 (d, J=7.6 Hz, 1H), 7.22 (dd, J=8.7, 5.7 Hz, 2H), 7.16 (t, J=8.9 Hz, 2H), 5.37 (s, 2H), 4.22 (t, J=7.0 Hz, 2H), 3.93-3.87 (m, 1H), 3.21 (q, J=6.3 Hz, 2H), 2.04 (t, J=6.8 Hz, 2H), 1.10 (d, J=6.6 Hz, 6H); MS (ESI(+)) m/e 444.5 (M+H)+.

The following examples were prepared as described in Example 6B followed by Example 46, substituting the appropriate amines in Example 6B and Example 46. Title compounds were purified by either flash chromatography (silica gel column eluting with a gradient of 0-10% methanol in dichloromethane) or reverse-phase HPLC (as described in Example 6C). Accordingly, some examples were isolated as trifluoroacetic acid salts.

MS EX NAME 1H NMR DATA DATA 63 2-{(4-fluorobenzyl)[(3- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) methylbutyl)carbamoyl]amino}- 9.15 (s, 1H), 8.70 (s, 1H), 7.83 (s, m/e 473 N-[3-(1H-imidazol-1- 1H), 7.32 (d, J = 20.0 Hz, 2H), (M + H)+ yl)propyl]-1,3-thiazole-5- 7.27 (dd, J = 9.4, 4.5 Hz, 2H), carboxamide 7.11 (s, 1H), 7.02 (t, J = 8.6 Hz, 2H), 5.15 (s, 2H), 4.30 (t, J = 6.5 Hz, 2H), 3.44-3.38 (m, 4H), 2.26-2.16 (m, 2H), 1.62 (dt, J = 13.4, 6.8 Hz, 1H), 1.48 (dd, J = 14.6, 7.1 Hz, 2H), 0.92 (t, J = 6.8 Hz, 6H). 64 2-{(4-fluorobenzyl)[(2- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) methylpropyl)carbamoyl]amino}- 9.15 (s, 1H), 8.80 (s, 1H), 7.84 (s, m/e 459 N-[3-(1H-imidazol-1- 1H), 7.35 (s, 1H), 7.30 (s, 1H), (M + H)+ yl)propyl]-1,3-thiazole-5- 7.27 (d, J = 4.4 Hz, 2H), 7.04 (s, carboxamide 1H), 7.02 (t, J = 8.5 Hz, 2H), 5.16 (s, 2H), 4.30 (t, J = 6.5 Hz, 2H), 3.44 (dd, J = 11.6, 6.0 Hz, 2H), 3.22 (t, J = 6.0 Hz, 2H), 2.28-2.17 (m, 2H), 1.85 (dd, J = 13.5, 6.7 Hz, 1H), 0.93 (d, J = 6.6 Hz, 6H). 65 N1-(4-fluorobenzyl)-N1-(5- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) {[3-(1H-imidazol-1- 9.16 (dd, J = 1.6, 1.0 Hz, 1H), m/e 514 yl)propyl]carbamoyl}-1,3- 7.79 (s, 1H), 7.34 (d, J = 0.5 Hz, (M + H)+ thiazol-2-yl)piperidine-1,3- 1H), 7.33-7.31 (m, 1H), 7.30 (d, dicarboxamide J = 5.4 Hz, 1H), 7.28 (s, 1H), 7.03-6.97 (m, 3H), 6.82-6.75 (m, 1H), 6.48-6.39 (m, 1H), 5.04 (d, J = 9.7 Hz, 2H), 4.36-4.30 (m, 2H), 3.69-3.62 (m, 1H), 3.56 (s, 1H), 3.50-3.42 (m, 3H), 3.04 (ddd, J = 11.6, 6.9, 2.5 Hz, 1H), 2.49 (d, J = 3.9 Hz, 1H), 2.26-2.21 (m, 2H), 1.42-1.33 (m, 2H), 0.97 (t, J = 7.4 Hz, 2H). 66 2-{(4-fluorobenzyl)[(3- 1H NMR (400 MHz, methanol-d4) (ESI(+)) hydroxyazetidin-1- δ 8.98 (s, 1H), 7.85 (s, 1H), m/e 459 yl)carbonyl]amino}-N-[3- 7.70 (d, J = 1.6 Hz, 1H), 7.57 (s, 1H), (M + H)+ (1H-imidazol-1-yl)propyl]- 7.21 (dd, J = 8.6, 5.3 Hz, 2H), 1,3-thiazole-5-carboxamide 7.05 (t, J = 8.7 Hz, 2H), 5.28 (s, 2H), 4.49 (ddd, J = 11.2, 5.6, 3.4 Hz, 1H), 4.31 (dd, J = 14.6, 7.2 Hz, 4H), 3.88 (dd, J = 9.6, 4.4 Hz, 2H), 3.37 (dd, J = 12.9, 6.5 Hz, 2H), 2.17 (p, J = 6.7 Hz, 2H). 67 N-(4-fluorobenzyl)-N-(5- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) {[3-(1H-imidazol-1- 9.07 (s, 1H), 7.84 (s, 1H), 7.34 (d, m/e 515 yl)propyl]carbamoyl}-1,3- J = 13.9 Hz, 2H), 7.30-7.24 (m, (M + H)+ thiazol-2-yl)-1,4-dioxa-7- 2H), 6.99 (t, J = 8.5 Hz, 2H), azaspiro[4.4]nonane-7- 6.86 (s, 1H), 5.09 (s, 2H), 4.29 (t, J = 6.3 Hz, carboxamide 2H), 3.96 (dd, J = 11.8, 3.4 Hz, 4H), 3.91 (dd, J = 12.4, 5.1 Hz, 2H), 3.61 (t, J = 7.2 Hz, 2H), 3.48-3.52 (m, 2H), 2.24-2.19 (m, 2H), 2.04 (t, J = 7.3 Hz, 2H). 68 2-{(4-fluorobenzyl)[(3- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) methoxypyrrolidin-1- 9.06 (s, 1H), 7.85 (s, 1H), 7.34 (s, m/e 487 yl)carbonyl]amino}-N-[3- 1H), 7.31 (s, 1H), 7.29-7.24 (m, (M + H)+ (1H-imidazol-1-yl)propyl]- 2H), 7.16 (s, 1H), 6.98 (t, J = 8.6 Hz, 1,3-thiazole-5-carboxamide 2H), 5.19-5.01 (m, 2H), 4.29 (t, J = 6.5 Hz, 2H), 3.94 (s, 1H), 3.56 (dt, J = 12.6, 7.3 Hz, 2H), 3.46 (dd, J = 13.5, 7.7 Hz, 4H), 3.27 (s, 3H), 2.23-2.16 (m, 2H), 2.09-2.03 (m, 1H), 1.98-1.81 (m, 1H). 69 2-{(4-fluorobenzyl)[(2- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) methoxyethyl)(methyl)carbamoyl]amino}- 9.10 (s, 1H), 7.82 (s, 1H), 7.34 (d, m/e 475 N-[3-(1H- J = 8.9 Hz, 3H), 7.28 (s, 1H), (M + H)+ imidazol-1-yl)propyl]-1,3- 7.11 (s, 1H), 6.98 (t, J = 8.6 Hz, 2H), thiazole-5-carboxamide 5.03 (s, 2H), 4.29 (t, J = 6.3 Hz, 2H), 3.49 (s, 4H), 3.43 (d, J = 5.4 Hz, 2H), 3.30 (s, 3H), 2.98 (s, 3H), 2.21-2.16 (m, 2H). 70 N-(4-fluorobenzyl)-N-(5- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) {[3-(1H-imidazol-1- 9.16-9.05 (m, 1H), 7.81 (s, 1H), m/e 501 yl)propyl]carbamoyl}-1,3- 7.38-7.28 (m, 4H), (M + H)+ thiazol-2-yl)-2,6- 7.03-6.95 (m, 2H), 6.96-6.88 (m, 1H), dimethylmorpholine-4- 5.06 (s, 2H), 4.30 (dd, J = 8.4, 4.0 Hz, carboxamide 2H), 3.65 (d, J = 12.8 Hz, 2H), 3.45 (dd, J = 6.9, 3.2 Hz, 4H), 2.66 (dd, J = 12.9, 10.8 Hz, 2H), 2.21-2.17 (m, 2H), 1.12 (d, J = 6.2 Hz, 6H). 71 2-{[ethyl(2- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) methoxyethyl)carbamoyl](4- 9.07 (s, 1H), 7.80 (s, 1H), m/e 489 fluorobenzyl)amino}-N-[3- 7.41-7.28 (m, 4H), 6.98 (t, J = 8.6 Hz, (M + H)+ (1H-imidazol-1-yl)propyl]- 3H), 5.04 (s, 2H), 4.29 (d, J = 6.1 Hz, 1,3-thiazole-5-carboxamide 2H), 3.50-3.39 (m, 6H), 3.37 (d, J = 7.0 Hz, 2H), 3.29 (s, 3H), 2.20-2.16 (m, 2H), 1.07 (t, J = 7.0 Hz, 3H). 72 N-(4-fluorobenzyl)-N-(5- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) {[3-(1H-imidazol-1- 9.12-9.04 (m, 1H), 7.80 (s, 1H), m/e 501 yl)propyl]carbamoyl}-1,3- 7.34 (dt, J = 4.2, 3.7 Hz, 3H), (M + H)+ thiazol-2-yl)-2,2- 7.29 (d, J = 0.4 Hz, 1H), dimethylmorpholine-4- 7.03-6.95 (m, 2H), 6.86-6.79 (m, 1H), carboxamide 5.06 (s, 2H), 4.29 (td, J = 6.4, 3.2 Hz, 2H), 3.64 (dd, J = 5.9, 3.7 Hz, 2H), 3.48-3.41 (m, 2H), 3.39-3.34 (m, 2H), 3.21 (d, J = 3.6 Hz, 2H), 2.23-2.17 (m, 2H), 1.10 (d, J = 4.9 Hz, 6H). 73 N-(4-fluorobenzyl)-N-(5- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) {[3-(1H-imidazol-1- 9.14-9.06 (m, 1H), 7.80 (s, 1H), m/e 487 yl)propyl]carbamoyl}-1,3- 7.38-7.33 (m, 3H), 7.28 (s, 1H), (M + H)+ thiazol-2-yl)-1,4-oxazepane- 7.00 (t, J = 8.6 Hz, 2H), 6.94 (s, 4-carboxamide 1H), 5.02 (s, 2H), 4.30 (dd, J = 7.9, 4.8 Hz, 2H), 3.66-3.62 (m, 2H), 3.62-3.58 (m, 2H), 3.53 (dd, J = 11.0, 5.9 Hz, 4H), 3.48-3.39 (m, 2H), 2.21-2.17 (m, 2H), 1.85 (dd, J = 10.1, 4.6 Hz, 2H). 78 2-{(4-fluorobenzyl)[(2- 1H NMR (400 MHz, DMSO-d6) δ (ESI(+)) propoxyethyl)carbamoyl]amino}- 9.11 (s, 1H), 8.46 (t, J = 5.7 Hz, m/e 489 N-[3-(1H-imidazol-1- 1H), 7.90 (s, 1H), 7.85 (t, J = 5.3 Hz, (M + H)+ yl)propyl]-1,3-thiazole-5- 1H), 7.81 (t, J = 1.4 Hz, 1H), carboxamide 7.69 (t, J = 1.4 Hz, 1H), 7.23 (dd, J = 8.6, 5.6 Hz, 2H), 7.13 (dd, J = 12.3, 5.4 Hz, 2H), 5.33 (s, 2H), 4.22 (t, J = 6.9 Hz, 2H), 3.40 (t, J = 5.6 Hz, 2H), 3.32 (dd, J = 10.9, 5.4 Hz, 2H), 3.26 (d, J = 6.6 Hz, 2H), 3.21 (dd, J = 12.3, 6.3 Hz, 2H), 2.03 (t, J = 6.8 Hz, 2H), 1.43 (dd, J = 14.1, 7.0 Hz, 2H), 1.33-1.09 (m, 1H), 0.80 (t, J = 7.4 Hz, 3H). 79 2-{(4- 1H NMR (400 MHz, DMSO-d6) δ (ESI(+)) fluorobenzyl)[(tetrahydrofuran- 9.12 (s, 1H), 8.46 (t, J = 5.7 Hz, m/e 487 2- 1H), 7.91 (s, 1H), 7.85 (t, J = 5.5 Hz, (M + H)+ ylmethyl)carbamoyl]amino}- 1H), 7.81 (t, J = 1.5 Hz, 1H), N-[3-(1H-imidazol-1- 7.70 (t, J = 1.5 Hz, 1H), yl)propyl]-1,3-thiazole-5- 7.28-7.20 (m, 2H), 7.20-7.10 (m, 2H), carboxamide 5.37 (q, J = 17.1 Hz, 2H), 4.23 (t, J = 7.0 Hz, 2H), 3.87 (dd, J = 12.2, 5.9 Hz, 1H), 3.28-3.17 (m, 4H), 2.08-2.00 (m, 2H), 1.82-1.65 (m, 3H), 1.42 (ddd, J = 9.1, 8.3, 6.0 Hz, 1H). 80 2-{(4-fluorobenzyl)[(1- 1H NMR (400 MHz, DMSO-d6) δ (ESI(+)) methoxypropan-2- 9.10 (s, 1H), 8.44 (t, J = 5.7 Hz, m/e 475 yl)carbamoyl]amino}-N-[3- 1H), 7.90 (s, 1H), 7.81 (t, J = 1.5 Hz, (M + H)+ (1H-imidazol-1-yl)propyl]- 1H), 7.69 (t, J = 1.4 Hz, 1H), 1,3-thiazole-5-carboxamide 7.54 (d, J = 7.9 Hz, 1H), 7.31-7.21 (m, 2H), 7.21-7.09 (m, 2H), 5.36 (d, J = 2.5 Hz, 2H), 4.22 (t, J = 7.0 Hz, 2H), 4.00 (dt, J = 18.2, 5.6 Hz, 1H), 3.32 (dd, J = 9.6, 6.6 Hz, 2H), 3.26-3.21 (m, 5H), 2.03 (t, J = 6.8 Hz, 2H), 1.08 (d, J = 6.8 Hz, 3H). 81 2-{(4- 1H NMR (400 MHz, DMSO-d6) δ (ESI(+)) fluorobenzyl)[(tetrahydro- 9.11 (s, 1H), 8.45 (t, J = 5.7 Hz, m/e 501 2H-pyran-2- 1H), 7.91 (s, 1H), 7.87-7.75 (m, (M + H)+ ylmethyl)carbamoyl]amino}- 2H), 7.69 (t, J = 1.4 Hz, 1H), N-[3-(1H-imidazol-1- 7.24 (dd, J = 8.6, 5.6 Hz, 2H), yl)propyl]-1,3-thiazole-5- 7.20-7.09 (m, 2H), 5.36 (s, 2H), carboxamide 4.22 (dd, J = 9.0, 5.0 Hz, 2H), 3.82 (dd, J = 11.0, 2.7 Hz, 1H), 3.32-3.24 (m, 2H), 3.23-3.15 (m, 4H), 2.09-1.98 (m, 2H), 1.76-1.66 (m, 1H), 1.46-1.33 (m, 4H), 1.09-0.98 (m, 1H). 82 2-{(4-fluorobenzyl)[(2- 1H NMR (400 MHz, DMSO-d6) δ (ESI(+)) methoxyethyl)carbamoyl]amino}- 9.12 (s, 1H), 8.46 (t, J = 5.7 Hz, m/e 461 N-[3-(1H-imidazol- 1H), 7.91 (s, 1H), 7.87 (t, J = 5.1 Hz, (M + H)+ 1-yl)propyl]-1,3-thiazole-5- 1H), 7.82 (t, J = 1.5 Hz, 1H), carboxamide 7.70 (t, J = 1.5 Hz, 1H), 7.30-7.20 (m, 2H), 7.20-7.12 (m, 2H), 5.35 (s, 2H), 4.23 (t, J = 7.0 Hz, 2H), 3.39 (dd, J = 8.4, 3.2 Hz, 2H), 3.34 (dd, J = 9.9, 4.6 Hz, 2H), 3.24-3.18 (m, 5H), 2.04 (t, J = 6.8 Hz, 2H). 83 2-{[(2- 1H NMR (400 MHz, DMSO-d6) δ (ESI(+)) ethoxyethyl)carbamoyl](4- 9.11 (s, 1H), 8.46 (t, J = 5.6 Hz, m/e 475 fluorobenzyl)amino}-N-[3- 1H), 7.90 (s, 1H), 7.85 (t, J = 5.3 Hz, (M + H)+ (1H-imidazol-1-yl)propyl]- 1H), 7.80 (d, J = 1.4 Hz, 1H), 1,3-thiazole-5-carboxamide 7.69 (d, J = 1.4 Hz, 1H), 7.29-7.18 (m, 2H), 7.18-7.09 (m, 2H), 5.34 (s, 2H), 4.22 (t, J = 7.0 Hz, 2H), 3.41-3.38 (m, 2H), 3.37 (d, J = 7.0 Hz, 2H), 3.33 (dd, J = 9.9, 4.7 Hz, 2H), 3.24-3.17 (m, 2H), 2.11-1.94 (m, 2H), 1.05 (t, J = 7.0 Hz, 3H). 84 2-{(4-fluorobenzyl)[(1- 1H NMR (400 MHz, DMSO-d6) δ (ESI(+)) methoxybutan-2- 9.11 (s, 1H), 8.44 (t, J = 5.8 Hz, m/e 489 yl)carbamoyl]amino}-N-[3- 1H), 7.90 (s, 1H), 7.81 (d, J = 1.4 Hz, (M + H)+ (1H-imidazol-1-yl)propyl]- 1H), 7.69 (d, J = 1.3 Hz, 1H), 1,3-thiazole-5-carboxamide 7.41 (d, J = 8.2 Hz, 1H), 7.24 (dd, J = 8.6, 5.6 Hz, 2H), 7.16 (t, J = 8.9 Hz, 2H), 5.39 (dd, J = 39.3, 17.0 Hz, 2H), 4.22 (t, J = 7.0 Hz, 2H), 3.85-3.78 (m, 1H), 3.30 (dt, J = 9.7, 3.7 Hz, 2H), 3.24-3.19 (m, 5H), 2.09-1.98 (m, 2H), 1.52 (ddd, J = 12.5, 7.2, 5.0 Hz, 1H), 1.42-1.32 (m, 1H), 0.73 (t, J = 7.4 Hz, 3H). 86 2-{[(1,3-dioxolan-2- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) ylmethyl)carbamoyl](4- 9.35-9.24 (m, 1H), m/e 489 fluorobenzyl)amino}-N-[3- 8.88-8.68 (m, 1H), 7.94-7.85 (m, 1H), (M + H)+ (1H-imidazol-1-yl)propyl]- 7.39-7.34 (m, 1H), 7.32-7.27 (m, 1,3-thiazole-5-carboxamide 3H), 7.21-7.08 (m, 1H), 7.01 (t, J = 8.6 Hz, 2H), 5.21-5.09 (m, 2H), 5.06 (t, J = 3.4 Hz, 1H), 4.35-4.25 (m, 2H), 3.99-3.82 (m, 4H), 3.64 (dd, J = 5.1, 3.5 Hz, 2H), 3.44 (dt, J = 10.2, 2.9 Hz, 2H), 2.24-2.19 (m, 2H). 87 2-[(4-fluorobenzyl){[2- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) (propan-2- 9.30 (ddd, J = 3.5, 2.1, 0.8 Hz, m/e 489 yloxy)ethyl]carbamoyl]amino}- 1H), 8.55-8.35 (m, 1H), (M + H)+ N-[3-(1H-imidazol-1- 7.94-7.86 (m, 1H), 7.35 (s, 1H), yl)propyl]-1,3-thiazole-5- 7.32-7.27 (m, 3H), 7.10-7.04 (m, 1H), carboxamide 7.03-6.95 (m, 2H), 5.18 (s, 2H), 4.32 (dd, J = 9.5, 3.5 Hz, 2H), 3.62-3.49 (m, 6H), 3.48-3.41 (m, 2H), 2.23-2.20 (m, 2H), 1.13 (t, J = 4.9 Hz, 6H). 88 2-{[(1,4-dioxan-2- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) ylmethyl)carbamoyl](4- 9.43-9.29 (m, 1H), m/e 503 fluorobenzyl)amino}-N-[3- 8.77-8.63 (m, 1H), 7.98-7.88 (m, 1H), (M + H)+ (1H-imidazol-1-yl)propyl]- 7.35 (s, 1H), 7.31-7.27 (m, 3H), 1,3-thiazole-5-carboxamide 7.22-7.11 (m, 1H), 7.06-6.95 (m, 2H), 5.27-5.06 (m, 2H), 4.33 (ddd, J = 5.9, 4.1, 3.0 Hz, 2H), 3.82-3.73 (m, 3H), 3.73-3.67 (m, 2H), 3.63-3.49 (m, 2H), 3.49-3.39 (m, 2H), 3.39-3.25 (m, 2H), 2.23-2.20 (m, 2H). 89 2-{[(1,3-dimethoxypropan- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) 2-yl)carbamoyl](4- 9.26-9.18 (m, 1H), 8.30 (s, 1H), m/e 505 fluorobenzyl)amino}-N-[3- 7.89 (s, 1H), 7.35 (s, 1H), 7.30 (d, (M + H)+ (1H-imidazol-1-yl)propyl]- J = 1.8 Hz, 1H), 7.28 (d, J = 3.0 Hz, 1,3-thiazole-5-carboxamide 2H), 7.13-7.04 (m, 1H), 7.02 (t, J = 8.6 Hz, 2H), 5.19 (s, 2H), 4.31 (t, J = 6.4 Hz, 2H), 4.24-4.13 (m, 1H), 3.55 (dd, J = 9.5, 4.5 Hz, 2H), 3.44 (dd, J = 9.6, 5.6 Hz, 4H), 3.34 (s, 6H), 2.27-2.15 (m, 2H). 90 2-{(4-fluorobenzyl)[(2- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) methoxybutyl)carbamoyl]amino}- 9.22 (s, 1H), 8.47-8.29 (m, 1H), m/e 489 N-[3-(1H-imidazol- 7.88 (s, 1H), 7.35 (s, 1H), 7.30 (s, (M + H)+ 1-yl)propyl]-1,3-thiazole-5- 1H), 7.29-7.26 (m, 2H), carboxamide 7.14-7.05 (m, 1H), 7.02 (t, J = 8.6 Hz, 2H), 5.19 (q, J = 16.6 Hz, 2H), 4.31 (t, J = 6.5 Hz, 2H), 3.68-3.59 (m, 1H), 3.48-3.40 (m, 2H), 3.32 (s, 3H), 3.30-3.23 (m, 2H), 2.27-2.15 (m, 2H), 1.66-1.53 (m, 1H), 1.47 (dt, J = 13.6, 6.9 Hz, 1H), 0.93 (dd, J = 9.4, 5.6 Hz, 3H). 91 2-[(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) fluorobenzyl)(tetrahydrofuran- 9.47-9.31 (m, 2H), m/e 473 3-ylcarbamoyl)amino]-N- 7.94-7.85 (m, 1H), 7.35 (s, 1H), 7.29 (d, J = 8.7 Hz, (M + H)+ [3-(1H-imidazol-1- 3H), 7.25-7.18 (m, 1H), yl)propyl]-1,3-thiazole-5- 7.08-6.95 (m, 2H), 5.12 (s, 2H), carboxamide 4.59-4.50 (m, 1H), 4.33 (td, J = 5.4, 1.1 Hz, 2H), 4.00-3.90 (m, 2H), 3.86 (td, J = 8.6, 5.5 Hz, 1H), 3.78 (dd, J = 9.4, 2.8 Hz, 1H), 3.44 (dt, J = 8.9, 3.6 Hz, 2H), 2.35-2.28 (m, 1H), 2.26-2.20 (m, 2H), 1.96-1.87 (m, 1H). 92 2-[(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) fluorobenzyl)(tetrahydro- 9.22 (s, 1H), 9.01-8.81 (m, 1H), m/e 487 2H-pyran-3- 7.88 (s, 1H), 7.35 (s, 1H), 7.29 (t, (M + H)+ ylcarbamoyl)amino]-N-[3- J = 6.9 Hz, 3H), 7.07 (dd, J = 8.5, (1H-imidazol-1-yl)propyl]- 3.5 Hz, 1H), 7.02 (t, J = 8.6 Hz, 1,3-thiazole-5-carboxamide 2H), 5.26 (d, J = 16.7 Hz, 1H), 5.08 (d, J = 16.6 Hz, 1H), 4.31 (t, J = 6.4 Hz, 2H), 3.99 (ddd, J = 8.8, 3.5, 1.6 Hz, 1H), 3.83-3.78 (m, 1H), 3.64 (dddd, J = 22.5, 16.6, 7.9, 3.3 Hz, 3H), 3.44 (dd, J = 11.4, 5.9 Hz, 2H), 2.29-2.14 (m, 2H), 1.91 (ddd, J = 8.1, 6.4, 2.7 Hz, 1H), 1.79-1.68 (m, 1H), 1.68-1.53 (m, 2H). 123 2-[(4-cyanobenzyl){[2- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) (propan-2- 9.22-9.13 (m, 1H), m/e 496 yloxy)ethyl]carbamoyl]amino}- 8.93-8.79 (m, 1H), 7.82 (s, 1H), 7.63 (d, J = 8.1 Hz, (M + H)+ N-[3-(1H-imidazol-1- 2H), 7.45-7.32 (m, 3H), yl)propyl]-1,3-thiazole-5- 7.29 (s, 1H), 7.07-6.96 (m, 1H), carboxamide 5.25 (s, 2H), 4.30 (t, J = 6.4 Hz, 2H), 3.65-3.54 (m, 5H), 3.46-3.40 (m, 2H), 2.23 (dd, J = 7.3, 3.9 Hz, 2H), 1.15 (d, J = 6.1 Hz, 6H). 124 2-{(4-cyanobenzyl)[(2- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) methoxypropyl)carbamoyl]amino}- 9.33-9.20 (m, 1H), m/e 482 N-[3-(1H-imidazol- 8.83-8.73 (m, 1H), 7.90-7.81 (m, 1H), (M + H)+ 1-yl)propyl]-1,3-thiazole-5- 7.63 (d, J = 8.2 Hz, 2H), 7.39 (dd, J = 15.0, carboxamide 7.1 Hz, 3H), 7.28 (s, 1H), 7.12-6.99 (m, 1H), 5.33-5.14 (m, 2H), 4.37-4.25 (m, 2H), 4.21-4.11 (m, 1H), 3.48-3.39 (m, 4H), 3.36 (s, 3H), 2.26-2.20 (m, 2H), 1.29-1.23 (m, 3H). 125 2-[(4-cyanobenzyl){[2-(2- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) hydroxyethoxy)ethyl]carbamoyl]amino}- 9.39-9.27 (m, 1H), m/e 498 N-[3-(1H- 9.26-9.16 (m, 1H), 7.81 (s, 1H), 7.62 (d, J = 8.2 Hz, (M + H)+ imidazol-1-yl)propyl]-1,3- 2H), 7.41-7.34 (m, 3H), thiazole-5-carboxamide 7.28 (s, 1H), 7.15-7.05 (m, 1H), 5.22 (s, 2H), 4.55-4.5 (m, 2H), 4.36-4.29 (m, 2H), 3.85-3.75 (m, 2H), 3.67 (d, J = 4.7 Hz, 3H), 3.65-3.60 (m, 2H), 3.46-3.40 (m, 2H), 2.25-2.19 (m, 2H). 126 2-[(4-cyanobenzyl){[3- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) (propan-2- 9.26-9.14 (m, 1H), 8.61 (s, 1H), m/e 510 yloxy)propyl]carbamoyl]amino}- 7.81 (s, 1H), 7.62 (d, J = 8.2 Hz, (M + H)+ N-[3-(1H-imidazol-1- 2H), 7.38 (d, J = 8.2 Hz, 3H), yl)propyl]-1,3-thiazole-5- 7.29 (s, 1H), 6.96 (s, 1H), 5.24 (s, carboxamide 2H), 4.35-4.30 (m, 2H), 3.53 (dt, J = 16.3, 5.8 Hz, 5H), 3.45-3.40 (m, 2H), 2.26-2.20 (m, 2H), 1.88-1.82 (m, 2H), 1.12 (d, J = 6.1 Hz, 6H). 127 2-{(4-cyanobenzyl)[(3- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) hydroxy-2,2- 9.67 (s, 1H), 9.34 (s, 1H), 7.87 (s, m/e 496 dimethylpropyl)carbamoyl]amino}- 1H), 7.63 (d, J = 8.2 Hz, 2H), (M + H)+ N-[3-(1H-imidazol- 7.45-7.34 (m, 3H), 1-yl)propyl]-1,3-thiazole-5- 7.25-7.18 (m, 1H), 5.20 (s, 2H), 4.32 (t, J = 6.1 Hz, carboxamide 2H), 4.18-4.12 (m, 2H), 3.42 (d, J = 4.4 Hz, 2H), 3.38 (d, J = 6.1 Hz, 2H), 2.25-2.20 (m, 2H), 1.06 (s, 6H). 128 2-{(4-cyanobenzyl)[(2- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) hydroxypropyl)carbamoyl]amino}- 9.85 (s, 1H), 9.32 (s, 1H), m/e 468 N-[3-(1H-imidazol- 7.85-7.74 (m, 1H), 7.63 (d, J = 8.2 Hz, (M + H)+ 1-yl)propyl]-1,3-thiazole-5- 2H), 7.42-7.35 (m, 3H), 7.24 (s, carboxamide 1H), 5.39-5.29 (m, 1H), 5.28-5.10 (m, 2H), 4.40-4.25 (m, 2H), 3.93-3.81 (m, 1H), 3.53-3.46 (m, 1H), 3.46-3.36 (m, 2H), 2.27-2.21 (m, 2H), 1.43 (d, J = 6.4 Hz, 3H). 129 2-{(4-cyanobenzyl)[(1- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) hydroxypropan-2- 9.74-9.65 (m, 1H), m/e 468 yl)carbamoyl]amino}-N-[3- 9.38-9.18 (m, 1H), 7.80 (d, J = 4.4 Hz, 1H), (M + H)+ (1H-imidazol-1-yl)propyl]- 7.63 (d, J = 8.3 Hz, 2H), 1,3-thiazole-5-carboxamide 7.42-7.35 (m, 3H), 7.23-7.08 (m, 1H), 5.20 (dt, J = 21.5, 9.8 Hz, 2H), 4.63-4.52 (m, 1H), 4.47-4.40 (m, 1H), 4.40-4.34 (m, 1H), 4.34-4.27 (m, 2H), 3.48-3.38 (m, 2H), 2.26-2.21 (m, 4H), 1.37 (d, J = 6.7 Hz, 3H). 130 2-{(4-cyanobenzyl)[(3- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) hydroxypropyl)carbamoyl]amino}- 9.58 (d, J = 4.9 Hz, 1H), 9.41 (d, J = 6.0 Hz, m/e 468 N-[3-(1H-imidazol- 1H), 7.90 (s, 1H), (M + H)+ 1-yl)propyl]-1,3-thiazole-5- 7.63 (d, J = 8.2 Hz, 2H), 7.39 (d, J = 8.3 Hz, carboxamide 2H), 7.35 (s, 1H), 7.24 (s, 1H), 5.19 (s, 2H), 4.47 (t, J = 6.1 Hz, 2H), 4.33 (dd, J = 7.1, 5.8 Hz, 2H), 3.54 (d, J = 5.9 Hz, 2H), 3.42 (d, J = 2.0 Hz, 2H), 2.27-2.21 (m, 2H), 2.13-2.08 (m, 2H). 131 2-[(4-cyanobenzyl){[(2S)-1- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) hydroxybut-3-en-2- 10.02 (s, 1H), 9.31 (s, 1H), m/e 480 yl]carbamoyl}amino]-N-[3- 7.84 (s, 1H), 7.63 (d, J = 8.2 Hz, 2H), (M + H)+ (1H-imidazol-1-yl)propyl]- 7.45-7.34 (m, 3H), 7.23 (s, 1H), 1,3-thiazole-5-carboxamide 6.01-5.84 (m, 1H), 5.38 (t, J = 14.8 Hz, 2H), 5.20 (dd, J = 39.0, 17.5 Hz, 2H), 4.98-4.90 (m, 1H), 4.61 (dd, J = 11.2, 4.3 Hz, 1H), 4.50 (dd, J = 11.1, 5.0 Hz, 1H), 4.31 (t, J = 6.4 Hz, 2H), 3.42 (d, J = 5.8 Hz, 2H), 2.26-2.21 (m, 2H). 132 2-{(4-cyanobenzyl)[(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) hydroxybutyl)carbamoyl]amino}- 9.53 (s, 1H), 9.30 (s, 1H), 7.85 (s, m/e 482 N-[3-(1H-imidazol-1- 1H), 7.62 (d, J = 8.2 Hz, 2H), (M + H)+ yl)propyl]-1,3-thiazole-5- 7.39 (d, J = 8.2 Hz, 2H), 7.35 (s, carboxamide 1H), 5.20 (s, 2H), 4.41 (t, J = 6.4 Hz, 2H), 4.32 (t, J = 6.3 Hz, 2H), 3.54-3.45 (m, 2H), 3.45-3.36 (m, 2H), 2.26-2.21 (m, 3H), 1.85 (dd, J = 15.1, 6.7 Hz, 2H), 1.75 (dd, J = 14.9, 6.5 Hz, 2H). 140 2-{[(3-amino-3- 1H NMR (400 MHz, methanol-d4) (ESI(+)) oxopropyl)carbamoyl](4- δ 8.97 (s, 1H), 7.79 (s, 1H), m/e 481 cyanobenzyl)amino}-N-[3- 7.73 (d, J = 8.2 Hz, 2H), 7.69 (s, 1H), (M + H)+ (1H-imidazol-1-yl)propyl]- 7.57 (s, 1H), 7.51 (d, J = 8.2 Hz, 1,3-thiazole-5-carboxamide 2H), 5.35 (s, 2H), 4.30 (t, J = 6.8 Hz, 2H), 3.47 (t, J = 6.4 Hz, 2H), 3.35 (t, J = 6.4 Hz, 2H), 2.41 (dd, J = 16.2, 9.2 Hz, 2H), 2.15 (p, J = 6.6 Hz, 2H). 141 2-[{[3-(acetylamino)-2- 1H NMR (400 MHz, methanol-d4) (ESI(+)) methylpropyl]carbamoyl}(4- δ 8.96 (s, 1H), 7.76 (d, J = 9.6 Hz, m/e 523 cyanobenzyl)amino]-N-[3- 2H), 7.73 (s, 1H), 7.69 (s, 1H), (M + H)+ (1H-imidazol-1-yl)propyl]- 7.57 (s, 1H), 7.52 (d, J = 8.1 Hz, 1,3-thiazole-5-carboxamide 2H), 5.36 (s, 2H), 4.30 (t, J = 6.8 Hz, 2H), 3.35 (t, J = 6.4 Hz, 2H), 3.10 (d, J = 6.4 Hz, 4H), 2.14 (p, J = 6.5 Hz, 2H), 1.95 (s, 3H), 1.85 (dd, J = 12.9, 6.4 Hz, 1H), 0.92 (d, J = 6.8 Hz, 3H). 142 2-[(4-cyanobenzyl){[3- 1H NMR (400 MHz, methanol-d4) (ESI(+)) (dimethylamino)-3- δ 8.97 (s, 1H), 7.78 (s, 1H), m/e 509 oxopropyl]carbamoyl}amino]- 7.73 (d, J = 8.3 Hz, 2H), 7.70 (s, 1H), (M + H)+ N-[3-(1H-imidazol-1- 7.57 (s, 1H), 7.49 (d, J = 8.0 Hz, yl)propyl]-1,3-thiazole-5- 2H), 5.34 (s, 2H), 4.30 (t, J = 6.8 Hz, carboxamide 2H), 3.47 (t, J = 6.8 Hz, 2H), 3.35 (t, J = 6.4 Hz, 2H), 3.03 (s, 3H), 2.92 (s, 3H), 2.64 (d, J = 14.3 Hz, 2H), 2.22-2.07 (m, 2H) 143 2-{(4-cyanobenzyl)[(3- 1H NMR (400 MHz, methanol-d4) (ESI(+)) ethoxy-2- δ 8.96 (s, 1H), 7.78 (s, 1H), m/e 512 hydroxypropyl)carbamoyl]amino}- 7.73 (t, J = 7.2 Hz, 2H), 7.69 (s, 1H), (M + H)+ N-[3-(1H-imidazol- 7.57 (s, 1H), 7.51 (d, J = 8.1 Hz, 1-yl)propyl]-1,3-thiazole-5- 2H), 5.36 (s, 2H), 4.30 (t, J = 6.8 Hz, carboxamide 2H), 3.82 (t, J = 4.8 Hz, 1H), 3.52 (q, J = 7.1 Hz, 2H), 3.48-3.38 (m, 2H), 3.35 (d, J = 6.6 Hz, 2H), 3.22 (dd, J = 13.7, 7.0 Hz, 2H), 2.15 (t, J = 6.6 Hz, 2H), 1.18 (t, J = 7.1 Hz, 3H). 144 2-[(4-cyanobenzyl){[3- 1H NMR (400 MHz, methanol-d4) (ESI(+)) (diethylamino)propyl]carbamoyl}amino]- δ 8.97 (s, 1H), 7.85 (s, 1H), m/e 523 N-[3-(1H- 7.73 (d, J = 8.2 Hz, 2H), 7.70 (s, 1H), (M + H)+ imidazol-1-yl)propyl]-1,3- 7.57 (s, 1H), 7.50 (d, J = 8.2 Hz, thiazole-5-carboxamide 2H), 5.36 (s, 2H), 4.31 (t, J = 6.9 Hz, 2H), 3.35 (dd, J = 11.6, 5.0 Hz, 4H), 3.23 (q, J = 7.3 Hz, 4H), 3.18-3.11 (m, 2H), 2.15 (p, J = 6.8 Hz, 2H), 2.03-1.85 (m, 2H), 1.31 (t, J = 7.3 Hz, 6H). 145 2-[{[2- 1H NMR (400 MHz, methanol-d4) (ESI(+)) (acetylamino)ethyl]carbamoyl}(4- δ 8.97 (s, 1H), 7.79 (s, 1H), m/e 495 cyanobenzyl)amino]- 7.74 (d, J = 8.2 Hz, 2H), 7.69 (s, 1H), (M + H)+ N-[3-(1H-imidazol-1- 7.57 (s, 1H), 7.51 (d, J = 8.1 Hz, yl)propyl]-1,3-thiazole-5- 2H), 5.35 (s, 2H), 4.30 (t, J = 6.8 Hz, carboxamide 2H), 3.35 (t, J = 6.5 Hz, 2H), 2.22-2.07 (m, 2H), 1.93 (s, 3H). 146 2-[(4-cyanobenzyl){[2- 1H NMR (400 MHz, methanol-d4) (ESI(+)) (diethylamino)ethyl]carbamoyl}amino]- δ 8.97 (s, 1H), 7.87 (s, 1H), m/e 509 N-[3-(1H- 7.74 (d, J = 8.2 Hz, 2H), 7.70 (s, 1H), (M + H)+ imidazol-1-yl)propyl]-1,3- 7.58 (s, 1H), 7.49 (d, J = 8.2 Hz, thiazole-5-carboxamide 2H), 5.37 (s, 2H), 4.31 (t, J = 6.9 Hz, 2H), 3.56 (t, J = 5.9 Hz, 2H), 3.35 (t, J = 6.5 Hz, 2H), 3.27 (dd, J = 7.3, 2.8 Hz, 4H), 2.15 (t, J = 6.7 Hz, 2H), 1.33 (t, J = 7.3 Hz, 6H). 147 2-[(4-cyanobenzyl)({2-[(2- 1H NMR (400 MHz, methanol-d4) (ESI(+)) methylpropanoyl)amino]ethyl}carbamoyl)amino]- δ 8.96 (s, 1H), 7.78 (s, 1H), m/e 523 N-[3- 7.73 (d, J = 8.2 Hz, 2H), 7.69 (s, 1H), (M + H)+ (1H-imidazol-1-yl)propyl]- 7.57 (s, 1H), 7.50 (d, J = 8.2 Hz, 1,3-thiazole-5-carboxamide 2H), 5.34 (s, 2H), 4.29 (t, J = 6.8 Hz, 2H), 3.34 (t, J = 6.5 Hz, 2H), 2.39 (dt, J = 13.9, 7.0 Hz, 1H), 2.14 (p, J = 6.6 Hz, 2H), 1.07 (d, J = 6.9 Hz, 6H). 148 2-[(4-cyanobenzyl){[(2R)-1- 1H NMR (400 MHz, methanol-d4) (ESI(+)) hydroxybut-3-en-2- δ 8.96 (s, 1H), 7.78 (s, 1H), m/e 480 yl]carbamoyl}amino]-N-[3- 7.74 (d, J = 8.2 Hz, 2H), 7.69 (s, 1H), (M + H)+ (1H-imidazol-1-yl)propyl]- 7.57 (s, 1H), 7.52 (d, J = 8.1 Hz, 1,3-thiazole-5-carboxamide 2H), 5.97-5.81 (m, 1H), 5.47-5.31 (m, 2H), 5.24 (d, J = 17.0 Hz, 1H), 5.16 (d, J = 10.6 Hz, 1H), 4.39-4.33 (m, 1H), 4.30 (t, J = 6.8 Hz, 2H), 3.64-3.50 (m, 2H), 3.35 (t, J = 6.4 Hz, 2H), 2.14 (p, J = 6.8 Hz, 2H). 149 2-[(4-cyanobenzyl){[3-(3- 1H NMR (400 MHz, methanol-d4) (ESI(+)) hydroxyazetidin-1- δ 8.97 (s, 1H), 7.84 (s, 1H), m/e 523 yl)propyl]carbamoyl}amino]- 7.74 (d, J = 8.2 Hz, 2H), 7.69 (d, J = 1.5 Hz, (M + H)+ N-[3-(1H-imidazol-1- 1H), 7.58 (t, J = 1.6 Hz, yl)propyl]-1,3-thiazole-5- 1H), 7.50 (d, J = 8.0 Hz, 2H), carboxamide 5.36 (s, 2H), 4.68-4.58 (m, 1H), 4.47 (dd, J = 10.2, 8.2 Hz, 1H), 4.30 (t, J = 6.9 Hz, 2H), 4.26-4.14 (m, 1H), 4.06 (d, J = 8.9 Hz, 1H), 3.87-3.79 (m, 1H), 3.35 (t, J = 6.5 Hz, 2H), 3.27 (t, J = 6.7 Hz, 3H), 3.23-3.16 (m, 1H), 2.15 (p, J = 6.7 Hz, 2H), 1.80 (dt, J = 13.9, 7.1 Hz, 2H). 159 ethyl N-[(4-cyanobenzyl)(5- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) {[3-(1H-imidazol-1- 9.15 (s, 1H), 8.04-7.96 (m, 1H), m/e 510 yl)propyl]carbamoyl}-1,3- 7.96-7.84 (m, 1H), 7.64 (d, J = 8.2 Hz, (M + H)+ thiazol-2-yl)carbamoyl]- 2H), 7.37 (d, J = 8.1 Hz, beta-alaninate 2H), 7.31 (s, 1H), 5.50-5.36 (m, 2H), 4.33 (t, J = 6.2 Hz, 2H), 4.14 (q, J = 7.2 Hz, 2H), 3.57 (t, J = 6.2 Hz, 2H), 3.41 (td, J = 5.6, 1.0 Hz, 2H), 2.61-2.51 (m, 2H), 2.21 (qd, J = 6.8, 3.4 Hz, 2H), 1.25 (t, J = 7.2 Hz, 3H). 160 ethyl 4-{[(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) cyanobenzyl)(5-{[3-(1H- 9.39 (s, 1H), 8.00 (d, J = 46.6 Hz, m/e 524 imidazol-1- 1H), 7.71-7.60 (m, 2H), (M + H)+ yl)propyl]carbamoyl}-1,3- 7.44-7.34 (m, 3H), 7.28 (d, J = 1.5 Hz, thiazol-2- 1H), 5.50-5.42 (m, 1H), yl)carbamoyl]amino}butanoate 4.41-4.31 (m, 2H), 4.18-4.05 (m, 2H), 3.46-3.37 (m, 2H), 3.38-3.26 (m, 2H), 2.39-2.34 (m, 3H), 2.24-2.20 (m, 3H), 1.96-1.82 (m, 2H), 1.33-1.18 (m, 3H). 161 ethyl 3-{[(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) cyanobenzyl)(5-{[3-(1H- 9.15 (s, 1H), 8.09-8.00 (m, 1H), m/e 524 imidazol-1- 7.65 (d, J = 8.2 Hz, 2H), 7.39 (dd, (M + H)+ yl)propyl]carbamoyl}-1,3- J = 11.3, 4.8 Hz, 3H), 7.33 (s, thiazol-2- 1H), 5.54-5.47 (m, 2H), yl)carbamoyl]amino}butanoate 4.40-4.23 (m, 3H), 4.12 (q, J = 7.1 Hz, 2H), 3.42 (dd, J = 10.1, 5.1 Hz, 2H), 2.65-2.43 (m, 2H), 2.28-2.18 (m, 2H), 1.29-1.18 (m, 6H). 162 ethyl 3-{[(4- 1H NMR NMR (400 MHz, CDCl3) δ (ESI(+)) cyanobenzyl)(5-{[3-(1H- 9.13 (s, 1H), 8.10 (dd, J = 6.0, 1.4 Hz, m/e 552 imidazol-1- 1H), 8.05 (s, 1H), 7.65 (d, J = 8.2 Hz, (M + H)+ yl)propyl]carbamoyl}-1,3- 2H), 7.39 (d, J = 8.6 Hz, thiazol-2- 3H), 7.33 (d, J = 7.9 Hz, 1H), yl)carbamoyl]amino}-4- 7.04-6.94 (m, 1H), 5.48 (d, J = 24.0 Hz, methylpentanoate 2H), 5.35-5.26 (m, 1H), 4.33 (t, J = 6.3 Hz, 2H), 4.16-3.94 (m, 3H), 3.46-3.34 (m, 2H), 2.64-2.41 (m, 2H), 2.26-2.15 (m, 2H), 1.20 (t, J = 7.1 Hz, 3H), 0.93 (d, J = 6.5 Hz, 6H). 163 ethyl 3-{[(4- 1H NMR NMR (400 MHz, CDCl3) δ (ESI(+)) cyanobenzyl)(5-{[3-(1H- 9.21-9.08 (m, 1H), m/e 538 imidazol-1- 8.06-7.96 (m, 1H), 7.91 (dd, J = 5.9, 1.8 Hz, (M + H)+ yl)propyl]carbamoyl}-1,3- 1H), 7.65 (d, J = 8.1 Hz, 2H), thiazol-2- 7.38 (d, J = 8.2 Hz, 3H), 7.31 (s, yl)carbamoyl]amino}-2,2- 1H), 6.90-6.64 (m, 1H), 5.44 (d, dimethylpropanoate J = 20.7 Hz, 2H), 4.33 (t, J = 6.1 Hz, 2H), 4.18-4.08 (m, 2H), 3.49-3.37 (m, 4H), 2.24-2.13 (m, 2H), 1.31-1.17 (m, 9H). 164 3-{[(4-cyanobenzyl)(5-{[3- 1H NMR NMR (400 MHz, methanol-d4) (ESI(+)) (1H-imidazol-1- δ 8.97 (s, 1H), 7.80 (s, 1H), m/e 508 yl)propyl]carbamoyl}-1,3- 7.74 (d, J = 8.0 Hz, 2H), 7.69 (s, 1H), (M + H)+ thiazol-2- 7.57 (s, 1H), 7.52 (d, J = 7.9 Hz, yl)carbamoyl]amino}cyclobutanecarboxylic 2H), 5.37 (d, J = 9.8 Hz, 2H), acid 4.30 (t, J = 6.8 Hz, 2H), 4.26-4.11 (m, 1H), 3.34 (d, J = 3.4 Hz, 2H), 2.80 (d, J = 8.4 Hz, 1H), 2.55 (d, J = 8.1 Hz, 2H), 2.25-2.04 (m, 4H). 165 ethyl 3-{[(4- 1H NMR NMR (400 MHz, CDCl3) δ (ESI(+)) cyanobenzyl)(5-{[3-(1H- 9.26 (s, 1H), 7.94 (s, 1H), m/e 524 imidazol-1- 7.78 (ddd, J = 3.7, 2.7, 2.0 Hz, 1H), (M + H)+ yl)propyl]carbamoyl}-1,3- 7.64 (d, J = 8.1 Hz, 2H), 7.38 (d, J = 7.2 Hz, thiazol-2- 3H), 7.29 (s, 1H), yl)carbamoyl]amino}-2- 6.52 (d, J = 1.6 Hz, 1H), 5.37 (s, 2H), methylpropanoate 4.34 (t, J = 6.2 Hz, 2H), 4.21-4.07 (m, 2H), 3.46-3.33 (m, 4H), 2.75-2.68 (m, 1H), 2.24-2.15 (m, 2H), 1.33-1.12 (m, 6H). 166 2-{(4-cyanobenzyl)[(3- 1H NMR NMR (400 MHz, CDCl3) δ (ESI(+)) methoxypropyl)carbamoyl]amino}- 8.96 (s, 1H), 7.75 (d, J = 5.6 Hz, m/e 482 N-[3-(1H-imidazol- 2H), 7.73 (s, 1H), 7.69 (s, 1H), (M + H)+ 1-yl)propyl]-1,3-thiazole-5- 7.57 (s, 1H), 7.51 (d, J = 8.2 Hz, carboxamide 2H), 5.35 (s, 2H), 4.33-4.24 (m, 2H), 3.44 (t, J = 6.3 Hz, 2H), 3.39-3.34 (m, 3H), 3.28-3.23 (m, 2H), 2.20-2.08 (m, 2H), 1.84-1.72 (m, 2H). 167 3-{[(4-cyanobenzyl)(5-{[3- 1H NMR NMR (400 MHz, methanol-d4) (ESI(+)) (1H-imidazol-1- δ 8.97 (s, 1H), 7.75 (d, J = 6.1 Hz, m/e 496 yl)propyl]carbamoyl}-1,3- 2H), 7.72 (s, 1H), 7.69 (s, 1H), (M + H)+ thiazol-2- 7.57 (s, 1H), 7.51 (d, J = 8.2 Hz, yl)carbamoyl]amino}butanoic 2H), 5.35 (s, 2H), 4.30 (t, J = 6.8 Hz, acid 3H), 4.25-4.12 (m, 1H), 3.39-3.33 (m, 2H), 2.59 (dd, J = 15.3, 6.2 Hz, 1H), 2.42 (dd, J = 15.3, 7.0 Hz, 1H), 2.20-2.09 (m, 2H), 1.23 (d, J = 6.7 Hz, 3H). 168 3-{[(4-cyanobenzyl)(5-{[3- 1H NMR NMR (400 MHz, methanol-d4) (ESI(+)) (1H-imidazol-1- δ 8.96 (s, 1H), 7.73 (d, J = 8.3 Hz, m/e 524 yl)propyl]carbamoyl}-1,3- 3H), 7.69 (s, 1H), 7.57 (s, 1H), (M + H)+ thiazol-2- 7.52 (d, J = 8.2 Hz, 2H), 5.37 (dt, yl)carbamoyl]amino}-4- J = 26.9, 11.8 Hz, 2H), methylpentanoic acid 4.36-4.24 (m, 2H), 4.08-3.93 (m, 1H), 3.35 (d, J = 6.6 Hz, 2H), 2.54 (dd, J = 15.4, 5.1 Hz, 1H), 2.49-2.38 (m, 1H), 2.22-2.07 (m, 2H), 1.91-1.79 (m, 1H), 0.94 (dd, J = 6.7, 2.6 Hz, 6H). 169 3-{[(4-cyanobenzyl)(5-{[3- 1H NMR NMR (400 MHz, methanol-d4) (ESI(+)) (1H-imidazol-1- δ 8.96 (s, 1H), 7.80-7.71 (m, m/e 510 yl)propyl]carbamoyl}-1,3- 3H), 7.69 (s, 1H), 7.57 (s, 1H), (M + H)+ thiazol-2- 7.51 (d, J = 8.2 Hz, 2H), 5.37 (s, yl)carbamoyl]amino}-2,2- 2H), 4.29 (t, J = 6.8 Hz, 2H), dimethylpropanoic acid 3.43-3.32 (m, 4H), 2.22-2.07 (m, 2H), 1.18 (s, 6H). 170 3-{[(4-cyanobenzyl)(5-{[3- 1H NMR NMR (400 MHz, methanol-d4) (ESI(+)) (1H-imidazol-1- δ 8.96 (s, 1H), 7.81-7.71 (m, m/e 496 yl)propyl]carbamoyl}-1,3- 3H), 7.69 (s, 1H), 7.57 (s, 1H), (M + H)+ thiazol-2- 7.51 (d, J = 8.1 Hz, 2H), 5.35 (s, yl)carbamoyl]amino}-2- 2H), 4.30 (t, J = 6.8 Hz, 2H), methylpropanoic acid 3.50-3.33 (m, 4H), 2.75-2.61 (m, 1H), 2.15 (dd, J = 12.9, 6.4 Hz, 2H), 1.17 (d, J = 7.2 Hz, 3H) 171 N-[(4-cyanobenzyl)(5-{[3- 1H NMR NMR (400 MHz, methanol-d4) (ESI(+)) (1H-imidazol-1- δ 8.97 (s, 1H), 7.77 (s, 1H), m/e 482 yl)propyl]carbamoyl}-1,3- 7.73 (d, J = 8.2 Hz, 2H), 7.70 (s, 1H), (M + H)+ thiazol-2-yl)carbamoyl]- 7.57 (s, 1H), 7.51 (d, J = 8.2 Hz, beta-alanine 2H), 5.35 (s, 2H), 4.30 (t, J = 6.8 Hz, 2H), 3.46 (t, J = 6.8 Hz, 2H), 3.39-3.33 (m, 2H), 2.54 (t, J = 6.8 Hz, 2H), 2.22-2.08 (m, 2H). 172 4-{[(4-cyanobenzyl)(5-{[3- 1H NMR NMR (400 MHz, methanol-d4) (ESI(+)) (1H-imidazol-1- δ 8.97 (s, 1H), 7.77 (s, 1H), m/e 496 yl)propyl]carbamoyl}-1,3- 7.74 (d, J = 8.2 Hz, 2H), 7.70 (s, 1H), (M + H)+ thiazol-2- 7.57 (s, 1H), 7.52 (d, J = 8.1 Hz, yl)carbamoyl]amino}butanoic 2H), 5.35 (s, 2H), 4.30 (t, J = 6.8 Hz, acid 2H), 3.39-3.33 (m, 2H), 3.24 (t, J = 6.9 Hz, 2H), 2.34 (t, J = 7.5 Hz, 2H), 2.14 (dd, J = 8.4, 4.9 Hz, 2H), 1.81 (dd, J = 8.4, 5.9 Hz, 2H).

Example 9 2-{(4-fluorobenzyl) [2-(pyrrolidin-1-yl)ethyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide

Example 6B (0.018 g, 0.05 mmol) was dissolved in acetonitrile (0.5 ml), and treated with potassium carbonate (0.021 g, 0.15 mmol) and 1-(2-chloroethyl)pyrrolidine (0.017 g, 0.1 mmol). The reaction mixture was heated via microwave at 180° C. for 30 minutes, concentrated in vacuo, and submitted to reverse-phase HPLC (as described in Example 6C) to provide the title compound. 1H NMR (400 MHz, CDCl3) δ 10.78 (s, 1H), 9.07 (s, 1H), 7.94 (s, 1H), 7.33 (dd, J=8.7, 5.1 Hz, 3H), 7.11 (s, 1H), 7.04 (t, J=8.6 Hz, 2H), 4.48-4.38 (m, 4H), 4.30 (t, J=5.8 Hz, 2H), 3.41 (dd, J=11.1, 5.5 Hz, 2H), 2.88 (d, J=5.4 Hz, 2H), 2.65-2.55 (m, 4H), 2.20-2.19 (m, 3H), 1.78 (t, J=3.2 Hz, 5H); MS (ESI(+)) m/e 456.6 (M+H)+.

The following examples were prepared as described in Example 6B followed by Example 9, substituting the appropriate amine in Example 6B and the appropriate alkyl halide in Example 9. Title compounds were purified by either flash chromatography (silica gel column eluting with a gradient of 0-10% methanol in dichloromethane) or reverse-phase HPLC (as in Example 6C). Accordingly, some examples were isolated as trifluoroacetic acid salts.

MS EX NAME 1H NMR DATA DATA 7 2-{(4-fluorobenzyl)[3- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) (morpholin-4- 10.52 (s, 1H), 8.75 (d, J = 5.5 Hz, m/e 487 yl)propyl]amino}-N-[3-(1H- 1H), 7.85 (s, 1H), 7.33 (dd, J = 8.5, (M + H)+ imidazol-1-yl)propyl]-1,3- 5.3 Hz, 2H), 7.20 (s, 1H), thiazole-5-carboxamide 7.10 (s, 1H), 7.04 (t, J = 8.6 Hz, 2H), 4.47-4.37 (m, 4H), 4.25 (t, J = 7.0 Hz, 2H), 3.74-3.66 (m, 5H), 3.42 (dd, J = 11.2, 5.6 Hz, 2H), 2.44-2.36 (m, 4H), 2.34 (t, J = 6.6 Hz, 2H), 2.22 (dd, J = 11.3, 5.7 Hz, 2H), 2.02-1.91 (m, 2H). 8 2-{(4-fluorobenzyl)[3- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) (piperidin-1- 10.69 (s, 1H), 8.90 (s, 1H), m/e 485 yl)propyl]amino}-N-[3-(1H- 7.90 (s, 1H), 7.33 (dd, J = 8.5, 5.3 Hz, (M + H)+ imidazol-1-yl)propyl]-1,3- 2H), 7.21 (s, 1H), 7.15 (s, 1H), thiazole-5-carboxamide 7.04 (t, J = 8.6 Hz, 2H), 4.42 (d, J = 10.4 Hz, 4H), 4.26 (t, J = 7.0 Hz, 2H), 3.42 (dd, J = 11.1, 5.6 Hz, 2H), 2.44 (d, J = 27.4 Hz, 4H), 2.26-2.18 (m, 2H), 2.02-1.93 (m, 4H), 1.64-1.61 (m, 4H), 1.46-1.5 (m, 2H). 10 2-[(4-fluorobenzyl){2-[4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) (propan-2-yl)piperazin-1- 7.56 (s, 1H), 7.48 (s, 1H), m/e 514 yl]ethyl}amino]-N-[3-(1H- 7.32 (dd, J = 8.5, 5.5 Hz, 2H), 7.07 (s, (M + H)+ imidazol-1-yl)propyl]-1,3- 1H), 7.01 (t, J = 8.7 Hz, 2H), thiazole-5-carboxamide 6.97 (s, 1H), 4.24 (s, 2H), 4.04 (t, J = 6.9 Hz, 2H), 3.93 (t, J = 6.1 Hz, 2H), 3.39 (d, J = 6.3 Hz, 2H), 2.85-2.78 (m, 2H), 2.75-2.65 (m, 5H), 2.10-2.05 (m, 4H), 1.11 (d, J = 6.4 Hz, 6H). 14 2-{[(5-chloro-1,3- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) benzodioxol-4-yl)methyl](4- 11.17 (s, 1H), 9.15 (t, J = 5.6 Hz, m/e 529 fluorobenzyl)amino}-N-[3- 1H), 7.99 (s, 1H), 7.38-7.29 (m, (M + H)+ (1H-imidazol-1-yl)propyl]- 2H), 7.14 (s, 1H), 7.09 (dt, J = 11.7, 1,3-thiazole-5-carboxamide 1.7 Hz, 2H), 7.06-6.98 (m, 2H), 6.86 (s, 1H), 6.02 (s, 2H), 5.38 (s, 2H), 4.45 (s, 2H), 4.43-4.38 (m, 2H), 3.41 (dd, J = 11.0, 5.6 Hz, 2H), 2.28-2.14 (m, 2H), 2.06 (s, 6H). 15 2-[(4-chlorobenzyl)(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) fluorobenzyl)amino]-N-[3- 11.45 (s, 1H), 9.23 (dd, J = 7.2, m/e 484 (1H-imidazol-1-yl)propyl]- 3.6 Hz, 1H), 8.02 (s, 1H), (M + H)+ 1,3-thiazole-5-carboxamide 7.43-7.36 (m, 2H), 7.36-7.31 (m, 2H), 7.29 (t, J = 5.4 Hz, 2H), 7.13 (t, J = 1.7 Hz, 1H), 7.09-6.95 (m, 2H), 6.89 (t, J = 1.7 Hz, 1H), 5.34 (s, 2H), 4.45 (s, 2H), 4.45-4.37 (m, 2H), 3.48-3.35 (m, 2H), 2.29-2.17 (m, 2H). 16 2-[(2-chlorobenzyl)(4- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) fluorobenzyl)amino]-N-[3- 11.25 (s, 1H), 9.21-9.12 (m, 1H), m/e 484 (1H-imidazol-1-yl)propyl]- 8.03 (s, 1H), 7.62 (dd, J = 6.8, 2.4 Hz, (M + H)+ 1,3-thiazole-5-carboxamide 1H), 7.46-7.41 (m, 1H), 7.40-7.30 (m, 4H), 7.10 (dt, J = 12.9, 1.6 Hz, 2H), 7.06-6.98 (m, 2H), 5.50 (s, 2H), 4.45 (s, 2H), 4.42 (d, J = 6.1 Hz, 2H), 3.41 (dd, J = 11.1, 5.6 Hz, 2H), 2.22 (ddd, J = 7.4, 5.9, 2.1 Hz, 2H). 17 2-[(2,5-dichlorobenzyl)(4- 1H NMR (400 MHz, DMSO-d6) δ (ESI(+)) fluorobenzyl)amino]-N-[3- 9.23 (s, 1H), 8.61 (t, J = 6.0 Hz, m/e 519 (1H-imidazol-1-yl)propyl]- 1H), 8.25 (t, J = 5.8 Hz, 1H), (M + H)+ 1,3-thiazole-5-carboxamide 7.81 (t, J = 1.7 Hz, 1H), 7.75 (t, J = 1.7 Hz, 1H), 7.63 (s, 1H), 7.59-7.55 (m, 2H), 7.53 (dd, J = 8.6, 2.4 Hz, 1H), 7.34 (dd, J = 8.6, 5.6 Hz, 2H), 7.15 (dd, J = 12.3, 5.5 Hz, 2H), 5.47 (s, 2H), 4.41 (d, J = 5.1 Hz, 2H), 4.18 (t, J = 7.0 Hz, 2H), 3.15 (s, 2H), 1.98 (t, J = 6.8 Hz, 2H). 23 2-[(4-fluorobenzyl)(4- 1H NMR (400 MHz, DMSO-d6) δ (ESI(+)) methylbenzyl)amino]-N-[3- 9.10 (d, J = 1.2 Hz, 1H), 8.28 (t, J = 5.7 Hz, m/e 464 (1H-imidazol-1-yl)propyl]- 1H), 7.79 (dd, J = 5.8, (M + H)+ 1,3-thiazole-5-carboxamide 4.1 Hz, 2H), 7.68 (t, J = 1.6 Hz, 1H), 7.38-7.27 (m, 2H), 7.21-7.11 (m, 6H), 4.72 (s, 2H), 4.68 (s, 2H), 4.20 (d, J = 7.0 Hz, 2H), 3.18 (q, J = 6.6 Hz, 3H), 2.01 (p, J = 6.8 Hz, 2H). 47 2-[(4-fluorobenzyl)(3- 1H NMR (400 MHz, DMSO-d6) δ (ESI(+)) methylbutyl)amino]-N-[3- 9.11 (s, 1H), 8.27 (t, J = 5.7 Hz, m/e 430 (1H-imidazol-1-yl)propyl]- 1H), 7.81 (d, J = 1.4 Hz, 1H), (M + H)+ 1,3-thiazole-5-carboxamide 7.75 (s, 1H), 7.69 (t, J = 1.5 Hz, 1H), 7.33 (dd, J = 8.6, 5.6 Hz, 2H), 7.23-7.08 (m, 2H), 4.69 (s, 2H), 4.22 (t, J = 7.0 Hz, 2H), 3.46-3.42 (m, 2H), 3.19 (dd, J = 11.6, 5.5 Hz, 2H), 2.02 (p, J = 6.8 Hz, 2H), 1.54 (dt, J = 12.9, 6.5 Hz, 1H), 1.46 (dd, J = 15.0, 7.1 Hz, 2H), 0.88 (d, J = 6.4 Hz, 6H). 55 2-[(2-fluorobenzyl)(3- 1H NMR (400 MHz, DMSO- (ESI(+)) methylbutyl)amino]-N-[3- d6/D2O) δ 9.22 (s, 1H), 7.78 (t, J = 1.7 Hz, m/e 430 (1H-imidazol-1-yl)propyl]- 1H), 7.73 (t, J = 1.7 Hz, (M + H)+ 1,3-thiazole-5-carboxamide 1H), 7.67 (s, 1H), 7.53-7.46 (m, 2H), 7.33-7.26 (m, 2H), 5.48 (s, 2H), 4.21 (t, J = 7.0 Hz, 2H), 3.31-3.22 (m, 2H), 3.20 (t, J = 6.6 Hz, 2H), 2.10-1.95 (m, 2H), 1.63 (dt, J = 13.3, 6.7 Hz, 1H), 1.45 (dd, J = 14.4, 7.0 Hz, 2H), 0.89 (d, J = 6.6 Hz, 6H). 56 2-[(3-fluorobenzyl)(3- 1H NMR (400 MHz, DMSO- (ESI(+)) methylbutyl)amino]-N-[3- d6/D2O) δ 9.03 (s, 1H), 7.74 (d, J = 2.1 Hz, m/e 430 (1H-imidazol-1-yl)propyl]- 2H), 7.64 (s, 1H), (M + H)+ 1,3-thiazole-5-carboxamide 7.41 (dd, J = 14.1, 7.9 Hz, 1H), 7.10 (dd, J = 17.6, 9.2 Hz, 3H), 4.73 (s, 2H), 4.22 (t, J = 7.0 Hz, 2H), 3.54-3.42 (m, 2H), 3.20 (t, J = 6.5 Hz, 2H), 2.03 (t, J = 6.8 Hz, 2H), 1.59-1.51 (m, 1H), 1.50-1.43 (m, 2H), 0.88 (d, J = 6.4 Hz, 6H). 57 2-[(2-chlorobenzyl)(3- 1H NMR (400 MHz, DMSO- (ESI(+)) methylbutyl)amino]-N-[3- d6/D2O) δ 9.22 (s, 1H), 7.80 (t, J = 1.7 Hz, m/e 447 (1H-imidazol-1-yl)propyl]- 1H), 7.71 (t, J = 1.7 Hz, (M + H)+ 1,3-thiazole-5-carboxamide 1H), 7.67 (s, 1H), 7.57 (d, J = 7.5 Hz, 1H), 7.51-7.42 (m, 3H), 5.51 (s, 2H), 4.22 (t, J = 7.0 Hz, 2H), 3.28-3.23 (m, 2H), 3.20 (t, J = 6.7 Hz, 2H), 2.03 (p, J = 6.7 Hz, 2H), 1.63 (dt, J = 13.3, 6.7 Hz, 1H), 1.45 (dd, J = 14.4, 7.0 Hz, 2H), 0.89 (d, J = 6.6 Hz, 6H). 58 2-[(3-chlorobenzyl)(3- 1H NMR (400 MHz, DMSO- (ESI(+)) methylbutyl)amino]-N-[3- d6/D2O) δ 9.02 (s, 1H), 7.74 (s, m/e 447 (1H-imidazol-1-yl)propyl]- 2H), 7.63 (s, 1H), 7.39 (dd, J = 13.9, (M + H)+ 1,3-thiazole-5-carboxamide 6.6 Hz, 3H), 7.32 (s, 1H), 7.25 (d, J = 7.4 Hz, 1H), 4.72 (s, 2H), 4.22 (t, J = 7.0 Hz, 2H), 3.47 (d, J = 7.1 Hz, 2H), 3.20 (t, J = 6.5 Hz, 2H), 2.09-1.97 (m, 2H), 1.54 (d, J = 6.2 Hz, 1H), 1.50-1.44 (m, 2H), 0.88 (d, J = 6.4 Hz, 6H). 59 2-[(4-chlorobenzyl)(3- 1H NMR (400 MHz, DMSO- (ESI(+)) methylbutyl)amino]-N-[3- d6/D2O) δ 7.73 (s, 2H), 7.62 (s, m/e 447 (1H-imidazol-1-yl)propyl]- 1H), 7.41 (d, J = 8.5 Hz, 3H), (M + H)+ 1,3-thiazole-5-carboxamide 7.38 (s, 1H), 7.30 (d, J = 8.5 Hz, 2H), 4.69 (s, 2H), 4.21 (t, J = 7.1 Hz, 2H), 3.47 (dd, J = 11.5, 4.4 Hz, 2H), 3.19 (t, J = 6.6 Hz, 2H), 2.03 (t, J = 6.8 Hz, 2H), 1.53 (d, J = 6.7 Hz, 1H), 1.51-1.44 (m, 2H), 0.88 (d, J = 6.4 Hz, 6H). 60 2-[(4-cyanobenzyl)(3- 1H NMR (400 MHz, DMSO- (ESI(+)) methylbutyl)amino]-N-[3- d6/D2O) δ 7.85-7.78 (m, 3H), m/e 437 (1H-imidazol-1-yl)propyl]- 7.74 (s, 1H), 7.72 (s, 1H), 7.64 (s, (M + H)+ 1,3-thiazole-5-carboxamide 1H), 7.46 (d, J = 8.2 Hz, 2H), 4.80 (s, 2H), 4.22 (t, J = 6.9 Hz, 2H), 3.49 (m, 2H), 3.19 (t, J = 6.7 Hz, 2H), 2.09-1.97 (m, 2H), 1.55 (s, 1H), 1.48 (d, J = 8.4 Hz, 2H), 0.89 (d, J = 6.4 Hz, 6H).

Example 18 2-{(4-fluorobenzyl)[2-(methylamino)-2-oxoethyl]amino}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide

Example 6B (0.018 g, 0.05 mmol) was dissolved in DMSO:CH3OH 1:1 (0.5 ml), Hunig's base (0.02 mL, 0.15 mmol) and 2-chloro-N-methylacetamide (0.006 g, 0.6 mmol). The reaction mixture was heated at 80° C. overnight and submitted to reverse-phase HPLC (as described in Example 6C) to afford the title compound. 1H NMR (400 MHz, methanol-d4) δ 7.70 (d, J=1.9 Hz, 1H), 7.64 (s, 1H), 7.59 (d, J=1.9 Hz, 1H), 7.36 (dd, J=8.4, 5.5 Hz, 2H), 7.06 (t, J=8.7 Hz, 2H), 4.97 (s, 2H), 4.48 (s, 2H), 4.29 (t, J=6.9 Hz, 2H), 3.35 (t, J=6.4 Hz, 2H), 2.79 (s, 3H), 2.14 (p, J=6.7 Hz, 2H); MS (ESI(+)) m/e 431 (M+H)+.

The following examples were prepared as described in Example 18, substituting the appropriate chloro-acetamide. Title compounds were purified by either flash chromatography (silica gel column eluting with a gradient of 0-10% methanol in dichloromethane) or reverse-phase HPLC (as described in Example 6C). Accordingly, some examples were isolated as trifluoroacetic acid salts.

MS EX NAME 1H NMR DATA DATA 19 2-{(4-fluorobenzyl)[2-oxo- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) 2-(propan-2- 10.95-10.86 (m, 1H), m/e 459 ylamino)ethyl]amino}-N-[3- 8.81-8.68 (m, 1H), 8.67-8.53 (m, 1H), (M + H)+ (1H-imidazol-1-yl)propyl]- 8.02-7.93 (m, 1H), 7.51 (ddd, J = 5.5, 1,3-thiazole-5-carboxamide 4.8, 1.7 Hz, 1H), 7.34 (dd, J = 8.4, 5.5 Hz, 2H), 7.14 (s, 1H), 7.07-6.99 (m, 2H), 5.04 (s, 2H), 4.46 (s, 2H), 4.38-4.27 (m, 2H), 3.96 (dd, J = 13.5, 6.8 Hz, 1H), 3.40-3.27 (m, 2H), 2.19-2.17 (m, 2H), 1.18 (d, J = 6.6 Hz, 6H). 20 2-{[2-(dimethylamino)-2- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) oxoethyl](4- 10.99-10.90 (m, 1H), m/e 445 fluorobenzyl)amino}-N-[3- 8.97-8.89 (m, 1H), 8.01 (s, 1H), (M + H)+ (1H-imidazol-1-yl)propyl]- 7.36-7.29 (m, 2H), 7.22 (t, J = 1.6 Hz, 1H), 1,3-thiazole-5-carboxamide 7.13 (t, J = 1.7 Hz, 1H), 7.07-6.99 (m, 2H), 5.36 (s, 2H), 4.45 (s, 2H), 4.41-4.32 (m, 2H), 3.38 (dd, J = 11.1, 5.7 Hz, 2H), 3.12 (s, 3H), 3.00 (s, 3H), 2.23-2.19 (m, 2H). 21 2-{[2-(diethylamino)-2- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) oxoethyl](4- 11.08-11.00 (m, 1H), m/e 473 fluorobenzyl)amino}-N-[3- 9.04-8.96 (m, 1H), 8.11-8.02 (m, 1H), (M + H)+ (1H-imidazol-1-yl)propyl]- 7.33 (dd, J = 8.5, 5.4 Hz, 2H), 7.25 (t, 1,3-thiazole-5-carboxamide J = 1.6 Hz, 1H), 7.13 (s, 1H), 7.04 (dd, J = 9.8, 7.5 Hz, 2H), 5.34 (s, 2H), 4.45 (s, 2H), 4.36 (dd, J = 7.8, 4.0 Hz, 2H), 3.44-3.37 (m, 6H), 2.24-2.19 (m, 2H), 1.29 (t, J = 5.4 Hz, 3H), 1.15 (t, J = 7.1 Hz, 3H). 22 2-{(4-fluorobenzyl)[2- 1H NMR (400 MHz, CDCl3) δ (ESI(+)) (morpholin-4-yl)-2- 11.09-11.00 (m, 1H), m/e 487 oxoethyl]amino}-N-[3-(1H- 8.92-8.79 (m, 1H), 8.11-8.02 (m, 1H), (M + H)+ imidazol-1-yl)propyl]-1,3- 7.36-7.29 (m, 2H), 7.24 (d, J = 1.5 Hz, thiazole-5-carboxamide 1H), 7.19-7.11 (m, 1H), 7.06-6.99 (m, 2H), 5.46 (dd, J = 4.8, 2.0 Hz, 2H), 4.45 (d, J = 3.3 Hz, 2H), 4.41-4.30 (m, 2H), 3.78 (ddd, J = 6.4, 5.3, 2.4 Hz, 2H), 3.75-3.70 (m, 2H), 3.63-3.57 (m, 4H), 3.37 (tdd, J = 7.3, 2.3, 1.4 Hz, 2H), 2.27-2.18 (m, 2H).

Example 26 2-[(N,N-dimethylglycyl)(4-fluorobenzyl)amino]-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide

Example 6B (0.036 g, 0.1 mmol) was dissolved in dichloromethane:pyridine 10:1 (1 ml), cooled to −10° C., and treated with chloroacetyl bromide (0.011 mL, 0.125 mmol). The resultant solution was stirred at room temperature for 30 minutes. The reaction mixture was then treated with an excess of dimethylamine in tetrahydrofuran (0.5 mL, 1M solution). The reaction mixture was heated at 80° C. overnight and purified by reverse-phase HPLC (as described in Example 6C) to afford the title compound. 1H NMR (400 MHz, methanol-d4) δ 8.98 (s, 1H), 8.03 (s, 1H), 7.71 (s, 1H), 7.58 (s, 1H), 7.35-7.23 (m, 2H), 7.10 (t, J=8.7 Hz, 2H), 5.48 (s, 2H), 4.60-4.45 (m, 2H), 4.32 (t, J=6.9 Hz, 2H), 3.40 (t, J=6.5 Hz, 2H), 2.98 (s, 6H), 2.18 (t, J=6.7 Hz, 2H); MS (ESI(+)) m/e 445 (M+H)+.

The following examples were prepared as described in Example 26, substituting the appropriate alkyl halide in Example 26. Title compounds were purified by either flash chromatography (silica gel column eluting with a gradient of 0-10% methanol in dichloromethane) or reverse-phase HPLC (as in described Example 6C). Accordingly, some examples were isolated as trifluoroacetic acid salts.

MS EX NAME 1H NMR DATA DATA 27 2-[(3,6-dihydropyridin- 1H NMR (400 MHz, methanol-d4) (ESI(+)) 1(2H)-ylacetyl)(4- δ 8.95 (s, 1H), 8.03 (s, 1H), m/e 483 fluorobenzyl)amino]-N-[3- 7.69 (s, 1H), 7.56 (s, 1H), 7.28 (s, 2H), (M + H)+ (1H-imidazol-1-yl)propyl]- 7.10 (t, J = 8.7 Hz, 2H), 5.98 (s, 1,3-thiazole-5-carboxamide 1H), 5.73 (s, 1H), 5.51 (s, 2H), 4.53-2.44 (m, 2H), 4.32 (t, J = 6.9 Hz, 2H), 3.88-3.78 (m, 1H), 3.57-3.42 (m, 1H), 3.40 (t, J = 6.6 Hz, 1H), 2.52-2.46 (m, 2H), 2.17 (dd, J = 13.5, 6.8 Hz, 2H). 28 2-{(4-fluorobenzyl)[(4- 1H NMR (400 MHz, methanol-d4) (ESI(+)) methylpiperidin-1- δ 8.98 (s, 1H), 8.03 (s, 1H), m/e 499 yl)acetyl]amino}-N-[3-(1H- 7.71 (s, 1H), 7.58 (s, 1H), 7.27 (s, 2H), (M + H)+ imidazol-1-yl)propyl]-1,3- 7.10 (t, J = 8.7 Hz, 2H), 5.49 (s, thiazole-5-carboxamide 2H), 4.45 (s, 2H), 4.32 (dd, J = 8.9, 4.9 Hz, 2H), 3.63 (d, J = 10.7 Hz, 2H), 3.40 (t, J = 6.5 Hz, 2H), 3.04 (t, J = 12.6 Hz, 2H), 2.21-2.14 (m, 2H), 1.92 (d, J = 15.0 Hz, 2H), 1.71 (s, 1H), 1.56 (d, J = 12.4 Hz, 2H), 1.03 (d, J = 6.4 Hz, 3H). 29 2-{(4-fluorobenzyl)[(4- 1H NMR (400 MHz, methanol-d4) (ESI(+)) hydroxypiperidin-1- δ 8.98 (s, 1H), 8.03 (s, 1H), m/e 501 yl)acetyl]amino}-N-[3-(1H- 7.71 (s, 1H), 7.58 (s, 1H), 7.28 (s, 2H), (M + H)+ imidazol-1-yl)propyl]-1,3- 7.10 (t, J = 8.7 Hz, 2H), 5.49 (s, thiazole-5-carboxamide 2H), 4.49 (s, 2H), 4.32 (t, J = 7.0 Hz, 2H), 3.46 (d, J = 5.3 Hz, 1H), 3.40 (t, J = 6.6 Hz, 2H), 2.19 (dd, J = 13.7, 6.8 Hz, 2H), 2.12 (d, J = 22.1 Hz, 2H), 1.91-1.85 (m, 2H). 30 2-{(4-fluorobenzyl)[(4- 1H NMR (400 MHz, methanol-d4) (ESI(+)) methylpiperazin-1- δ 8.99 (s, 1H), 7.99 (s, 1H), m/e 500 yl)acetyl]amino}-N-[3-(1H- 7.71 (d, J = 1.4 Hz, 1H), 7.59 (s, 1H), (M + H)+ imidazol-1-yl)propyl]-1,3- 7.27-7.15 (m, 2H), 7.08 (t, J = 8.7 Hz, thiazole-5-carboxamide 2H), 5.54 (s, 2H), 4.33 (t, J = 7.0 Hz, 2H), 3.71 (s, 2H), 3.40 (t, J = 6.5 Hz, 2H), 3.13-2.91 (m, 4H), 2.88 (s, 3H), 2.82-2.66 (m, 2H), 2.19 (p, J = 7.0 Hz, 2H). 31 2-[(4-fluorobenzyl){[4- 1H NMR (400 MHz, methanol-d4) (ESI(+)) (propan-2-yl)piperazin-1- δ 8.99 (s, 1H), 7.99 (s, 1H), m/e 528 yl]acetyl}amino]-N-[3-(1H- 7.72 (t, J = 1.6 Hz, 1H), 7.59 (t, J = 1.6 Hz, (M + H)+ imidazol-1-yl)propyl]-1,3- 1H), 7.21 (dd, J = 8.6, 5.3 Hz, thiazole-5-carboxamide 2H), 7.08 (dd, J = 12.2, 5.3 Hz, 2H), 5.55 (s, 2H), 4.33 (t, J = 6.9 Hz, 2H), 3.71 (s, 2H), 3.51-3.37 (m, 4H), 3.15-2.91 (m, 4H), 2.75-2.67 (m, 1H), 2.19 (t, J = 6.7 Hz, 2H), 1.33 (d, J = 6.7 Hz, 6H). 32 2-{(4-fluorobenzyl)[(4- 1H NMR (400 MHz, methanol-d4) (ESI(+)) formylpiperazin-1- δ 8.99 (s, 1H), 8.05 (s, 1H), m/e 514 yl)acetyl]amino}-N-[3-(1H- 8.00 (d, J = 9.0 Hz, 1H), 7.72 (s, 1H), (M + H)+ imidazol-1-yl)propyl]-1,3- 7.59 (s, 1H), 7.31-7.19 (m, 2H), thiazole-5-carboxamide 7.15-7.03 (m, 2H), 5.66-5.41 (m, 2H), 4.33 (t, J = 7.0 Hz, 2H), 4.21-4.03 (m, 2H), 3.68 (tdd, J = 5.0, 4.5, 1.3 Hz, 2H), 3.66-3.60 (m, 2H), 3.46-3.38 (m, 2H), 3.16-2.93 (m, 4H), 2.25-2.13 (m, 2H). 33 2-[(4- 1H NMR (400 MHz, methanol-d4) (ESI(+)) fluorobenzyl)(hexahydropyrrolo[1, δ 8.99 (s, 1H), 7.99 (s, 1H), m/e 526 2-a]pyrazin-2(1H)- 7.72 (t, J = 1.6 Hz, 1H), 7.59 (t, J = 1.5 Hz, (M + H)+ ylacetyl)amino]-N-[3-(1H- 1H), 7.21 (dd, J = 8.5, 5.3 Hz, imidazol-1-yl)propyl]-1,3- 2H), 7.08 (t, J = 8.7 Hz, 2H), thiazole-5-carboxamide 5.54 (s, 2H), 4.33 (t, J = 6.9 Hz, 2H), 3.81-3.68 (m, 2H), 3.39 (d, J = 6.5 Hz, 2H), 3.26-2.68 (m, 6H), 2.28-2.01 (m, 5H). 34 2-[{[4- 1H NMR (400 MHz, methanol-d4) (ESI(+)) (cyclopropylmethyl)piperazin- δ 8.99 (s, 1H), 8.00 (s, 1H), m/e 540 1-yl]acetyl}(4- 7.72 (t, J = 1.7 Hz, 1H), 7.59 (s, 1H), (M + H)+ fluorobenzyl)amino]-N-[3- 7.27-7.15 (m, 2H), (1H-imidazol-1-yl)propyl]- 7.15-7.02 (m, 2H), 5.55 (s, 2H), 4.33 (t, J = 6.9 Hz, 1,3-thiazole-5-carboxamide 2H), 3.72 (s, 2H), 3.65-3.50 (m, 2H), 3.40 (dd, J = 8.0, 5.1 Hz, 2H), 3.17-2.97 (m, 6H), 2.88-2.68 (m, 2H), 2.26-2.11 (m, 2H), 1.06 (d, J = 7.2 Hz, 1H), 0.83-0.70 (m, 2H), 0.43 (dd, J = 5.6, 4.9 Hz, 2H). 35 2-[{[4-(2- 1H NMR (400 MHz, methanol-d4) (ESI(+)) ethoxyethyl)piperazin-1- δ 8.99 (s, 1H), 7.99 (s, 1H), m/e 558 yl]acetyl}(4- 7.72 (s, 1H), 7.59 (s, 1H), 7.21 (dd, J = 8.6, (M + H)+ fluorobenzyl)amino]-N-[3- 5.2 Hz, 2H), 7.09-7.06 (m, (1H-imidazol-1-yl)propyl]- 2H), 5.55 (s, 2H), 4.39-4.24 (m, 1,3-thiazole-5-carboxamide 2H), 3.74 (dd, J = 6.4, 3.6 Hz, 2H), 3.71 (s, 2H), 3.57 (q, J = 7.1 Hz, 2H), 3.40 (t, J = 6.5 Hz, 2H), 2.95 (d, J = 58.3 Hz, 6H), 2.26-2.09 (m, 2H), 1.22 (t, J = 7.0 Hz, 3H). 37 2-[(4-fluorobenzyl){[4- 1H NMR (400 MHz, methanol-d4) (ESI(+)) (prop-2-en-1-yl)piperazin-1- δ 8.99 (s, 1H), 8.00 (s, 1H), m/e 526 yl]acetyl}amino]-N-[3-(1H- 7.71 (d, J = 7.5 Hz, 1H), 7.58 (s, 1H), (M + H)+ imidazol-1-yl)propyl]-1,3- 7.21 (dd, J = 8.5, 5.3 Hz, 2H), thiazole-5-carboxamide 7.08 (t, J = 8.7 Hz, 2H), 6.01-5.82 (m, 1H), 5.62 (s, 1H), 5.59 (d, J = 6.2 Hz, 1H), 5.54 (s, 2H), 4.33 (t, J = 6.9 Hz, 2H), 3.74 (d, J = 7.3 Hz, 2H), 3.75-3.70 (m, 2H), 3.40 (t, J = 6.5 Hz, 2H), 2.95-2.9 (m, 4H), 2.19 (p, J = 6.9 Hz, 2H). 38 2-[(4-fluorobenzyl){[4-(3- 1H NMR (400 MHz, methanol-d4) (ESI(+)) methoxypropyl)piperazin-1- δ 8.99 (s, 1H), 8.00 (s, 1H), m/e 558 yl]acetyl}amino]-N-[3-(1H- 7.71 (s, 1H), 7.58 (s, 1H), 7.21 (dd, J = 8.5, (M + H)+ imidazol-1-yl)propyl]-1,3- 5.3 Hz, 2H), 7.08 (t, J = 8.7 Hz, thiazole-5-carboxamide 2H), 5.55 (s, 2H), 4.33 (t, J = 6.9 Hz, 2H), 3.71 (s, 2H), 3.48 (t, J = 5.6 Hz, 2H), 3.40 (t, J = 6.5 Hz, 2H), 3.34 (s, 3H), 3.23 (t, J = 8.0 Hz, 2H), 2.26-2.09 (m, 2H), 1.97 (dd, J = 9.7, 5.8 Hz, 2H). 39 2-[{[3- 1H NMR (400 MHz, methanol-d4) (ESI(+)) (dimethylamino)pyrrolidin- δ 8.99 (s, 1H), 8.01 (s, 1H), m/e 514 1-yl]acetyl}(4- 7.71 (s, 1H), 7.58 (s, 1H), 7.24 (dd, J = 8.5, (M + H)+ fluorobenzyl)amino]-N-[3- 5.3 Hz, 2H), 7.08 (t, J = 8.7 Hz, (1H-imidazol-1-yl)propyl]- 2H), 5.51 (s, 2H), 4.33 (t, J = 6.9 Hz, 1,3-thiazole-5-carboxamide 2H), 4.06 (d, J = 32.5 Hz, 2H), 3.97-3.90 (m, 1H), 3.52-3.43 (m, 1H), 3.40 (t, J = 6.5 Hz, 2H), 3.13 (s, 1H), 2.91 (s, 6H), 2.40 (dd, J = 13.1, 4.6 Hz, 1H), 2.26-2.06 (m, 3H). 40 2-[(4- 1H NMR (400 MHz, methanol-d4) (ESI(+)) fluorobenzyl)(morpholin-4- δ 8.99 (s, 1H), 8.04 (s, 1H), m/e 487 ylacetyl)amino]-N-[3-(1H- 7.71 (s, 1H), 7.58 (s, 1H), (M + H)+ imidazol-1-yl)propyl]-1,3- 7.35-7.23 (m, 2H), 7.10 (t, J = 8.7 Hz, 2H), thiazole-5-carboxamide 5.50 (s, 2H), 4.54 (s, 2H), 4.33 (t, J = 6.9 Hz, 2H), 3.99-3.90 (m, 4H), 3.53-3.33 (m, 6H), 2.19 (p, J = 6.8 Hz, 2H). 41 2-{(4-fluorobenzyl)[(3- 1H NMR (400 MHz, methanol-d4) (ESI(+)) hydroxypiperidin-1- δ 8.99 (s, 1H), 8.04 (s, 1H), m/e 501 yl)acetyl]amino}-N-[3-(1H- 7.71 (s, 1H), 7.59 (s, 1H), (M + H)+ imidazol-1-yl)propyl]-1,3- 7.34-7.23 (m, 2H), 7.10 (t, J = 8.7 Hz, 2H), thiazole-5-carboxamide 5.50 (s, 2H), 4.50 (m, 1H), 4.33 (t, J = 7.0 Hz, 2H), 4.15-4.1 (m, 1H), 3.76-3.49 (m, 1H), 3.40 (t, J = 6.6 Hz, 2H), 3.27-2.95 (m, 2H), 2.19 (p, J = 6.8 Hz, 2H), 1.79 (d, J = 15.5 Hz, 2H). 42 2-[(4-fluorobenzyl){[4-(2- 1H NMR (400 MHz, methanol-d4) (ESI(+)) hydroxyethyl)piperazin-1- δ 8.99 (s, 1H), 8.00 (s, 1H), m/e 530 yl]acetyl}amino]-N-[3-(1H- 7.72 (s, 1H), 7.58 (s, 1H), 7.22 (dd, J = 8.6, (M + H)+ imidazol-1-yl)propyl]-1,3- 5.3 Hz, 2H), 7.08 (t, J = 8.7 Hz, thiazole-5-carboxamide 2H), 5.55 (s, 2H), 4.33 (t, J = 6.9 Hz, 2H), 3.91-3.80 (m, 2H), 3.75-3.65 (m, 2H), 3.40 (t, J = 6.5 Hz, 2H), 3.26-3.21 (m, 2H), 2.98-2.88 (m, 4H), 2.19 (p, J = 6.7 Hz, 2H). 43 2-[(1,4-dioxa-7- 1H NMR (400 MHz, methanol-d4) (ESI(+)) azaspiro[4.4]non-7- δ 8.99 (s, 1H), 8.03 (s, 1H), m/e 529 ylacetyl)(4- 7.71 (s, 1H), 7.58 (s, 1H), (M + H)+ fluorobenzyl)amino]-N-[3- 7.35-7.23 (m, 2H), 7.10 (t, J = 8.7 Hz, 2H), (1H-imidazol-1-yl)propyl]- 5.48 (s, 2H), 4.64 (s, 2H), 4.33 (t, 1,3-thiazole-5-carboxamide J = 6.9 Hz, 2H), 3.99 (d, J = 3.7 Hz, 4H), 3.72-3.63 (m, 2H), 3.6-3.5 (m, 2H), 3.40 (t, J = 6.5 Hz, 2H), 2.29 (t, J = 7.7 Hz, 2H), 2.19 (p, J = 6.7 Hz, 2H).

Example 212 2-{(5S)-5-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-2-oxo-1,3-oxazolidin-3-yl}-N-[3-(1H-imidazol-1-yl)propyl]-1,3-thiazole-5-carboxamide

Example 6A (0.095 g, 0.3 mmol), (R)-2-((2-oxooxazolidin-5-yl)methyl)isoindoline-1,3-dione (0.049 g, 0.2 mmol), and potassium phosphate (0.127 g, 0.6 mmol) were suspended in dry dioxane, and nitrogen was bubbled through for 5 minutes. Tris(dibenzylideneacetone)dipalladium(0) (0.018 g. 0.02 mmol) and 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (XantPhos, 0.035 g, 0.06 mmol) were added to the reaction, and the vial capped. The reaction was stirred at 90° C. for 5 hours, concentrated and submitted to reverse phase HPLC (as described in Example 6C) to afford the title compound. 1H NMR (400 MHz, methanol-d4) δ 8.98 (s, 1H), 7.95 (s, 1H), 7.90 (dt, J=7.3, 3.7 Hz, 2H), 7.87-7.80 (m, 2H), 7.71 (d, J=1.6 Hz, 1H), 7.58 (t, J=1.6 Hz, 1H), 5.16 (dt, J=12.7, 5.8 Hz, 1H), 4.40 (dd, J=10.2, 8.8 Hz, 1H), 4.33 (t, J=6.8 Hz, 2H), 4.20 (dd, J 10.4, 5.8 Hz, 1H), 4.10 (ddd, J=19.6, 14.6, 5.9 Hz, 2H), 3.39 (dd, J=11.2, 6.1 Hz, 2H), 2.18 (p, J=6.7 Hz, 2H); MS (ESI(+)) m/e 480.5 (M+H)+.

The following examples were prepared as described in Example 212, substituting the appropriate imidazolidinone for the oxazolidinone. Title compounds were purified by either flash chromatography (silica gel column eluting with a gradient of 0-10% methanol in dichloromethane) or reverse-phase HPLC (as described in Example 6C). Accordingly, some examples were isolated as trifluoroacetic acid salts.

MS EX NAME 1H NMR DATA DATA 203 2-[3-(2-hydroxyethyl)-2- 1H NMR (400 MHz, methanol-d4) (ESI(+)) oxoimidazolidin-1-yl]-N-[3- δ 7.89 (s, 1H), 7.70 (s, 1H), m/e 365 (1H-imidazol-1-yl)propyl]- 7.18 (s, 1H), 6.97 (s, 1H), 4.10 (dd, J = 11.6, (M + H)+ 1,3-thiazole-5-carboxamide 4.7 Hz, 4H), 3.74 (dd, J = 12.9, 7.2 Hz, 4H), 3.43 (t, J = 5.4 Hz, 2H), 3.34 (t, J = 6.8 Hz, 2H), 2.07 (p, J = 6.8 Hz, 2H). 204 2-[3-(4-fluorophenyl)-2- 1H NMR (400 MHz, methanol-d4) (ESI(+)) oxoimidazolidin-1-yl]-N-[3- δ 8.99 (s, 1H), 7.95 (s, 1H), m/e 415 (1H-imidazol-1-yl)propyl]- 7.76-7.54 (m, 4H), 7.15 (t, J = 8.8 Hz, (M + H)+ 1,3-thiazole-5-carboxamide 2H), 4.34 (t, J = 6.8 Hz, 2H), 4.24 (dd, J = 10.0, 6.5 Hz, 2H), 4.13 (dd, J = 9.9, 6.7 Hz, 2H), 3.40 (dd, J = 11.5, 6.0 Hz, 2H), 2.19 (p, J = 6.6 Hz, 2H).

Claims

1-9. (canceled)

10. A method of treating inflammatory and tissue repair disorders; particularly rheumatoid arthritis, inflammatory bowel disease, asthma and COPD (chronic obstructive pulmonary disease), osteoarthritis, osteoporosis and fibrotic diseases; dermatosis, including psoriasis, atopic dermatitis and ultra-violet induced skin damage; autoimmune diseases including systemic lupus erythematosis, multiple sclerosis, psoriatic arthritis, ankylosing spondylitis, tissue and organ rejection, Alzheimer's disease, stroke, athersclerosis, restenosis, diabetes, glomerulonephritis, cancer, particularly wherein the cancer is selected from breast, prostate, lung, colon, cervix, ovary, skin, CNS, bladder, pancreas, leukemia, lymphoma or Hodgkin's disease, cachexia, inflammation associated with infection and certain viral infections, including Acquired Immune Deficiency Syndrome (AIDS), adult respiratory distress syndrome, and ataxia telengiectasia in a patient, said method comprising administering to the patient a therapeutically effective amount of a compound of formula (I), or a therapeutically acceptable salt thereof, wherein

R1 and R2 are each independently selected from the group consisting of R6, C(O)R6, C(O)NHR6, and C(O)N(R6)2: wherein at least one of R1 and R2 is R6; or
R1 and R2, together with the nitrogen to which they are attached form a heterocycloalkyl or heterocycloalkenyl ring: wherein the ring formed with R1 and R2 together with the nitrogen to which they are attached is optionally substituted with one or more substituents independently selected from the group consisting of R7, OR7, SR7, S(O)R7, SO2R7, C(O)R7, CO(O)R7, OC(O)R7, OC(O)OR7, NH2, NHR7, N(R7)2, NHC(O)R7, NR7C(O)R7, NHS(O)2R7, NR7S(O)2R7, NHC(O)OR7, NR7C(O)OR7, NHC(O)NH2, NHC(O)NHR7, NHC(O)N(R7)2, NR7C(O)NHR7, NR7C(O)N(R7)2, C(O)NH2, C(O)NHR7, C(O)N(R7)2, C(O)NHOH, C(O)NHOR7, C(O)NHSO2R7, C(O)NR7SO2R7, SO2NH2, SO2NHR7, SO2N(R7)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR7, C(N)N(R7)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;
R3, R4, and R5 are each independently selected from the group consisting of hydrogen, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6 haloalkyl, C1-6 hydroxyalkyl, F, Cl, Br and I;
R6, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, SR8, S(O)R8, SO2R8, C(O)R8, CO(O)R8, OC(O)R8, OC(O)OR8, NH2, NHR8, N(R8)2, NHC(O)R8, NR8C(O)R8, NHS(O)2R8, NR8S(O)2R8, NHC(O)OR8, NR8C(O)OR8, NHC(O)NH2, NHC(O)NHR8, NHC(O)N(R8)2, NR8C(O)NHR8, NR8C(O)N(R8)2, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)NHOH, C(O)NHOR8, C(O)NHSO2R8, C(O)NR8SO2R8, SO2NH2, SO2NHR8, SO2N(R8)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR8, C(N)N(R8)2, CNOH, CNOCH3, OH, CN, N, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R6 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, SR9, S(O)R9, SO2R9, C(O)R9, CO(O)R9, OC(O)R9, OC(O)OR9, NH2, NHR9, N(R9)2, NHC(O)R9, NR9C(O)R9, NHS(O)2R9, NR9S(O)2R9, NHC(O)OR9, NR9C(O)OR9, NHC(O)NH2, NHC(O)NHR9, NHC(O)N(R9)2, NR9C(O)NHR9, NR9C(O)N(R9)2, C(O)NH2, C(O)NHR9, C(O)N(R9)2, C(O)NHOH, C(O)NHOR9, C(O)NHSO2R9, C(O)NR9SO2R9, SO2NH2, SO2NHR9, SO2N(R9), C(O)H, C(O)OH, C(N)NH2, C(N)NHR9, C(N)N(R9)2, CNOH, CNOCH3, OH, CN, N3, NO2, F Cl, Br and I;
R7, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R7 are each independently optionally substituted with one or more substituents independently selected from the group consisting of aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R7 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I;
R8, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl: wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R10, OR10, SR10, S(O)R10, SO2R10, C(O)R10, CO(O)R10, OC(O)R10, OC(O)OR10, NH2, NHR10, N(R10)2, NHC(O)R10, NR10C(O)R10, NHS(O)2R10, NR10S(O)2R10, NHC(O)OR10, NR10C(O)OR10, NHC(O)NH2, NHC(O)NHR10, NHC(O)N(R10)2, NR10C(O)NHR10, NR10C(O)N(R10)2, C(O)NH2, C(O)NHR10, C(O)N(R10)2, C(O)NHOH, C(O)NHOR10, C(O)NHSO2R10, C(O)NR10SO2R10, SO2NH2, SO2NHR10, SO2N(R10)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR10, C(N)N(R10)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R8 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, SR11, S(O)R11, SO2R11, C(O)R11, CO(O)R11, OC(O)R11, OC(O)OR11, NH2, NHR11, N(R11)2, NHC(O)R11, NR11C(O)R11, NHS(O)2R11, NR11S(O)2R11, NHC(O)OR11, NR11C(O)OR11, NHC(O)NH2, NHC(O)NHR11, NHC(O)N(R11)2, NR11C(O)NHR11, NR11C(O)N(R11)2, C(O)NH2, C(O)NHR11, C(O)N(R11)2, C(O)NHOH, C(O)NHOR11, C(O)NHSO2R11, C(O)NR11SO2R11, SO2NH2, SO2NHR11, SO2N(R11)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR11, C(N)N(R11)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;
R9, at each occurrence, is independently selected from the group consisting of C1-6 alkyl C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C1-6 alkenyl, and C2-6 alkynyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R12, OR12, SR12, S(O)R12, SO2R12, C(O)R12, CO(O)R12, OC(O)R12, OC(O)OR12, NH2, NHR12, N(R12)2, NHC(O)R12, NR12C(O)R12, NHS(O)2R12, NR12S(O)2R12, NHC(O)OR12, NR12C(O)OR12, NHC(O)NH2, NHC(O)NHR12, NHC(O)N(R12)2, NR12C(O)NHR12, NR12C(O)N(R12)2, C(O)NH2, C(O)NHR12, C(O)N(R12)2, C(O)NHOH, C(O)NHOR12, C(O)NHSO2R12, C(O)NR12SO2R12, SO2NH2, SO2NHR12, SO2N(R12)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR12, C(N)N(R12)2, CNOH, CNOCH3s OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R9 are each independently optionally substituted with one or more substituents independently selected from the group consisting of R13, OR13, SR13, S(O)R13, SO2R13, C(O)R13, CO(O)R13, OC(O)R13, OC(O)OR13, NH2, NHR13, N(R13)2, NHC(O)R13, NR13C(O)R13, NHS(O)2R13, NR13S(O)2R13, NHC(O)OR13, NR13C(O)OR13, NHC(O)NH2, NHC(O)NHR13, NHC(O)N(R13)2, NR13C(O)NHR13, NR13C(O)N(R13)2C(O)NH2, C(O)NHR13, C(O)N(R13)2, C(O)NHOH, C(O)NHOR13, C(O)NHSO2R13, C(O)NR13SO2R13, SO2NH2, SO2NHR13, SO2N(R13)2, C(O)H, C(O)OH, C(N)NH2, C(N)NHR13, C(N)N(R13)2, CNOH, CNOCH3, OH, CN, N3, NO2, F, Cl, Br and I;
R10, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6 haloalkyl, and C1-6 hydroxyalkyl;
R11, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R11 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I;
R12, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl; wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of C1-6 alkoxy, aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, cycloalkenyl, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; wherein the aryl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, cycloalkyl, and cycloalkenyl represented by R12 are each independently optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I; and
R13, at each occurrence, is independently selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl: wherein the C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl represented by R13 are each independently optionally substituted with one or more substituents independently selected from the group consisting of alkoxy, NH2, C(O)H, C(O)OH, OH, CN, N3, NO2, F, Cl, Br and I.

11-13. (canceled)

Patent History
Publication number: 20160193209
Type: Application
Filed: Mar 11, 2016
Publication Date: Jul 7, 2016
Applicant: AbbVie Inc. (North Chicago, IL)
Inventors: Ramzi F. Sweis (Lake Bluff, IL), Michael L. Curtin (Pleasant Prairie, WI), Marina A. Pliushchev (Vernon Hills, IL), Todd M. Hansen (Grayslake, IL), Kenton Longenecker (Grayslake, IL)
Application Number: 15/068,131
Classifications
International Classification: A61K 31/506 (20060101); A61K 31/496 (20060101); A61K 31/497 (20060101); A61K 31/4439 (20060101); A61K 31/427 (20060101);