IMIDAZOPYRIDINYL COMPOUNDS AND USE THEREOF FOR TREATMENT OF PROLIFERATIVE DISORDERS

Info

Publication number: 20220242861
Type: Application
Filed: Feb 21, 2020
Publication Date: Aug 4, 2022
Inventors: Jinhwa LEE (Gyeonggi-do), Suyeon JO (Gyeonggi-do), Keonseung LIM (Gyeonggi-do), A Yeong PARK (Gyeonggi-do), Jae Eun KIM (Gyeonggi-do), Misoon KIM (Gyeonggi-do), Inyoung YANG (Seoul)
Application Number: 17/432,497

Abstract

The present disclosure provides a compound of Formula (I) or pharmaceutically acceptable salt, stereoisomers thereof, a pharmaceutical composition comprising the compound, and a method to treat or prevent cancer diseases and/or proliferative disorders using the compound.

Description

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit and priority to U.S. Provisional Patent Application No. 62/809,230, filed on 22 Feb. 2019. The entire disclosure of the application identified in this paragraph is incorporated herein by reference.

FIELD

The present disclosure generally relates to compounds having enzyme inhibitory activity, pharmaceutical compositions comprising the compound, and methods of using the compounds for treating cancer and/or proliferative disorders.

BACKGROUND

The c-Abl protein is a tightly regulated nonreceptor tyrosine kinase that is involved in the regulation of cell proliferation, cell survival, cell adhesion, cell migration and apoptosis. The c-Abl protein is located both in the nucleus and the cytoplasm. In the nucleus, c-Abl protein is known to be activated in response to DNA damage and contributes to apoptosis (Wang, 2000). Cytoplasmic c-Abl is associated with growth factor receptor signaling that can affect cell mobility and cell adhesion (Taagepera et al., 1998). The oncogenic effects of Abl are believed to reside in cytoplasmic forms of c-Abl. Several studies have shown that c-Abl is downregulated in part by intramolecular interactions that provide autoinhibitory kinase effects (Pendergast, 2002; Pluk et al., 2002; Hantschel et al., 2003). Studies have also found that c-Abl kinase activity is regulated by intermolecular interactions with negative regulators, which include Bcr (Liu et al., 1996; Ling et al., 2003), PAG (Wen and Van Etten, 1997), F-actin (Woodring et al., 2003) and phosphoinositides (Plattner and Pendergast, 2003).

The c-Abl protein is widely expressed in all tissues and until recently oncogenically activated forms of Abl were believed to be restricted to hematopoietic malignancies, principally chronic myeloid leukemia (CML) and to a lesser degree in acute lymphocytic B-cell leukemia. Over 95% of CML patients have an abnormal chromosome 22 known as the Philadelphia chromosome (Ph). The Ph fuses 50 portions of BCR to the second exon of the c-ABL gene. The first exon of c-ABL encodes sequences involved in the autoinhibition of the c-Abl tyrosine kinase, so deletion of these sequences is thought to contribute to the activated state of the Abl tyrosine kinase domain.

Recent findings demonstrate that activated c-Abl tyrosine kinase may also play a role in non-small cell lung cancer (NSCLC) (Lin et al., 2005, 2007). Activation of c-Abl tyrosine kinase in some solid tumors is further supported by studies from Plattner and co-workers (Srinivasan and Plattner, 2006; Srinivasan et al., 2008), whose findings indicate active c-Abl tyrosine kinase plays a role in aggressive human breast cancer cell lines (J Lin and R Arlinghaus; Oncogene 2008, 27, 4385).

The enzyme KIT (also called CD 117) is a receptor tyrosine kinase expressed on a wide variety of cell types. The KIT molecule contains a long extracellular domain, a transmembrane segment, and an intracellular portion. The ligand for KIT is stem cell factor (SCF), whose binding to the extracellular domain of KIT induces receptor dimerization and activation of downstream signaling pathways. KIT mutations generally occur in the DNA encoding the juxtumembrane domain (exon 11). They also occur, with less frequency, in exons 7, 8, 9, 13, 14, 17, and 18. Mutations make KIT function independent of activation by SCF, leading to a high cell division rate and possibly genomic instability. Mutant KIT has been implicated in the pathogenesis of several disorders and conditions including systemic mastocytosis, GIST (gastrointestinal stromal tumors), AML (acute myeloid leukemia), melanoma, and seminoma. As such, there is a need for therapeutic agents that inhibit KIT, and especially agents that inhibit mutant KIT.

Platelet-derived growth factor (PDGF) has been studied in relation to tumor angiogenesis binds to a large spectrum of mesoderm-derived cells such as fibroblasts, pericytes, glial or mesangial cells. PDGF isoforms bind two distinct receptors, PDGF-alpha and -beta, and this mechanism induces receptor autophosphorylation and activation of several signaling molecules. PDGF receptors are expressed in tumor cells and stromal cells in both normal and tumoral tissue. They play an important role in tumor progression as being part of a group of receptors that are expressed along the membrane of tumor cells (Adina Octavia Due et al. Rom J Morphol Embryol 2012, 53(3 Suppl):749) including Non-Hodgkin lymphoma (NHL) especially B cell lymphoma (BCLs), T cell lymphoma and natural killer cell lymphoma.

And PDGFRA D842V mutation has been found in a distinct subset of GIST, typically from the stomach. The D842V mutation is known to be associated with tyrosine kinase inhibitor resistance. As such, there is a need for agents that target this mutation. (Valentina et al., Int. J. Mol. Sci. 2018, 19, 732).

SUMMARY

The present disclosure provides a compound having c-abl, KIT and/or PDGFR inhibitory activity, a composition comprising the compound and a method useful to treat cancer and/or proliferative disorders.

In an embodiment, there are provided a compound of Formula (I) and a pharmaceutically acceptable salt thereof:

wherein R¹, R², R³, R⁴, and R⁵are as defined herebelow.

In another embodiment, the present disclosure provides pharmaceutical compositions comprising a therapeutically effective amount of a compound described herein and a pharmaceutically acceptable carrier.

In yet another embodiment, the present disclosure provides methods of inhibiting or treating cancer and/or a proliferative disorder comprising administering to a subject in need thereof a therapeutically effective amount of one or more compounds described herein.

DETAILED DESCRIPTION

The following description is merely exemplary in nature and is not intended to limit the present disclosure, application, or uses.

Definitions

The generic terms used in the present disclosure are herein defined for clarity.

This specification uses the terms “substituent”, “radical”, “group”, “moiety”, and “fragment” interchangeably.

As used herein, the term “alkenyl” refers to a straight or branched hydrocarbonyl group with at least one site of unsaturation, i.e., a carbon-carbon, sp2 double bond. In an embodiment, alkenyl has from 2 to 12 carbon atoms. In some embodiments, alkenyl is a C₂—C₁₀alkenyl group or a C₂—C₆alkenyl group. Examples of alkenyl group include, but are not limited to, ethylene or vinyl (CH═CH₂), allyl (—CH₂CH═CH₂), cyclopentenyl (—C₅H₇), and 5-hexenyl (—CH₂CH₂CH₂CH₂CH═CH₂).

As used herein, the term “alkoxy” is RO— where R is alkyl. Non-limiting examples of alkoxy groups include methoxy, ethoxy and propoxy.

As used herein, the term “alkoxyalkyl” refers to an alkyl moiety substituted with an alkoxy group. Examples of alkoxyalkyl groups include methoxymethyl, methoxyethyl, methoxypropyl and ethoxyethyl.

As used herein, the term “alkoxycarbonyl” is ROC(O)—, where R is an alkyl group as defined herein. In various embodiments, R is a C₁-C₁₀alkyl group or a C₁-C₆alkyl group.

As used herein, the term “alkyl” refers to a straight or branched chain hydrocarbonyl group. In an embodiment, alkyl has from 1 to 12 carbon atoms. In some embodiments, alkyl is a C₁-C₁₀alkyl group or a C₁-C₆alkyl group. Examples of alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, pentyl, hexyl, heptyl, octyl, nonyl and decyl. “lower alkyl” means alkyl having from 1 to 4 carbon atoms.

As used herein, the term “alkylamino” refers to an amino group substituted with one or more alkyl groups. “N-(alkyl)amino” is RNH— and “N,N-(alkyl)2amino” is R₂N—, where the R groups are alkyl as defined herein and are the same or different. In various embodiments, R is a C₁-C₁₀alkyl group or a C₁-C₆alkyl group. Examples of alkylamino groups include methylamino, ethylamino, propylamino, butylamino, dimethylamino, diethylamino, and methylethylamno.

As used herein, the term “alkylaminoalkyl” refers to an alkyl moiety substituted with an alkylamino group, wherein alkylamino is as defined herein. Examples of alkylaminoakyl groups include methylaminomethyl and ethylaminomethyl.

As used herein, the term “alkynyl” refers to a straight or branched carbon-chain group with at least one site of unsaturation, i.e., a carbon-carbon, sp triple bond. In an embodiment, alkynyl has from 2 to 12 carbon atoms. In some embodiments, alkynyl is a C₂—C₁₀alkynyl group or a C₂—C₆alkynyl group. Examples of alkynyl groups include acetylenic (—C≡CH) and propargyl (—CH₂C≡CH).

As used herein, the term “aryl” refers to any monocyclic or bicyclic carbon ring of up to 7 atoms in each ring, wherein at least one ring is aromatic, or an aromatic ring system of 5 to 14 carbon atoms which includes a carbocyclic aromatic group fused with a 5-or 6-membered cycloalkyl group. Representative examples of aryl groups include, but are not limited to, phenyl, tolyl, xylyl, naphthyl, tetrahydronaphthyl, anthracenyl, fluorenyl, indenyl, azulenyl and indanyl. A carbocyclic aromatic group can be unsubstituted or optionally substituted.

As used herein, the term “cycloalkyl” is a hydrocarbyl group containing at least one saturated or partially unsaturated ring structure, and attached via a ring carbon. In various embodiments, it refers to a saturated or a partially unsaturated C₃—C₁₂cyclic moiety, examples of which include cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl and cyclooctyl. “Cycloalkyloxy” is RO—, where R is cycloalkyl.

As used herein, the terms “halogen” and “halo” refers to chloro (—Cl), bromo (—Br), fluoro (—F) or iodo (—I). “Haloalkoxy” refers to an alkoxy group substituted with one or more halo groups and examples of haloalkoxy groups include, but are not limited to, —OCF₃, —OCHF₂and —OCH₂F. “Haloalkoxyalkyl” refers to an alkyl moiety substituted with a haloalkoxy group, wherein haloalkoxy is as defined herein. Examples of haloalkoxyalkyl groups include trifluoromethoxymethyl, trifluoroethoxymethyl and trifluoromethoxyethyl. “Haloalkyl” refers to an alkyl moiety substituted with one or more halo groups. Examples of haloalkyl groups include —CF₃and CHF₂.

As used herein, the term “heteroalkyl” refers to a straight- or branched-chain alkyl group having from 2 to 14 carbons (in some embodiments, 2 to 10 carbons) in the chain, one or more of which has been replaced by a heteroatom selected from S, 0, P and N. Exemplary heteroalkyls include alkyl ethers, secondary and tertiary alkyl amines, amides, alkyl sulfides, and the like.

As used herein, the term “heterocyclyl” includes the heteroaryls defined below and refers to a saturated or partially unsaturated monocyclic, bicyclic or tricyclic group of 2 to 14 ring-carbon atoms and, in addition to ring-carbon atoms, 1 to 4 heteroatoms selected from P, N, O and S. In various embodiments the heterocyclic group is attached to another moiety through carbon or through a heteroatom, and is optionally substituted on carbon or a heteroatom. Examples of heterocyclyl include azetidinyl, benzoimidazolyl, benzofuranyl, benzofurazanyl, benzopyrazolyl, benzotriazolyl, benzothiophenyl, benzoxazolyl, carbazolyl, carbolinyl, cinnolinyl, furanyl, imidazolyl, indolinyl, indolyl, indolazinyl, indazolyl, isobenzofuranyl, isoindolyl, isoquinolyl, isothiazolyl, isoxazolyl, naphthpyridinyl, oxadiazolyl, oxazolyl, oxazoline, isoxazoline, oxetanyl, pyranyl, pyrazinyl, pyrazolyl, pyridazinyl, pyridopyridinyl, pyridazinyl, pyridyl, pyrimidyl, pyrrolyl, quinazolinyl, quinolyl, quinoxalinyl, tetrahydropyranyl, tetrahydrothiopyranyl, tetrahydroisoquinolinyl, tetrazolyl, tetrazolopyridyl, thiadiazolyl, thiazolyl, thienyl, triazolyl, azetidinyl, 1,4-dioxanyl, hexahydroazepinyl, piperazinyl, piperidinyl, pyridin-2-onyl, pyrrolidinyl, morpholinyl, thiomorpholinyl, dihydrobenzoimidazolyl, dihydrobenzofuranyl, dihydrobenzothiophenyl, dihydrobenzoxazolyl, dihydrofuranyl, dihydroimidazolyl, dihydroindolyl, dihydroisooxazolyl, dihydroisothiazolyl, dihydrooxadiazolyl, dihydrooxazolyl, dihydropyrazinyl, dihydropyrazolyl, dihydropyridinyl, dihydropyrimidinyl, dihydropyrrolyl, dihydroquinolinyl, dihydrotetrazolyl, dihydrothiadiazolyl, dihydrothiazolyl, dihydrothienyl, dihydrotriazolyl, dihydroazetidinyl, methylenedioxybenzoyl, tetrahydrofuranyl, and tetrahydrothienyl, and N-oxides thereof. “Heterocyclyloxy” is RO—, where R is heterocyclyl. “Heterocyclylthio” is RS, where R is heterocyclyl.

As used herein, the term “3- or 4-membered heterocyclyl” refers to a monocyclic ring having 3 or 4 ring atoms wherein at least one ring atom is heteroatom selected from the group consisting of N, O and S. Non-limiting examples of 3- or 4-membered heterocyclyl include aziridinyl, 2H-azirinyl, oxiranyl, thiiranyl, azetidinyl, 2,3-dihyroazetyl, azetyl, 1,3-diazetidinyl, oxetanyl, 2H-oxetyl, thietanyl, and 2H-thietyl.

As used herein, the term “heteroaryl” refers to a monocyclic, bicyclic or tricyclic ring having up to 7 atoms in each ring, wherein at least one ring is aromatic and contains from 1 to 4 heteroatoms in the ring selected from the group consisting of N, O and S. Non-limiting examples of heteroaryl include pyridyl, thienyl, furanyl, pyrimidyl, imidazolyl, pyranyl, pyrazolyl, thiazolyl, thiadiazolyl, isothiazolyl, oxazolyl, isoxazoyl, pyrrolyl, pyridazinyl, pyrazinyl, quinolinyl, isoquinolinyl, benzofuranyl, dibenzofuranyl, dibenzothiophenyl, benzothienyl, indolyl, benzothiazolyl, benzooxazolyl, benzimidazolyl, isoindolyl, benzotriazolyl, purinyl, thianaphthenyl and pyrazinyl. Attachment of heteroaryl can occur via an aromatic ring, or, if heteroaryl is bicyclic or tricyclic and one of the rings is not aromatic or contains no heteroatoms, through a non-aromatic ring or a ring containing no heteroatoms. “Heteroaryl” is also understood to include the N-oxide derivative of any nitrogen containing heteroaryl. “Heteroaryloxy” is RO—, where R is heteroaryl.

As used herein, the term “hydroxyalkoxy” refers to an alkoxy group substituted with a hydroxyl group (OH), wherein alkoxy is as defined herein. An example of hydroxyalkoxy is hydroxyethoxy.

As used herein, the term “hydroxyalkyl” refers to a linear or branched monovalent C₁-C₁₀hydrocarbon group substituted with at least one hydroxy group and examples of hydroxyalkyl groups include, but are not limited to, hydroxymethyl, hydroxyethyl, hydroxypropyl and hydroxybutyl.

As used herein, the term “pharmaceutically acceptable” means suitable for use in pharmaceutical preparations, generally considered as safe for such use, officially approved by a regulatory agency of a national or state government for such use, or being listed in the U.S. Pharmacopoeia or other generally recognized pharmacopoeia for use in animals, and more particularly in humans.

As used herein, the term “pharmaceutically acceptable carrier” refers to a diluent, adjuvant, excipient, or carrier, or other ingredient which is pharmaceutically acceptable and with which a compound of the invention is administered.

As used herein, the term “pharmaceutically acceptable salt” refers to a salt which may enhance desired pharmacological activity. Examples of pharmaceutically acceptable salts include acid addition salts formed with inorganic or organic acids, metal salts and amine salts. Examples of acid addition salts formed with inorganic acids include salts with hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid and phosphoric acid. Examples of acid addition salts formed with organic acids such as acetic acid, propionic acid, hexanoic acid, heptanoic acid, cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, o-(4-hydroxy-benzoyl)-benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, 1,2-ethanedisulfonic acid, 2-hydroxyethane-sulfonic acid, benzenesulfonic acid, p-chlorobenzenesulfonic acid, 2-naphthalenesulfonic acid, p-toluenesulfonic acid, camphorsulfonic acid, 4-methyl-bicyclo[2.2.2]oct-2-ene1-carboxylic acid, gluco-heptonic acid, 4,4′-methylenebis(3-hydroxy-2-naphthoic) acid, 3-phenylpropionic acid, trimethyl-acetic acid, tertiary butylacetic acid, lauryl sulfuric acid, gluconic acid, glutamic acid, hydroxy-naphthoic acids, salicylic acid, stearic acid and muconic acid. Examples of metal salts include salts with sodium, potassium, calcium, magnesium, aluminum, iron, and zinc ions. Examples of amine salts include salts with ammonia and organic nitrogenous bases strong enough to form salts with carboxylic acids.

As used herein, the term “therapeutically effective amount” means when applied to a compound of the invention is intended to denote an amount of the compound that is sufficient to ameliorate, palliate, stabilize, reverse, slow or delay the progression of a disorder or disease state, or of a symptom of the disorder or disease. In an embodiment, the method of the present invention provides for administration of combinations of compounds. In such instances, the “therapeutically effective amount” is the amount of a compound of the present invention in the combination sufficient to cause the intended biological effect.

As used herein, the term “treatment” or “treating” as used herein means ameliorating or reversing the progress or severity of a disease or disorder, or ameliorating or reversing one or more symptoms or side effects of such disease or disorder. “Treatment” or “treating”, as used herein, also means to inhibit or block, as in retard, arrest, restrain, impede or obstruct, the progress of a system, condition or state of a disease or disorder. For purposes of this invention, “treatment” or “treating” further means an approach for obtaining beneficial or desired clinical results, where “beneficial or desired clinical results” include, without limitation, alleviation of a symptom, diminishment of the extent of a disorder or disease, stabilized (i.e., not worsening) disease or disorder state, delay or slowing of a disease or disorder state, amelioration or palliation of a disease or disorder state, and remission of a disease or disorder, whether partial or total.

In another embodiment, the compounds of Formula (I) are used for modulating the activity of a protein kinase c-abl, KIT and PDGFR.

As used herein, the term “modulating” or “modulation” refers to the alteration of the catalytic activity of a protein kinase. In particular, modulating refers to the activation or inhibition of the catalytic activity of a protein kinase, depending on the concentration of the compound or salt to which the protein kinase is exposed or, more preferably, the inhibition of the catalytic activity of a protein kinase. The term “catalytic activity” as used herein refers to the rate of phosphorylation of tyrosine, serine or threonine under the influence, direct or indirect, of a protein kinase.

The three main classes that pharmacological inhibitors of kinase activity are categorized by are (1) Type I, or “DFG-in” ATP competitive inhibitors, which directly compete with ATP in the ATP binding site (i.e., Src and Abl inhibitor dasatinib, (2) Type II, or “DFG-out” ATP competitive inhibitors, which, in addition to binding the ATP binding site also engage an adjacent hydrophobic binding site that is only accessible when the kinase is in an inactivated configuration (i.e., the activation loop is oriented in a conformation that would block substrate binding) (i.e., imatinib, nilotinib), and (3) non-ATP competitive inhibitors that bind at sites outside the ATP binding site that affect the activity of the kinase (i.e. GNF-2).

As used herein, the phrase “compound(s) of this/the disclosure” includes any compound(s) of Formula (I), as well as clathrates, hydrates, solvates, or polymorphs thereof. And, even if the term “compound(s) of the disclosure” does not mention its pharmaceutically acceptable sat, the term includes salts thereof. In one embodiment, the compounds of this disclosure include stereochemically pure compounds, e.g., those substantially free (e.g., greater than 85% ee, greater than 90% ee, greater than 95% ee, greater than 97% ee, or greater than 99% ee) of other stereoisomers. That is, if the compounds of Formula (I) according to the present disclosure or salts thereof are tautomeric isomers and/or stereoisomers (e.g., geometrical isomers and conformational isomers), such isolated isomers and their mixtures also are included in the scope of this disclosure. If the compounds of the present disclosure or salts thereof have an asymmetric carbon in their structures, their active optical isomers and their racemic mixtures also are included in the scope of this disclosure.

As used herein, the term “polymorph” refers to solid crystalline forms of a compound of this disclosure or complex thereof. Different polymorphs of the same compound can exhibit different physical, chemical and/or spectroscopic properties. Different physical properties include, but are not limited to stability (e.g., to heat or light), compressibility and density (important in formulation and product manufacturing), and dissolution rates (which can affect bioavailability). Differences in stability can result from changes in chemical reactivity (e.g., differential oxidation, such that a dosage form discolors more rapidly when comprised of one polymorph than when comprised of another polymorph) or mechanical characteristics (e.g., tablets crumble on storage as a kinetically favored polymorph converts to thermodynamically more stable polymorph) or both (e.g., tablets of one polymorph are more susceptible to breakdown at high humidity). Different physical properties of polymorphs can affect their processing. For example, one polymorph might be more likely to form solvates or might be more difficult to filter or wash free of impurities than another due to, for example, the shape or size distribution of particles of it.

As used herein, the term “solvate” means a compound or its salt according to this disclosure that further includes a stoichiometric or non-stoichiometric amount of a solvent bound by non-covalent intermolecular forces. Preferred solvents are volatile, non-toxic, and/or acceptable for administration to humans in trace amounts.

As used herein, the term “hydrate” means a compound or its salt according to this disclosure that further includes a stoichiometric or non-stoichiometric amount of water bound by non-covalent intermolecular forces.

As used herein, the term “clathrate” means a compound or its salt in the form of a crystal lattice that contains spaces (e.g., channels) that have a guest molecule (e.g., a solvent or water) trapped within.

Compounds of the Present Disclosure

The present disclosure provides compounds according to Formula (I):

or a pharmaceutically acceptable salt thereof, wherein:

R¹is cyclopropyl, cyclobutyl, or 4-membered heterocyclyl, wherein R¹is optionally substituted with one or more groups selected from the group consisting of halo, alkyl, hydroxyalkyl, haloalkyl, and monoalkylaminoalkyl,

R²and R³are independently —H, halo, alkyl, alkoxy, —CF₃,—CHF₂, —CH₂F, or —OCF₃,

R⁴is aryl, heteroaryl, cycloalkyl, heterocyclyl, or heteroalkyl, wherein R⁴is optionally substituted with one or more groups selected from the group consisting of halo, hydroxyl, alkyl, alkenyl, alkynyl, cycloalkyl, haloalkyl, hydroxyalkyl, dialkylaminoalkyl, trimethylsilylethoxymethyl, —CH₂NHC(O)CH₃, —NO₂, —NR_aR_b, —NR_aC(═O)R_b, —NR_aC(═O)NR_aR_b, —NR_aC(═O)OR_b, —OR_a, —CN, —C(═O)R_a, —C(═O)OR_a, —C(═O)NR_aR_b, —OC(═O)R_a, —OC(═O)OR_a, —OC(═O)NR_aR_b, —SR_a, azetidinyl, oxetanyl, tetrahydrofuranyl, furanyl, pyrrolidinyl, pyrrolyl, pyrazolyl, thiophenyl, imidazolyl, oxazolyl, isoxazolyl, thiazolyl, furazanyl, oxadiazolyl, thiadiazolyl, phenyl, tetrahydropyranyl, pyranyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, piperidinyl, piperazinyl, morpholinyl and thiomorpholinyl, R_aand R_bare independently —H, halo, amino, alkyl, or haloalkyl, and

R⁵is H, halo, or alkyl.

In some embodiments, R¹is cyclopropyl or cyclobutyl, wherein R¹is optionally substituted with one or more groups selected from the group consisting of halo, C₁-C₃alkyl, C₁-C₃hydroxyalkyl and C₁-C₃haloalkyl; R²and R³are independently —H, halo, C₁-C₃alkyl, C₁-C₃alkoxy, —CF₃, —CHF₂, —CH₂F, or —OCF₃; R⁴is aryl, heteroaryl, cycloalkyl, or heterocyclyl, wherein R⁴is optionally substituted with one or more groups selected from the group consisting of halo, hydroxyl, C₁-C₃alkyl, C₂—C₃alkenyl, C₂—C₃alkynyl, C₃—C₄cycloalkyl, C₁-C₃haloalkyl, mono-C₁-C₃alkylamino, di-C₁-C₃alkylamino, —NO₂, —NR_aR_b, —NR_aC(═O)R_b, —NR_aC(═O)NR_aR_b, —NR_aC(═O)OR_b, —OR_a, —CN, —C(═O)R_a, —C(═O)OR_a, —C(═O)NR_aR_b, —OC(═O)R_a, —OC(═O)0 R_a, —OC(═O)NR_aR_b, —SR_a, azetidinyl, oxetanyl, tetrahydrofuranyl, furanyl, pyrrolidinyl, pyrrolyl, pyrazolyl, thiophenyl, imidazolyl, oxazolyl, isoxazolyl, thiazolyl, furazanyl, oxadiazolyl, thiadiazolyl, phenyl, tetrahydropyranyl, pyranyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, piperidinyl, piperazinyl, morpholinyl and thiomorpholinyl; R_aand R_bare independently —H, halo, amino, C₁-C₃alkyl, or C₁-C₃haloalkyl; and R⁵is H, F—, Cl—, Br— or methyl

In various embodiments, R¹is cyclopropyl or cyclobutyl, wherein R¹is optionally substituted with one or more groups selected from the group consisting of halo, C₁-C₃alkyl, C₁-C₃hydroxyalkyl and C₁-C₃haloalkyl. In particular embodiments, R¹is cyclopropyl, fluorocyclopropyl, hydroxycyclopropyl, hydroxymethylcyclopropyl, difluorocyclopropyl, methylaminomethylcyclopropyl, cyclobutyl, fluorocyclobutyl, or difluorocyclobutyl. In other particular embodiments, R¹is cyclopropyl, fluorocyclopropyl, cyclobutyl, or fluorocyclobutyl.

In some other embodiments, R¹is 4-membered heterocyclyl which is optionally substituted with one or more groups selected from the group consisting of halo, C₁-C₃alkyl, C₁-C₃hydroxyalkyl and C₁-C₃haloalkyl. In particular embodiments, the 4-membered heterocyclyl is selected from the group consisting of aziridinyl, 2H-azirinyl, oxiranyl, thiiranyl, azetidinyl, 2,3-dihyroazetyl, azetyl, 1,3-diazetidinyl, oxetanyl, 2H-oxetyl, thietanyl, and 2H-thietyl.

In some embodiments, R²and R³are independently H, methyl, or fluoro.

In some embodiments, R⁴is phenyl, pyridinyl, pyrimidinyl, indolinyl, pyrazolyl, thiazolyl, oxoindolinyl, pyrrolopyridinyl, pyrazolyl, pyrazolopyridinyl, oxodihydropyrrolopyridinyl, oxodihydrobenzothiazolyl, benzoimidazolyl, bezooxazolyl, beznothiazolyl, thiophenyl, pyrrolopyridinyl or isothiazolyl, wherein R⁴is optionally substituted with one or more groups selected from the group consisting of halo, alkyl, alkenyl, alkynyl, hydroxyalkyl, amino, cyano, acetyl, hydroxy, and haloalkyl. In particular embodiments, R⁴is fluoro-methylphenyl, fluoro-hydroxymethylphenyl, chloro-hydroxymethylphenyl, methyl-hydroxymethylphenyl, difluoro-hydroxymethylphenyl, chloro-fluoro-hydroxymethylphenyl, fluoro-methyl-hydroxymethylphenyl, chloro-methylphenyl, dimethylphenyl, acetamido-methylphenyl, hydroxy-methylphenyl, hydroxypropanyl-methylphenyl, methyl-propenylphenyl, methyl-pyridinylethynylphenyl, methyl-pyrrolylphenyl, methyl-thiazolylphenyl, imidazolyl-methylphenyl, cyano-methylphenyl, methyl-pyrazolylphenyl, ethynyl-methylphenyl, methylpyridinyl, fluoro-methyl-methylaminophenyl, dimethylpyridinyl, fluoro-methylpyridinyl, fluoromethyl-methylpyridinyl, cyanopyridinyl, trifluoromethyl-methylpyridinyl, hydroxymethylpyridinyl, hydroxymethyl-methylpyridinyl, hydroxyethyl-methylpyridinyl, chloro-methylpyridinyl, aminopyridinyl, acetyl-methylpyridinyl, amino-dimethylpyridinyl, hydroxyethyl-methylprydinyl, methylindolyl, methyloxoindolyl, trimethylsilylethoxymethylindolyl, acetyl-methylindolinyl, methylpyrimidinyl, dimethylpyrimidinyl, trifluoromethylpyrimidinyl, pyrazolyl, methylthiazolyl, methyloxoindolinyl, pyrrolopyridinyl, methylpyrrolopyridinyl, methyl-tetrahydropyranyl, methylpyrazolyl, methyl-oxodihydrobibenzothiazolyl, pyrazolopyridinyl, oxodihydropyrrolopyridinyl, methylisothiazolyl, chloro-methylisothiazolyl, dimethylisothiazolyl, or fluoro-methylindolyl. In particular embodiments, R⁴is fluoro-methylphenyl, fluoro-hydroxymethylphenyl, chloro-hydroxymethylphenyl, methyl-hydroxymethylphenyl, difluoro-hydroxymethylphenyl, chloro-fluoro-hydroxymethylphenyl, fluoro-methyl-hydroxymethylphenyl, chloro-methylphenyl, dimethylphenyl, acetam ido-methylphenyl, hydroxyl-methylphenyl, methyl-propenylphenyl, ethynyl-methylphenyl, fluoro-methyl-methylaminophenyl, fluoro-hydroxyl-methylphenyl, methyl-methylaminophenyl, methyl-pyrrolylphenyl, methyl-thiazolylphenyl, cyano-methylphenyl, imidazolyl-methylphenyl, methylpyridinyl, chloro-methylpyridinyl, fluoro-methylpyridinyl, fluoromethyl-methylpyridinyl, bimethylpyridinyl, aminopyridinyl, amino-dimethylpyridinyl, methoxypyridinyl, acetyl-methylpyridinyl, hydroxymethylpyridinyl, hydroxymethyl-methylpyridinyl, hydroxyethyl-methylpyridinyl, cyanopyridinyl, trifluoromethylpyridinyl, methylthiophenyl, methylindolinyl, methylpyrimidinyl, dimethylpyrimidinyl, pyrazolyl, methylpyrazolyl, methylindolinyl, methyloxoindolinyl, pyrrolopyridinyl, methylpyrrolopyridinyl, methylpyrrolyl, pyrazolopyridinyl, dihydropyrrolopyridinyl, methylisothiazolyl, dimethylisothiazolyl, methyl indazolyl, or methyl-benzothiazolyl. In particular embodiments, R⁴is pyridinyl or phenyl that has one or more substitutions selected from the group consisting of alkyl, alkenyl, alkynyl, cycloalkyl, halo, hydroxyl, hydroxyalkyl, haloalkyl, cyano, amino, alkoxy, alkoxyalkoxyalkyl, alkoxyalkyl, and haloalkoxy. In some particular embodiments, R⁴is selected from the group consisting of:

In some embodiments, R¹is cyclopropyl, fluorocyclopropyl, difluorocyclopropyl, cyclobutyl, fluorocyclobutyl, or difluorocyclobutyl; R²and R³are independently H, methyl, or fluoro; and R⁴is fluoro-methylphenyl, fluoro-hydroxymethylphenyl, chloro-methylphenyl, dimethylphenyl, acetamido-methylphenyl, hydroxyl-methylphenyl, methyl-propenylphenyl, ethynyl-methylphenyl, fluoro-methyl-methylaminophenyl, methyl-pyrrolylphenyl, methyl-thiazolylphenyl, cyano-methylphenyl, imidazolyl-methylphenyl, methylpyridinyl, chloro-methylpyridinyl, fluoro-methylpyridinyl, fluoromethyl-methylpyridinyl, bimethylpyridinyl, aminopyridinyl, amino-dimethylpyridinyl, methoxypyridinyl, acetyl-methylpyridinyl, hydroxymethylpyridinyl, hydroxymethyl-methylpyridinyl, hydroxyethyl-methylpyridinyl, cyanopyridinyl, trifluoromethylpyridinyl, methylthiophenyl, methylindolinyl, methylpyrimidinyl, dimethylpyrimidinyl, pyrazolyl, methylpyrazolyl, methylindolinyl, methyloxoindolinyl, pyrrolopyridinyl, methylpyrrolopyridinyl, methylpyrrolyl, pyrazolopyridinyl, dihydropyrrolopyridinyl, methylisothiazolyl, dimethylisothiazolyl, methylindazolyl, or methyl-bibenzothiazolyl.

The compounds described herein have c-abl inhibition activity and selectivity against c-abl. The compounds are effective to treat cancer and/or a proliferative disorder.

In an embodiment, R¹is cyclopropyl, fluorocyclopropyl, cyclobutyl, fluorocyclobutyl, or difluorocyclobutyl; R²and R³are H; R⁴is phenyl, pyridinyl, pyrazolyl, pyrrolopyridinyl, indolinyl, oxoindolinyl, bezothiazolyl, benzoimidazolyl, benzooxazolyl, or thiophenyl, wherein R⁴is optionally substituted with one or more groups selected from the group consisting of halo, hydroxyl, alkyl, haloalkyl, hydroxyalkyl, cycloalkyl, alkoxyalkyl, alkoxyalkoxy, alkylaminoalkyl, —NR_aR_b, —NR_aC(═O)R_b, —OR_a, -SR_a, —CN, —C(═O)R_a, —C(═O)OR_a, —C(═O)NR_aR_b, —OC(═O)R_a, furanyl, or pyrrolyl; R_aand R_bare independently —H, halo, amino, alkyl, or haloalkyl; and R⁵is —H, halo, or C₁-C₃alkyl.

In various embodiments, R¹is fluorocyclopropyl, and such compounds include, but are not limited to, the following compounds and salts thereof:

2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(2-fluoro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(3-chloro-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(3-chloro-6-(2-fluoro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(3-methyl-6-(4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(3-chloro-6-(4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(3-fluoro-2-methylphenyl)-3-methylimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(2-fluoro-6-methylphenyl)-3-methylimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(5-fluoro-4-methylpyridin-3-yI)-3-methylimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(5-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(5-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
methyl3-(2-(2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-4-methylbenzoate;
2-fluoro-N-(6-(5-fluoro-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(5-methyl-1H-indol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(3-chloro-6-(5-fluoro-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(5-cyano-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(1H-pyrazol-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(4-methyl-1H-pyrazol-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(3-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(4-chloropyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(2,3-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(5-amino-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(2-methyl-5-(methylamino)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(5-acetamido-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(5-chloro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(1H-pyrrolo[2,3-b]pyridin-5-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(2-methyl-5-(1H-pyrazol-3-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(4-chloro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(3-chloro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(4-(trifluoromethyl)pyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(2,4-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(3-fluoro-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(2,5-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(2-oxoindolin-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(4-cyanopyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(4-fluoro-2,3-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(4-fluoro-2,6-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(4-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(2-methyl-5-(1H-pyrrol-3-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(3-methylthiophen-2-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(2,6-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(4-fluoro-5-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(3,4-difluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(3,6-difluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(4-chloro-3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(2-fluoro-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(4-methoxypyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(6-amino-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(5-amino-3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(5-methyl-2-oxoindolin-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(2-chloro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(3-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(2-oxo-2,3-dihydrobenzo[d]thiazol-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(6-aminopyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(2-methyl-5-(1H-pyrazol-1-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(3-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(3-bromo-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(3-fluoro-2-methoxyphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(2-cyano-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
N-(6-(2-chloro-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
N-(6-(2,3-difluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
N-(6-(3,5-dimethyl-1H-indol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-(methoxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-(furan-2-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-(methylthio)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(6-fluoro-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(2-acetyl-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
N-(6-(6-(dimethylamino)-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(2-(aminomethyl)-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
N-(6-(2-(acetamidomethyl)-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
2,2-difluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-((methylamino)methyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-((isopropylamino)methyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-((2-methoxyethoxy)methyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-((2-hydroxyethoxy)methyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(2-((dimethylamino)methyl)-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
N-(6-(1H-pyrrolo[2,3-b]pyridin-5-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
2-fluoro-N-(6-(4-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)imidazo[1,2-a]pyridin-2-yl)pcyclopropanecarboxamide;
N-(6-(4-chloro-1H-pyrrolo[2,3-b]pyridin-5-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
2-fluoro-N-(6-(o-tolyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-hydroxyphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(2-amino-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
2-fluoro-N-(6-(5-methyl-1H-indol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(6-methyl-1H-indol-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(2-(dimethylamino)-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
2-fluoro-N-(6-(5-methyl-1H-benzo[d]imidazol-6-yl)imidazo[1,2-a]pyridin-2-yl)pcyclopropanecarboxamide;
N-(6-(2-ethyl-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-(trifluoromethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(2-cyclopropyl-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-(methylamino)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(5-methylbenzo[d]oxazol-6-yl)imidazo[1,2-a]pyridin-2-yl)pcyclopropanecarboxamide;
2-fluoro-N-(6-(5-methyl-1H-benzo[d]imidazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(6-methylbenzo[d]thiazol-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(5-methylbenzo[d]oxazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(5-methylbenzo[d]thiazol-6-yl)imidazo[1,2-a]pyridin-2-yl)pcyclopropanecarboxamide;
2-fluoro-N-(6-(7-methylbenzo[d]thiazol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-isopropylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(2-methyl-3-(trifluoromethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(3-fluoro-2-(trifluoromethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(3-fluoro-2,6-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(2-ethyl-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide
N-(6-(4-acetyl-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(2-chloro-3,4-difluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(2-chloro-3,6-difluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(furan-2-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(thiophen-2-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(thiazol-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(3-methylisothiazol-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(5-methylthiazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(3-fluoro-2-methylphenyl)-8-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(8-(difluoromethyl)-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(3-fluoro-2-methylphenyl)-8-(fluoromethyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(8-fluoro-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(7-fluoro-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(4-fluoro-2-methylphenyl)-8-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(8-(difluoromethyl)-6-(4-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(4-fluoro-2-methylphenyl)-8-(fluoromethyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(8-fluoro-6-(4-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(7-fluoro-6-(4-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(5-fluoro-2-methylphenyl)-8-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(8-(difluoromethyl)-6-(5-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(5-fluoro-2-methylphenyl)-8-(fluoromethyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(8-fluoro-6-(5-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(7-fluoro-6-(5-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(2-fluoro-6-methylphenyl)-8-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(8-(difluoromethyl)-6-(2-fluoro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(2-fluoro-6-methylphenyl)-8-(fluoromethyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(8-fluoro-6-(2-fluoro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(7-fluoro-6-(2-fluoro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(3-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(4-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(4-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(5-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(5-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(2-fluoro-6-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(2-fluoro-6-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(3-chloro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(3-chloro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(4-chloro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(4-chloro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(5-chloro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(5-chloro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(2-chloro-6-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(2-chloro-6-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(2-(hydroxymethyl)-3-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(2-(hydroxymethyl)-3-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(2-(hydroxymethyl)-4-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(2-(hydroxymethyl)-4-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(2-(hydroxymethyl)-5-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(2-(hydroxymethyl)-5-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(2-(hydroxymethyl)-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(2-(hydroxymethyl)-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(3,4-difluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(3,4-difluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(4,5-difluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(4,5-difluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(2,3-difluoro-6-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(2,3-difluoro-6-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(3,6-difluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(3,6-difluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(3-chloro-4-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(3-chloro-4-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(4-chloro-5-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(4-chloro-5-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(3-chloro-2-fluoro-6-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(3-chloro-2-fluoro-6-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(6-chloro-3-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(6-chloro-3-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(4-fluoro-2-(hydroxymethyl)-3-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(4-fluoro-2-(hydroxymethyl)-3-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(5-fluoro-2-(hydroxymethyl)-4-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(5-fluoro-2-(hydroxymethyl)-4-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(2-fluoro-6-(hydroxymethyl)-3-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(2-fluoro-6-(hydroxymethyl)-3-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(3-fluoro-2-(hydroxymethyl)-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)pcyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-(hydroxymethyl)-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(4-chloro-3-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(4-chloro-3-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(3-fluoro-2-(hydroxymethyl)-4-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-(hydroxymethyl)-4-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(3,5-difluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(3,5-difluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(5-chloro-3-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(5-chloro-3-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(3-fluoro-2-(hydroxymethyl)-5-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-(hydroxymethyl)-5-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(5-chloro-4-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(5-chloro-4-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(3,4-difluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(3,4-difluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(2,4-difluoro-6-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(2,4-difluoro-6-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(2-chloro-4-fluoro-6-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(2-chloro-4-fluoro-6-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(4-fluoro-2-(hydroxymethyl)-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(4-fluoro-2-(hydroxymethyl)-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(2-chloro-3-fluoro-6-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(2-chloro-3-fluoro-6-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(3,5-difluoro-2-(hydroxymethyl)-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(3,5-difluoro-2-(hydroxymethyl)-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(3-chloro-5-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(3-chloro-5-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(5-fluoro-2-(hydroxymethyl)-3-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(5-fluoro-2-(hydroxymethyl)-3-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(5-fluoro-2-(hydroxymethyl)-4-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(5-fluoro-2-(hydroxymethyl)-4-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(3-chloro-6-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(3-chloro-6-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(6-fluoro-2-(hydroxymethyl)-3-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(6-fluoro-2-(hydroxymethyl)-3-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(4-chloro-2-fluoro-6-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
N-(6-(4-chloro-2-fluoro-6-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(2-fluoro-6-(hydroxymethyl)-4-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(2-fluoro-6-(hydroxymethyl)-4-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(5-(hydroxymethyl)-1H-indol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(5-(hydroxymethyl)-1H-indol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(4-(hydroxymethyl)-1H-pyrazol-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(4-(hydroxymethyl)-1H-pyrazol-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(2-(hydroxymethyl)-5-(1H-pyrazol-3-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(2-(hydroxymethyl)-5-(1H-pyrazol-3-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(2-(hydroxymethyl)-5-(1H-pyrrol-3-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(2-(hydroxymethyl)-5-(1H-pyrrol-3-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(3-(hydroxymethyl)thiophen-2-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(3-(hydroxymethyl)thiophen-2-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(5-(hydroxymethyl)-2-oxoindolin-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(5-(hydroxymethyl)-2-oxoindolin-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(3-(hydroxymethyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(3-(hydroxymethyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(2-(hydroxymethyl)-5-(1H-pyrazol-1-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(2-(hydroxymethyl)-5-(1H-pyrazol-1-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(5-(hydroxymethyl)-3-methyl-1H-indol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(5-(hydroxymethyl)-3-methyl-1H-indol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(4-(hydroxymethyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(4-(hydroxymethyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(5-(hydroxymethyl)-1H-indol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(5-(hydroxymethyl)-1H-indol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(6-(hydroxymethyl)-1H-indol-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(6-(hydroxymethyl)-1H-indol-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(5-(hydroxymethyl)-1H-benzo[d]imidazol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(5-(hydroxymethyl)-1H-benzo[d]imidazol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(5-(hydroxymethyl)benzo[d]oxazol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(5-(hydroxymethyl)benzo[d]oxazol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(5-(hydroxymethyl)-1H-benzo[d]imidazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(5-(hydroxymethyl)-1H-benzo[d]imidazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(5-(hydroxymethyl)benzo[d]thiazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(5-(hydroxymethyl)benzo[d]thiazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(5-(hydroxymethyl)benzo[d]oxazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(5-(hydroxymethyl)benzo[d]oxazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(5-(hydroxymethyl)benzo[d]thiazol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(5-(hydroxymethyl)benzo[d]thiazol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(7-(hydroxymethyl)benzo[d]thiazol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(7-(hydroxymethyl)benzo[d]thiazol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(5-(hydroxymethyl)thiazol-4-Amidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; and
2-fluoro-N-(6-(5-(hydroxymethyl)thiazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide.

In an embodiment, R¹is fluorocyclopropyl; R²and R³are H; R⁴is phenyl, indolinyl, oxoindolinyl, or benzothiazolyl, wherein R⁴is optionally substituted with one or more groups selected from the group consisting of halo, hydroxyl, alkyl, alkylamino, and pyrrolyl; and R⁵is —H, halo, or C₁-C₃alkyl. In various embodiments, such compounds include, but are not limited to, the following compounds and salts thereof:

2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(2-fluoro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(3-chloro-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(3-chloro-6-(2-fluoro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(3-fluoro-2-methylphenyl)-3-methylimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(2-fluoro-6-methylphenyl)-3-methylimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(5-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(5-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(5-methyl-1H-indol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(3-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(2,3-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(2-methyl-5-(methylamino)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(2,4-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(3-fluoro-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(2,5-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(2-oxoindolin-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(2-methyl-5-(1H-pyrrol-3-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(6-(2,6-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
2-fluoro-N-(6-(4-fluoro-5-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
2-fluoro-N-(6-(5-methyl-2-oxoindolin-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
N-(3-bromo-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
N-(6-(3,5-dimethyl-1H-indol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(5-methyl-1H-indol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
2-fluoro-N-(6-(6-methyl-1H-indol-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; and
2-fluoro-N-(6-(5-methylbenzo[d]thiazol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide.

In one embodiment, the compound of Formula (I) is selected from compounds according to Formula (II) and pharmaceutically acceptable salts thereof:

wherein R⁶is selected from the group consisting of halo, C₁-C₃alkyl, C₁-C₃hydroxyalkyl and C₁-C₃haloalkyl and R², R³, R⁴, and R⁵are as defined above.

In one embodiment, the compound of Formula (I) is a compound of which R¹is cyclopropyl. In an embodiment, the compound of Formula (I) is N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide or a salt thereof.

In another embodiment, the compound of Formula (I) is a compound of which R¹is cyclobutyl which is optionally substituted with one or more groups selected from the group consisting of halo, alkyl, hydroxyalkyl, haloalkyl, and monoalkylaminoalkyl; and R², R³, R⁴, and R⁵are as defined above. In various embodiments, the compound of Formula (I) is selected from the group consisting of the following compounds and salts thereof:

N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclobutanecarboxamide;
3-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclobutanecarboxamide; and
3,3-difluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclobutanecarboxamide.

The compounds of the present disclosure include stereoisomers of the compounds described herein. In some embodiments, the compounds are stereochemically pure compounds such as those substantially free (e.g., greater than 85% ee, greater than 90% ee, greater than 95% ee, greater than 97% ee, or greater than 99% ee) of other stereoisomers. Examples of such stereoisomers include, but are not limited to,

wherein R², R³, R⁴, R⁵, and R⁶are as defined above.

In one embodiment, the compound of Formula (I) is selected from compounds according to Formula (III) and pharmaceutically acceptable salts thereof:

wherein R⁶is selected from the group consisting of halo, C₁-C₃alkyl, C₁-C₃hydroxyalkyl and C₁-C₃haloalkyl and R², R³, R⁴, and R⁵are as defined above. Table 1 shows exemplary compounds having the stereochemistry of Formula (III). Examples of the compound of Formula (III) include, but are not limited to, the following compounds and salts thereof:

(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(2-fluoro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-N-(3-chloro-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-N-(3-chloro-6-(2-fluoro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(3-methyl-6-(4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-N-(3-chloro-6-(4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-methylphenyl)-3-methylimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(2-fluoro-6-methylphenyl)-3-methylimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(5-fluoro-4-methylpyridin-3-yl)-3-methylimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(5-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(5-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
methyl 3-(2-((1 S,2 S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-4-methylbenzoate;
(1 S,2 S)-2-fluoro-N-(6-(5-fluoro-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(5-methyl-1H-indol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-N-(3-chloro-6-(5-fluoro-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(5-cyano-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(1H-pyrazol-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(4-methyl-1H-pyrazol-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(3-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(4-chloropyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(2,3-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(5-amino-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(2-methyl-5-(methylamino)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(5-acetamido-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(5-chloro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(1H-pyrrolo[2,3-b]pyridin-5-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(2-methyl-5-(1H-pyrazol-3-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(4-chloro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(3-chloro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(4-(trifluoromethyl)pyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(2,4-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(3-fluoro-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(2,5-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(2-oxoindolin-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(4-cyanopyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(4-fluoro-2,3-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(4-fluoro-2,6-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(4-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(2-methyl-5-(1H-pyrrol-3-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(3-methylthiophen-2-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(2,6-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(4-fluoro-5-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(3,4-difluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(3,6-difluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(4-chloro-3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(2-fluoro-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(4-methoxypyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(6-amino-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(5-amino-3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(5-methyl-2-oxoindolin-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(2-chloro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(3-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(2-oxo-2,3-dihydrobenzo[d]thiazol-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(6-aminopyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(2-methyl-5-(1H-pyrazol-1-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-N-(3-bromo-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-methoxyphenyl)imidazo[1,2-a] pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-N-(6-(2-cyano-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
(1 S,2 S)-N-(6-(2-chloro-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
(1 S,2 S)-N-(6-(2,3-difluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
(1 S,2 S)-N-(6-(3,5-dimethyl-1H-indol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-(methoxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-(furan-2-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-(methylthio)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(6-fluoro-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-N-(6-(2-acetyl-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
(1 S,2 S)-N-(6-(6-(dimethylamino)-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide
(1 S,2 S)-N-(6-(2-(aminomethyl)-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
(1 S,2 S)-N-(6-(2-(acetamidomethyl)-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-((methylamino) methyl) phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-((isopropylamino)methyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-24(2-methoxyethoxy)methyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-((2-hydroxyethoxy)methyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-N-(6-(2-((dimethylamino)methyl)-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
(1 S,2 S)-N-(6-(1H-pyrrolo[2,3-b]pyridin-5-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(4-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-N-(6-(4-chloro-1H-pyrrolo[2,3-b]pyridin-5-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(o-tolyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-hydroxyphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-N-(6-(2-amino-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(5-methyl-1H-indol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(6-methyl-1H-indol-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-N-(6-(2-(dimethylamino)-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(5-methyl-1H-benzo[d]imidazol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-N-(6-(2-ethyl-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-(trifluoromethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-N-(6-(2-cyclopropyl-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-(methylamino)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(5-methylbenzo[d]oxazol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(5-methyl-1H-benzo[d]imidazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(6-methylbenzo[d]thiazol-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(5-methylbenzo[d]oxazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(5-methylbenzo[d]thiazol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;
(1 S,2 S)-2-fluoro-N-(6-(7-methylbenzo[d]thiazol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; and
(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-isopropylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide.

In particular embodiments, the compound of Formula (I) is selected from the group consisting of the following compounds and salts thereof:

(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(5-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(5-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(5-methyl-1H-indol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(2-methyl-5-(methylamino)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-N-(6-(2,5-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(2-methyl-5-(1H-pyrrol-3-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(4-fluoro-5-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;
(1 S,2 S)-2-fluoro-N-(6-(6-methyl-1H-indol-5-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; and
(1 S,2 S)-2-fluoro-N-(6-(5-methylbenzo[d]thiazol-6-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide.

The present disclosure provides pharmaceutically acceptable salts of the compounds described above. The pharmaceutically acceptable salts are as defined above in the definition section. In some embodiments, the salt is hydrochloric acid salt, tartaric acid salt, phosphoric acid salt, or maleic acid salt.

Methods of Treatment

The present disclosure further provides methods for treating cancer and/or proliferative disorders in a subject having or susceptible to having such a disease or disorder, by administering to the subject a therapeutically effective amount of one or more compounds as described above.

1. Diseases or Conditions

The compound of the present disclosure for inhibiting c-abl, KIT and PDGFR activity is useful for treatment or prevention of cancer diseases and proliferative disorders. The compound can be used for inhibiting or hindering c-abl, KIT and/or PDGFR kinase activity, and for treating cancer diseases and proliferative disorders, or for preventing aggravation of such disease. Thus, the present disclosure provides a method for inhibiting or hindering c-abl, KIT and/or PDGFR activity in a cell, wherein the cell is contacted with an effective amount of a compound of the present disclosure. In one embodiment, such cell is present in a subject (for example, CML patients). In another embodiment, there is provided a medical use for treating or preventing cancer diseases and proliferative disorders in a subject, using the compound according to the present disclosure. The method of the present disclosure comprises administering to a subject in need of treatment or prevention of cancer diseases and proliferative disorders with a pharmaceutical composition containing a therapeutically or prophylactically effective amount of c-abl, KIT and/or PDGFR inhibitor. The cancer diseases and proliferative disorders include, but is not limited to, breast cancer, ovarian cancer, NSCLC, acute lymphocytic leukemia acute myelogeneous leukemia, chronic myelogenous leukemia and chronic lymphocytic leukemia.

In another aspect, the compounds also described herein can be useful for treating conditions associated with aberrant KIT activity, in humans or non-humans. Activating mutations in KIT are found in multiple indications, including systemic mastocytosis, GIST (gastrointestinal stromal tumors), AML (acute myeloid leukemia), melanoma, seminoma, intercranial germ cell tumors, and Non-Hodgkin lymphoma (NHL) such as B cell lymphoma (BCLs), T cell lymphoma and natural killer cell lymphoma. In addition, mutations in KIT have been linked to Ewing's sarcoma, DLBCL (diffuse large B cell lymphoma), dysgerminoma, MDS (myelodysplastic syndrome), NKTCL (nasal NK/T-cell lymphoma), CMML (chronic myelomonocytic leukemia), and brain cancers.

Mastocytosis refers to a group of disorders characterized by excessive mast cell accumulation in one tissue, or in multiple tissues. Mastocytosis is subdivided into two groups of disorders: (1) cutaneous mastocytosis (CM) describes forms that are limited to the skin; and (2) systemic mastocytosis (SM) describes forms in which mast cells infiltrate extracutaneous organs, with or without skin involvement. SM is further subdivided into five forms: indolent (ISM), smoldering (SSM), aggressive (ASM), SM with associated hematologic non-mast cell lineage disease (SM-AHNMD), and mast cell leukemia (MCL).

Diagnosis of systemic mastocytosis is based in part on histological and cytological studies of bone marrow showing infiltration by mast cells of frequently atypical morphology, which frequently abnormally express non-mast cell markers (CD25 and/or CD2). Diagnosis of SM is confirmed when bone marrow mast cell infiltration occurs in the context of one of the following: (1) abnormal mast cell morphology (spindle-shaped cells); (2) elevated level of serum tryptase above 20 ng/mL; or (3) the presence of the activating KIT D816V mutation.

Activating mutations at the D816 position are found in the vast majority of mastocytosis cases (90-98%), with the most common mutations being D816V and D816H, and D816Y. The D816V mutation is found in the activation loop of the kinase domain and leads to constitutive activation of KIT kinase.

The compounds described herein may also be useful to treat GIST. Complete surgical resection remains the principal treatment of choice for patients with a primary GIST. Surgery is effective in approximately 50% of patients with GIST; of the remaining patients, tumor recurrence is frequent. Primary treatment with a KIT inhibitor such as imatinib has also been shown to be sufficient for initial treatment. However, resistance to imatinib occurs within months through somatic mutation. These secondary imatinib resistant mutations are most frequently located on Exon 11, 13, 14, 17 or 18. Sunitinib is the standard of care second line treatment for most imatinib resistant tumors and is effective for those containing mutations in exons 11, 13 and 14. However, secondary KIT mutations in exons 17 and 18 are resistant to sunitinib treatment and furthermore, tumors containing tertiary resistance mutations in exon 17 and 18 emerge several months after sunitinib treatment. Regorafenib has shown promising results in a phase 3 clinical trial of imatinib, sunitinib resistant GISTs with activity against several but not all exon 17 and 18 mutations, of which D816 is one. Thus, there is a need for therapeutic agents to treat GIST patients with exon 17 mutations not addressed by regorafenib. In addition to the use of the compounds described herein as single agents in the refractory GIST setting, the use of combinations of imatinib, sunitinib and/or regorafenib with the compounds disclosed herein may allow for the prevention of emergence of resistance to exon 17 mutations.

The compounds described herein may also be useful in treating AML. AML patients harbor KIT mutations as well, with the majority of these mutations at the D816 position.

There is a subset of GIST patients with a D842V mutation in PDGFRa; this subgroup of GIST patients can be stratified by identifying this mutation. This subset of patients is refractory to all tyrosine kinase inhibitors currently available. The compounds described herein, due to their activity against PDGFRα D842V, can be useful in treating these patients.

In various embodiments, the method above is used to treat gastrointestinal stromal tumor(GIST), GI tract cancers such as stomach cancer and colorectal cancer, melanoma, chronic lymphocytic leukemia (CLL), acute lymphocytic leukem ia(ALL), or acute myelogeneous leukemia(AML). In particular embodiments, the method is used to treat gastrointestinal stromal tumor(GIST), melanoma or chronic lymphocytic leukemia (CLL).

2. Subjects

Suitable subjects to be treated according to the present disclosure include mammalian subjects. Mammals according to the present disclosure include, but are not limited to, human, canine, feline, bovine, caprine, equine, ovine, porcine, rodents, lagomorphs, primates, and the like, and encompass mammals in utero. Subjects may be of either gender and at any stage of development. In one embodiment, the suitable subject to be treated according to the present disclosure is human.

3. Administration and Dosing

The compounds of the present disclosure are generally administered in a therapeutically effective amount. The compounds of the present disclosure can be administered by any suitable route in the form of a pharmaceutical composition adapted to such a route, and in a dose effective for the treatment intended. An effective dosage is typically in the range of about 0.001 to about 100 mg per kg body weight per day, preferably about 0.01 to about 50 mg/kg/day, in single or divided doses. Depending on age, species and disease or condition being treated, dosage levels below the lower limit of this range may be suitable. In other cases, still larger doses may be used without harmful side effects. Larger doses may also be divided into several smaller doses, for administration throughout the day. Methods for determining suitable doses are well known in the art to which the present disclosure pertains. For example, Remington: The Science and Practice of Pharmacy, Mack Publishing Co., 20th ed., 2000 can be used.

Pharmaceutical Compositions, Dosage Forms and Administration Routes

For the treatment of the diseases or conditions referred to above, the compounds described herein or pharmaceutically acceptable salts thereof can be administered as follows:

Oral Administration

The compounds of the present disclosure may be administered orally, including by swallowing, so that the compound enters the gastrointestinal tract, or absorbed into the blood stream directly from the mouth (e.g., buccal or sublingual administration).

Suitable compositions for oral administration include solid, liquid, gel or powder formulations, and have a dosage form such as tablet, lozenge, capsule, granule or powder.

Compositions for oral administration may be formulated as immediate or modified release, including delayed or sustained release, optionally with enteric coating.

Liquid formulations can include solutions, syrups and suspensions, which can be used in soft or hard capsules. Such formulations may include a pharmaceutically acceptable carrier, for example, water, ethanol, polyethylene glycol, cellulose, or an oil. The formulation may also include one or more emulsifying agents and/or suspending agents.

In a tablet dosage form the amount of drug present may be from about 0.05% to about 95% by weight, more typically from about 2% to about 50% by weight of the dosage form. In addition, tablets may contain a disintegrant, comprising from about 0.5% to about 35% by weight, more typically from about 2% to about 25% of the dosage form. Examples of disintegrants include, but are not limited to, lactose, starch, sodium starch glycolate, crospovidone, croscarmellose sodium, maltodextrin, or mixtures thereof.

Suitable lubricants, for use in a tablet, may be present in amounts from about 0.1% to about 5% by weight, and include, but are not limited to, talc, silicon dioxide, stearic acid, calcium, zinc or magnesium stearate, sodium stearyl fumarate and the like.

Suitable binders, for use in a tablet, include, but are not limited to, gelatin, polyethylene glycol, sugars, gums, starch, polyvinyl pyrrolidone, hydroxypropyl cellulose, hydroxypropylmethyl cellulose and the like. Suitable diluents, for use in a tablet, include, but are not limited to, mannitol, xylitol, lactose, dextrose, sucrose, sorbitol, microcrystalline cellulose and starch.

Suitable solubilizers, for use in a tablet, may be present in amounts from about 0.1% to about 3% by weight, and include, but are not limited to, polysorbates, sodium lauryl sulfate, sodium dodecyl sulfate, propylene carbonate, diethyleneglycol monoethyl ether, dimethyl isosorbide, polyethylene glycol (natural or hydrogenated) castor oil, HCOR™ (Nikkol), oleyl ester, Gelucire™, caprylic/caprylic acid mono/diglyceride, sorbitan fatty acid esters, and Solutol HS™.

Parenteral Administration

Compounds of the present disclosure may be administered directly into the blood stream, muscle, or internal organs. Suitable means for parenteral administration include intravenous, intra-muscular, subcutaneous intraarterial, intraperitoneal, intrathecal, intracranial, and the like. Suitable devices for parenteral administration include injectors (including needle and needle-free injectors) and infusion methods.

Compositions for parenteral administration may be formulated as immediate or modified release, including delayed or sustained release. Most parenteral formulations are aqueous solutions containing excipients, including salts, buffering agents and isotonic agents. Parenteral formulations may also be prepared in a dehydrated form (e.g., by lyophilization) or as sterile non-aqueous solutions. These formulations can be used with a suitable vehicle, such as sterile water. Solubility-enhancing agents may also be used in preparation of parenteral solutions.

Transdermal Administration

Compounds of the present disclosure may be administered topically to the skin or transdermally. Formulations for this topical administration can include lotions, solutions, creams, gels, hydrogels, ointments, foams, implants, patches and the like. Pharmaceutically acceptable carriers for topical administration formulations can include water, alcohol, mineral oil, glycerin, polyethylene glycol and the like. Topical or transdermal administration can also be performed by electroporation, iontophoresis, phonophoresis and the like.

Compositions for topical administration may be formulated as immediate or modified release, including delayed or sustained release.

Combination Therapy

A pharmaceutical composition according to the present disclosure may contain one or more additional therapeutic agents, for example, to increase the efficacy or decrease the side effects. In some embodiments, accordingly, a pharmaceutical composition further contains one or more additional therapeutic agents selected from active ingredients useful to treat or inhibit diseases mediated directly or indirectly by c-abl, c-abl, KIT and/or PDGFR kinase. Examples of such active ingredients are, without limitation, agents such asimatinib, sunitinib and regorafenib. Other agents include the compounds described in WO 2014/039714 and WO 2014/100620.

References for Preparing Pharmaceutical Compositions

Methods for preparing pharmaceutical compositions for treating or preventing a disease or condition are well known in the art to which the present disclosure pertains. For example, based on Handbook of Pharmaceutical Excipients (7th ed.), Remington: The Science and Practice of Pharmacy (20th ed.), Encyclopedia of Pharmaceutical Technology (3^rded.), or Sustained and Controlled Release Drug Delivery Systems (1978), pharmaceutically acceptable excipients, carriers, additives and so on can be selected and then mixed with the compounds of the present disclosure for making the pharmaceutical compositions.

The present disclosure provides a compound having various pharmacological effects by inhibiting c-abl, KIT and/or PDGFR activity, a pharmaceutical composition having the compound as an effective agent, a medical use, particularly for treating cancer diseases and proliferative disorders, of the compound, and a method of treatment or prevention comprising administering the compound to a subject in need of such treatment or prevention. The compounds of the present disclosure and pharmaceutically acceptable salts thereof have good safety and high selectivity for c-abl, KIT and/or PDGFR, and thus exhibit superior properties as a drug.

EXAMPLES

Hereinafter, the present disclosure is described in considerable detail with examples to help those skilled in the art understand the present disclosure. However, the following examples are offered by way of illustration and are not intended to limit the scope of the invention. It is apparent that various changes may be made without departing from the spirit and scope of the invention or sacrificing all of its material advantages.

Synthesis of Formula (I) Compounds

Synthetic methods A to N were used to prepare the compounds of the following. Below, the illustrating synthetic examples of some compounds of the present disclosure are described, and other compounds can be prepared by the similar method to the one described below with different starting or reacting materials.

Synthetic Method A

Example 1 (1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1, 2-a]pyridin-2-yl)cyclopropane-1-carboxamide hydrochloride

Step 1) 6-iodoimidazo[1,2-a]pyridin-2-amine

A mixture of Compound 1 (10.000 g, 28.164 mmol) and lithium hydroxide monohydrate (4.727 g, 112.657 mmol) in water (100 mL)/methanol (300 mL) was heated at reflux for 18 hr, cooled down to the room temperature, concentrated under the reduced pressure, and partitioned between ethyl acetate and saturated aqueous ammonium chloride solution. The organic layer was washed with aqueous saturated sodium chloride solution, separated, dried with anhydrous MgSO₄, filtered, and concentrated in vacuo. The residue was diluted with dichloromethane (30 mL) and hexane (200 mL) and stirred at the ambient temperature. The resulting precipitates were collected by filtration, washed by hexane, and dried to give Compound 2 as brown solid (5.890 g, 80.7%).

Step 2) (1 S,2 S)-2-fluoro-N-(6-iodoimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide

A mixture of Compound 2 (5.890 g, 22.737 mmol), (1 S,2 S)-2-fluorocyclopropane-1-carboxylic acid (3.076 g, 29.558 mmol) and 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC-HCl, 6.538 g, 34.105 mmol) in dichloromethane (100 mL) was treated at the room temperature with N,N-diisopropylethylamine (2.376 mL, 13.642 mmol), stirred at the same temperature for 40 hr. The precipitates were collected by filtration, washed by dichloromethane, and dried to give Compound 3 as beige solid (3.870 g, 49.3%).

1H NMR (400 MHz, DMSO-d6) δ10.99 (s, 1H), 8.87 (s, 1H), 8.02 (s, 1H), 7.36˜7.23 (m, 2H), 4.97˜4.77 (m, 1H), 2.09˜2.07 (m, 1H), 1.65˜1.57 (m, 1H), 1.16˜1.09 (m, 1H).

Step 3) (1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1, 2-a]pyrid in-2-yl)cyclopropane-1-carboxamide

Compound 3 (1.000 g, 2.898 mmol), (3-fluoro-2-methylphenyl)boronic acid (0.535 g, 3.477 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (Pd(dppf)Cl₂, 0.212 g, 0.290 mmol) and cesium carbonate (1.416 g, 4.346 mmol) in tetrahydrofuran (12 mL)/water (3 mL) was mixed at the room temperature and then heated at 100° C. under the microwaves for 30 min, cooled down to the room temperature, filtered through a celite pad to remove solids, and partitioned between ethyl acetate and saturated aqueous sodium bicarbonate solution. The organic layer was washed with aqueous saturated sodium chloride solution, separated, dried (anhydrous MgSO₄), filtered, and concentrated in vacuo. The residue was chromatographed (SiO₂, 45 g cartridge; ethyl acetate/hexane =70% to 100%) to give the crude product which was crystallized at the room temperature using diethylether (5 mL). The resulting precipitates were filtered, washed by diethylether, and dried to give Compound 4 as white solid (0.700 g, 73.8%)

Step 4) (1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1, 2-a]pyridin-2-yl)cyclopropane-1-carboxamide hydrochloride

A solution of Compound 4 (0.600 g, 1.833 mmol) in ethyl acetate (100 mL) was mixed at the room temperature with hydrochloric acid (1.00 M solution in EtOAc, 1.925 mL, 1.925 mmol). The reaction mixture was stirred at the same temperature for 3 hr. The precipitates were collected by filtration, washed by diethylether, and dried to give Example 1 as white solid (0.665 g, 99.7%).

1H NMR (400 MHz, DMSO-d6) δ11.67 (s, 1H), 8.74 (s, 1H), 8.13 (s, 1H), 7.69 (d, J=9.2 Hz, 1H), 7.55 (d, J=9.2 Hz, 1H), 7.35˜7.30 (m, 1H), 7.23 (t, J=9.2 Hz, 1H), 7.15 (d, J=7.2 Hz, 1H), 5.05˜4.85 (m, 1H), 7.21˜7.14 (m, 4H), 1.69˜1.63 (m, 1H), 1.21˜1.18 (m, 1H).

Synthetic Method B

Example 3 (1 S,2 S)-N-(3-chloro-6-(3-fluoro-2-methylphenyl)imidazo[1, 2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide

Step 1) (1 S,2 S)-N-(3-chloro-6-(3-fluoro-2-methylphenyl)imidazo[1, 2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide

A solution of Example 1 (0.060 g, 0.183 mmol) in acetonitrile (8 mL) was mixed at the room temperature with 1-chloropyrrolidine-2,5-dione (NCS, 0.027 g, 0.202 mmol), stirred at the same temperature for 3 hr, and partitioned between ethyl acetate and saturated aqueous sodium bicarbonate solution. The organic layer was washed with aqueous saturated sodium chloride solution, separated, dried (anhydrous MgSO₄), filtered, and concentrated in vacuo. The residue was chromatographed (SiO₂, 12 g cartridge; ethyl acetate/hexane =70% to 100%) to give the crude product which was crystallized at the room temperature using diethylether (5 mL). The resulting precipitates were filtered, washed by diethylether, and dried to give Example 3 as white solid (0.015 g, 22.6%).

1H NMR (400 MHz, DMSO-d6) δ10.44 (s, 1H), 8.21 (s, 1H), 7.62 (d, J=9.6 Hz, 1H), 7.35 (dd, J=9.2, 1.6 Hz, 1H), 7.30 (t, J=7.0 Hz, 1H), 7.24˜7.19 (m, 2H), 5.01˜4.83 (m, 1H), 2.15 (d, J=2.4 Hz, 3H), 2.06˜2.03 (m, 1H), 1.64˜1.56 (m, 1H), 1.15 1.08 (m, 1H).

Synthetic Method C

Example 5 (1 S,2 S)-2-fluoro-N-(3-methyl-6-(4-methylpyridin-3-yl)imidazo [1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide

Step 1) (E)-2-(5-iodo-2-(tosylim ino)pyridin-1(2H)-yl)propanamide

A mixture of Compound 5 and 2-bromopropanamide (4.549 g, 29.931 mmol) in N,N-dimethylformamide (40 mL) was treated at the room temperature with N,N-diisopropylethylamine (5.213 mL, 29.931 mmol), stirred at the same temperature for 24 hr. The reaction mixture was diluted with water (500 mL) and stirred at the ambient temperature. The resulting precipitates were collected by filtration, washed by water, and dried to give the crude product which was re-dissolved in ethyl acetate (100 mL) and diethylether (300 mL) and stirred at the ambient temperature. The resulting precipitates were collected by filtration, washed by diethylether, and dried to give Compound 6 as pale pink solid (4.220 g, 35.5%).

1H NMR (400 MHz, DMSO-d6) δ8.15 (d, J=1.6 Hz, 1H), 7.87 (dd, J=9.6, 2.4 Hz, 1H), 7.75 (s, 1H), 7.62 (d, J=8.0 Hz, 2H), 7.38 (s, 1H), 7.24 (d, J=8.4 Hz, 2H), 7.16 (d, J=9.6 Hz, 1H), 5.63 (m, 1H), 2.30 (s, 3H), 1.60 (d, J=7.2 Hz, 3H).

Step 2) 2,2,2-trifluoro-N-(6-iodo-3-methylimidazo[1,2-a]pyridin-2-yl)acetamide

A stirred slurry of Compound 6 (4.220 g, 9.477 mmol) in dichloromethane (50 mL) was mixed at the room temperature with trifluoroacetic anhydride (8.032 mL, 56.863 mmol). The reaction mixture was heated at reflux for 4 hr, cooled down to the room temperature, and concentrated under the reduced pressure. The residue was diluted with diethylether (300 mL) and stirred at the ambient temperature. The resulting precipitates were collected by filtration, washed by diethylether, and dried to give the crude product which was re-dissolved in water (300 mL) and stirred at the ambient temperature. The resulting precipitates were collected by filtration, washed by water, and dried to give Compound 7 as beige solid (3.098 g, 88.6%).

Step 3) 6-iodo-3-methylimidazo[1,2-a]pyridin-2-amine

Compound 7 (3.098 g, 8.394 mmol) and lithium hydroxide monohydrate (1.057 g, 25.181 mmol) in water (15 mL)/ethanol (30 mL) was mixed at the room temperature and then heated at 140° C. under the microwaves for 30 min, cooled down to the room temperature, and concentrated under the reduced pressure. The residue was diluted with aqueous saturated ammonium chloride solution (20 mL) and stirred at the ambient temperature. The resulting precipitates were collected by filtration, washed by water, and dried to give Compound 8 as light yellow solid (1.400 g, 61.1%).

Step 4) (1 S,2 S)-2-fluoro-N-(6-iodo-3-methylimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide

A mixture of Compound 8 (1.400 g, 5.127 mmol), (1 S,2 S)-2-fluorocyclopropane-1-carboxylic acid (0.640 g, 6.152 mmol) and 1-[bis (dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxide hexafluorophosphate (HATU, 2.924 g, 7.690 mmol) in N,N-dimethylformamide (20 mL) was treated at the room temperature with N,N-diisopropylethylamine (2.679 mL, 15.380 mmol), stirred at 60° C. for 48 hr, cooled down to the room temperature, and concentrated under the reduced pressure. The residue was diluted with water (100 mL) and stirred at the ambient temperature. The resulting precipitates were collected by filtration, washed by water, and dried to give the crude product which was re-dissolved in ethyl acetate (50 mL) and stirred at the ambient temperature. The resulting precipitates were collected by filtration, washed by ethyl acetate, and dried to give Compound 9 as white solid (1.070 g, 58.1%).

1H NMR (400 MHz, DMSO-d6) δ10.24 (s, 1H), 8.51 (s, 1H), 7.36 (dd, J=9.2, 1.6 Hz, 1H), 7.27 (d, J=9.2 Hz, 1H), 4.97˜4.80 (m, 1H), 2.25 (s, 3H), 2.03 (m, 1H), 1.60˜1.53 (m, 1H), 1.11˜1.06 (m, 1H).

Step 5) (1 S,2 S)-2-fluoro-N-(3-methyl-6-(4-methylpyridin-3-yl)imidazo[1, 2-a]pyrid in-2-yl)cyclopropane-1-carboxamide

Compound 9 (0.200 g, 0.557 mmol), (4-methylpyridin-3-yl)boronic acid (0.099 g, 0.724 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (Pd(dppf)Cl₂, 0.041 g, 0.056 mmol) and potassium carbonate (0.231 g, 1.671 mmol) in water (3 mL)/tetrahydrofuran (12 mL) was mixed at the room temperature and then heated at 120° C. under the microwaves for 1 hr, cooled down to the room temperature, and partitioned between ethyl acetate and water. The organic layer was washed with aqueous saturated sodium chloride solution, separated, dried (anhydrous MgSO₄), filtered, and concentrated in vacuo. The residue was chromatographed (SiO₂, 10 g cartridge; tetrahydrofuran/ethyl acetate =0% to 10%) to give the crude product which was dissolved in diethylether (5 mL) and hexane (20 mL) and stirred at the ambient temperature. The resulting precipitates were collected by filtration, washed by hexane, and dried to give Example 5 as beige solid (0.100 g, 55.4%).

1H NMR (400 MHz, DMSO-d6) δ10.25 (s, 1H), 8.47 (s, 1H), 8.44 (d, J=5.2 Hz, 1H), 8.26 (s, 1H), 7.51 (d, J=9.2 Hz, 1H), 7.34 (d, J=5.2 Hz, 1H), 7.24 (d, J=9.2 Hz, 1H), 4.99˜4.81 (m, 1H), 2.29 (s, 6H), 2.07˜2.03 (m, 1H), 1.63˜1.56 (m, 1H), 1.15 1.05 (m, 1H).

Synthetic Method D

Example 29 (1 S,2 S)-2-fluoro-N-(6-(2-methyl-5-(1H-pyrazol-3-yl)phenyl)imidazol[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide

Step 1) (1 S,2 S)-2-fluoro-N-(6-(2-methyl-5-(1 H-pyrazol-3-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide

Example 26 (0.100 g, 0.291 mmol), (1H-pyrazol-3-yl)boronic acid (0.042 g, 0.378 mmol), [1,1′-bis(di-tert-butylphosphino)ferrocene]palladium(II) dichloride (Pd(dtbpf)Cl₂, 0.019 g, 0.029 mmol) and cesium carbonate (0.284 g, 0.873 mmol) in 1,4-dioxane (12 mL) /water (3 mL) was mixed at the room temperature and then heated at 140° C. under the microwaves for 1 hr, cooled down to the room temperature, and partitioned between ethyl acetate and water. The organic layer was washed with aqueous saturated sodium chloride solution, separated, dried (anhydrous MgSO₄), filtered, and concentrated in vacuo. The residue was chromatographed (SiO2, 10 g cartridge; tetrahydrofuran/ethyl acetate =0% to 20%) to give the crude product which was dissolved in dichloromethane (3 mL) and hexane (20 mL) and stirred at the ambient temperature. The resulting precipitates were collected by filtration, washed by diethylether, and dried to give Example 29 as beige solid (0.005 g, 4.6%).

1H NMR (400 MHz, DMSO-d6) δ12.82 (s, 1H), 10.99 (s, 1H), 8.58 (s, 1H), 8.08 (s, 1H), 7.73˜7.69 (m, 2H), 7.46˜7.23 (m, 4H), 6.70 (s, 1H), 4.97˜4.80 (m, 1H), 2.25 (s, 3H), 2.14˜2.09 (m, 1H), 1.66˜1.59 (m, 1H), 1.13˜1.08 (m, 1H).

Synthetic Method E

Example 34. (1 S,2 S)-2-fluoro-N-(3-fluoro-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide

Step 1) (1 S,2 S)-2-fluoro-N-(3-fluoro-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide

A solution of Example 1 (0.1 g, 0.3055 mmol) in tetrahydrofuran (4 mL) was mixed at 0° C. with 1-(chloromethyl)-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane ditetrafluoroborate (Selectfluor®, 0.162 g, 0.4582 mmol), stirred at the room temperature for 3 hr, and partitioned between dichloromethane and saturated aqueous sodium bicarbonate solution. The organic layer was washed with aqueous saturated sodium chloride solution, separated, dried (anhydrous Na₂SO₄), filtered, and concentrated in vacuo. The residue was chromatographed (SiO₂, 12 g cartridge; ethyl acetate/hexane =0% to 30%) to give Example 34 as yellow solid (0.021 g, 15%).

1H NMR (400 MHz, DMSO-d6) δ10.56 (s, 1H), 8.23 (s, 1H), 7.49 (d, J=9.6 Hz, 1H), 7.33˜7.27 (m, 1H), 7.24˜7.16 (m, 3H), 5.01˜4.81 (m, 1H), 2.15 (s, 3H), 2.05˜2.05 (m, 1H), 1.63˜1.56 (m, 1H), 1.17˜1.09 (m, 1H).

Synthetic Method F

Example 41 (1 S,2 S)-2-fluoro-N-(6-(2-methyl-5-(1H-pyrrol-3-yl)phenyl)imidazol[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide

Step 1) 3-(2-((1 S,2 S)-2-fluorocyclopropane-1-carboxamido)imidazo[1, 2-a]pyridin-6-yl)-4-methylphenyl trifluoromethanesulfonate

A mixture of Example 12 (0.842 g, 2.588 mmol) and pyridine (0.313 mL, 3.882 mmol) in dichloromethane (100 mL) was treated at 0° C. with Trifluoromethanesulfonic anhydride (0.479 mL, 2.847 mmol), stirred at the same temperature for 1 hr, and partitioned between dichloromethane and saturated aqueous sodium bicarbonate solution. The organic layer was washed with aqueous saturated sodium chloride solution, separated, dried (anhydrous MgSO₄), filtered, and concentrated in vacuo. The residue was chromatographed (SiO₂, 10 g cartridge; ethyl acetate/hexane=80% to 100%) to give Compound 10 as purple solid (0.056 g, 4.7%).

Step 2) (1 S,2 S)-2-fluoro-N-(6-(2-methyl-5-(1H-pyrrol-3-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide

Compound 10 (0.056 g, 0.122 mmol), 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole (0.031 g, 0.159 mmol), [1,1′-bis(diphenylphosphino) ferrocene]dichloropalladium(11) (Pd(dppf)Cl₂, 0.009 g, 0.012 mmol) and potassium carbonate (0.051 g, 0.367 mmol) in water (3 mL)/tetrahydrofuran (12 mL) was mixed at the room temperature and then heated at 120° C. under the microwaves for 30 min, cooled down to the room temperature, and partitioned between ethyl acetate and water. The organic layer was washed with aqueous saturated sodium chloride solution, separated, dried (anhydrous MgSO₄), filtered, and concentrated in vacuo. The residue was chromatographed (SiO₂, 10 g cartridge; tetrahydrofuran/ethyl acetate =0% to 10%) to give the crude product which was dissolved in diethylether (5 mL) and hexane (5 mL) and stirred at the ambient temperature. The resulting precipitates were collected by filtration, washed by diethylether, and dried to give Example 41 as white solid (0.005 g, 10.9%).

1H NMR (400 MHz, DMSO-d6) δ10.97 (s, 1H), 10.86 (bs, 1H), 8.54 (s, 1H), 8.07 (s, 1H), 7.44˜7.40 (m, 3H), 7.23˜7.19 (m, 3H), 6.74 (dd, J=4.4, 2.8 Hz, 1H), 6.41 (dd, J=4.4, 2.8 Hz, 1H), 4.97 4.79 (m, 1H), 2.20 (s, 3H), 2.11 (m, 1H), 1.66˜1.59 (m, 1H), 1.15˜1.10 (m, 1H).

Synthetic Method G

Example 44 (15 ,25)-2-fluoro-N-(6-(4-fluoro-5-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide

Step 1) (15,25)-2-fluoro-N-(6-(4,4, 5, 5-tetramethyl-1, 3,2-d ioxaborolan-2-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide

Compound 3 (0.800 g, 2.318 mmol), 4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi(1,3,2-dioxaborolane, 1.177 g, 4.636 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (Pd(dppf)Cl2, 0.169 g, 0.231 mmol) and potassium acetate (0.796 g, 8.113 mmol) were mixed at the room temperature in DMSO (20 mL) and then stirred at 90° C. for 24 hr, cooled down to the room temperature, filtered through a celite pad to remove solids, and partitioned between ethyl acetate and water. The organic layer was washed with aqueous saturated sodium chloride solution, separated, dried with anhydrous MgSO₄, filtered, and concentrated in vacuo. The residue was chromatographed (SiO2, 12 g cartridge; ethyl acetate/hexane =0% to 100%) to give Compound 11 as brown solid (0.560 g, 69.9%).

Step 2) (15 , 25)-2-fluoro-N-(6-(4-fluoro-5-hydroxy-2-methylphenyl) imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide

Compound 11 (0.080 g, 0.231 mmol), 5-bromo-2-fluoro-4-methylphenol (0.056 g, 0.277 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (Pd(dppf)Cl₂, 0.017 g, 0.023 mmol) and Na₂CO₃(0.049 g, 0.462 mmol) in dioxane (2 mL)/water (0.5 mL) was mixed at the room temperature and then the mixture was degassed and purged with N₂for 1 minutes, after then the mixture was stirred at 80° C. for 12 hours under N₂atmosphere. The reaction mixture was concentrated to give a residue. The residue was purified. The residue was chromatographed (SiO₂, 12 g cartridge; ethyl acetate/hexane =80% to 100%) to give Example 44 as white solid (0.031 g, 39.8%).

1H NMR (400 MHz, DMSO-d6) δ10.98 (s, 1H), 9.75 (bs, 1H), 8.47 (s, 1H), 8.05 (s, 1H), 7.40 (d, J=9.2 Hz, 1H), 7.13 (dd, J=9.2, 2.0 Hz, 1H), 7.06 (d, J=12.4 Hz, 1H), 6.81 (d, J=9.2 Hz, 1H), 4.98˜4.78 (m, 1H), 2.14˜2.07 (m, 4H), 1.65˜1.58 (m, 1H), 1.16˜1.07 (m, 1H).

Synthetic Method H

Example 66 (1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-(methoxymethyl)phenyl) imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide

Step 1) 1-bromo-3-fluoro-2-(methoxymethyl)benzene

To a solution of Compound 12 (500 mg, 2.44 mmol, 1 eq) in THF (10 mL) was added NaH (146.31 mg, 3.66 mmol, 60% purity, 1.5 eq) in portions at 0° C. under N₂, and reaction mixture was stirred at 0° C. for 0.5 hour under N2, after then Mel (692.30 mg, 4.88 mmol, 303.64 μL, 2 eq) was added dropwise, then the mixture was stirred at 20° C. for another 1 hour under N₂. Saturated aqueous solution of NH₄Cl (30 mL) was added into the reaction mixture, then the mixture was extracted with ethyl acetate (20 mL*2), the combined organic layers were dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. Compound 13 (510 mg, crude) was obtained as a yellow oil.

1H NMR (400MHz, CDCl₃) δ7.41 (d, J=8.1 Hz, 1H), 7.18 (dt, J=5.9, 8.2 Hz, 1H), 7.10˜7.00 (m, 1H), 4.64 (d, J=2.3 Hz, 2H), 3.42 (s, 3H).

Step 2) (1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-(methoxymethyl)phenyl) imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide

To a solution of Compound 13 (80 mg, 365.21 μmol, 1 eq) and Compound 11 (151.27 mg, 438.25 μmol, 1.2 eq) in dioxane (2 mL) and H₂O (0.4 mL) were added Pd(dppf)Cl₂(26.72 mg, 36.52 μmol, 0.1 eq) and Na₂CO₃(77.42 mg, 730.42 μmol, 2 eq), then the mixture was stirred at 90° C. for 12 hours under N₂. The reaction mixture was diluted with ethyl acetate (300 mL), then the mixture was filtered with silica gel, and the filtrate was concentrated to give a residue. The residue was purified by prep-HPLC (column: Phenomenex luna C18 150*40mm* 15um; mobile phase: [water(0.1%TFA)-ACN];B%: 17%-47%,10min). Example 66 (91.3 mg, 193.69 μmol, 53.03% yield, 100% purity, TFA) was obtained as a white solid.

1H NMR (400MHz, DMSO-d6) δ11.25 (s, 1H), 8.68 (s, 1H), 8.14 (s, 1H), 7.60 (d, J=9.2 Hz, 1H), 7.52 (dt, J=6.0, 7.9 Hz, 1H), 7.44 (dd, J=1.6, 9.2 Hz, 1H), 7.33 (d, J=8.7 Hz, 1H), 7.30˜7.25 (m, 1H), 5.11˜4.76 (m, 1H), 4.30 (br d, J=1.3 Hz, 2H), 3.25 (s, 3H), 2.23˜2.08 (m, 1H), 1.76˜1.59 (m, 1H), 1.20 (tdd, J=6.3, 9.1, 12.4 Hz, 1H).

Synthetic Method I

Example 67 (1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-(furan-2-yl)phenyl)imidazo [1,2-a]pyridin-2-yl)cyclopropanecarboxamide

Step 1) 2-(2-bromo-6-fluorophenyl)furan

To a solution of Compound 14 (511.74 mg, 1.70 mmol, 1.1 eq) and 2-(furan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (300 mg, 1.55 mmol, 1 eq) in dioxane (3 mL) and H₂O (0.6 mL) were added Pd(dppf)Cl₂(113.13 mg, 154.61 μmol, 0.1 eq) and Na₂CO₃(491.61 mg, 4.64 mmol, 3 eq), then the reaction mixture was stirred at 80° C. for 3 hr under N₂. The reaction mixture was poured into water (50 mL), then the mixture was extracted with ethyl acetate (50 mL*2), the combined organic layers were dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by prep-TLC (SiO₂, Petroleum ether: Ethyl acetate=3:1). The residue was purified by prep-TLC (SiO₂, Petroleum ether: Ethyl acetate=1:0). Compound 15 (70 mg, 290.39 μmol, 18.78% yield) was obtained as a yellow oil.

1H NMR (400 MHz, CDCl₃) δ7.61 (dd, J=0.8, 1.8 Hz, 1H), 7.48 (td, J=1.1, 8.0 Hz, 1H), 7.21 (dt, J=5.8, 8.1 Hz, 1H), 7.15˜7.08 (m, 1H), 6.70 (td, J=0.9, 3.3 Hz, 1H), 6.56 (dd, J=1.8, 3.3 Hz, 1H).

Step 2) (1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-(furan-2-yl)phenyl)imidazo[1, 2-a]pyridin-2-yl)cyclopropanecarboxamide

To a solution of Compound 15 (70 mg, 290.39 μmol, 1 eq) and Compound 11 (110.26 mg, 319.43 μmol, 1.1 eq) in dioxane (1 mL) and H₂O (0.2 mL) were added Pd(dppf)Cl₂(21.25 mg, 29.04 μmol, 0.1 eq) and Na₂CO₃(92.33 mg, 871.17 pmol, 3 eq), then the reaction mixture was stirred at 80° C. for 12 hr under N₂. The reaction mixture was poured into brine (10 mL), then the mixture was extracted with ethyl acetate (10 mL*2), the combined organic layers were dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was dissolved with methanol: dichloromethane (1:10, 100 mL), then the mixture was filtered with silica gel, and the filtrate was concentrated to give a residue. The residue was purified by prep-HPLC (column: Phenomenex Synergi C18 150*2510 um; mobile phase: [water(0.1%TFA)-ACN];B%: 34%-54%,9min). Example 67 (38.3 mg, 77.63 μmol, 26.73% yield, 100% purity, TFA) was obtained as a white solid.

1H NMR (400 MHz, DMSO-d6) δ11.20 (s, 1H), 8.61 (s, 1H), 8.08 (s, 1H), 7.61 (dd, J=0.9, 1.6 Hz, 1H), 7.60˜7.54 (m, 1H), 7.45˜7.41 (m, 1H), 7.40˜7.36 (m, 2H), 6.93 (dd, J=1.3, 9.3 Hz, 1H), 6.56˜6.48 (m, 2H), 5.05˜4.83 (m, 1H), 2.19˜2.09 (m, 1H), 1.75˜1.59 (m, 1H), 1.19 (tdd, J=6.3, 9.1, 12.4 Hz, 1H).

Synthetic Method J

Example 72 N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide

Step 1) 2,2,2-trifluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)acetamide

To a solution of Compound 1 (1 g, 2.82 mmol, 1 eq) in dioxane (10 mL) and H₂O (1 mL) was added Compound 2 (520.30 mg, 3.38 mmol, 1.2 eq), Pd(dppf)Cl₂(206.08 mg, 281.65 μmol, 0.1 eq) and Na₂CO₃(298.52 mg, 2.82 mmol, 1 eq). The mixture was stirred at 80° C. for 16 hr under N₂atmosphere. The reaction mixture diluted with water 30 mL and extracted with Ethyl acetate (30 mL*2). The combined organic layers were washed with brine (30 mL*2), dried over Na₂SO₄, filtered and the filtrate was concentrated under reduced pressure to give a residue. The residue was purified by column chromatography (Silica gel, Petroleum ether: Ethyl acetate=20:1 to 5:1). Compound 16 (500 mg, 1.48 mmol, 52.64% yield) was obtained as a white solid.

Step 2) 6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-amine

To a solution of Compound 16 (500 mg, 1.48 mmol, 1 eq) in MeOH (10 mL) and H₂O (10 mL) was added K₂CO₃(1.02 g, 7.41 mmol, 5 eq). The mixture was stirred at 75° C. for 2 hr. The reaction mixture was added with water 50 m L, and extracted with Ethyl acetate (50 mL*2). The combined organic layers were washed with brine (50 mL*2), dried over Na₂SO₄, filtered and the filtrate was concentrated under reduced pressure to give a residue. Compound 17 (300 mg, 1.24 mmol, 83.88% yield) was obtained as a yellow solid

Step 3) N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide

To a solution of Compound 17 (100 mg, 414.49 μmol, 1 eq) in EtOAc (2 mL) was added cyclopropanecarboxylic acid (53.52 mg, 621.73 μmol, 49.10 μL, 1.5 eq) and DCC (85.52 mg, 414.49 μmol, 83.84 μL, 1 eq). The mixture was stirred at 20° C. for 32 hr. Then DMAP (5.06 mg, 41.45 μmol, 0.1 eq) was added to the mixture and stirred at 20° C. for 16 hr. The reaction mixture was diluted with water 20 mL and extracted with Ethyl acetate (20 mL*2). The combined organic layers were washed with brine (20 mL*2), dried over Na₂SO₄, filtered and the filtrate was concentrated under reduced pressure to give a residue. The residue was purified by prep-HPLC (column: Phenomenex Luna C18 150*25mm*10 um;mobile phase: [water(0.1%TFA)-ACN]; B%: 22%-52%,10min). Example 72 (45.9 mg, 106.25 μmol, 25.63% yield, 98% purity, TFA) was obtained as a pink solid.

1H NMR (400MHz, DMSO-d6) δ11.22 (br s, 1H), 8.66 (s, 1H), 8.09 (s, 1H), 7.59 (d, J=9.2 Hz, 1H), 7.40 (br d, J=9.3 Hz, 1H), 7.38˜7.30 (m, 1H), 7.28˜7.21 (m, 1H), 7.17 (d, J=7.5 Hz, 1H), 2.18 (d, J=2.3 Hz, 3H), 1.94 (quin, J=6.2 Hz, 1H), 0.85 (d, J=6.1 Hz, 4H).

Synthetic Method K

Example 77 (1 S,2 S)-N-(6-(2-(acetam idomethyl)-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide

Step 1) N-(2-bromo-6-fluorobenzyl)acetamide

To a solution of Compound 18 (200 mg, 695.94 μmol, 1 eq) in Py (5 mL) was added Ac₂O (85.26 mg, 835.13 μmol, 78.22 μL, 1.2 eq). The mixture was stirred at 25° C. for 3 hr. Desired MS was detected by LC-MS. The mixture was concentrated under reduced pressure to give a residue. The residue was adjusted to pH=6 with HCI, and extracted with EA (30 mL*3). The organic phase was concentrated under reduced pressure to give a residue. Compound 19 (130 mg, 412.07 μmol, 59.21% yield, 78% purity) was obtained as light yellow solid.

Step 2) (1 S,2 S)-N-(6-(2-(acetam idomethyl)-3-fluorophenyl)imidazo[1, 2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide

A mixture of Compound 19 (100 mg, 361.68 μmol, 1 eq), Compound 11 (122.35 mg, 354.44 μmol, 0.98 eq), Pd(dppf)Cl₂(26.46 mg, 36.17 μmol, 0.1 eq) and Na₂CO₃(76.67 mg, 723.35 μmol, 2 eq) in Water (1 mL) and dioxane (4 mL) was degassed and purged with N₂for 3 times, and then the mixture was stirred at 80° C. for 16 hr under N₂atmosphere. Desired MS was detected by LC-MS. The mixture was filtered, and the filtrate was concentrated under reduced pressure to give a residue. The residue was purified by prep-HPLC (column: Phenomenex luna C18 250*50mm*10 um ;mobile phase: [water(0.1%TFA)-ACN]; B′)/0: 10%-40%,9m in). Example 77 (15.3 mg, 29.84 μmol, 8.25% yield, 97.2% purity, TFA) was obtained as white solid

1H NMR (400 MHz, CD3OD) δ8.67 (s, 1H), 7.81˜7.71 (m, 2H), 7.49-7.47 (m, 1H), 7.31-7.22 (m, 2H), 5.04˜5.01 (m, 0.5H), 4.87-4.85 (m, 0.5H), 4.38 (s, 2H), 2.16-2.12 (m, 1H), 1.90-1.84 (m, 1H), 1.31-1.28 (m, 1H).

Synthetic Method L

Example 84 (1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2)-((2-methoxyethoxy)methyl) phenyl)imidazof1,2-alpyridin-2-yl)cyclopropanecarboxamide. TFA salt

Step 1) 1-bromo-3-fluoro-2-((2-methoxyethoxy)methyl)benzene

Compound 20 (445.00 mg, 2.17 mmol, 1 eq) was dissolved in DMF (15 mL), to which NaH (130.22 mg, 3.26 mmol, 60% purity, 1.5 eq) was added at 0° C. in portions. The resulting mixture was then stirred under N₂atmosphere for 30 min, before 1-bromo-2-methoxy-ethane (362.01 mg, 2.60 mmol, 244.60 μL, 1.2 eq) was added at 0° C. The mixture was then stirred under N₂atmosphere at 15° C. for another 11.5 hr. The mixture was quenched with EtOH (5 mL), diluted with water (20 mL) and extracted with EA (20 mL×3). The combined organic layers were concentrated under reduced pressure. The residue was purified by silica gel chromatography (pure PE to PE/EA=4/1) to afford Compound 21 (178 mg, 676.54 μmol, 31.17% yield) as a light yellow oil.

Step 2) (15,25)-2-fluoro-N-(6-(3-fluoro-2-((2-methoxyethoxy)methyl) phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide. TFA salt

The mixture of Compound 21 (178 mg, 676.54 μmol, 1 eq) and Compound 11 (210.17 mg, 608.89 μmol, 0.9 eq) was dissolved in dioxane (10 mL) and H₂O (2 mL), to which Pd(dppf)Cl₂(99.01 mg, 135.31 μmol, 0.2 eq) and Na₂CO₃(215.12 mg, 2.03 mmol, 3 eq) were added in portions. The resulting mixture was then stirred under N₂atmosphere at 80° C. for 16 hr. Desired m/z was detected by LC-MS. The mixture was filtered and the filtrate was diluted with water (20 mL) and extracted with EA (20 mL×3). The combined organic layers were concentrated under reduced pressure. The residue was purified by silica gel chromatography (PE/EA=10/1 to 1/1) and then Prep-HPLC (column: Phenomenex Gemini-NX C18 75*30mm*3um;mobile phase: [water(0.1%TFA)-ACN]; B%: 18%-48%,7m in) and lyophilized to afford Example 84 (32.2 mg, 62.10 μmol, 9.18% yield, 99.4% purity, TFA) as an off-white solid.

1H NMR (400 MHz, DMSO) δ11.23˜11.19 (br s, 1H), 8.72 (s, 1H), 8.10 (s, 1H), 7.56-7.50 (m, 3H), 7.32˜7.28 (m, 2H), 5.04˜4.84 (m, 1H), 4.35 (s, 2H), 3.47-3.44 (m, 4H), 3.25 (s, 3H), 2.16˜2.11 (m, 1H), 1.70-1.64 (m, 1H), 1.21-1.16 (m, 1H).

Synthetic Method M

Example 85 (15,25)-2-fluoro-N-(6-(3-fluoro-24(2-hydroxyethoxy)methyl) phenyl)imidazof1,2-alpyridin-2-yl)cyclopropanecarboxamide

Step 1) (2-((2-bromo-6-fluorobenzyl)oxy)ethoxy)(tert-butyl)dimethylsilane

Compound 22 (1 g, 4.88 mmol, 1 eq) was dissolved in DMF (50 mL), NaH (292.65 mg, 7.32 mmol, 60% purity, 1.5 eq) was added at 0° C. in portions. The resulting mixture was then stirred under N₂atmosphere for 30 min, before 2-bromoethoxy-tert-butyl-dimethyl-silane (1.40 g, 5.85 mmol, 109.93 μL, 1.2 eq) was added at 0° C. The mixture was then stirred under N₂atmosphere at 15° C. for another 11.5 hr. New spots were formed according to the result of TLC (PE/EA =4/1). The mixture was quenched with EtOH (5 mL), diluted with water (20 mL) and extracted with EA (20 mL×3). The combined organic layers were concentrated under reduced pressure. The residue was purified together with the former batch by silica gel chromatography (pure PE to PE/EA=4/1) to afford Compound 23 (372 mg, 1.02 mmol, 20.99% yield) as a white solid.

1H NMR (400 MHz, DMSO-d6) δ7.52-7.50 (m, 1H), 7.37-7.36 (m, 1H), 7.34-7.30 (m, 1H), 4.61-4.60 (m, 2H), 3.90-3.80 (m, 2H), 3.58-3.47 (m, 2H), 0.835 (s, 9H), 0.02 (s, 6H).

Step 2) 2-((2-bromo-6-fluorobenzyl)oxy)ethanol

Compound 23 (352 mg, 968.80 μmol, 1 eq) was dissolved in DMF (10 mL), CsF (147.16 mg, 968.80 μmol, 35.72 μL, 1 eq) was added. The resulting mixture was then stirred at 80° C. for 12 hr. The starting material was consumed according to the result of TLC (PE/EA=4/1). The mixture was filtered and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel chromatography (PE to PE/EA=5/1) to afford Compound 24 (120 mg, 481.78 μmol, 49.73% yield) as an off-white solid.

1H NMR (400 MHz, DMSO-d6) δ7.52-7.50 (m, 1H), 7.36-7.28 (m, 2H), 4.60-4.59 (m, 2H), 3.52-3.47 (m, 4H).

Step 3 (15 , 25)-2-fluoro-N-(6-(3-fluoro-2-((2-hydroxyethoxy)methyl)phenyl) imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide

The mixture of Compound 24 (120 mg, 481.78 μmol, 1 eq) and Compound 11 (149.67 mg, 433.60 μmol, 0.9 eq) was dissolved in the mixture of dioxane (10 mL) and H₂O (2 mL), Pd(dppf)Cl₂(35.25 mg, 48.18 μmol, 0.1 eq) and Na₂CO₃(153.19 mg, 1.45 mmol, 3 eq) were added in portions. The resulting mixture was then stirred under N₂atmosphere at 80° C. for 12 hr. Desired m/z was detected by LC-MS. The mixture was filtered and the filtrate was diluted with water (20 mL) and extracted with EA (20 mL×3). The combined organic layers were concentrated under reduced pressure. The residue was purified by silica gel chromatography (PE/EA =2/1 to EA/MeOH=10/1) and then by Prep-HPLC (column: Phenomenex Gemini-NX C18 75*30mm*3um;mobile phase: [water(0.1%TFA)-ACN]; B%: 12%-42%,9m in) and lyophilized to afford Example 85 (74.1 mg, 143.65 μmol, 29.82% yield, 97.2% purity, TFA) as an off-white solid .

1H NMR (400 MHz, DMSO-d6) δ11.21 (s, 1H), 8.78 (s, 1H), 8.14 (s, 1H), 7.58-7.47 (m, 3H), 7.33-7.29 (m, 2H), 5.05-4.85 (m, 1H), 4.36 (s, 2H), 3.55-3.52 (m, 2H), 3.47-3.45 (m, 2H), 2.16-2.13 (m, 1H), 1.71-1.69 (m, 1H), 1.65-1.64 (m, 1H).

Synthetic Method N

Example 105 (1 S,2 S)-2-fluoro-N-(6-(2-methyl-5-(1H-pyrazol-1-yl)phenyl) imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide

Step 1) 3-bromo-4-methyl-2-nitrophenol

To a solution of Compound 25 (5 g, 26.73 mmol, 1 eq) in CHCl₃(50 mL) was added HNO₃(2.85 g, 29.41 mmol, 2.04 mL, 1.1 eq) dropwise at −50° C., then the reaction mixture was stirred at -50° C. for 1 hr. The reaction mixture was slowly poured into ice water (200 mL), then the mixture was extracted with dichloromethane (100 mL* 2), the combined organic layers were dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by column chromatography (SiO₂, Petroleum ether/Ethyl acetate=1/0 to 100/1). Compound 26 (550 mg, 2.37 mmol, 8.87% yield) was obtained as a yellow oil.

1H NMR (400 MHz, CDCl₃) δ8.84-8.20 (m, 1H), 7.31 (d, J=8.7 Hz, 1H), 7.00 (d, J=8.6 Hz, 1H), 2.41 (s, 3H).

Step 2) 2-amino-3-bromo-4-methylphenol

To a solution of Compound 26 (450 mg, 1.94 mmol, 1 eq) in EtOH (5 mL) and H₂O (5 mL) were added Fe (649.83 mg, 11.64 mmol, 6 eq) and NH₄Cl (622.44 mg, 11.64 mmol, 6 eq). The suspension was degassed and purged with N₂for 3 times. The reaction mixture was stirred under N₂at 80° C. for 2 hours. The reaction mixture was filtered, the filter cake was washed with methanol (50 mL* 3) and the filtrate was concentrated under reduced pressure to give a residue. The residue was poured into water (50 mL), then the mixture was extracted with ethyl acetate (50 mL* 2), the combined organic layers were dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by reverse flase (MeCN/H₂O, CF₃COOH), then the mixture was concentrated to remove MeCN, after then the mixture's pH was adjust to pH=7 by using saturated aqueous solution of sodium bicarbonate, then the mixture was extracted with ethyl acetate (100 mL*2), the combined organic layers were dried over saturated sodium sulfate, filtered and concentrated under reduced pressure to give a residue. Compound 27 (210 mg, 1.02 mmol, 52.52% yield, 98% purity) was obtained as a yellow solid.

1H NMR (400 MHz, CDCl₃) δ6.64-6.59 (m, 1H), 6.54-6.50 (m, 1H), 2.30 (s, 3H).

Step 3) 4-bromo-5-methylbenzo[d]oxazole

To a solution of Compound 27 (210 mg, 1.02 mmol, 1 eq) and trimethoxymethane (162.14 mg, 1.53 mmol, 167.50 μL, 1.5 eq) in EtOH (3 mL) was added tris(trifluoromethylsulfonyloxy)ytterbium (14.19 mg, 22.87 μmol, 2.25e-2 eq), then the reaction mixture was stirred at 90° C. for 12 hr. LCMS showed 19% of Compound 3 was remained and 81% of desired mass was detected. trimethoxymethane (108.09 mg, 1.02 mmol, 111.66 μL, 1 eq) was added to the reaction mixture, then the reaction mixture was stirred at 90° C. for another 2 hr. The reaction mixture was concentrated under reduced pressure to remove solvent. Saturated aqueous solution of NaHCO₃(50 mL) was added into the residue, then the mixture was extracted with ethyl acetate (30mL* 3), the combined organic layers were dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. Compound 28 (160 mg, crude) was obtained as a brown solid.

1H NMR (400 MHz, CDCl₃) δ8.12 (s, 1H), 7.43 (d, J=8.3 Hz, 1H), 7.29 (d, J=8.4 Hz, 1H), 2.54 (s, 3H).

Step 4) (1 S,2 S)-2-fluoro-N-(6-(5-methylbenzo[d]oxazol-4-yl)imidazo[1, 2-a]pyridin-2-yl)cyclopropanecarboxamide

To a solution of Compound 28 (130 mg, 613.08 μmol, 1 eq) and Compound 11 (253.95 mg, 735.70 μmol, 1.2 eq) in dioxane (2 mL) and H₂O (0.4 mL) were added Pd(dppf)Cl₂(44.86 mg, 61.31 μmol, 0.1 eq) and Na₂CO₃(194.94 mg, 1.84 mmol, 3 eq), then the reaction mixture was stirred at 90° C. for 12 hr under N₂. The reaction mixture was poured into brine (30 mL), then the mixture was extracted with ethyl acetate (30 mL* 2), the combined organic layers were dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was dissolved with methanol: dichloromethane (1:10, 100 mL), then the mixture was filtered with silica gel, and the filtrate was concentrated to give a residue. The residue was purified by prep-HPLC (column: Xtimate C18 150*40mml Oum;mobile phase: [water (0.05% ammonia hydroxide v/v)-ACN];B%: 25%-55%,10min). Example 105 (118.4 mg, 333.33 pmol, 54.37% yield, 98.633% purity) was obtained as a white solid.

1H NMR (400 MHz, DMSO-d6) δ11.07 (s, 1H), 8.70 (s, 1H), 8.65 (s, 1H), 8.13 (s, 1H), 7.71 (d, J=8.3 Hz, 1H), 7.53 (d, J=9.2 Hz, 1H), 7.43 (d, J=8.4 Hz, 1H), 7.29 (dd, J=1.6, 9.2 Hz, 1H), 5.05-4.81 (m, 1H), 2.38 (s, 3H), 2.20-2.10 (m, 1H), 1.73-1.59 (m, 1H), 1.17 (tdd, J=6.2, 9.1, 12.2 Hz, 1H).

Table 1 below shows the compounds of Examples along with general synthetic methods used to make the compound and characterization data.

TABLE 1 Compounds of Examples Synthetic Ex # Structure/Name 1H NMR/MS (M + 1) Method 1 1H NMR (400 MHz, DMSO-d6) δ 11.67 (s, 1H), 8.74 (s, 1H), 8.13 (s, 1H), 7.69 (d, J = 9.2 Hz, 1H), 7.55 (d, J = 9.2 Hz, 1H), 7.35~7.30 (m, 1H), 7.23 (t, J = 9.2 Hz, 1H), 7.15 (d, J = 7.2 Hz, 1H), 5.05~4.85 (m, 1H), 7.21~7.14 (m, 4H), 1.69~1.63 (m, 1H), 1.21~1.18 (m, 1H); LCMS (electrospray) m/z 327.88 (M + H)+. A 2 1H NMR (400 MHz, DMSO-d6) δ 11.00 (s, 1H), 8.53 (s, 1H), 8.06 (s, 1H), 7.46 (d, J = 9.2 Hz, 1H), 7.35~7.29 (m, 1H), 7.17~7.09 (m, 3H), 4.98~4.78 (m, 1H), 2.16~2.09 (m, 4H), 1.66~1.59 (m, 1H), 1.16~1.08 (m, 1H); LCMS (electrospray) m/z 327.96 (M + H)+. A 3 1H NMR (400 MHz, DMSO-d6); δ 10.44 (s, 1H), 8.21 (s, 1H), 7.62 (d, J = 9.6 Hz, 1H), 7.35 (dd, J = 9.2, 1.6 Hz, 1H), 7.30 (d, J = 7.0 Hz, 1H), 7.24~7.19 (m, 2H), 5.01~4.83 (m, 1H), 2.15 (d, J = 2.4 Hz, 3H), 2.06~2.03 (m, 1H), 1.64~1.56 (m, 1H), 1.15~1.08 (m, 1H); LCMS (electrospray) m/z 361.95 (M + H))+. B 4 1H NMR (400 MHz, DMSO-d6); δ 10.46 (s, 1H), 8.27 (s, 1H), 7.64 (d, J = 8.4 Hz, 1H), 7.38~7.33 (m, 1H), 7.27 (d, J = 8.8 Hz, 1H), 7.19~7.12 (m, 2H), 5.01~4.83 (m, 1H), 2.17 (s, 3H), 2.12~2.05 (m, 1H), 1.63~1.56 (m, 1H), 1.20~1.10 (m, 1H); LCMS (electrospray) m/z 361.95 (M + H)+. B 5 1H NMR (400 MHz, DMSO-d6); δ 10.25 (s, 1H), 8.47 (s, 1H), 8.44 (d, J = 5.2 Hz, 1H), 8.26 (s, 1H), 7.51 (d, J = 9.2 Hz, 1H), 7.34 (d, J = 5.2 Hz, 1H), 7.24 (d, J = 9.2 Hz, 1H), 4.99~4.81 (m, 1H), 2.29 (s, 6H), 2.07~2.03 (m, 1H), 1.63~1.56 (m, 1H), 1.15~1.05 (m, 1H); LCMS (electrospray) m/z 324.95 (M + H)+. C 6 1H NMR (400 MHz, DMSO-d6); δ 11.01 (s, 1H), 8.61 (s, 1H), 8.44~8.42 (m, 2H), 7.47 (d, J = 9.2 Hz, 1H), 7.33 (d, J = 5.2 Hz, 1H), 7.25 (dd, J = 9.2, 2.0 Hz, 1H), 4.99~4.78 (m, 1H), 2.28 (s, 3H), 2.15~2.08 (m, 1H), 1.66~1.59 (m, 1H), 1.15~1.12 (m, 1H)); LCMS (electrospray) m/z 311.00 (M + H)+. A 7 1H NMR (400 MHz, DMSO-d6); δ 10.46 (s, 1H), 8.47 (s, 1H), 8.30 (s, 1H), 7.63 (d, J = 9.2 Hz, 1H), 7.40 (dd, J = 9.2, 1.6 Hz, 1H), 7.35 (d, J = 4.8 Hz, 1H), 5.01~4.83 (m, 1H), 2.28 (s, 3H), 2.08~2.01 (m, 1H), 1.63~1.56 (m, 1H), 1.20~1.05 (m, 1H); LCMS (electrospray) m/z 344.91 (M + H)+. B 8 1H NMR (400 MHz, DMSO-d6); δ 10.24 (s, 1H), 8.19 (s, 1H), 7.49 (d, J = 9.2 Hz, 1H), 7.29 (m, 1H), 7.22~7.18 (m, 3H), 4.99~4.81 (m, 1H), 2.29 (s, 3H), 2.15 (s, 3H), 2.07~2.03 (m, 1H), 1.63~1.56 (m, 1H), 1.12~1.05 (m, 1H); LCMS (electrospray) m/z 341.99 (M + H)+. C 9 1H NMR (400 MHz, DMSO); δ 10.25 (s, 1H), 8.22 (s, 1H), 7.51 (d, J = 8.0 Hz, 1H), 7.33 (dd, J = 14.2, 7.8 Hz, 1H), 7.18~7.08 (m, 3H), 4.99~4.81 (m, 1H), 2.27 (s, 3H), 2.17 (s, 3H), 2.06 (m, 1H), 1.64~1.56 (m, 1H), 1.12~1.05 (m, 1H); LCMS (electrospray) m/z 341.99 (M + H)+. C 10 1H NMR (400 MHz, DMSO-d₆) δ 10.27 (s, 1H), 8.52 (s, 1H), 8.41 (s, 1H), 8.32 (s, 1H), 7.53 (d, J = 9.2 Hz, 1H), 7.26 (dd, J = 9.4, 1.4 Hz, 1H), 4.99~4.81 (m, 1H), 2.30 (s, 3H), 2.23 (s, 3H), 2.07~2.04 (m, 1H), 1.63~1.56 (m, 1H), 1.10~1.09 (m, 1H); LCMS (electrospray) m/z 342.96 (M + H)+. C 11 ¹H NMR (400 MHz, DMSO-d₆) δ 11.00 (s, 1H), 8.56 (s, 1H), 8.06 (s, 1H), 7.44 (d, J = 9.2 Hz, 1H), 7.32 (t, J = 7.2 Hz, 1H), 7.22 (dd, J = 9.2, 2.0 Hz, 1H), 7.12~7.09 (m, 2H), 4.99~4.78 (m, 1H), 2.21 (s, 3H), 2.11~2.10 (m, 1H), 1.66~1.59 (m, 1H), 1.17~1.12 (m, 1H); LCMS (electrospray) m/z 327.92 (M + H)+. A 12 ¹H NMR (400 MHz, DMSO-d₆) δ 10.97 (s, 1H), 8.48 (s, 1H), 8.06 (s, 1H), 7.41 (d, J = 8.8 Hz, 1H), 7.15 (dd, J = 9.4, 1.4 Hz, 1H), 7.06 (d, J = 8.4 Hz, 1H), 6.69~6.64 (m, 2H), 4.98~4.78 (m, 1H), 2.12~2.07 (m, 4H), 1.66~1.58 (m, 1H), 1.16~1.09 (m, 1H); LCMS (electrospray) m/z 325.90 (M + H)+. A 13 ¹H NMR (400 MHz, DMSO-d₆) δ 11.00 (s, 1H), 8.59 (s, 1H), 7.86 (dd, J = 7.8, 1.8 Hz, 1H), 7.81 (d, J = 1.6 Hz, 1H), 7.48~7.44 (m, 2H), 7.22 (dd, J = 9.2, 1.6 Hz, 1H), 4.99~4.78 (m, 1H), 3.82 (s, 3H), 2.32 (s, 3H), 2.12~2.11 (m, 1H), 1.65~1.59 (m, 1H), 1.15~1.10 (m, 1H); LCMS (electrospray) m/z 367.98 (M + H)+. A 14 ¹H NMR (400 MHz, DMSO-d₆) δ 11.03 (s, 1H), 8.66 (s, 1H), 8.50 (s, 1H), 8.35 (s, 1H), 8.35 (s, 1H), 8.08 (s, 1H), 7.49 (d, J = 9.2 Hz, 1H), 7.27 (dd, J = 9.0, 1.8 Hz, 1H), 4.99~4.79 (m, 1H), 2.23 (s, 3H), 2.12~2.11 (m, 1H), 1.66~1.59 (m, 1H), 1.16~1.10 (m, 1H); LCMS (electrospray) m/z 328.96 (M + H)+. A 15 ¹H NMR (400 MHz, DMSO-d₆) δ 11.68 (bs, 1H), 1.16 (s, 1H), 8.74 (s, 1H), 8.15 (s, 1H), 7.75 (d, J = 9.2 Hz, 1H), 7.59 (d, J = 9.2 Hz, 1H), 7.34 (d, J = 8.4 Hz, 1H), 7.29 (t, J = 2.8 Hz, 1H), 7.04 (d, J = 8.4 Hz, 1H), 6.08 (s, 1H), 5.07~4.87 (m, 1H), 2.24 (s, 3H), 2.17 (m, 1H), 1.71~1.65 (m, 1H), 1.25~1.19 (m, 1H); LCMS (electrospray) m/z 349.04 (M + H)+. A 16 ¹H NMR (400 MHz, DMSO-d₆) δ 10.48 (s, 1H), 8.53 (s, 1H), 8.40 (s, 1H), 8.37 (s, 1H), 7.66 (d, J = 10.0 Hz, 1H), 7.41 (dd, J = 9.0, 1.4 Hz, 1H), 5.01~4.83 (m, 1H), 2.22 (d, J = 2.0 Hz, 3H), 2.11~2.03 (m, 1H), 1.63~1.56 (m, 1H), 1.14~1.11 (m, 1H); LCMS (electrospray) m/z 362.92 (M + H)+. B 17 ¹H NMR (400 MHz, DMSO-d₆) δ 8.59 (s, 1H), 8.06 (s, 1H), 7.76~7.74 (m, 2H), 7.52 (d, J = 8.4 Hz, 1H), 7.46 (d, J = 9.2 Hz, 1H), 7.23 (dd, J = 9.2, 1.6 Hz, 1H), 4.99~4.78 (m, 1H), 2.33 (s, 3H), 2.14~2.08 (m, 1H), 1.66~1.59 (m, 1H), 1.17~1.03 (m, 1H); LCMS (electrospray) m/z 335.01 (M + H)+. A 18 ¹H NMR (400 MHz, DMSO-d₆) δ 12.90 (s, 1H), 10.97 (s, 1H), 8.94 (s, 1H), 8.05 (s, 1H), 7.78 (s, 1H), 7.67 (d, J = 9.2 Hz, 1H), 7.41 (d, J = 9.2 Hz, 1H), 6.67 (s, 1H), 4.98~4.78 (m, 1H), 2.11~2.09 (m, 1H), 1.65~1.59 (m, 1H), 1.51~1.09 (m, 1H); LCMS (electrospray) m/z 285.93 (M + H)+. A 19 ¹H NMR (400 MHz, DMSO-d₆) δ 12.50 (s, 1H), 10.67 (s, 1H), 8.65 (s, 1H), 8.09 (s, 1H), 7.53~7.39 (m, 3H), 4.93~4.76 (m, 1H), 2.19~2.11 (m, 4H), 1.69~1.62 (m, 1H), 1.15~1.07 (m, 1H); LCMS (electrospray) m/z 299.96 (M + H)+ A 20 ¹H NMR (400 MHz, DMSO-d₆) δ 10.69 (s, 1H), 9.44 (s, 1H), 8.45 (s, 1H), 8.05 (s, 1H), 7.40 (d, J = 9.2 Hz, 1H), 7.13 (dd, J = 9.2, 2.0 Hz, 1H), 7.08~7.01 (m, 1H), 6.81 (d, J = 7.6 Hz, 1H), 6.89 (d, J = 6.8 Hz, 1H), 4.98~4.79 (m, 1H), 2.13~2.09 (m, 1H), 2.02 (s, 3H), 1.65~1.58 (m, 1H), 1.14~1.09 (m, 1H); LCMS (electrospray) m/z 326.00 (M + H)+ A 21 ¹H NMR (400 MHz, DMSO-d₆) δ 11.04 (s, 1H), 8.73 (s, 1H), 8.65 (s, 1H), 8.55 (d, J = 5.2 Hz, 1H), 8.09 (s, 1H), 7.68 (d, J = 5.6 Hz, 1H), 7.50 (d, J = 9.2 Hz, 1H), 7.32 (dd, J = 9.2, 2.0 Hz, 1H), 4.99~4.79 (m, 1H), 2.11~2.10 (m, 1H), 1.65~1.59 (m, 1H), 1.17~1.10 (m, 1H); LCMS (electrospray) m/z 330.88 (M + H)+ A 22 ¹H NMR (400 MHz, DMSO-d₆) δ 10.97 (s, 1H), 8.45 (s, 1H), 8.06 (s, 1H), 7.42 (d, J = 9.2 Hz, 1H), 7.19~7.06 (m, 4H), 4.98~4.78 (m, 1H), 2.27 (s, 3H), 2.21~2.11 (m, 4H), 1.66~1.58 (m, 1H), 1.16~1.11 (m, 1H); LCMS (electrospray) m/z 323.83 (M + H)+. A 23 ¹H NMR (400 MHz, DMSO-d₆) δ 10.96 (s, 1H), 8.44 (s, 1H), 8.06 (s, 1H), 7.39 (d, J = 8.0 Hz, 1H), 7.12 (dd, J = 9.2, 1.6 Hz, 1H), 6.91 (d, J = 8.4 Hz, 1H), 6.50~6.46 (m, 2H), 4.98~4.78 (m, 3H), 2.12~2.09 (m, 1H), 2.05 (s, 3H), 1.66~1.58 (m, 1H), 1.14~1.11 (m, 1H); LCMS (electrospray) m/z 324.95 (M + H)+. A 24 ¹H NMR (400 MHz, DMSO-d₆) δ 10.97 (s, 1H), 8.46 (s, 1H), 8.06 (s, 1H), 7.39 (d, J = 9.2 Hz, 1H), 7.14 (d, J = 9.2 Hz, 1H), 6.98 (d, J = 8.0 Hz, 1H), 6.46 (d, J = 7.6 Hz, 1H), 6.41 (s, 1H), 5.49 (d, J = 5.2 Hz, 1H), 4.96-~4.80 (m, 1H), 2.63 (d, J = 4.4 Hz, 3H), 2.10~2.07 (m, 4H), 1.64~1.59 (m, 1H), 1.12 (m, 1H); LCMS (electrospray) m/z 338.99 (M + H)+. A 25 ¹H NMR (400 MHz, DMSO-d₆) δ 10.99 (s, 1H), 9.90 (s, 1H), 8.50 (s, 1H), 8.07 (s, 1H), 7.49~7.42 (m, 3H), 7.19 (d, J = 8.4 Hz, 1H), 7.16 (dd, J = 9.2, 1.6 Hz, 1H), 4.99~4.78 (m, 1H), 2.17 (s, 3H), 2.13~2.11 (m, 1H), 1.99 (s, 3H), 1.66~1.58 (m, 1H), 1.15~1.10 (m, 1H); LCMS (electrospray) m/z 366.98 (M + H)+. A 26 ¹H NMR (400 MHz, DMSO-d₆) δ 11.00 (s, 1H), 8.56 (s, 1H), 8.05 (s, 1H), 7.43 (d, J = 9.2 Hz, 1H), 7.36~7.31 (m, 3H), 7.20 (dd, J = 9.2, 1.6 Hz, 1H), 4.99~4.78 (m, 1H), 2.22 (s, 3H), 2.12~2.10 (m, 1H), 1.66~1.59 (m, 1H), 1.13~1.07 (m, 1H); LCMS (electrospray) m/z 343.94 (M + H)+. A 27 ¹H NMR (400 MHz, DMSO-d₆) δ 11.71 (s, 1 H), 10.99 (s, 1 H), 8.89 (s, 1 H), 8.50 (d, J = 1.6 Hz, 1 H), 8.20 (d, J = 1.6 Hz, 1 H), 8.07 (s, 1 H), 7.59 (d, J = 1.6 Hz, 1 H), 7.50~7.47 (m, 2 H), 4.99~4.79 (m, 1 H), 2.12~2.11 (m, 1 H), 1.67~1.59 (m, 1 H), 1.17~1.09 (m, 1 H); LCMS (electrospray) m/z 335.91 (M + H)+. A 28 ¹H NMR (400 MHz, DMSO-d₆) δ 12.82 (s, 1H), 10.99 (s, 1H), 8.58 (s, 1H), 8.08 (s, 1H), 7.73~7.69 (m, 2H), 7.46~7.23 (m, 4H), 6.70 (s, 1H), 4.97~4.80 (m, 1H), 2.25 (s, 3H), 2.14~2.09 (m, 1H), 1.66~1.59 (m, 1H), 1.13~1.08 (m, 1H); LCMS (electrospray) m/z 376.00 (M + H)+. D 29 ¹H NMR (400 MHz, DMSO-d₆) δ 10.99 (s, 1H), 8.52 (dd, J = 1.8, 1.0 Hz, 1H), 8.06 (s, 1H), 7.44~7.40 (m, 2H), 7.33~7.26 (m, 2H), 7.18 (dd, J = 9.2, 2.0 Hz, 1H), 4.98~4.78 (m, 1H), 2.24 (s, 3H), 2.11 (m, 1H), 1.66~1.58 (m, 1H), 1.13~1.09 (m, 1H); LCMS (electrospray) m/z 343.94 (M + H)+. A 30 ¹H NMR (400 MHz, DMSO-d₆) δ 11.00 (s, 1H), 8.53 (s, 1H), 8.06 (s, 1H), 7.48~7.43 (m, 2H), 7.30~7.24 (m, 2H), 7.18 (dd, J = 9.2, 1.2 Hz, 1H), 4.98~4.79 (m, 1H), 2.25 (s, 3H), 2.11 (m, 1H), 1.65~1.58 (m, 1H), 1.15~1.10 (m, 1H); LCMS (electrospray) m/z 343.94 (M + H)+. A 31 ¹H NMR (400 MHz, DMSO-d₆) δ 11.05 (s, 1H), 8.89 (d, J = 5.6 Hz, 1H), 8.65 (s, 1H), 8.10 (s, 1H), 7.86 (d, J = 5.6 Hz, 1H), 7.49 (d, J = 9.2 Hz, 1H), 7.19 (d, J = 10.0 Hz, 1H), 4.99~4.79 (m, 1H), 2.13~2.10 (m, 1H), 1.66~1.59 (m, 1H), 1.16~1.11 (m, 1H); LCMS (electrospray) m/z 364.86 (M + H)+. A 32 ¹H NMR (400 MHz, DMSO-d₆) δ 10.97 (s, 1H), 8.47 (s, 1H), 8.05 (s, 1H), 7.41 (d, J = 9.2 Hz, 1H), 7.16~7.04 (m, 4H), 4.97~4.79 (m, 1H), 2.28 (s, 3H), 2.20 (s, 3H), 2.14~2.10 (m, 1H), 1.65~1.58 (m, 1H), 1.16~1.05 (m, 1H); LCMS (electrospray) m/z 323.75 (M + H)+. A 33 ¹H NMR (400 MHz, DMSO-d₆) δ 10.56 (s, 1H), 8.23 (s, 1H), 7.49 (d, J = 9.6 Hz, 1H), 7.33~7.27 (m, 1H), 7.24~7.16 (m, 3H), 5.01~4.81 (m, 1H), 2.15 (s, 3H), 2.05~2.05 (m, 1H), 1.63~1.56 (m, 1H), 1.17~1.09 (m, 1H); LCMS (electrospray) m/z 345.96 (M + H)+. E 34 ¹H NMR (400 MHz, DMSO-d₆) δ 10.97 (s, 1H), 8.49 (s, 1H), 8.05 (s, 1H), 7.41 (d, J = 8.8 Hz, 1H), 7.17 (dd, J = 9.2, 1.6 Hz, 2H), 7.08 (d, J = 7.6 Hz, 2H), 4.98~4.78 (m, 1H), 2.27 (s, 3H), 2.19 (s, 3H), 2.11~2.11 (m, 1H), 1.65~1.58 (m, 1H), 1.15~1.09 (m, 1H); LCMS (electrospray) m/z 323.68 (M + H)+. A 35 ¹H NMR (400 MHz, DMSO-d₆) δ 10.98 (s, 1H), 10.50 (s, 1H), 8.83 (t, J = 1.2 Hz, 1H), 8.08 (s, 1H), 7.45 (d, J = 1.2 Hz, 2H), 7.27 (d, J = 7.2 Hz, 1H), 7.20 (dd, J = 7.6, 1.6 Hz, 1H), 7.02 (d, J = 1.2 Hz, 1H), 4.99~4.78 (m, 1H), 3.49 (s, 2H), 2.12~2.09 (m, 1H), 1.66~1.59 (m, 1H), 1.15~1.10 (m, 1H); LCMS (electrospray) m/z 350.99 (M + H)+. A 36 ¹H NMR (400 MHz, DMSO-d₆) δ 11.09 (s, 1H), 8.95 (s, 1H), 8.91 (s, 1H), 8.82 (d, J = 4.8 Hz, 1H), 8.13 (s, 1H), 7.99 (dd, J = 4.8, 0.8 Hz, 1H), 7.58 (d, J = 9.2 Hz, 1H), 7.49 (dd, J = 9.2, 2.0 Hz, 1H), 5.00~4.79 (m, 1H), 2.14~2.10 (m, 1H), 1.67~1.60 (m, 1H), 1.18~1.10 (m, 1H); LCMS (electrospray) m/z 321.95 (M + H)+. A 37 ¹H NMR (400 MHz, DMSO-d₆) δ 10.98 (s, 1H), 8.44 (dd, J = 1.8, 1.0 Hz, 1H), 8.05 (s, 1H), 7.42 (d, J = 9.2 Hz, 1H), 7.14~7.09 (m, 2H), 7.04 (m, 1H), 4.98~4.78 (m, 1H), 2.18 (d, J = 2.0 Hz, 3H), 2.14~2.08 (m, 4H), 1.65~1.58 (m, 1H), 1.15~1.09 (m, 1H); LCMS (electrospray) m/z 341.99 (M + H)+. A 38 ¹H NMR (400 MHz, DMSO-d₆) δ 10.99 (s, 1H), 8.35 (s, 1H), 8.03 (s, 1H), 7.45 (d, J = 9.2 Hz, 1H), 6.99~6.94 (m, 3H), 4.97~4.79 (m, 1H), 2.11 (m, 1H), 2.03 (s, 3H), 2.02 (s, 3H), 1.66~1.58 (m, 1H), 1.13~1.11 (m, 1H); LCMS (electrospray) m/z 341.84 (M + H)+. A 39 ¹H NMR (400 MHz, DMSO-d₆) δ 10.98 (s, 1H), 8.50 (s, 1H), 8.05 (s, 1H), 7.42 (d, J = 9.2 Hz, 1H), 7.31~7.27 (m, 1H), 7.17 (dd, J = 9.2, 1.6 Hz, 2H), 7.08 (dt, J = 14.4, 4.2 Hz, 1H), 4.98~4.78 (m, 1H), 2.24 (s, 3H), 2.11~2.09 (m, 1H), 1.66~1.58 (m, 1H), 1.16~1.08 (m, 1H); LCMS (electrospray) m/z 328.10 (M + H)+. A 40 ¹H NMR (400 MHz, DMSO-d₆) δ 10.97 (s, 1H), 10.86 (bs, 1H), 8.54 (s, 1H), 8.07 (s, 1H), 7.44~7.40 (m, 3H), 7.23~7.19 (m, 3H), 6.74 (dd, J = 4.4, 2.8 Hz, 1H), 6.41 (dd, J = 4.4, 2.8 Hz, 1H), 4.97~4.79 (m, 1H), 2.20 (s, 3H), 2.11 (m, 1H), 1.66~1.59 (m, 1H), 1.15~1.10 (m, 1H); LCMS (electrospray) m/z 375.10 (M + H)+. F 41 ¹H NMR (400 MHz, DMSO-d₆) δ 11.00 (s, 1H), 8.66 (t, J = 0.8 Hz, 1H), 8.11 (s, 1H), 7.47~7.44 (m, 2H), 7.26 (dd, J = 9.2, 2.0 Hz, 1H), 6.99 (d, J = 4.8 Hz, 1H), 4.99~4.78 (m, 1H), 2.26 (s, 3H), 2.11 (m, 1H), 1.66~1.59 (m, 1H), 1.15~1.10 (m, 1H); LCMS (electrospray) m/z 316.10 (M + H)+. A 42 ¹H NMR (400 MHz, DMSO-d6) δ 10.98 (s, 1H), 8.35 (s, 1H), 8.03 (s, 1H), 7.45 (d, J = 9.2 Hz, 1H), 7.19~7.10 (m, 3H), 6.97 (dd, J = 9.0, 1.8 Hz, 1H), 4.98~4.78 (m, 1H), 2.11~2.10 (m, 1H), 2.02 (s, 3H), 2.01 (s, 3H), 1.64~1.58 (m, 1H), 1.44~1.10 (m, 1H); LCMS (electrospray) m/z 325.00 (M + H)+. A 43 ¹H NMR (400 MHz, DMSO-d₆) δ 10.98 (s, 1H), 9.75 (bs, 1H), 8.47 (s, 1H), 8.05 (s, 1H), 7.40 (d, J = 9.2 Hz, 1H), 7.13 (dd, J = 9.2, 2.0 Hz, 1H), 7.06 (d, J = 12.4 Hz, 1H), 6.81 (d, J = 9.2 Hz, 1H), 4.98~4.78 (m, 1H), 2.14~2.07 (m, 4H), 1.65~1.58 (m, 1H), 1.16~1.07 (m, 1H); LCMS (electrospray) m/z 343.90 (M + H)+. G 44 ¹H NMR (400 MHz, DMSO-d₆) δ 11.00 (s, 1H), 8.54 (s, 1H), 8.07 (s, 1H), 7.45 (d, J = 9.2 Hz, 1H), 7.36 (m, 1H), 7.19~7.13 (m, 2H), 4.99~4.78 (m, 1H), 2.19 (d, J = 2.8 Hz, 3H), 2.11 (m, 1H), 1.66~1.58 (m, 1H), 1.15~1.10 (m, 1H); LCMS (electrospray) m/z 346.00 (M + H)+. G 45 ¹H NMR (400 MHz, DMSO-d₆) δ 11.02 (s, 1H), 8.57 (s, 1H), 8.07 (s, 1H), 7.49 (d, J = 9.2 Hz, 1H), 7.26 (m, 1H), 7.19 (m, 1H), 7.12 (dd, J = 9.0, 1.0 Hz, 1H), 4.99~4.78 (m, 1H), 2.10 (m, 1H), 2.06 (d, J = 2.4 Hz, 3H), 1.66~1.59 (m, 1H), 1.15~1.10 (m, 1H); LCMS (electrospray) m/z 345.96 (M + H)+. G 46 1H NMR (400 MHz, DMSO-d6) δ 11.01 (s, 1H), 8.56 (s, 1H), 8.07 (s, 1H), 7.49~7.44 (m, 2H), 7.20~7.15 (m, 2H), 4.98~4.79 (m, 1H), 2.19 (d, J = 2.8 Hz, 3H), 2.11 (m, 1H), 1.65~1.59 (m, 1H), 1.15~1.10 (m, 1H); LCMS (electrospray) m/z 362.00 (M + H)+. G 47 ¹H NMR (400 MHz, DMSO-d₆) δ 11.03 (s, 1H), 8.61 (s, 1H), 8.11 (d, J = 5.2 Hz, 1H), 8.06 (s, 1H), 7.49 (d, J = 9.2 Hz, 1H), 7.34 (d, J = 5.2 Hz, 1H), 7.16 (d, J = 9.2 Hz, 1H), 4.99~4.78 (m, 1H), 2.24 (s, 3H), 2.17~2.09 (m, 1H), 1.66~1.59 (m, 1H), 1.17~1.11 (m, 1H); LCMS (electrospray) m/z 329.01 (M + H)+. A 48 ¹H NMR (400 MHz, DMSO-d₆) 11.00 (s, 1H), 8.46 (s, 1H), 8.06 (s, 1H), 7.47 (d, J = 9.2 Hz, 1H), 7.40~7.38 (m, 1H), 7.31~7.30 (m, 2H), 7.02 (dd, J = 9.2, 1.6 Hz, 1H), 4.99~4.78 (m, 1H), 2.13~2.09 (m, 4H), 1.71~1.58 (m, 1H), 1.15~1.10 (m, 1H); LCMS (electrospray) m/z 343.94 (M + H)+. A 49 ¹H NMR (400 MHz, DMSO-d₆) δ 11.03 (s, 1H), 8.55 (s, 1H), 7.88 (s, 1H), 7.80 (bs, 2H), 7.47 (d, J = 9.2 Hz, 1H), 7.21 (dd, J = 9.2, 2.0 Hz, 1H), 6.84 (s, 1H), 4.99~4.79 (m, 1H), 2.25 (s, 3H), 2.14~2.07 (m, 1H), 1.65~1.58 (m, 1H), 1.16~1.05 (m, 1H); LCMS (electrospray) m/z 325.70 (M + H)+. A 50 ¹H NMR (400 MHz, DMSO-d₆) δ 10.98 (s, 1H), 8.48 (dd, J = 1.6, 0.8 Hz, 1H), 8.07 (s, 1H), 7.41 (d, J = 9.2 Hz, 1H), 7.12 (dd, J = 9.2, 2.0 Hz, 1H), 6.35~6.31 (m, 2H), 5.26 (bs, 2H), 4.97~4.78 (m, 1H), 2.10 (m, 1H), 1.93 (d, J = 2.0 Hz, 3H), 1.65~1.58 (m, 1H), 1.15~1.09 (m, 1H); LCMS (electrospray) m/z 343.10 (M + H)+. G 51 ¹H NMR (400 MHz, DMSO-d₆) δ 10.97 (s, 1H), 10.32 (s, 1H), 8.50 (s, 1H), 8.03 (s, 1H), 7.43 (d, J = 9.2 Hz, 1H), 7.14~7.10 (m, 2H), 6.73 (d, J = 8.0 Hz, 1H), 4.98~4.78 (m, 1H), 3.30 (s, 2H), 2.11~2.09 (m, 4H), 1.66~1.59 (m, 1H), 1.16~1.11 (m, 1H); LCMS (electrospray) m/z 365.02 (M + H)+. G 52 ¹H NMR (400 MHz, DMSO-d₆) δ 11.00 (s, 1H), 8.46 (s, 1H), 8.06 (s, 1H), 7.47 (d, J = 9.2 Hz, 1H), 7.40~7.38 (m, 1H), 7.31~7.30 (m, 2H), 7.02 (dd, J = 9.2, 1.6 Hz, 1H), 4.99~4.78 (m, 1H), 2.13~2.09 (m, 4H), 1.71~1.58 (m, 1H), 1.15~1.10 (m, 1H); LCMS (electrospray) m/z 343.94 (M + H)+. A 53 ¹H NMR (400 MHz, DMSO-d₆) δ 11.35 (s, 1H), 10.99 (s, 1H), 8.91 (d, J = 0.8 Hz, 1H), 8.48 (d, J = 2.0 Hz, 1H), 8.16 (d, J = 2.4 Hz, 1H), 8.07 (s, 1H), 7.61 (dd, J = 9.2, 1.6 Hz, 1H), 7.48 (d, J = 9.2 Hz, 1H), 7.25 (s, 1H), 4.99~4.49 (m, 1H), 2.28 (s, 3H), 2.11 (m, 1H), 1.66~1.60 (m, 1H), 1.16~1.10 (m, 1H); LCMS (electrospray) m/z 350.17 (M + H)+. G 54 ¹H NMR (400 MHz, DMSO-d₆) δ 11.00 (s, 1H), 8.86 (s, 1H), 7.64 (d, J = 8.4 Hz, 1H), 7.47 (s, 2H), 7.39 (dd, J = 8.4, 1.2 Hz, 1H), 7.30 (s, 1H), 4.99~4.78 (m, 1H), 2.14~2.07 (m, 1H), 1.67~1.59 (m, 1H), 1.17~1.08 (m, 1H); LCMS (electrospray) m/z 369.00 (M + H)+. G 55 ¹H NMR (400 MHz, DMSO-d₆) δ 10.96 (s, 1H), 8.73 (s, 1H), 8.21 (d, J = 2.4 Hz, 1H), 8.01 (s, 1H), 7.66 (dd, J = 8.8, 2.8 Hz, 1H), 7.42 (s, 2H), 6.51 (s, 1H), 6.06 (s, 2H), 4.98~4.78 (m, 1H), 2.12~2.04 (m, 1H), 1.66~1.58 (m, 1H), 1.16~1.58 (m, 1H); LCMS (electrospray) m/z 311.67 (M + H)+. G 56 ¹H NMR (400 MHz, DMSO-d₆) δ 11.00 (s, 1H), 8.62 (t, J = 0.8 Hz, 1H), 8.50 (d, J = 2.4 Hz, 1H), 8.08 (s, 1H), 7.77~7.74 (m, 2H), 7.69 (d, J = 2.0 Hz, 1H), 7.47~7.40 (m, 2H), 7.27 (dd, J = 9.2, 2.0 Hz, 1H), 6.50 (t, J = 2.0 Hz, 1H), 4.99-4.78 (m, 1H), 2.27 (s, 3H), 2.13-2.09 (m, 4H), 1.66-1.58 (m, 1H), 1.15-1.09 (m, 1H); LCMS (electrospray) m/z 376.13 (M + H)+. D 57 ¹H NMR (400 MHz, DMSO-d₆) δ 11.34 (br s, 1H), 8.74 (s, 1H), 8.14 (s, 1H), 7.66- 7.55 (m, 2H), 7.46 (dt, J = 5.9, 8.0 Hz, 1H), 7.30 (d, J = 8.6 Hz, 1H), 7.28-7.22 (m, 1H), 5.09-4.84 (m, 1H), 4.41 (d, J = 1.4 Hz, 2H), 2.20-2.11 (m, 1H), 1.76-1.61 (m, 1H), 1.29-1.13 (m, 1H); LCMS (electrospray) m/z 344.40 (M + H)+. G 58 1H NMR (400 MHz, DMSO-d6); δ 10.42 (s, 1H), 8.20 (s, 1H), 7.65 (d, J = 9.6 Hz, 1H), 7.40 (dd, J = 9.2, 1.6 Hz, 1H), 7.39~7.35 (m, 1H), 7.25~7.22 (m, 1H), 5.03~4.86 (m, 1H), 2.17 (d, J = 2.4 Hz, 3H), 2.10~2.05 (m, 1H), 1.66~1.58 (m, 1H), 1.15~1.08 (m, 1H); LCMS (electrospray) m/z 408.00 (M + H)+. B (NBS reagent) 59 ¹H NMR (400 MHz, DMSO-d₆) δ 11.31 (s, 1H), 8.81 (s, 1H), 8.17 (s, 1H), 7.62- 7.57 (m, 2H), 7.35-7.22 (m, 3H), 5.11- 4.82 (m, 1H), 3.75 (s, 3H), 2.19-2.09 (m, 1H), 1.72-1.65 (m, 1H), 1.23-1.13 (m, 1H); LCMS (electrospray) m/z 344.1 (M + H)+. G 60 ¹H NMR (400 MHz, DMSO-d₆) δ 11.14 (s, 1H), 8.92 (s, 1H), 8.17 (s, 1H), 7.90- 7.88 (m, 1H), 7.65-7.54 (m, 3H), 7.46 (s, 1H), 5.12-4.79 (m, 1H), 2.23-2.12 (m, 1H), 1.76-1.56 (m, 1H), 1.32-1.08 (m, 1H); LCMS (electrospray) m/z 339.1 (M + H)+. G 61 ¹H NMR (400 MHz, DMSO-d₆) δ 11.14 (s, 1H), 8.74 (s, 1H), 8.14 (s, 1H), 7.58- 7.49 (m, 3H), 7.40-7.39 (m, 2H), 5.11-4.78 (m, 1H), 2.17-2.12 (m, 1H), 1.70- 1.63 (m, 1H), 1.21-1.15 (m, 1H); LCMS (electrospray) m/z 348.0 (M + H)+. G 62 ¹H NMR (400 MHz, DMSO-d₆) δ 11.16 (s, 1H), 8.89 (s, 1H), 8.16 (s, 1H), 7.60- 7.57 (m, 1H), 7.52-7.44 (m, 3H), 7.42- 7.36 (m, 1H), 5.09-4.85 (m, 1H), 2.17- 2.13 (m, 1H), 1.78-1.63 (m, 1H), 1.21- 1.16 (m, 1H); LCMS (electrospray) m/z 332.1 (M + H)+. G 63 ¹H NMR (400 MHz, DMSO-d₆) δ 11.20 (s, 1H), 10.75 (s, 1H), 8.45 (s, 1H), 8.11 (s, 1H), 7.55 (d, J = 8.8 Hz, 1H), 7.32- 7.24 (m, 2H), 7.05-6.99 (m, 2H), 5.05- 4.85 (m, 1H), 2.19-2.16 (m, 1H), 2.14 (d, J = 2.9 Hz, 3H), 1.73-1.66 (m, 1H), 1.63 (dd, J = 0.7, 4.4 Hz, 3H), 1.25-1.12 (m, 1H); LCMS (electrospray) m/z 363.2 (M + H)+. G 64 ¹H NMR (400 MHz, DMSO-d₆) δ 11.25 (s, 1H), 8.68 (s, 1H), 8.14 (s, 1H), 7.60 (d, J = 9.2 Hz, 1H), 7.52 (dt, J = 6.0, 7.9 Hz, 1H), 7.44 (dd, J = 1.6, 9.2 Hz, 1H), 7.33 (d, J = 8.7 Hz, 1H), 7.30-7.25 (m, 1H), 5.11- 4.76 (m, 1H), 4.30 (br d, J = 1.3 Hz, 2H), 3.25 (s, 3H), 2.23-2.08 (m, 1H), 1.76- 1.59 (m, 1H), 1.20 (tdd, J = 6.3, 9.1, 12.4 Hz, 1H); LCMS (electrospray) m/z 358.5 (M + H)+. H 65 ¹H NMR (400 MHz, DMSO-d₆) δ 11.20 (s, 1H), 8.61 (s, 1H), 8.08 (s, 1H), 7.61 (dd, J = 0.9, 1.6 Hz, 1H), 7.60-7.54 (m, 1H), 7.45-7.41 (m, 1H), 7.40-7.36 (m, 2H), 6.93 (dd, J = 1.3, 9.3 Hz, 1H), 6.56-6.48 (m, 2H), 5.05-4.83 (m, 1H), 2.19-2.09 (m, 1H), 1.75-1.59 (m, 1H), 1.19 (tdd, J = 6.3, 9.1, 12.4 Hz, 1H); LCMS (electrospray) m/z 380.5 (M + H)+. I 66 ¹H NMR (400 MHz, DMSO-d₆) δ 11.16 (s, 1H), 8.65 (s, 1H), 8.13 (s, 1H), 7.56- 7.50 (m, 1H), 7.50-7.45 (m, 1H), 7.41- 7.33 (m, 2H), 7.29 (dd, J = 1.0, 7.6 Hz, 1H), 5.05-4.82 (m, 1H), 2.28 (s, 3H), 2.21-2.09 (m, 1H), 1.77-1.59 (m, 1H), 1.26-1.11 (m, 1H); LCMS (electrospray) m/z 360.1 (M + H)+. G 67 ¹H NMR (400 MHz, DMSO-d₆) δ 11.21 (s, 1H), 8.69 (s, 1H), 8.13 (m, 1H), 8.12 (s, 1H), 7.62-7.55 (m, 1H), 7.43-7.35 (m, 1H), 7.25-7.20 (m, 1H), 5.06-5.03 (m, 1H), 4.89-4.86 (m, 1H), 2.38 (s, 3H), 2.22-2.11 (m, 1H), 1.76-1.59 (m, 1H), 1.26-1.13 (m, 1H); LCMS (electrospray) m/z 329.1 (M + H)+. G 68 ¹H NMR (400 MHz, DMSO-d₆) δ 11.81 (s, 1H), 8.66 (br s, 1H), 8.15 (s, 1H), 7.67- 7.58 (m, 1H), 7.53 (d, J = 9.2 Hz, 1H), 7.41 (t, J = 9.2 Hz, 1H), 7.36 (dd, J = 0.7, 7.7 Hz, 1H), 7.25-7.18 (m, 1H), 5.03 (td, J = 3.1, 6.2 Hz, 1H), 4.88-4.85 (m, 1H), 2.40 (s, 3H), 2.20-2.09 (m, 1H), 1.74- 1.60 (m, 1H), 1.25-1.12 (m, 1H); LCMS (electrospray) m/z 356.1 (M + H)+. G 69 ¹H NMR (400 MHz, DMSO-d₆) δ 11.00 (s, 1H), 8.55 (s, 1H), 8.08 (s, 1H), 7.96 (s, 1H), 7.44 (d, J = 9.2 Hz, 1H), 7.20 (dd, J = 9.2, 1.6 Hz, 1H), 6.60 (s, 1H), 5.01- 4.82 (m, 1H), 3.05 (s, 6H), 2.23 (s, 3H), 2.18-2.09 (m, 1H), 1.73-1.58 (m, 1H), 1.22-1.08 (m, 1H); LCMS (electrospray) m/z 354.2 (M + H)+. G 70 ¹H NMR (400 MHz, DMSO-d₆) δ 11.22 (br s, 1H), 8.66 (s, 1H), 8.09 (s, 1H), 7.59 (d, J = 9.2 Hz, 1H), 7.40 (br d, J = 9.3 Hz, 1H), 7.38-7.30 (m, 1H), 7.28-7.21 (m, 1H), 7.17 (d, J = 7.5 Hz, 1H), 2.18 (d, J = 2.3 Hz, 3H), 1.94 (quin, J = 6.2 Hz, 1H), 0.85 (d, J = 6.1 Hz, 4H); LCMS (electrospray) m/z 310.1 (M + H)+. J 71 ¹H NMR (400 MHz, DMSO-d₆) δ 11.34 (s, 1H), 8.65 (s, 1H), 8.09 (s, 1H), 7.58 (d, J = 9.2 Hz, 1H), 7.40-7.35 (m, 1H), 7.35- 7.30 (m, 1H), 7.28-7.20 (m, 1H), 7.17 (d, J = 7.5 Hz, 1H), 5.03-4.80 (m, 1H), 2.53- 2.42 (m, 1H), 2.18 (d, J = 2.2 Hz, 3H), 1.62- 1.49 (m, 1H), 1.27 (qd, J = 6.5, 13.1 Hz, 1H); LCMS (electrospray) m/z 328.1 (M + H)+. J 72 ¹H NMR (400 MHz, DMSO-d₆) δ 11.31 (s, 1H), 8.64 (d, J = 0.6 Hz, 1H), 8.08 (s, 1H), 7.56 (d, J = 9.1 Hz, 1H), 7.38-7.30 (m, 2H), 7.27-7.21 (m, 1H), 7.17 (d, J = 7.5 Hz, 1H), 5.03-4.81 (m, 1H), 2.54- 2.42 (m, 1H, 2.18 (d, J = 2.3 Hz, 3H), 1.62- 1.49 (m, 1H), 1.26 (qd, J = 6.5, 13.1 Hz, 1H); LCMS (electrospray) m/z 328.5 (M + H)+. J 73 ¹H NMR (400 MHz, DMSO-d₆) δ 11.27 (s, 1H), 8.67 (s, 1H), 8.13 (s, 1H), 7.59 (d, J = 9.2 Hz, 1H), 7.40 (dd, J = 1.6, 9.2 Hz, 1H), 7.38-7.31 (m, 1H), 7.28-7.21 (m, 1H), 7.18 (d, J = 7.5 Hz, 1H), 5.07-4.85 (m, 1H), 2.18 (d, J = 2.2 Hz, 3H), 2.16- 2.12 (m, 1H), 1.74-1.61 (m, 1H), 1.20 (tdd, J = 6.2, 9.1, 12.5 Hz, 1H); LCMS (electrospray) m/z 328.1 (M + H)+. J 74 ¹H NMR (400 MHz, DMSO-d₆) δ 11.15 (s, 1H), 8.61 (s, 1H), 8.14 (s, 1H), 8.13- 8.10 (m, 2H), 7.62-7.56 (m, 2H), 7.46- 7.43 (m, 1H), 7.31-7.29 (m, 2H), 5.05- 5.01 (m, 0.5H), 4.88-4.86 (m, 0.5H), 4.06-4.04 (m, 2H), 2.18-2.14 (m, 1H), 1.69-1.63 (m, 1H), 1.21-1.16 (m, 1H); LCMS (electrospray) m/z 343.2 (M + H)+. G 75 ¹H NMR (400 MHz, CD3OD) δ = 8.67 (s, 1H), 7.81-7.71 (m, 2H), 7.49-7.47 (m, 1H), 7.31-7.22 (m, 2H), 5.04-5.01 (m, 0.5H), 4.87-4.85 (m, 0.5H), 4.38 (s, 2H), 2.16-2.12 (m, 1H), 1.90-1.84 (m, 1H), 1.31-1.28 (m, 1H); LCMS (electrospray) m/z 385.1 (M + H)+. K 76 ¹H NMR (400 MHz, DMSO-d₆) δ 10.80 (s, 1H), 8.69 (s, 1H), 8.15 (s, 1H), 7.59 (d, J = 9.1 Hz, 1H), 7.41 (dd, J = 1.5, 9.3 Hz, 1H), 7.38-7.31 (m, 1H), 7.29-7.21 (m, 1H), 7.18 (d, J = 7.5 Hz, 1H), 3.35 (quin, J = 8.3 Hz, 1H), 2.30-2.20 (m, 2H), 2.18 (d, J = 2.3 Hz, 3H), 2.17-2.07 (m, 2H), 2.02-1.90 (m, 1H), 1.88-1.77 (m, 1H); LCMS (electrospray) m/z 324.5 (M + H)+. J 77 ¹H NMR (400 MHz, DMSO-d₆) δ 11.35 (s, 1H), 8.64 (s, 1H), 8.14 (s, 1H), 7.56 (d, J = 9.1 Hz, 1H), 7.38-7.29 (m, 2H), 7.28- 7.21 (m, 1H), 7.18 (d, J = 7.5 Hz, 1H), 2.93 (ddd, J = 8.3, 10.7, 13.5 Hz, 1H), 2.18 (d, J = 2.3 Hz, 3H), 2.11-1.96 (m, 2H); LCMS (electrospray) m/z 364.4 (M + H)+. J 78 ¹H NMR (400 MHz, DMSO-d₆) δ 11.01 (s, 2H), 8.68 (d, J = 0.9 Hz, 2H), 8.17 (d, J = 4.1 Hz, 2H), 7.58 (dd, J = 2.0, 9.1 Hz, 2H), 7.42-7.37 (m, 2H), 7.36-7.31 (m, 2H), 7.28-7.21 (m, 2H), 7.18 (d, J = 7.5 Hz, 2H), 5.37-5.15 (m, 1H), 5.14-4.92 (m, 1H), 3.41-3.29 (m, 1H), 2.88-2.76 (m, 1H), 2.61-2.52 (m, 4H), 2.49-2.26 (m, 4H), 2.18 (d, J = 2.1 Hz, 6H); LCMS (electrospray) m/z 342.5 (M + H)+. J 79 ¹H NMR (400 MHz, DMSO-d₆) δ 11.10 (s, 1H), 8.67 (s, 1H), 8.18 (s, 1H), 7.56 (d, J = 9.3 Hz, 1H), 7.39-7.30 (m, 2H), 7.27- 7.21 (m, 1H), 7.18 (d, J = 7.5 Hz, 1H), 3.23 (dquin, J = 3.3, 8.4 Hz, 1H), 2.88-2.75 (m, 4H), 2.18 (d, J = 2.3 Hz, 3H); LCMS (electrospray) m/z 360.5 (M + H)+. J 80 ¹H NMR (400 MHz, DMOS-d₆) δ 11.22 (s, 1H), 8.75 (br s, 2H), 8.64 (s, 1H), 8.14 (s, 1H), 7.63-7.60 (m, 2H), 7.50-7.40 (m, 1H), 7.34-7.30 (m, 1H), 5.05-5.03 (m, 0.5H), 4.88-4.84 (m, 0.5H), 4.19 (s, 2H), 2.47 (s, 3H), 2.18-2.14 (m, 1H), 1.70-1.63 (m, 1H), 1.22-1.16 (m, 1H); LCMS (electrospray) m/z 357.2 (M + H)+. G 81 ¹H NMR (400 MHz, DMSO-d₆) δ 11.15 (s, 1H), 8.64 (s, 1H), 8.60 (br s, 2H), 8.15 (s, 1H), 7.62-7.59 (m, 2H), 7.50-7.40 (m, 2H), 7.33-7.30 (m, 2H), 5.05-5.03 (m, 0.5H), 4.87-4.86 (m, 0.5H), 4.18 (m, 2H), 3.31-3.25 (m, 1H), 2.18-2.15 (m, 1H), 1.71-1.60 (m, 1H), 1.21-1.16 (m, 1H), 1.12 (d, J = 6.8 Hz, 6 H); LCMS (electrospray) m/z 385.2 (M + H)+. G 82 ¹H NMR (400 MHz, DMSO-d₆) δ 11.23- 11.19 (br s, 1H), 8.72 (s, 1H), 8.10 (s, 1H), 7.56-7.50 (m, 3H), 7.32-7.28 (m, 2H), 5.04-4.84 (m, 1H), 4.35 (s, 2H), 3.47-3.44 (m, 4H), 3.25 (s, 3H), 2.16- 2.11 (m, 1H), 1.70-1.64 (m, 1H), 1.21- 1.16 (m, 1H); LCMS (electrospray) m/z 402.0 (M + H)+. L 83 ¹H NMR (400 MHz, DMSO-d₆) δ 11.21 (s, 1H), 8.78 (s, 1H), 8.14 (s, 1H), 7.58- 7.47 (m, 3H), 7.33-7.29 (m, 2H), 5.05- 4.85 (m, 1H), 4.36 (s, 2H), 3.55-3.52 (m, 2H), 3.47-3.45 (m, 2H), 2.16-2.13 (m, 1H), 1.71-1.69 (m, 1H), 1.65-1.64 (m, 1H); LCMS (electrospray) m/z 387.9 (M + H)+. M 84 ¹H NMR (400 MHz, CD3OD) δ 8.65 (s, 1H), 7.74-7.70 (m, 2H), 7.60-7.55 (m, 1H), 7.48-7.38 (m, 2H), 5.05-5.00 (m, 0.5H), 4.86-4.84 (m, 0.5H), 4.53 (s, 2H), 2.74 (s, 6H), 2.16 (br s, 1H), 1.87-1.81 (m, 1H), 1.31-1.25 (m, 1H); LCMS (electrospray) m/z 371.2 (M + H)+. G 85 ¹H NMR (400 MHz, DMSO-d₆) δ = 11.86 (s, 1H), 11.40 (s, 1H), 9.07 (s, 1H), 8.58 (d, J = 2.1 Hz, 1H), 8.30 (d, J = 1.9 Hz, 1H), 8.14 (s, 1H), 7.91-7.83 (m, 1H), 7.75-7.65 (m, 1H), 7.60-7.55 (m, 1H), 6.60-6.53 (m, 1H), 5.10-4.87 (m, 1H), 2.23-2.12 (m, 1H), 1.78-1.63 (m, 1H), 1.30-1.16 (m, 1H); LCMS (electrospray) m/z 336.1 (M + H)+. G 86 ¹H NMR (400 MHz, DMSO-d₆) δ 11.94 (s, 1H), 11.48 (s, 1H), 8.76 (s, 1H), 8.20 (s, 1H), 8.18-8.14 (m, 1H), 7.77-7.65 (m, 1H), 7.60 (dd, J = 1.6, 9.2 Hz, 1H), 7.58-7.54 (m, 1H), 6.72-6.59 (m, 1H), 5.11-4.80 (m, 1H), 2.52 (s, 3H), 2.25- 2.08 (m, 1H), 1.80-1.58 (m, 1H), 1.34- 1.11 (m, 1H); LCMS (electrospray) m/z 350.1 (M + H)+. G 87 ¹H NMR (400 MHz, DMSO-d₆) δ 12.18 (s, 1H), 11.24 (s, 1H), 8.78 (s, 1H), 8.29 (s, 1H), 8.15 (s, 1H), 7.72-7.66 (m, 1H), 7.64-7.59 (m, 1H), 7.54-7.49 (m, 1H), 6.59 (dd, J = 1.9, 3.4 Hz, 1H), 5.10-4.84 (m, 1H), 2.21-2.13 (m, 1H), 1.78-1.59 (m, 1H), 1.31-1.09 (m, 1H); LCMS (electrospray) m/z 370.1 (M + H)+. G 88 ¹H NMR (400 MHz, DMSO-d₆) δ 11.26 (s, 1H), 8.64 (s, 1H), 8.12 (s, 1H), 7.58 (d, J = 9.2 Hz, 1H), 7.41 (br d, J = 9.0 Hz, 1H), 7.36-7.27 (m, 4H), 5.08-4.84 (m, 1H), 2.28 (s, 3H), 2.19-2.10 (m, 1H), 1.74-1.62 (m, 1H), 1.25-1.16 (m, 1H); LCMS (electrospray) m/z 310.1 (M + H)+. G 89 ¹H NMR (400 MHz, DMSO-d₆) δ = 11.22 (s, 1H), 9.94-9.83 (m, 1H), 8.79 (s, 1H), 8.13 (s, 1H), 7.57 (s, 2H), 7.24 (br d, J = 8.9 Hz, 1H), 7.19 (br d, J = 7.9 Hz, 1H), 6.93 (dt, J = 5.3, 7.9 Hz, 1H), 5.08-4.83 (m, 1H), 2.21-2.09 (m, 1H), 1.76-1.60 (m, 1H), 1.27-1.12 (m, 1H); LCMS (electrospray) m/z 329.8 (M + H)+. G 90 ¹H NMR (400 MHz, DMSO-d₆) δ 11.31 (s, 1H), 8.69 (s, 1H), 8.12 (s, 1H), 7.62 (d, J = 9.0 Hz, 1H), 7.45 (br d, J = 9.2 Hz, 1H), 7.09 (ddd, J = 1.4, 8.1, 11.4 Hz, 1H), 6.93 (d, J = 7.5 Hz, 1H), 6.66 (dt, J = 5.3, 7.9 Hz, 1H), 5.11-4.81 (m, 1H), 2.23- 2.05 (m, 1H), 1.79-1.59 (m, 1H), 1.34- 1.11 (m, 1H); LCMS (electrospray) m/z 328.8 (M + H)+. G 91 ¹H NMR (400 MHz, DMSO-d₆) δ 1.27 (br s, 1H), 11.08 (br s, 1H), 8.64 (s, 1H), 8.13 (s, 1H), 7.58 (d, J = 9.1 Hz, 1H), 7.45 (br s, 2H), 7.36 (t, J = 2.7 Hz, 1H), 7.29 (s, 1H), 6.39 (t, J = 2.0 Hz, 1H), 5.19-4.74 (m, 1H), 5.35-4.58 (m, 1H), 2.30 (s, 3H), 2.20-2.12 (m, 1H), 1.75-1.63 (m, 1H), 1.26-1.15 (m, 1H); LCMS (electrospray) m/z 348.9 (M + H)+. G 92 ¹H NMR (400 MHz, DMSO-d₆) δ 11.28- 11.20 (m, 1H), 11.05 (br s, 1H), 8.60 (s, 1H), 8.11 (s, 1H), 7.55 (br d, J = 9.4 Hz, 1H), 7.44 (s, 2H), 7.35-7.30 (m, 2H), 6.44-6.39 (m, 1H), 5.09-4.79 (m, 1H), 2.32 (s, 3H), 2.19-2.10 (m, 1H), 1.77- 1.56 (m, 1H), 1.29-1.07 (m, 1H); LCMS (electrospray) m/z 348.8 (M + H)+. G 93 ¹H NMR (400 MHz, DMSO-d₆) δ 11.30 (br s, 1H), 8.70 (s, 1H), 8.13 (s, 1H), 7.62- 7.49 (m, 2H), 7.27-7.16 (m, 3H), 5.07- 4.86 (m, 2H), 2.63 (d, J = 2.0 Hz, 6H), 2.20-2.11 (m, 1H), 1.75-1.62 (m, 1H), 1.26-1.14 (m, 1H); LCMS (electrospray) m/z 357.5 (M + H)+. G 94 ¹H NMR (400 MHz, DMSO-d₆) δ 11.14 (s, 1H), 9.45 (s, 1H), 8.64 (s, 1H), 8.14 (s, 1H), 7.80 (s, 1H), 7.74 (s, 1H), 7.55 (d, J = 9.3 Hz, 1H), 7.33 (dd, J = 1.6, 9.3 Hz, 1H), 5.14-4.79 (m, 1H), 2.41 (s, 3H), 2.16 (td, J = 7.1, 14.0 Hz, 1H), 1.74-1.60 (m, 1H), 1.27-1.08 (m, 1H); LCMS (electrospray) m/z 349.9 (M + H)+. G 95 ¹H NMR (400 MHz, DMSO-d₆) δ 11.13 (br s, 1H), 8.60 (s, 1H), 8.13 (s, 1H), 7.54 (d, J = 9.0 Hz, 1H), 7.39-7.28 (m, 1H), 7.28-7.20 (m, 2H), 7.15-7.11 (m, 1H), 5.08-4.79 (m, 1H), 2.61-2.53 (m, 2H), 2.23-2.09 (m, 1H), 1.75-1.57 (m, 1H), 1.25-1.12 (m, 1H), 1.05 (t, J = 7.6 Hz, 3H); LCMS (electrospray) m/z 342.1 (M + H)+. G 96 ¹H NMR (400 MHz, DMSO-d₆) δ 11.20 (s, 1H), 8.62 (s, 1H), 8.12 (s, 1H), 7.89 (d, J = 7.8 Hz, 1H), 7.81-7.74 (m, 1H), 7.72- 7.65 (m, 1H), 7.58-7.50 (m, 2H), 7.25 (d, J = 9.2 Hz, 1H), 5.06-4.83 (m, 1H), 2.20-2.10 (m, 1H), 1.75-1.60 (m, 1H), 1.28-1.10 (m, 1H); LCMS (electrospray) m/z 364.0 (M + H)+. G 97 ¹H NMR (400 MHz, DMSO-d₆) δ 11.16 (br s, 1H), 8.69 (s, 1H), 8.11 (s, 1H), 7.57- 7.42 (m, 2H), 7.39-7.32 (m, 1H), 7.24- 7.16 (m, 2H), 5.11-4.76 (m, 1H), 2.23- 2.07 (m, 1H), 1.99-1.85 (m, 1H), 1.77- 1.56 (m, 1H), 1.31-1.05 (m, 1H), 0.80- 0.69 (m, 2H), 0.44-0.30 (m, 2H); LCMS (electrospray) m/z 353.9 (M + H)+. G 98 ¹H NMR (400 MHz, DMSO-d₆) δ 11.25 (br s, 1H), 8.63 (s, 1H), 8.11 (s, 1H), 7.57 (br d, J = 9.0 Hz, 1H), 7.36 (br d, J = 9.0 Hz, 1H), 7.12 (ddd, J = 1.3, 8.1, 13.0 Hz, 1H), 6.95 (d, J = 7.7 Hz, 1H), 6.77 (dt, J = 5.0 7.8 Hz, 1H), 5.06-4.85 (m, 1H), 2.66 (d, J = 3.6 Hz, 3H), 2.19-2.09 (m, 1H), 1.74- 1.60 (m, 1H), 1.20 (ddd, J = 2.8, 6.2, 12.2 Hz, 1H); LCMS (electrospray) m/z 343.3.00 (M + H)+. G 99 ¹H NMR (400 MHz, DMSO-d₆) δ 11.05 (s, 1H), 8.76 (s, 1H), 8.60 (dd, J = 0.9, 1.6 Hz, 1H), 8.11 (s, 1H), 7.77 (s, 1H), 7.73 (s, 1H), 7.49 (d, J = 9.2 Hz, 1H), 7.27 (dd, J = 1.8, 9.2 Hz, 1H), 5.04-4.82 (m, 1H), 2.36 (s, 3H), 2.19-2.10 (m, 1H), 1.71- 1.59 (m, 1H), 1.16 (tdd, J = 6.2, 9.1, 12.3 Hz, 1H); LCMS (electrospray) m/z 351.5 (M + H)+. G 100 ¹H NMR (400 MHz, DMSO-d₆) δ 11.13 (s, 1H), 9.42 (s, 1H), 8.68 (s, 1H), 8.13 (s, 1H), 7.79 (d, J = 8.4 Hz, 1H), 7.68-7.51 (m, 2H), 7.27 (dd, J = 1.6, 9.0 Hz, 1H), 5.11-4.80 (m, 1H), 2.39-2.37 (s, 3H), 2.19-2.14 (m, 1H), 1.74-1.60 (m, 1H), 1.23-1.12 (m, 1H); LCMS (electrospray) m/z 350.2 (M + H)+. G 101 ¹H NMR (400 MHz, DMSO-d₆) δ 11.27 (s, 1H), 9.30 (s, 1H), 8.70 (s, 1H), 8.08- 8.05 (m, 2H), 7.67-7.61 (m, 1H), 7.48- 7.44 (m, 1H), 7.43-7.39 (m, 1H), 5.06- 4.86 (m, 1H), 2.37 (s, 3H), 2.18-2.15 (m, 1H), 1.75-1.60 (m, 1H), 1.23-1.17 (m, 1H); LCMS (electrospray) m/z 367.2 (M + H)+. G 102 ¹H NMR (400 MHz, DMSO-d₆) δ 11.07 (s, 1H), 8.70 (s, 1H), 8.65 (s, 1H), 8.13 (s, 1H), 7.71 (d, J = 8.3 Hz, 1H), 7.53 (d, J = 9.2 Hz, 1H), 7.43 (d, J = 8.4 Hz, 1H), 7.29 (dd, J = 1.6, 9.2 Hz, 1H), 5.05-4.81 (m, 1H), 2.38 (s, 3H), 2.20-2.10 (m, 1H), 1.73-1.59 (m, 1H), 1.17 (tdd, J = 6.2, 9.1, 12.2 Hz, 1H); LCMS (electrospray) m/z 351.2 (M + H)+. N 103 ¹H NMR (400 MHz, DMSO-d₆) δ 11.07 (s, 1H), 9.40 (s, 1H), 8.64 (dd, J = 0.9, 1.6 Hz, 1H), 8.12 (s, 1H), 8.11 (s, 1H), 8.07 (s, 1H), 7.51 (d, J = 9.2 Hz, 1H), 7.30 (dd, J = 1.8, 9.2 Hz, 1H), 5.05-4.82 (m, 1H), 2.42 (s, 3H), 2.21-2.10 (m, 1H), 1.74- 1.59 (m, 1H), 1.24-1.12 (m, 1H); LCMS (electrospray) m/z 367.5 (M + H)+ G 104 ¹H NMR (400 MHz, DMSO-d₆) δ 11.07 (s, 1H), 9.45 (s, 1H), 8.67-8.61 (m, 1H), 8.13 (s, 1H), 8.03 (d, J = 8.3 Hz, 1H), 7.52 (dd, J = 7.2, 8.7 Hz, 2H), 7.30 (dd, J = 1.8, 9.2 Hz, 1H), 5.05-4.80 (m, 1H), 2.54 (s, 3H), 2.20-2.10 (m, 1H), 1.74-1.59 (m, 1H), 1.24-1.11 (m, 1H); LCMS (electrospray) m/z 367.5 (M + H)+. G 105 ¹H NMR (400 MHz, DMSO-d₆) δ 11.12 (br s, 1H), 8.55 (s, 1H), 8.12 (s, 1H), 7.51 (br d, J = 8.9 Hz, 1H), 7.35-7.27 (m, 1H), 7.26-7.20 (m, 1H), 7.20-7.16 (m, 1H), 7.10 (d, J = 7.3 Hz, 1H), 5.12-4.78 (m, 1H), 3.07-2.82 (m, 1H), 2.22-2.09 (m, 1H), 1.74-1.58 (m, 1H), 1.25 (br d, J = 6.8 Hz, 6H), 1.20-1.13 (m, 1H); LCMS (electrospray) m/z 355.9 (M + H)+. G

Evaluation of Compounds

c-abl Kinase Assay

ADP-Glo assay kit was purchased from Promega. Magnesium chloride (MgCl₂), bovine serum albumin (BSA), ethylene glycol-bis(p-aminoethyl ether)-N,N,N′-tetraacetic acid (EGTA), triton X-100, 1,4-dithiothreitol (DTT) and dimethyl sulfoxide (DMSO) were purchased from Sigma-Aldrich. HEPES buffer was purchased from Gibco. ABL1 kinase and Abltide were purchased from Signalchem.

c-Abl kinase activity was measured by Promega's ADP-Glo™ Assay. In this assay, His-tagged recombinant human ABL1 (0.25 ng/μl) is incubated with 5 μL of compounds (0.5% DMSO), 5 μL of Abltide (0.01 μg/μl) and 5 μL of ATP (25 pM) in buffer (50 mM HEPES,7.5; 10 mM MgCl2; 1 mM EGTA; 0.05% BSA; 0.01% Triton X-100; 2 mM DTT.). The assay was started by incubating the reaction mixture in a 96-well plate at 30° C. for 30-min. After the incubation, 25 μL ADP-Glo reagent was added and the reaction was incubated at room temperature for 40-min to stop the reaction and degrade residual ATP. The ADP product was then converted to ATP by adding 50 μL per well of detection reagent. Luminescence was detected after 30-min room temperature incubation with the Molecular device I3X plate reader. The IC50 values were calculated from a series of percent inhibition values determined at a range of inhibitor concentration using software routines as implemented in the GraphPad Prism 7 software and Sigma Plot 13.0.

c-Kit Kinase Assay

ADP-Glo assay kit was purchased from Promega. Magnesium chloride (MgCl₂), ethylene glycol-bis(8-aminoethyl ether)-N,N,N′,N′-tetraacetic acid (EGTA), manganese (II) chloride (MnCl₂), bovine serum albumin (BSA), 1,4-dithiothreitol (DTT) and dimethyl sulfoxide (DMSO) were purchased from Sigma-Aldrich. HEPES buffer was purchased from Gibco. c-Kit kinase and poly (4:1 Glu, Tyr) peptide were purchased from Signalchem.

c-Kit kinase activity was measured by Promega's ADP-Glo™ Assay. In this assay, 100ng of recombinant human c-Kit is incubated with 5 μL of compounds (0.5% DMSO), 5 μL of Poly (4:1 Glu, Tyr) peptide (50 ng/μl) and 5 μL of ATP (50 μM) in buffer (50 mM HEPES, pH7.5; 10 mM MgCl₂; 1 mM EGTA; 0.05% BSA; 50μM DTT; 2mM MnCl₂). The assay was started by incubating the reaction mixture in a 96-well plate at 30° C. for 120-min. After the incubation, 25 μL ADP-Glo reagent was added and the reaction was incubated at room temperature for 40-min to stop the reaction and degrade residual ATP. The ADP product was then converted to ATP by adding 50 μL per well of detection reagent. Luminescence was detected after 30-min room temperature incubation with the Molecular device I3X plate reader. The IC50 values were calculated from a series of percent inhibition values determined at a range of inhibitor concentration using software routines as implemented in the GraphPad Prism 8 software and Sigma Plot 13.0.

c-Kit (D816V) Kinase Assay

ADP-Glo assay kit was purchased from Promega. Magnesium chloride (MgCl₂), ethylene glycol-bis(β-aminoethyl ether)-N,N,N′,N′-tetraacetic acid (EGTA), bovine serum albumin (BSA), 1,4-dithiothreitol (DTT) and dimethyl sulfoxide (DMSO) were purchased from Sigma-Aldrich. HEPES buffer was purchased from Gibco. c-Kit (D816V) kinase and poly (4:1 Glu, Tyr) peptide were purchased from Signalchem.

c-Kit (D816V) kinase activity was measured by Promega's ADP-GIoTM Assay. In this assay, 2.5ng of recombinant human c-Kit (D816V) is incubated with 5 μL of compounds (0.5% DMSO), 5 μL of Poly (4:1 Glu, Tyr) peptide (50 ng/μl) and 5 μL of ATP (15 μM) in buffer (50 mM HEPES, pH7.5; 10 mM MgCl₂; 1 mM EGTA; 0.05% BSA; 50 μM DTT). The assay was started by incubating the reaction mixture in a 96-well plate at 30° C. for 120-min. After the incubation, 25 μL ADP-Glo reagent was added and the reaction was incubated at room temperature for 40-min to stop the reaction and degrade residual ATP. The ADP product was then converted to ATP by adding 50 μL per well of detection reagent. Luminescence was detected after 30-min room temperature incubation with the Molecular device I3X plate reader. The IC50 values were calculated from a series of percent inhibition values determined at a range of inhibitor concentration using software routines as implemented in the GraphPad Prism 8 software and Sigma Plot 13.0.

PDGFRα Kinase Assay

ADP-Glo assay kit was purchased from Promega. Magnesium chloride (MgCl₂), ethylene glycol-bis(p-aminoethyl ether)-N,N,N′,N′-tetraacetic acid (EGTA), bovine serum albumin (BSA), 1,4-dithiothreitol (DTT) and dimethyl sulfoxide (DMSO) were purchased from Sigma-Aldrich. HEPES buffer was purchased from Gibco. PDGFRα Kinase and poly (4:1 Glu, Tyr) peptide were purchased from Signalchem.

PDGFRα kinase activity was measured by Promega's ADP-Glo™ Assay. In this assay, 40ng of recombinant human PDGFRα is incubated with 5 μL of compounds (0.5% DMSO), 5 μL of Poly (4:1 Glu, Tyr) peptide (100 ng/μl) and 5 μL of ATP (25 pM) in buffer (50 mM HEPES, pH7.5; 10 mM MgCl₂; 1 mM EGTA; 0.05% BSA; 50 μM DTT). The assay was started by incubating the reaction mixture in a 96-well plate at 30° C. for 60-min. After the incubation, 25 μL ADP-Glo reagent was added and the reaction was incubated at room temperature for 40-min to stop the reaction and degrade residual ATP. The ADP product was then converted to ATP by adding 50 μL per well of detection reagent. Luminescence was detected after 30-min room temperature incubation with the Molecular device I3X plate reader. The IC₅₀values were calculated from a series of percent inhibition values determined at a range of inhibitor concentration using software routines as implemented in the GraphPad Prism 8 software and Sigma Plot 13.0.

PDGFRα (D842V) Kinase Assay

ADP-Glo assay kit was purchased from Promega. Magnesium chloride (MgCl₂), ethylene glycol-bis(p-aminoethyl ether)-N, N, N′, N′-tetraacetic acid (EGTA), bovine serum albumin (BSA), 1,4-dithiothreitol (DTT) and dimethyl sulfoxide (DMSO) were purchased from Sigma-Aldrich. HEPES buffer was purchased from Gibco. PDGFRα (D842V) Kinase and poly (4:1 Glu, Tyr) peptide were purchased from Signalchem.

PDGFRα (D842V) kinase activity was measured by Promega's ADP-Glo™ Assay. In this assay, 10 ng of recombinant human PDGFRα (D842V) is incubated with 5 μL of compounds (0.5% DMSO), 5 μL of Poly (4:1 Glu, Tyr) peptide (100 ng/μl) and 5 μL of ATP (3 pM) in buffer (50 mM HEPES, pH7.5; 10 mM MgCl₂; 1 mM EGTA; 0.05% BSA; 50pM DTT). The assay was started by incubating the reaction mixture in a 96-well plate at 30° C. for 120-min. After the incubation, 25 μL ADP-Glo reagent was added and the reaction was incubated at room temperature for 40-min to stop the reaction and degrade residual ATP. The ADP product was then converted to ATP by adding 50 μL per well of detection reagent. Luminescence was detected after 30-min room temperature incubation with the Molecular device I3X plate reader. The IC₅₀values were calculated from a series of percent inhibition values determined at a range of inhibitor concentration using software routines as implemented in the GraphPad Prism 8 software and Sigma Plot 13.0.

Table 2 shows IC₅₀values of the invented compounds which represent +for >1000 nM, ++for 101-1000 nM, +++for 10-100 nM, ++++for <10 nM.

TABLE 2 In vitro kinase activity c-KIT PDGFRα c-Abl c-KIT D816V PDGFRa D842V IC₅₀ IC₅₀ IC₅₀ IC₅₀ IC₅₀ Example (nM) (nM) (nM) (nM) (nM) 1 ++++ Not tested Not tested Not tested Not tested 57 ++++ + ++ ++ +++ 64 ++++ + + + ++ 65 +++ + + + + 68 +++ + + + + 74 + + + + + 75 ++ + + + + 80 + + + + + 81 + + + + + 82 +++ + + ++ ++ 83 ++ + + ++ ++ 84 + + + Not tested Not tested

K562 Cell Proliferation Assay

K562 human leukemia cell line purchased from Korean cell line bank (KCLB) and were cultured in Roswell Park Memorial Institute (RPMI) 1640 Medium supplemented with 10% fetal bovine serum (FBS) and 1% penicillin-streptomycin in a humidified incubator in an atmosphere of 5% CO₂at 37° C. Cells were seeded in 96-well plates at a density of 2×103 cells/well in 100 p1 media. Compounds were diluted as two times concentration in 100 μl of media and added to each well. Compounds were 5-fold serially diluted for 6 points and treated from 5 μM to 1.6 nM in K562 cells. After 48 hr incubation, Compound treated cells were analyzed for anti-proliferation assay. Cell viability was investigated using the Cell Titer 96 Aqueous One Solution Reagent. Briefly, 200 μl of media were supplemented with 40 μl of MTS solution, incubated for 4hr, and then the absorbance was recorded at 490 nm with a 96-well plate reader. G150 values were calculated from a series of percent of cell viability at a range of compound concentration. GraphPad Prism 8 software or SigmaPlot 13.0 was used to generate G150 values.

Table 3 shows 1050 values of the invented compounds which represent +for >1000 nM, ++for 101-1000 nM, +++for 10-100 nM, ++++for <10 nM.

TABLE 3 K562 cell activity K562 IC₅₀ Example (nM) 1 ++ 11 ++ 12 +++ 15 +++ 24 +++ 40 +++ 57 ++ 70 ++ 77 ++ 85 ++ 92 +++ 94 ++ 103 +++

Claims

1. A method for treating cancer in a subject, comprising: wherein the 6-membered aryl or 6-membered heteroaryl is optionally substituted with one or more groups selected from the group consisting of halo, hydroxyl, alkyl, alkenyl, alkynyl, cycloalkyl, haloalkyl, hydroxyalkyl, dialkylaminoalkyl, trimethylsilylethoxymethyl, —CH2NHC(O)CH3, —NO2, —NRaRb, —NRaC(═O)Rb, —NRaC(═O)NRaRb, —NRaC(═O)ORb, —ORa, —CN, —C(═O)Ra, —C(═O)ORa, —C(═O)NRaRb, —OC(═O)Ra, —OC(═O)ORa, —OC(═O)NRaRb, —SRa, azetidinyl, oxetanyl, tetrahydrofuranyl, furanyl, pyrrolidinyl, pyrrolyl, pyrazolyl, thiophenyl, imidazolyl, oxazolyl, isoxazolyl, thiazolyl, furazanyl, oxadiazolyl, thiadiazolyl, phenyl, tetrahydropyranyl, pyranyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, piperidinyl, piperazinyl, morpholinyl and thiomorpholinyl;

administering to the subject in need thereof a therapeutically effective amount of a compound of Formula (I) or a pharmaceutically acceptable salt thereof.

wherein

R1 is cyclopropyl substituted with one or more groups selected from the group consisting of halo, alkyl, hydroxyalkyl, haloalkyl, and monoalkylaminoalkyl;

R2 and R3 are independently —H, halo, alkyl, alkoxy, —CF3, —CHF2, —CH2F, or —OCF3;

R4 is selected from the group consisting of 6-membered aryl, 6-membered heteroaryl,

Ra and Rb are independently —H, halo, amino, alkyl, or haloalkyl; and

R5 is H, halo, or alkyl.

2. The method of claim 1, wherein

R1 is cyclopropyl substituted with one or more groups selected from the group consisting of halo, C1-C3 alkyl, C1-C3 hydroxyalkyl and C1-C3 haloalkyl;

R2 and R3 are independently —H, halo, C1-C3 alkyl, C1-C3 alkoxy, —CF3, —CHF2, —CH2F, or —OCF3;

R4 is 6-membered aryl or 6-membered heteroaryl, wherein R4 is optionally substituted with one or more groups selected from the group consisting of halo, hydroxyl, C1-C3 alkyl, C2—C3 alkenyl, C2—C3 alkynyl, C3—C4 cycloalkyl, C1-C3 haloalkyl, mono-C1-C3 alkylamino, di-C1-C3 alkylamino, —CH2NHC(O)CH3, —NO2, —NRaRb, —NRaC(═O)Rb, —NRaC(═O)NRaRb, —NRaC(═O)ORb, —ORa, —CN, —C(═O)Ra, —C(═O)ORa, —C(═O)NRaRb, —OC(═O)Ra, —OC(═O)ORa, —OC(═O)NRaRb, —SRa, azetidinyl, oxetanyl, tetrahydrofuranyl, furanyl, pyrrolidinyl, pyrrolyl, pyrazolyl, thiophenyl, imidazolyl, oxazolyl, isoxazolyl, thiazolyl, furazanyl, oxadiazolyl, thiadiazolyl, phenyl, tetrahydropyranyl, pyranyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, piperidinyl, piperazinyl, morpholinyl and thiomorpholinyl;

Ra and Rb are independently —H, halo, amino, C1-C3 alkyl, or C1-C3 haloalkyl; and

R5 is H, F—, Cl—, Br— or methyl.

3. The method of claim 1, wherein

R1 is cyclopropyl substituted with one or more selected from the group consisting of fluoro, C1-C3 alkyl, C1-C3 hydroxyalkyl and C1-C3 fluoroalkyl;

R2 and R3 are independently —H, —F, —Br, —Cl, C1-C3 alkyl, or —CF3;

R4 is phenyl, pyridinyl, pyrimidinyl, pyrazinyl, or pyridazinyl, wherein R4 is optionally substituted with one or more groups selected from the group consisting of halo, hydroxyl, C1-C3 alkyl, C1-C3 haloalkyl, mono(C1-C3)alkylamino, di(C1-C3)alkylamino, —NRaRb, —ORa, —CN, —C(═O)Ra, —C(═O)ORa, —OC(═O)Ra, —OC(═O)ORa, —SRa, furanyl, pyrazolyl, imidazolyl, isothiazolyl, thiazolyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl and pyrrolyl; and

Ra and Rb are independently —H, halo, amino, C1-C3 alkyl, or C1-C3 haloalkyl.

4. The method of claim 1, wherein R1 is cyclopropyl or substituted with one or more groups selected from the group consisting of fluoro, methyl, ethyl, hydroxymethyl, hydroxyethyl, and methylaminom ethyl.

5. The method of claim 1, wherein R1 is fluorocyclopropyl, hydroxycyclopropyl, hydroxymethylcyclopropyl, difluorocyclopropyl, or methylaminomethylcyclopropyl; and R2 and R3 are independently —H, methyl, or fluoro.

6. The method of claim, wherein R4 is fluoro-methylphenyl, fluoro-hydroxymethylphenyl, chloro-methylphenyl, dimethylphenyl, acetamido-methylphenyl, hydroxy-methylphenyl, hydroxypropanyl-methylphenyl, methyl-propenylphenyl, methyl-pyridinylethynylphenyl, methyl-pyrrolylphenyl, methyl-thiazolylphenyl, imidazolyl-methylphenyl, cyano-methylphenyl, methyl-pyrazolylphenyl, ethynyl-methylphenyl, methylpyridinyl, fluoro-methyl-methylaminophenyl, dimethylpyridinyl, fluoro-methylpyridinyl, fluoromethyl-methylpyridinyl, cyanopyridinyl, trifluoromethyl-methylpyridinyl, hydroxymethylpyridinyl, hydroxymethyl-methylpyridinyl, hydroxyethyl-methylpyridinyl, chloro-methylpyridinyl, aminopyridinyl, acetyl-methylpyridinyl, amino-dimethylpyridinyl, hydroxyethyl-methylpyridinyl, methylpyrimidinyl, dimethylpyrimidinyl, or trifluoromethylpyrimidinyl.

7. The method of claim 1, wherein R4 is fluoro-methylphenyl, fluoro-hydroxymethylphenyl, chloro-methylphenyl, dimethylphenyl, acetamido-methylphenyl, hydroxyl-methylphenyl, methyl-propenylphenyl, ethynyl-methylphenyl, fluoro-methyl-methylaminophenyl, fluoro-hydroxyl-methylphenyl, methyl-methylaminophenyl, methyl-pyrrolylphenyl, methyl-thiazolylphenyl, cyano-methylphenyl, imidazolyl-methylphenyl, methylpyridinyl, chloro-methylpyridinyl, fluoro-methylpyridinyl, fluoromethyl-methylpyridinyl, bimethylpyridinyl, aminopyridinyl, amino-dimethylpyridinyl, methoxypyridinyl, acetyl-methylpyridinyl, hydroxymethylpyridinyl, hydroxymethyl-methylpyridinyl, hydroxyethyl-methylpyridinyl, cyanopyridinyl, trifluoromethylpyridinyl, methylpyrimidinyl, or dimethylpyrimidinyl.

8. The method of claim 1, wherein R4 is selected from the group consisting of phenyl, pyridinyl, and pyrimidinyl, wherein R4 is optionally substituted with one or more groups selected from the group consisting of halo, alkyl, alkynyl, hydroxyalkyl, amino, cyano, acetyl, hydroxy, and haloalkyl.

9. The method of claim 1, wherein R4 is selected from the group consisting of:

10. The method of claim 1, wherein R1 is fluorocyclopropyl.

11. The method of claim 10, wherein R2 and R3 are H; R4 is phenyl, pyridinyl, or indolinyl, wherein R4 is optionally substituted with one or more groups selected from the group consisting of halo, hydroxyl, alkyl, haloalkyl, hydroxyalkyl, cycloalkyl, alkoxyalkyl, alkoxyalkoxy, alkylaminoalkyl, —NRaRb, —NRaC(═O)Rb, —ORa, —SRa, —CN, —C(═O)Ra, —C(═O)ORa, —C(═O)NRaRb, —OC(═O)Ra, furanyl, or pyrrolyl; Ra and Rb are independently —H, halo, amino, alkyl, or haloalkyl; and R5 is —H, halo, or methyl.

12. The method of claim 1, wherein the compound is a compound of Formula (II):

wherein R6 is selected from the group consisting of halo, C1-C3 alkyl, C1-C3 hydroxyalkyl and C1-C3 haloalkyl.

13. The method of claim 12, wherein R2 and R3 are —H; R4 is phenyl or pyridinyl, wherein R4 is optionally substituted with one or more groups selected from the group consisting of halo, hydroxyl, alkyl, haloalkyl, hydroxyalkyl, cycloalkyl, alkoxyalkyl, alkoxyalkoxy, alkylaminoalkyl, —NRaRb, —NRaC(═O)Rb, —ORa, —SRa, —CN, —C(═O)Ra, —C(═O)ORa, —C(═O)NRaRb, —OC(═O)Ra, furanyl, or pyrrolyl; Ra and Rb are independently —H, halo, amino, alkyl, or haloalkyl; and R5 is —H, halo, or alkyl.

14. The method of claim 12, wherein the compound is selected from the group consisting of:

2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(2-fluoro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(3-chloro-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

N-(3-chloro-6-(2-fluoro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(3-methyl-6-(4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(3-chloro-6-(4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(6-(3-fluoro-2-methylphenyl)-3-methylimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(2-fluoro-6-methylphenyl)-3-methylimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(5-fluoro-4-methylpyridin-3-yI)-3-methylimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(5-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(5-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

methyl-3-(2-(2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-4-methylbenzoate;

2-fluoro-N-(6-(5-fluoro-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(3-chloro-6-(5-fluoro-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

N-(6-(5-cyano-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(6-(3-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(6-(4-chloropyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

N-(6-(2,3-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

N-(6-(5-amino-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(6-(2-methyl-5-(methylamino)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(6-(5-acetamido-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

N-(6-(5-chloro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

N-(6-(3-chloro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(6-(4-(trifluoromethyl)pyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(6-(2,4-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(3-fluoro-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(6-(2,5-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

N-(6-(4-cyanopyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(6-(4-fluoro-2,3-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(4-fluoro-2,6-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(4-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(2-methyl-5-(1 H-pyrrol-3-yl)phenyl)imidazo[l,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(6-(2,6-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(6-(4-fluoro-5-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(6-(3,4-difluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

N-(6-(3,6-difluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

N-(6-(4-chloro-3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(6-(2-fluoro-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(4-methoxypyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(6-(6-amino-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

N-(6-(5-amino-3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

N-(6-(2-chloro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

N-(6-(6-aminopyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(6-(2-methyl-5-(1H-pyrazol-1-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(3-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(3-bromo-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(6-(3-fluoro-2-methoxyphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

N-(6-(2-cyano-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

N-(6-(2-chloro-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

N-(6-(2,3-difluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

2-fluoro-N-(6-(3-fluoro-2-(methoxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

2-fluoro-N-(6-(3-fluoro-2-(furan-2-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

2-fluoro-N-(6-(3-fluoro-2-(methylthio)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

2-fluoro-N-(6-(6-fluoro-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

N-(6-(2-acetyl-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

N-(6-(6-(dimethylamino)-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

N-(6-(2-(aminomethyl)-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

N-(6-(2-(acetam idomethyl)-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

2,2-difluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

2-fluoro-N-(6-(3-fluoro-2-((methylamino)methyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

2-fluoro-N-(6-(3-fluoro-2-((isopropylamino)methyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

2-fluoro-N-(6-(3-fluoro-2-((2-methoxyethoxy)methyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

2-fluoro-N-(6-(3-fluoro-2-((2-hydroxyethoxy)methyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

N-(6-(2-((dimethylamino)methyl)-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

2-fluoro-N-(6-(o-tolyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

2-fluoro-N-(6-(3-fluoro-2-hydroxyphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

N-(6-(2-amino-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

N-(6-(2-(dimethylamino)-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

N-(6-(2-ethyl-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

2-fluoro-N-(6-(3-fluoro-2-(trifluoromethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

N-(6-(2-cyclopropyl-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

2-fluoro-N-(6-(3-fluoro-2-(methylamino)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

2-fluoro-N-(6-(3-fluoro-2-isopropylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

2-fluoro-N-(6-(3-fluoro-2-(trifluoromethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(3-fluoro-2,6-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(6-(2-ethyl-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide

N-(6-(4-acetyl-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

N-(6-(2-chloro-3,4-difluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

N-(6-(2-chloro-3,6-difluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(6-(3-fluoro-2-methylphenyl)-8-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(8-(difluoromethyl)-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(6-(3-fluoro-2-methylphenyl)-8-(fluoromethyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(8-fluoro-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(7-fluoro-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(4-fluoro-2-methylphenyl)-8-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(8-(difluoromethyl)-6-(4-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(6-(4-fluoro-2-methylphenyl)-8-(fluoromethyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(8-fluoro-6-(4-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(7-fluoro-6-(4-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(5-fluoro-2-methylphenyl)-8-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(8-(difluoromethyl)-6-(5-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(6-(5-fluoro-2-methylphenyl)-8-(fluoromethyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(8-fluoro-6-(5-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(7-fluoro-6-(5-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(2-fluoro-6-methylphenyl)-8-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(8-(difluoromethyl)-6-(2-fluoro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(6-(2-fluoro-6-methylphenyl)-8-(fluoromethyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(8-fluoro-6-(2-fluoro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; and

2-fluoro-N-(7-fluoro-6-(2-fluoro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide.

15. The method of claim 12, wherein the compound is selected from the group consisting of:

2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(2-fluoro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(3-chloro-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

N-(3-chloro-6-(2-fluoro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide′

2-fluoro-N-(6-(3-fluoro-2-methylphenyl)-3-methylimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(2-fluoro-6-methylphenyl)-3-methylimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(5-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(5-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

2-fluoro-N-(6-(3-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(6-(2,3-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(6-(2-methyl-5-(methylamino)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(6-(2,4-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(3-fluoro-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(6-(2,5-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(6-(2-methyl-5-(1H-pyrrol-3-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(6-(2,6-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(6-(4-fluoro-5-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

N-(3-bromo-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; and

2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide.

16. The method of claim 1, wherein the compound is a compound of Formula (III):

wherein R6 is selected from the group consisting of halo, C1-C3 alkyl, C1-C3 hydroxyalkyl and C1-C3 haloalkyl.

17. The method of claim 16, wherein R2 and R3 are —H; R4 is phenyl or pyridinyl wherein R4 is optionally substituted with one or more groups selected from the group consisting of halo, hydroxyl, alkyl, haloalkyl, hydroxyalkyl, cycloalkyl, alkoxyalkyl, alkoxyalkoxy, alkylaminoalkyl, —NRaRb, —NRaC(═O)Rb, —ORa, —SRa, —CN, —C(═O)Ra, —C(═O)ORa, —C(═O)NRaRb, —OC(═O)Ra, furanyl, or pyrrolyl; Ra and Rb are independently —H, halo, amino, alkyl, or haloalkyl; and R5 is —H, halo, or alkyl.

18. The method of claim 16, wherein the compound is selected from the group consisting of:

(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(2-fluoro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-N-(3-chloro-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-N-(3-chloro-6-(2-fluoro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(3-methyl-6-(4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-N-(3-chloro-6-(4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-methylphenyl)-3-methylimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(2-fluoro-6-methylphenyl)-3-methylimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(5-fluoro-4-methylpyridin-3-yl)-3-methylimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(5-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(5-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

methyl 3-(2-((1 S,2 S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-4-methylbenzoate;

(1 S,2 S)-2-fluoro-N-(6-(5-fluoro-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-N-(3-chloro-6-(5-fluoro-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(5-cyano-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(3-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(4-chloropyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(2,3-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(5-amino-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(2-methyl-5-(methylamino)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(5-acetamido-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(5-chloro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(2-methyl-5-(1H-pyrazol-3-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(4-chloro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(3-chloro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(4-(trifluoromethyl)pyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(2,4-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(3-fluoro-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(2,5-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(4-cyanopyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(4-fluoro-2,3-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(4-fluoro-2,6-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(4-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(2-methyl-5-(1H-pyrrol-3-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(3-methylthiophen-2-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(2,6-dimethylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(4-fluoro-5-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(3,4-difluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(3,6-difluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(4-chloro-3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(2-fluoro-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(4-methoxypyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(6-amino-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(5-amino-3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(2-chloro-6-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(6-aminopyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(2-methyl-5-(1H-pyrazol-1-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-(hydroxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-N-(3-bromo-6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-methoxyphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

(1 S,2 S)-N-(6-(2-cyano-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

(1 S,2 S)-N-(6-(2-chloro-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

(1 S,2 S)-N-(6-(2,3-difluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-(methoxymethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-(furan-2-yl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-(methylthio)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

(1 S,2 S)-2-fluoro-N-(6-(6-fluoro-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

(1 S,2 S)-N-(6-(2-acetyl-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

(1 S,2 S)-N-(6-(6-(dimethylamino)-4-methylpyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

(1 S,2 S)-N-(6-(2-(aminomethyl)-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

(1 S,2 S)-N-(6-(2-(acetamidomethyl)-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-((methylamino)methyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-((isopropylamino)methyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-((2-methoxyethoxy)methyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-((2-hydroxyethoxy)methyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

(1 S,2 S)-N-(6-(2-((dimethylamino)methyl)-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

(1 S,2 S)-2-fluoro-N-(6-(o-tolypimidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-hydroxyphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

(1 S,2 S)-N-(6-(2-amino-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

(1 S,2 S)-N-(6-(2-(dimethylamino)-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

(1 S,2 S)-N-(6-(2-ethyl-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-(trifluoromethyl)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

(1 S,2 S)-N-(6-(2-cyclopropyl-3-fluorophenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropanecarboxamide;

(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-(methylamino)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide;

(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-isopropylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide.

19. The method of claim 16, which is selected from the group consisting of:

(1 S,2 S)-2-fluoro-N-(6-(3-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(5-fluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(5-hydroxy-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-N-(6-(4-chloropyridin-3-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(2-methyl-5-(methylamino)phenyl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide;

(1 S,2 S)-2-fluoro-N-(6-(3-methylthiophen-2-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; and

(1 S,2 S)-N-(6-(3,4-difluoro-2-methylphenyl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide.

20. (canceled)

21. (canceled)

22. (canceled)

23. (canceled)

24. The method of claim 1, wherein the salt is hydrochloric acid salt, tartaric acid salt, phosphoric acid salt, or maleic acid salt.

25. The method of claim 1, wherein the compound is administered in a form of a pharmaceutical composition comprising at least one pharmaceutically acceptable carrier.

26. The method of claim 25, wherein the composition further comprises one or more active ingredient that is useful to treat cancer.

27. The method of claim 1, wherein the cancer is selected from the group consisting of acute lymphocytic leukemia, acute myelogeneous leukemia, chronic myelogenous leukemia, chronic lymphocytic leukemia, gastrointestinal stromal tumors, systemic mastocytosis, melanoma, seminoma, intercranial germ cell tumors, and Non-Hodgkin lymphoma (NHL).

28. The method of claim 1, wherein the cancer is selected from the group consisting of breast cancer, ovarian cancer, and non-small cell lung cancer.

29. The method of claim 1, wherein the cancer is selected from the group consisting of systemic mastocytosis, gastrointestinal stromal tumor, acute myeloid leukemia, melanoma, and seminoma.

30. The method of claim 1, wherein the cancer is selected from the group consisting of Ewing's sarcoma, diffuse large B cell lymphoma, dysgerminoma, myelodysplastic syndrome, nasal NK/T-cell lymphoma, chronic myelomonocytic leukemia, and brain cancer.

31. The method of claim 1, wherein the cancer is selected from the group consisting of gastrointestinal stromal tumor (GIST), stomach cancer, colorectal cancer, melanoma, chronic lymphocytic leukemia (CLL), acute lymphocytic leukemia (ALL), and acute myelogeneous leukem ia(AML).

32. The method of claim 1, wherein the cancer is selected from the group consisting of gastrointestinal stromal tumor (GIST), melanoma and chronic lymphocytic leukemia (CLL).

33. The method of claim 1, wherein the subject is a human.