CHIRAL REAGENTS FOR PREPARATION OF HOMOGENEOUS OLIGOMERS

Abstract

We provide diastereomerically pure or substantially diastereomerically pure activated phosphoramidochloridate morpholino nucleosides, methods of their preparation, and methods of their use in stereospecific coupling for stereospecific synthesis of diastereomerically pure phosphorodiamidate morpholino oligomers (PMOs).

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional application of U.S. patent application Ser. No. 16/573,185, filed on Sep. 17, 2019, which was a divisional application of U.S. patent application Ser. No. 15/750,087 (now U.S. Pat. No. 10,457,698 B2), filed on Feb. 2, 2018, as the United States national stage under 35 U.S.C. § 371 of PCT International Patent App. No. PCT/US2016/045876, having an international filing date of Aug. 5, 2016, which claims benefit of priority of U.S. Provisional Patent App. No. 62/201,510, filed on Aug. 5, 2015. That application is incorporated by reference herein.

BACKGROUND

Field

Embodiments may relate to preparation of substantially diastereomerically pure activated monomers that are phosphoramidochloridate morpholino subunits. Embodiments may also relate to use of substantially diastereomerically pure activated phosphorylated morpholino monomers for preparation of molecules through stereospecific coupling reactions.

Background

Synthesis of diastereomerically pure phosphorodiamidate oligonucleotides is substantially complicated by the existence of chiral phosphorous linkages. This is contrasted with, for example, phosphodiester linkages, which do not have a chiral phosphorous. Examples may be seen in FIG. 1, which compares phosphodiester, phosphorothioate (which also includes a chiral phosphorous), and phosphorodiamidate

The existence of the chiral phosphorous presents substantial challenges to synthetic routes that involve connection of a series of phosphorodiamidate nucleotides. Lack of stereochemically pure reagents (templates, subunits, building blocks) that enable stereospecific formation of phosphorodiamidate linkages leads to reaction at the stereocenter in which the phosphorus chirality of the resulting compound may not be controlled.

As shown graphically in FIG. 2, the use of diastereomeric mixtures of nucleotides for stereochemically uncontrolled coupling to prepare an oligonucleotide of any significant length and sequence creates a heterogeneous mixture of many diastereomers. The number of diastereomers is theoretically 2⁽ⁿ⁻¹⁾, where n is the number of nucleotides that are connected to form the oligonucleotide. As shown in FIG. 2, even a modest four-nucleotide oligonucleotide (tetranucleotide) can result in formation of a mixture of eight separate diastereomers.

Formation of a significant number of diastereomers can create the need for sensitive separation techniques following synthesis. Yield of desired product may be adversely impacted by use of raw materials to prepare multiple diastereomers that are not desired.

It would be useful to be able to select a specific diastereomer prior to synthesis, then to synthesize the selected diastereomer in a stereochemically pure or substantially-pure form.

BRIEF SUMMARY

Embodiments may provide one or more stereochemically pure or substantially stereochemically pure compounds of Table 1. Further embodiments may also provide enantiomers of the compounds of Table 1. Typically the stereochemistry of those enantiomers varies from that of the compounds of Table 1 by the alteration of the stereochemistry of the morpholino ring.

TABLE 1
Compound Formula #
         20
         21
         22
         23
         24
         25
         26
         27
         28
         29
         30
         31

R₁ and R₂ may be the same or different, and may be —H, optionally substituted C1-C3 alkyl, optionally substituted phenyl, optionally substituted naphthyl, or, with the nitrogen to which they are attached, form an optionally substituted heterocycle, which may be, for example, pyrrolidine, piperazine, or morpholine.

Optionally substituted moieties may be substituted with one or more of methyl, ethyl, halogen, nitro, methoxy, or cyano.

R₃ may be trityl (Tr), which may be substituted trityl, including but not limited to such as MMTr (p-methoxyphenyldiphenylmethyl), optionally substituted benzyl, 4-methoxybenzyl (PMB, MPM), 3,4-dimethoxybenzyl, diphenylmethyl (Dpm), or sulfonyl, which may be a cleavable sulfonyl. In some embodiments, sulfonyl is 2-nitrobenzenesulfonyl, 4-nitrobenzenesulfonyl, or 2,4-dinitrobenzenesulfonyl.

R₄, R₅, R₆ may be —H, —C(O)R₇, or —C(O)OR₇, where R₇ is alkyl (methyl, ethyl, isopropyl, or other C1-C6 alkyl), benzyl, 2,2,2-trichloroethyl, or aryl (including but not limited to phenyl, 4-methoxy phenyl, 4-bromophenyl, and 4-nitrophenyl). R₉ may be optionally substituted alkyl, cyanoethyl, acyl, carbonate, carbamate, optionally substituted benzyl, 4-pivaloyloxy benzyl, and silyl.

In further embodiments, morpholino nucleosides in addition to those shown in Table 1 may be prepared in diastereomerically pure or substantially diastereomerically pure form.

Embodiments may also provide methods for separation of diastereomeric mixtures of the above-disclosed compounds into stereochemically pure or substantially stereochemically pure compounds. Further embodiments may provide pharmaceutical compositions comprising stereochemically pure or substantially stereochemically pure compounds as reported herein. Further embodiments may provide pharmaceutical compositions comprising pharmaceutically acceptable salts of stereochemically pure or substantially stereochemically pure compounds as reported herein. Pharmaceutical compositions may be administered in effective amounts to patients in need of treatment. Pharmaceutical compositions may further include pharmaceutically acceptable carriers.

In some embodiments the following moiety in each of the compounds of Table 1 may be substituted at positions a, b, and e with one or two methyl groups, and may be substituted at positions c and d with one methyl group. In each case the methyl group may be oriented on either side of the plan of the morpholino ring. In further embodiments, an additional methylene, optionally substituted with one or more methyl groups, may be inserted adjacent to the nitrogen in the morpholino group to allow for expansion to a seven-membered ring.

Embodiments further provide for preparation of stereochemically pure oligonucleotides through stereospecific coupling of activated monomers. Further embodiments provide substantially diastereomerically pure oligomer made by stereospecific coupling of activated monomers. Still further embodiments provide substantially diastereomerically pure compositions comprising substantially diastereomerically pure compounds as reported herein.

DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS

FIG. 1 shows phosphodiester, phosphorothioate, and phosphorodiamidate oligonucleotide linkages.

FIG. 2 shows the R- and S-phosphorous linkages in a phosphorodiamidate morpholino oligomer (PMO). FIG. 2 also shows the proliferation of diastereomers that typically results when diastereomeric mixtures of phosphorodiamidate oligomer precursors are used to synthesize dinucleotides (2-mers), trinucleotides (3-mers), tetranucleotides (4-mers), and N-mers.

FIG. 3 shows preparation of diastereomerically pure dinucleotides both by using diastereomerically pure phosphoramidochloridates and by using diastereomeric mixture of phosphoramidochloridates.

FIG. 4A and FIG. 4B show generalized diastereomeric mixtures of phosphoramidochloridates that may be useful for preparation of diastereomerically pure or substantially diastereomerically pure diastereomeric subunits.

FIG. 5 shows preparation of diastereomerically pure (homogeneous) oligonucleotides using diastereomerically pure phosphoramidochloridates as reported herein.

FIG. 6 shows a scheme for stereospecific synthesis of 16-mer PMOs and differentiation of stereoisomers by biophysical assay.

FIG. 7 shows melting points for Stereoisomers 1 and 2 of the example showing stereospecific synthesis of 16-mer PMOs and differentiation of stereoisomers by biophysical assay, as reported below.

FIG. 8 shows an ORTEP plot of crystalline Compound 100, as reported below.

FIG. 9A and FIG. 9B show ORTEP plots of two fragments of Compound 100, as reported below.

DETAILED DESCRIPTION

We have found that two diastereomers of activated morpholino subunits may be sorted by their physical properties, allowing preparation of diastereometrically pure isomers. This permits preparation of stereochemically pure or substantially stereochemically pure PMOs under controlled reaction conditions, which may then be used to selectively prepare oligonucleotides with a desired stereochemistry.

Embodiments may also provide methods for separation of diastereomeric mixtures of the above-disclosed compounds into stereochemically pure or substantially stereochemically pure compounds. Once separated, the pure diastereomers from the formerly diastereomeric mixture may be used to prepare diastereomerically pure compounds through stereospecific coupling reactions.

Diastereomerically pure compounds and substantially diastereomerically pure compounds prepared as set forth herein may be diastereomerically pure phosphorodiamidate oligonucleotides. These diastereomerically pure and substantially diastereomerically pure phosphorodiamidate oligonucleotides may have multiple uses. For example, they may be useful as pharmaceuticals. They may be selected for properties that are potentially superior to those of heterogeneous mixtures (stereo-random mixtures) of diastereomers of phosphorodiamidate oligonucleotides. For example, they may be selected for differences in potency, efficacy, stability, safety, and specificity. Diastereomerically pure and substantially diastereomerically pure oligomers may have physical, chemical, and biological properties that differ from those of stereochemically heterogeneous mixtures of oligomers.

“Stereoisomers” refers to isomers that differ only in the arrangement of the atoms in space.

“Diastereomers” refers to stereoisomers that are not mirror images of each other.

“Enantiomers” refers to stereoisomers that are non-superimposable mirror images of one another. Enantiomers include “enantiomerically pure” isomers that comprise substantially a single enantiomer, for example, greater than or equal to 90%, 92%, 95%, 98%, or 99%, or equal to 100% of a single enantiomer.

“Activated monomer” refers to 5′-O-phosphorylated morpholino subunits that bear reactive phosphorous having leaving groups, including but not limited to chloride and halide leaving groups, that undergo displacement reaction with nucleophiles, including but not limited to amines and alcohols.

“R” and “S” as terms describing isomers are descriptors of the stereochemical configuration at asymmetrically substituted atoms, including but not limited to: carbon, sulfur, phosphorous and ammonium nitrogen. The designation of asymmetrically substituted atoms as “R” or “S” is done by application of the Cahn-Ingold-Prelog priority rules, as are well known to those skilled in the art, and described in the International Union of Pure and Applied Chemistry (IUPAC) Rules for the Nomenclature of Organic Chemistry. Section E, Stereochemistry.

An enantiomer can be characterized by the direction in which it rotates the plane of plane polarized light, as is well known to those in the chemical arts. If it rotates the light clockwise (as seen by a viewer towards whom the light is traveling), that enantiomer is labeled (+), and is denoted dextrorotatory. Its mirror-image will rotate plane polarized light in a counterclockwise direction, and is labeled (−), or levorotatory. The direction of rotation of plane polarized light by an enantiomerically pure compound, termed the sign of optical rotation, may be readily measured in standard device known as a polarimeter.

“Racemic” refers to a mixture containing equal parts of individual enantiomers.

“Non-racemic” refers to a mixture containing unequal parts of individual enantiomers. A non-racemic mixture may be enriched in the R- or S-configuration, including, without limitation, about 50/50, about 60/40, and about 70/30 R- to S-enantiomer, or S- to R-enantiomer, mixtures.

“Substantially stereochemically pure” and “substantial stereochemical purity” refer to enantiomers or diastereomers that are in enantiomeric excess or diastereomeric excess, respectively, equal to or greater than 80%. In some embodiments, “Substantially stereochemically pure” and “substantial stereochemical purity” refer to enantiomers or diastereomers that are in enantiomeric excess or diastereomeric excess, respectively, equal to or greater than 87%, equal to or greater than 90%, equal to or greater than 95%, equal to or greater than 96%, equal to or greater than 97%, equal to or greater than 98%, or equal to or greater than 99%. “Substantially Diastereomerically Pure” refers to diastereomers that are in diastereomeric excess equal to or greater than 87%, equal to or greater than 90%, equal to or greater than 95%, equal to or greater than 96%, equal to or greater than 97%, equal to or greater than 98%, or equal to or greater than 99%.

“Enantiomeric excess” (ee) of an enantiomer is [(the mole fraction of the major enantiomer) minus the (mole fraction of the minor enantiomer)]×100. Diastereomeric excess (de) of a diastereomer in a mixture of two diastereomers is defined analogously.

“Pharmaceutically acceptable salt” as used herein refers to acid addition salts or base addition salts of the compounds in the present disclosure. A pharmaceutically acceptable salt is any salt which retains the activity of the parent compound and does not impart any unduly deleterious or undesirable effect on a subject to whom it is administered and in the context in which it is administered. Pharmaceutically acceptable salts include, but are not limited to, metal complexes and salts of both inorganic and carboxylic acids. Pharmaceutically acceptable salts also include metal salts such as aluminum, calcium, iron, magnesium, manganese and complex salts. In addition, pharmaceutically acceptable salts include, but are not limited to, acid salts such as acetic, aspartic, alkylsulfonic, arylsulfonic, axetil, benzenesulfonic, benzoic, bicarbonic, bisulfuric, bitartaric, butyric, calcium edetate, camsylic, carbonic, chlorobenzoic, citric, edetic, edisylic, estolic, esyl, esylic, formic, fumaric, gluceptic, gluconic, glutamic, glycolic, glycolylarsanilic, hexamic, hexylresorcinoic, hydrabamic, hydrobromic, hydrochloric, hydroiodic, hydroxynaphthoic, isethionic, lactic, lactobionic, maleic, malic, malonic, mandelic, methanesulfonic, methylnitric, methylsulfuric, mucic, muconic, napsylic, nitric, oxalic, p nitromethanesulfonic, pamoic, pantothenic, phosphoric, monohydrogen phosphoric, dihydrogen phosphoric, phthalic, polygalactouronic, propionic, salicylic, stearic, succinic, sulfamic, sulfanlic, sulfonic, sulfuric, tannic, tartaric, teoclic, toluenesulfonic, and the like.

An “effective amount” of a combination of therapeutic agents (e.g., Compound 1 and a CDK 4/6 inhibitor) is an amount sufficient to provide an observable therapeutic benefit compared to HCC or IHCC left untreated in a subject or patient.

Active agents as reported herein can be combined with a pharmaceutically acceptable carrier to provide pharmaceutical formulations thereof. The particular choice of carrier and formulation will depend upon the particular route of administration for which the composition is intended.

“Pharmaceutically acceptable carrier” as used herein refers to a nontoxic carrier, adjuvant, or vehicle that does not destroy the pharmacological activity of the compound with which it is formulated. Pharmaceutically acceptable carriers, adjuvants or vehicles that may be used in the compositions of this invention include, but are not limited to, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substances, polyethylene glycol, sodium carboxymethylcellulose, polyacrylates, waxes, polyethylene glycol and wool fat.

The compositions of the present invention may be suitable for parenteral, oral, inhalation spray, topical, rectal, nasal, buccal, vaginal or implanted reservoir administration, etc. In some embodiments, the formulation comprises ingredients that are from natural or non-natural sources. In some embodiments, the formulation or carrier may be provided in a sterile form. Non-limiting examples of a sterile carrier include endotoxin-free water or pyrogen-free water.

The term “parenteral” as used herein includes subcutaneous, intravenous, intramuscular, intra-articular, intra-synovial, intrasternal, intrathecal, intrahepatic, intralesional and intracranial injection or infusion techniques. In particular embodiments, the compounds are administered intravenously, orally, subcutaneously, or via intramuscular administration. Sterile injectable forms of the compositions of this invention may be aqueous or oleaginous suspension. These suspensions may be formulated according to techniques known in the art using suitable dispersing or wetting agents and suspending agents. The sterile injectable preparation may also be a sterile injectable solution or suspension in a nontoxic parenterally acceptable diluent or solvent. Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium.

Embodiments of the invention provide for preparation of stereochemically pure isomers or substantially stereochemically pure isomers, followed by use of the pure isomers to stereospecifically prepare diastereomerically pure phosphorodiamidate morpholino oligomers (PMOs). Preparation may be by separation of the diastereomeric mixture of phosphoramidochloridate nucleotides. Separation may be made by, for example, chromatography; for example, high performance liquid chromatography or “HPLC.” Separation may also be accomplished through crystallization.

Separated monomers may be referred to as “active” monomers. By “active” it is meant that the monomers include phosphoramidochloridate moiety that is reactive towards a variety of nucleophiles, which include but not limited to: amines, alcohols/alkoxides, thiol/thiolate, alkyllithium, and Grignard reagents.

I. Preparation of Diastereometric Isomers

In one embodiment, stereochemically pure or substantially stereochemically pure activated monomers may be prepared by separation of a diastereomeric mixture of monomers. Separation may be accomplished by methods that permit distinction of stereoisomers using physical properties. For example, separation may be accomplished through chromatography or crystallization. Suitable types of chromatography include, for example, but are not limited to high performance liquid chromatography (HPLC), simulated moving bed chromatography, countercurrent chromatography, and other types of separative chromatography. For example, a diastereomeric mixture may be subjected to HPLC, eluting a fast-moving fraction and a slow-moving fraction. Each of these fractions is a different stereochemically pure or substantially stereochemically pure amount of a monomer. As described below, these monomers may be used to prepare oligomers with desired stereochemistry through stereospecific coupling using controlled reaction conditions.

We have further determined that, once separated, the stereochemically pure activated monomers have sufficient stability for use in further chemical reactions. Furthermore, we have determined that the stereochemically pure activated monomers can undergo stereospecific chemical reactions. Thus, as discussed in more detail below, these stereochemically pure activated monomers may be used for stereospecific coupling reactions to prepare stereochemically pure products.

As noted above, embodiments may provide one or more stereochemically pure or substantially stereochemically pure compounds of Table 1, which may be prepared by taking advantage of different physical properties in the stereoisomers. Further embodiments may also provide enantiomers of the compounds of Table 1. Typically the stereochemistry of those enantiomers varies from that of the compounds of Table 1 by the alteration of the stereochemistry of the morpholino ring.

TABLE 1
Compound Formula #
         20
         21
         22
         23
         24
         25
         26
         27
         28
         29
         30
         31

wherein R3 is optionally substituted triphenylmethyl (also referred to as “trityl”), optionally substituted benzyl, or sulfonyl. R4, R5, and R6 may be —C(O)R7 or —C(O)OR8, where R7 is methyl, ethyl, or phenyl, and R8 is benzyl or 2,2,2-trichloroethyl. R9 may be optionally substituted alkyl, cyanoethyl (for use as a protecting group see, for example, U.S. Patent Application Pub. No. US2013/0197220), acyl, sulfonyl, acetal/ketal, carbonate, carbamate, optionally substituted benzyl, 4-pivaloyloxy benzyl, and silyl.

In some embodiments, the optionally substituted benzyl is 4-methoxybenzyl (PMB, MPM). In some embodiments, sulfonyl is a cleavable sulfonyl. In some embodiments, sulfonyl is 2-nitrobenzenesulfonyl, 4-nitrobenzenesulfonyl, or 2,4-dinitrobenzenesulfonyl.

R1 and R2 may be the same or different, and may be —H, optionally substituted C1-C3 alkyl, optionally substituted phenyl, optionally substituted naphthyl, or, with the nitrogen to which they are attached, form an optionally substituted heterocycle, which may be, for example, pyrrolidine, piperazine, or morpholine.

Optionally substituted moieties may be substituted with one or more of methyl, ethyl, halogen, nitro, or cyano.

R3 may be trityl (Tr), which may be substituted trityl, including but not limited to such as MMTr (p-methoxyphenyldiphenylmethyl), benzyl, 4-methoxybenzyl (PMB, MPM), and 3,4-dimethoxybenzyl, diphenylmethyl (Dpm),

R4, R5, R6 may be —H, —C(O)R7, or —C(O)OR7, where R7 is alkyl (methyl, ethyl, isopropyl, or other C1-C6 alkyl) or aryl (including but not limited to phenyl, 4-methoxy phenyl, 4-bromophenyl, and 4-nitrophenyl).

II. Stereospecific Coupling

In addition to determining that separation technology might be used to prepare substantially stereochemically pure amounts of activated monomer, we have determined that these activated monomers may, under some reaction conditions, be used to accomplish stereospecific coupling for the preparation of stereochemically pure dinucleotides, stereochemically pure trinucleotides, and larger stereochemically pure oligomers. Through use of methods reported herein, chirality of newly formed PMO linkage may be specifically coded by chirality of stereochemically pure active monomers used to form the oligomer.

Typical reaction conditions for stereospecific coupling include reaction in aprotic solvents. These solvents may be, for example, but are not limited to, acetonitrile, tetrahydrofuran (THF), 1,3-dimethylimidazolidinone (DMI), dimethylformamide (DMF), N-methyl-2-pyrrolidinone (NMP), dimethylacetamide (DMAc), dichloromethane (DCM), 1,2-dichloroethane (DCE), chloroform, 1,4-dioxane, ethyl acetate, 2-methyltetrahydrofuran, and isopropyl acetate. Coupling reactions may be conducted in the presence of non-nucleophilic tertiary amine bases and aromatic bases. Suitable bases include, but are not limited to, diisopropylethylamine, triethylamine, 2,6-lutidine, trimethylpyridines (collidines), and N-ethylmorpholine. Reaction temperatures may range from room temperature (about 20° C.) to 50° C. Sonication may be applied in some cases to help dissolution of substrate(s).

To demonstrate the feasibility of stereospecific coupling, multiple substantially stereochemically pure PMO dinucleotides were prepared by stereospecific PMO coupling of the fast- and slow-eluting substantially stereochemically pure active monomers (phosphoramidochloridates). Table 2, below, summarizes HPLC retention profiles of these substantially stereochemically pure PMO dinucleotides The table compares retention times for dinucleotides that were prepared from combinations of the 5′-end monomers listed on the left of the table with both faster-eluting and slower-eluting isomers of 3′-end monomers listed on the top. The table demonstrates that stereospecific coupling of substantially stereochemically pure active monomers produces different diastereomerically pure dinucleotides having different physical properties.

TABLE 2

U

Cc

Ad

Gb

T

fast

slow

fast

slow

fast

slow

fast

slow

fast

slow

U1

U2

C1

C2

A1

A2

G1

G2

T1

T2

U

UU1

UU2

UC1

UC2

UA1

UA2

UG1

UG2

UT1

UT2

dinucleotide

9

<

27

9.1

>

6.5

12.6

>

10.9

12.5

<

18.8

8.4

<

27

RT (min)

Ca

CU1

CU2

CC1

CC2

CA1

CA2

CG1

CG2

CT1

CT2

dinucleotide

5.6

<

6.6

6.7

>

5.7

8

>

7.4

10.4

<

13.3

5.6

<

6.1

RT (min)

Aa

Au1

Au2

AC1

AC2

AA1

AA2

AG1

AG2

AT1

AT2

dinucleotide

3.5

<

3.6

3.6

=

3.6

4.2

>

4.1

7.6

<

8.5

3.5

<

3.6

RT (min)

Gb

Gu1

Gu2

GC1

GC2

GA1

GA2

GG1

GG2

GT1

GT2

dinucleotide

7.6

<

8.1

7.2

=

7.2

9.7

>

8.9

14.2

>

11.3

7.4

<

7.5

RT (min)

T

Tu1

Tu2

TC1

TC2

TA1

TA2

TG1

TG2

TT1

T21

dinucleotide

9.7

<

23.9

8.9

>

5.6

13.2

>

11.4

13.2

<

20.0

9

<

24

RT (min)

anucleobases unprotected

bguanine amino group protected with isobutyryl group

ccytosine amino group protected with: (1) acetyl group for coupling with U, C, A and G, (2) benzoyl group for coupling with T

dadenine amino group protected with benzoyl group

Analytical HPLC conditions for profiling of the substantially stereochemically pure PMO dinucleotides of Table 2 are reported below:

HPLC column      Chiralpak IC 4.6 × 250 mm 5 μm
Temperature      30° C.
Flow rate        1.0 mL/min
Mobile phase     10% n-heptane, 80% EtOAc
                 and 10% MeOH-EtOH 1:1 with 0.1% diethylamine
Gradient         Isocratic
Run time         30 min
Injection volume 1-2 μL (0.2 mg/ml, dichloromethane)
Detection        UV 260 nm

EXAMPLES

III. Examples of Diastereomeric Separation of Activated Monomers

The following examples show diastereomer separation of activated monomers according to certain embodiments as presented herein.

A. U-Monomers

Analytical HPLC Conditions for Activated U Monomers:

HPLC column	Chiralpak IC, 4.6 × 250 mm, 5 u
Temperature	35° C.
Flow rate	1 mL/min
Mobile phase	Ethyl acetate
Gradient	Isocratic
Run time	15 min
Injection volume	10 μL (5 mg/ml, ethyl acetate)
Detection	260 nm
Retention Time	U1	5 min
	U2	7.5 min

Preparative HPLC Conditions for Activated U Monomers:

Chiralpak IC, 21×250 mm, 5μ; Elute column at 11 ml/minute with ethyl acetate, room temperature, 260 nm detection.

[¹H-NMR Data for U₁]

¹H NMR (400 MHz, CDCl₃) δ 8.18 (br, 1H), 7.45 (m, 6H), 7.15-7.32 (m, 10H), 6.12 (dd, 1H, J=2.0 & 9.6 Hz), 5.62 (d, 1H, J=8.0 Hz), 4.39 (m, 1H), 4.11 (m, 2H), 3.39 (d, 1H, J=11 Hz), 3.15 (d, 1H, J=11 Hz), 2.65 (s, 3H), 2.62 (s, 3H), 1.49 (t, 1H, J=11 Hz), 1.39 (t, 1H, J=11 Hz)

[¹H-NMR Data for U₂]

¹H NMR (400 MHz, CDCl₃) δ 8.07 (br, 1H), 7.44 (m, 6H), 7.14-7.34 (m, 10H), 6.12 (dd, 1H, J=2 & 9 Hz), 5.61 (d, 1H, 8.0 Hz), 4.39 (m, 1H), 4.08 (m, 2H), 3.39 (d, 1H, J=12 Hz), 3.15 (d, 1H, J=12 Hz), 2.66 (s, 3H), 2.62 (s, 3H), 1.46 (t, 1H, J=11 Hz), 1.38 (t, 1H, J=11 Hz),

B. A-Monomers

Analytical HPLC Conditions for Activated a Monomers:

HPLC column	Chiralpak IC, 4.6 × 250 mm, 5 u
Temperature	35° C.
Flow rate	1 mL/min
Mobile phase	Ethyl acetate
Gradient	Isocratic
Run time	15 min
Injection volume	10 μL (5 mg/ml, ethyl acetate)
Detection	260 nm
Retention Time	A1	8.1 min
	A2	11.7 min

Preparative HPLC Conditions for Activated a Monomers:

Chiralpak IC, 21×250 mm, 5u; Elute with 100% ethyl acetate at 15 ml/minute, room temperature, uv 260 nm detection.

[1H-NMR Data for A₁]

¹H NMR (400 MHz, CDCl₃) δ 9.01 (br, 1H), 8.79 (s, 1H), 8.00 (m, 3H), 7.58 (m, 1H), 7.4-7.6 (m, 8H), 7.2-7.4 (m, 10H), 6.42 (d, 1H, J=8.4 Hz), 4.51 (m, 1H), 4.12 (m, 3H), 3.54 (d, 1H, J=12 Hz), 3.25 (d, 1H, J=12 Hz), 2.62 (s, 3H), 2.59 (s, 3H), 1.81 (t, 1H, J=11 Hz), 1.62 (t, 1H, J=11 Hz)

[¹H-NMR Data for A₂]

¹H NMR (400 MHz, CDCl₃) δ 9.04 (br, 1H), 8.79 (s, 1H), 8.00 (m, 3H), 7.56 (m, 1H), 7.4-7.6 (m, 8H), 7.2-7.4 (m, 10H), 6.41 (d, 1H, J=8.4 Hz), 4.51 (m, 1H), 4.12 (m, 3H), 3.54 (d, 1H, J=12 Hz), 3.25 (d, 1H, J=12 Hz), 2.64 (s, 3H), 2.61 (s, 3H), 1.82 (t, 1H, J=11 Hz), 1.63 (t, 1H, J=11 Hz)

C. C-Monomers

Analytical HPLC Conditions for Activated C Monomers:

HPLC column	Chiralpak IC, 4.6 × 250 mm, 5 u
Temperature	35° C.
Flow rate	1.0 mL/min
Mobile phase	90% ethyl acetate 10% n-heptane
Gradient	Isocratic
Run time	12 min
Injection volume	10 μL (5 mg/ml, dichloromethane)
Detection	260 nm
Retention Time	C1	6.0 min
	C2	6.2 min

Preparative HPLC Conditions for Activated C Monomers:

Chiralpak IC eluted at 15 ml/minute with 75% ethyl acetate and 25% n-heptane. Room temperature and uv 260 nm detection.

[¹H-NMR Data for C₁]

¹H NMR (400 MHz, CDCl₃) δ 7.66 (d, 1H, J=7.8 Hz), 7.43 (m, 6H), 7.33 (d, 1H, J=7.4 Hz), 7.15-7.32 (m, 9H), 6.18 (dd, 1H, J=2.2 & 9.2 Hz), 4.42 (m, 1H), 4.08-4.16 (m, 2H), 3.54 (d, 1H, J=11 Hz), 3.14 (d, 1H, J=12 Hz), 2.64 (s, 3H), 2.60 (s, 3H), 2.23 (s, 3H), 1.51 (t, 1H, J=11 Hz), 1.25 (m, 1H).

[¹H-NMR Data for C₂]

¹H NMR (400 MHz, CDCl₃) δ 7.64 (d, 1H, J=7.8 Hz), 7.43 (m, 6H), 7.32 (d, 1H, J=7.4 Hz), 7.15-7.32 (m, 9H), 6.19 (dd, 1H, J=2.1 & 9.2 Hz), 4.41 (m, 1H), 4.06-4.15 (m, 2H), 3.54 (d, 1H, J=11 Hz), 3.15 (d, 1H, J=12 Hz), 2.64 (s, 3H), 2.61 (s, 3H), 2.22 (s, 3H), 1.49 (t, 1H, J=11 Hz), 1.25 (m, 1H)

D. G-Monomers (Guanine Mono-Protected)

Analytical HPLC Conditions for Activated G Monomers:

HPLC column	Chiralpak IC, 4.6 × 250 mm, 5 u
Temperature	35° C.
Flow rate	1.0 mL/min
Mobile phase	ethyl acetate
Gradient	Isocratic
Run time	30 min
Injection volume	10 μL (5 mg/ml, ethyl acetate)
Detection	260 nm
Retention Time	G1	17.8 min
	G2	22.3 min

Preparative HPLC Conditions for Activated G Monomers:

Chiralpak IC eluted at 15 ml/minute with 100% ethyl acetate. Room temperature and uv 260 nm detection.

E. T-Monomers

Analytical HPLC Conditions for Activated T Monomers:

HPLC column	Chiralpak IC, 4.6 × 250 mm, 5 u
Temperature	35° C.
Flow rate	1 mL/min
Mobile phase	Ethyl acetate
Gradient	lsocratic
Run time	10 min
Injection volume	10 μL (5 mg/ml, methylene chloride)
Detection	260 nm
Retention Time	T1	4.5 min
	T2	7.0 min

Preparative HPLC Conditions for Activated T Monomers:

Chiralpak IC, 50×500 mm, 20u. Elute column at 60 ml/minute with ethyl acetate, room temperature, 260 nm detection. Retention times are 25 and 40 minutes.

[1H-NMR Data for T1]

¹H NMR (400 MHz, CDCl₃) δ 7.4-7.5 (m, 5H), 7.26-7.33 (m, 6H), 7.16-7.22 (m, 3H), 7.04 (d, 1H, J=1 Hz), 6.12 (dd, 1H, J=2 & 10 Hz), 4.39 (m, 1H), 4.12 (m, 2H), 3.37 (d, 1H, J=12 Hz), 3.15 (d, 1H, J=12 Hz), 2.66 (s, 3H), 2.63 (s, 3H), 1.83 (d, 1H, J=1 Hz), 1.49 (t, 1H, J=11 Hz), 1.41 (t, 1H, J=11 Hz))

[1H-NMR Data for T2]

¹H NMR (400 MHz, CDCl₃) δ 7.4-7.5 (m, 6H), 7.24-7.35 (m, 6H), 7.14-7.22 (m, 3H), 7.03 (s, 1H), 6.12 (dd, 1H, J=2 & 10 Hz), 4.39 (m, 1H), 4.09 (m, 2H), 3.37 (d, 1H, J=11 Hz), 3.15 (d, 1H, J=11 Hz), 2.66 (s, 3H), 2.62 (s, 3H), 1.82 (s, 3H), 1.48 (t, 1H, J=11 Hz), 1.40 (t, 1H, J=11 Hz)

F. C-Monomers (NBz)

Analytical HPLC Conditions for Activated C Monomers (NBz):

HPLC column	Chiralpak IB, 4.6 × 150 mm, 5 u
Temperature	35° C.
Flow rate	1.0 mL/min
Mobile phase	100% acetonitrile
Gradient	Isocratic
Run time	5 min
Injection volume	10 μL (5 mg/ml, acetonitrile)
Detection	260 nm
Retention Time	C1	3.4 min
	C2	4.5 min

Preparative HPLC Conditions for Activated C Monomers (NBz):

Chiralpak IB, 20×250 mm 5u, eluted at 9 ml/minute with 100% acetonitrile. Room temperature and uv 260 nm detection. Retention times are 13 and 16 minutes.

G. G-Monomers (Guanine Doubly Protected)

Analytical HPLC Conditions for Activated G Monomers (Guanine Doubly Protected):

	HPLC column	Chiralpak IA, 4.6 × 250 mm, 5 u
	Temperature	35° C.
	Flow rate	1.0 mL/min
	Mobile phase	70% ethyl acetate/30% methylene chloride
	Gradient	Isocratic
	Run time	8 min
	Injection volume	10 μL (5 mg/ml, ethyl acetate)
	Detection	260 nm
	Retention Time	G1	3.9 min
		G2	4.3 min

Preparative HPLC Conditions for Activated G Monomers (Guanine Doubly Protected):

Chiralpak IA 50×500 mm, eluted at 60 ml/minute with 100% ethyl acetate. Room temperature and uv 260 nm detection. Retention times are 20 and 24 minutes.

[¹H-NMR Data for G₁ (Guanine Doubly Protected)]

¹H NMR (400 MHz, CDCl₃) δ 7.76 (s, 2H), 7.50 (d, 2H, J=9 Hz), 7.4-7.5 (m, 6H), 7.26-7.32 (m, 6H), 7.16-7.22 (m, 3H), 7.02 (d, 2H, J=9 Hz), 6.24 (dd, 1H, J=2 & 10 Hz), 5.61 (d, 1H, J=12 Hz), 5.56 (d, 1H, J=12 Hz), 4.48 (m, 1H), 4.1 (m, 2H), 3.47 (d, 1H, J=11 Hz), 3.23 (d, 1H, J=12 Hz), 3.2 (m, 1H), 2.62 (s, 3H), 2.59 (s, 3H), 1.75 (t, 1H, J=11 Hz), 1.57 (t, 1H, J=12 Hz), 1.33 (s, 9H), 1.33 (t, 6H, J=7 Hz)

[¹H-NMR Data for G₂ (Guanine Doubly Protected)]

¹H NMR (400 MHz, CDCl₃) δ 7.78 (s, 1H), 7.77 (s, 1H), 7.50 (d, 2H, J=9 Hz), 7.4-7.5 (m, 6H), 7.26-7.33 (m, 6H), 7.15-7.22 (m, 3H), 7.02 (d, 2H, J=9 Hz), 6.23 (dd, 1H, J=2 & 10 Hz), 5.61 (d, 1H, J=12 Hz), 5.56 (d, 1H, J=12 Hz), 4.47 (m, 1H), 4.1 (m, 2H), 3.47 (d, 1H, J=11 Hz), 3.22 (d, 1H, J=12 Hz), 3.2 (m, 1H), 2.64 (s, 3H), 2.60 (s, 3H), 1.75 (t, 1H, J=11 Hz), 1.58 (t, 1H, J=11 Hz), 1.33 (s, 9H), 1.33 (t, 6H, J=7 Hz)

IV. Examples of Stereospecific PMO Coupling with Diastereomerically Pure Activated Monomers

The following examples report use of stereospecific coupling to prepare stereochemically homogeneous products.

A. Activated U-Monomers (U₁ & U₂)+U-Morpholine-NH (1)

U₁ (11 mg, 0.018 mmol, 1 eq, 99.0% de) was dissolved in acetonitrile (0.11 ml) and mixed with diisopropylethylamine (8 μL, 0.05 mmol, 2.5 eq). U-morpholine-NH (1; 14 mg, 0.030 mmol, 1.6 eq) was added and sonication was applied to aid for dissolution. After 0.5 h stirring, a small aliquot of reaction mixture was diluted with CDCl₃ and analyzed by ¹H NMR. All the rest of reaction mixture was diluted with acetonitrile (8 ml) for HPLC analysis and kept in freezer. Stereospecific formation of 2 was confirmed by HPLC analysis (99.4% de). The above protocol was employed also for the coupling of U₂ (95.6% de) to stereospecifically give 3 (96.0% de).

Analytical HPLC Conditions for U/U-Coupling:

	HPLC column	Chiralpak IC, 4.6 × 250 mm, 5 u
	Temperature	35° C.
	Flow rate	1.0 mL/min
	Mobile phase	80% methanol 20% acetonitrile
	Gradient	Isocratic
	Run time	30 min
	Injection volume	10 μL (2 mg/ml, acetonitrile)
	Detection	260 nm
	Retention Time	U1		11.5 min
		U2		21.5 min
		2		12.0 min
		3		22.1 min
	nucleophile	activated U		Product
		monomer		(UU dinucleotide)
	U morpholine-NH	U1	→	2
	(1)	(99.0% de)		(99.4% de)
		U2	→	3
		(95.6% de)		(96.0% de)

[¹H-NMR Data for 2]

¹H NMR (400 MHz, CDCl₃) δ 7.6 (m, 4H), 7.2-7.5 (m, 20H), 7.1-7.2 (m, 3H), 6.15 (d, 1H, J=8.0 Hz), 5.73 (d, 1H, J=8.0 Hz), 5.66 (d, 1H, J=8.0 Hz), 5.54 (d, 1H, J=8.0 Hz), 4.40 (m, 1H), 3.93 (m, 2H), 3.81 (m, 1H), 3.70 (m, 2H), 3.41 (m, 2H), 3.40 (m, 3H), 3.11 (d, 1H, J=12 Hz), 2.78 (m, 1H), 2.56 (s, 3H; NMe), 2.54 (s, 3H; NMe), 2.48 (m, 1H), 1.47 (t, 1H, J=11 Hz), 1.35 (t, 1H, J=11 Hz), 1.04 (s, 9H)

[¹H-NMR Data for 3]

¹H NMR (400 MHz, CDCl₃) δ 7.6 (m, 4H), 7.3-7.5 (m, 11H), 7.2-7.3 (m, 9H), 7.1 (m, 3H), 6.12 (dd, 1H, J=2.0 & 9.6 Hz), 5.71 (d, 1H, J=8.4 Hz), 5.70 (d, 1H, J=8.0 Hz), 5.47 (dd, 1H, J=2.0 & 10.4 Hz), 4.31 (m, 1H), 3.97 (m, 1H), 3.85 (m, 1H), 3.73 (m, 2H), 3.65 (m, 1H), 3.31 (m, 2H), 3.24 (m, 1H), 3.07 (d, 1H, J=12 Hz), 2.68 (m, 1H), 2.65 (s, 3H; NMe), 2.62 (s, 3H; NMe), 2.26 (m, 1H), 1.45 (t, 1H, J=12 Hz), 1.29 (t, 1H, J=11 Hz), 1.04 (s, 9H)

B. Activated C-Monomers (C₁ & C₂)+C-Morpholine-NH (4)

C₁ (20 mg, 0.031 mmol, 1 eq, 93.5% de) was dissolved/suspended in THF (0.40 ml) and mixed with diisopropylethylamine (12 μL, 0.069 mmol, 2.3 eq). The morpholino-cytosine (4; 16 mg, 0.035 mmol, 1.1 eq) dissolved in THF (0.20 mL) was added. After 1.0-2.0 h stirring, a small aliquot of reaction mixture was diluted with acetonitrile and analyzed by LC/MS. An aliquot (30-50 μL) of reaction mixture was diluted with dichloromethane (0.6 ml) for HPLC analysis. Stereospecific formation of 6 was confirmed by HPLC analysis (94.3% de). The reaction mixture was directly loaded onto a silica gel column and eluted with a gradient mobile phase of 0-15% of methanol in ethyl acetate. The above protocol was employed also for the C/C coupling of C₂ (90.2% de) to stereospecifically give 5 (90.0% de).

Analytical HPLC Conditions for C/C-Coupling:

HPLC column	Chiralpak IC, 4.6 × 250 mm, 5 u
Temperature	35° C.
Flow rate	1.0 mL/min
Mobile phase	Solvent A		n-heptane
	Solvent B		1:1 ethanol: methanol
			0.1%
			diethylamine (DEA)
	Isocratic
Gradient	% A		% B
	50		50
Run time	20 min
Injection volume	5 μL (3 mg/ml, dichloromethane)
Detection	260 nm
Retention Time	4		5.4 min
	5		10.5 min
	6		12.9 min
nucleophile	activated C		Product
	monomer		(CC dinucleotide)
C morpholine-	C1	→	6
NH (4)	(93.5% de)		(94.3% de)
	C2	→	5
	(90.2% de)		(90.0% de)

[¹H-NMR Data for 5]

¹H NMR (400 MHz, CDCl₃) δ 10.9 (br, 1H), 7.69 (d, 1H, J=7.4 Hz), 7.62 (m, 5H), 7.35-7.44 (m, 13H), 7.21-7.35 (m, 6H), 7.15 (m, 4H), 6.14 (br d, 1H, J=7.8 Hz), 5.58 (dd, 1H, J=2.4 & 9.4 Hz), 5.53 (br, 1H), 4.51 (dd, 1H, J=8.6 & 10 Hz), 4.09 (m, 1H), 3.70-3.80 (m, 4H), 3.60 (dd, 1H, J=6.3 & 10 Hz), 3.56 (d, 1H, J=11 Hz), 3.28 (m, 1H), 2.96 (d, 1H, J=11 Hz), 2.69 (s, 3H; NMe), 2.67 (s, 3H; NMe), 2.65 (m, 1H), 2.25 (m, 1H), 2.07 (s, 3H), 1.31 (t, 1H, J=11 Hz), 1.13 (t, 1H, J=11 Hz), 1.04 (s, 9H).

[¹H-NMR Data for 6]

¹H NMR (400 MHz, CDCl₃) δ 9.57 (br, 1H), 7.62-7.70 (m, 7H), 7.35-7.50 (m, 14H), 7.23-7.35 (m, 4H), 7.12 (m, 4H), 6.31 (m, 1H), 5.79 (m, 1H), 5.70 (m, 1H), 4.61 (m, 1H), 4.03 (m, 1H), 3.80-3.90 (m, 2H), 3.72 (m, 2H), 3.58 (m, 1H), 3.48 (m, 1H), 3.09 (m, 1H), 2.75 (m, 1H), 2.58 (s, 3H; NMe), 2.55 (s, 3H; NMe), 2.53 (m, 1H), 2.38 (m, 1H), 2.21 (s, 3H), 1.47 (t, 1H, J=10 Hz), 1.22 (t, 1H, J=10 Hz), 1.06 (s, 9H).

C. Activated A-Monomers (A₁ & A₂)+U-Morpholine-NH (1)

A₁ (5.9 mg, 0.008 mmol) was suspended in acetonitrile (118 μL). Diisopropylethylamine (5 μL, 0.03 mmol) was added followed by morpholino-uracil (1; 4.6 mg, 0.01 mmol). Sonication was applied for 1 min and resultant homogeneous mixture was stirred at ambient temperature. After overnight stirring, the mixture (thick white paste) was diluted with a mixture of acetonitrile (5.0 ml) and methanol (0.30 ml) to give homogeneous clear solution. A small aliquot was directly analyzed by HPLC without further dilution.

A₂ (F2; 5.0 mg, 0.007 mmol) was suspended in acetonitrile (100 μl). Diisopropylethylamine (4 μl, 0.02 mmol) was added followed by morpholino-uracil (4.1 mg, 0.009 mmol). Sonication was applied for 1 min and resultant thick suspension was stirred at ambient temperature. After overnight stirring, acetonitrile (5.0 ml) was added and sonication was applied to give homogeneous clear solution. A small aliquot was directly analyzed by HPLC without further dilution.

Analytical HPLC Conditions for U/A-Coupling:

HPLC column	Chiralpak IC, 4.6 × 250 mm, 5 u
Temperature	35° C.
Flow rate	1 mL/min
Mobile phase	Solvent A		Ethyl acetate
	Solvent B		1:1 ethanol/methanol
			with 0.1% diethylamine
Gradient	Isocratic: 98% solvent A, 2% solvent B
Run time	30 min
Injection volume	5 μL (1 mg/ml, acetonitrile-methanol)
Detection	260 nm
Retention Time	7 (S isomer)		21.7 min
	8 (R isomer)		24.9 min
nucleophile	activated A		Product
	monomer		(UA dinucleotide)
U morpholine-NH (1)	A1	→	8
	(97.8% de)		(R isomer, 96.2% de)
	A2	→	7
	(98.4% de)		(S isomer 98.3% de)

D. Activated G-Monomers (G₁ & G₂)+U-Morpholine-NH (1)

G₁ (6.5 mg, 0.009 mmol, 1 eq, 99.9% de) was dissolved/suspended in THF (0.13 ml) and mixed with diisopropylethylamine (3.6 μL, 0.02 mmol, 2.2 eq). The morpholino-uracil (1; 4.7 mg, 0.010 mmol, 1.1 eq) dissolved in THF (0.07 mL) was added. After 1.0-2.0 h stirring, a small aliquot of reaction mixture was diluted with acetonitrile and analyzed by LC/MS. An aliquot (100 μL) of reaction mixture was diluted with dichloromethane (0.4 ml) for HPLC analysis. Stereospecific formation of 9 was confirmed by HPLC analysis (99.9% de).

Analytical HPLC Conditions for U/G-Coupling:

HPLC column	Chiralpak IA, 4.6 × 250 mm, 5 u
Temperature	35° C.
Flow rate	1.0 mL/min
Mobile phase	Solvent A		n-heptane
	Solvent B		Ethyl acetate
	Solvent C		1:1 ethanol:
			methanol 0.1%
			diethylamine (DEA)
Gradient	Isocratic
	% A	% B	% C
	55	40	5
Run time	30 min
Injection volume	5 μL (2 mg/ml, dichloromethane)
Detection	260 nm
Retention Time	1		8.4 min
	9		14.0 min
	10		16.3 min
nucleophile	activated G monomer		Product
			(UG dinucleotide)
U morpholine-NH	G1	→	9
(1)	(99.9% de)		(99.9% de)

Diastereomerically substantially pure compounds as reported above may be used to prepare stereochemically pure oligonucleotides and other compounds. Examples of potential oligonucleotides are shown, for example, in Summerton, J (1999). “Morpholino Antisense Oligomers: The Case for an RNase-H Independent Structural Type.”. Biochimica et Biophysica Acta 1489 (1): 141-58; and in Summerton, J; Weller D. (1997). “Morpholino Antisense Oligomers: Design, Preparation and Properties”. Antisense & Nucleic Acid Drug Development 7 (3): 187-95. Both of those documents are incorporated by reference herein.

V. Example of Stereospecific Synthesis of 16-mer PMOs and Differentiation of Stereoisomers by Biophysical Assay

This example reports a synthesis that targets a pair of stereopure 16-mer PMOs through stereospecific coupling using activated monomers. These PMOs have opposite stereochemical arrays for their phosphorous linkages.

Target Sequence:

Stereopure Active Monomers (Building Blocks):

Target PMOs    Stereopure active monomers used for coupling
Stereoisomer 1 A2, C2, G1 and T1
Stereoisomer 2 A1, C1, G2 and T2

A scheme for stereospecific synthesis of 16-mer PMOs and differentiation of stereoisomers by biophysical assay is shown in FIG. 6. The 16-mer PMO stereoisomers 1 and stereoisomer 2 were prepared manually by solid-phase synthesis on aminomethylpolystyrene-disulfide resin (˜300 μmol/g loading, see U.S. Patent App. Pub. No. 20090131624A1, which is incorporated by reference herein) at 50 mg scale (starting resin weight).

Stock Solutions for Solid-Phase Synthesis:

De-tritylation 4 cyanopyridine trifluoroacetate
               (CYTFA) 2% (w/v) and 0.9% ethanol
               (v/v) in 20% trifluoroethanol/DCM (v/v).
Neutralization 5% diisopropylethylamine (v/v)
               in 25% isopropanol/DCM (v/v).
Coupling       Freshly prepared 55 mM solution in
               NEM-DMI* for each of stereopure
               active monomers (A2, C2, G1 and T1 for
               stereoisomer 1; A1, C1, G2 and T2
               for stereoisomer 2)
               * 0.11M N-ethylmorpholine in
               1,3-dimethylimidazolidinone (DMI)

Operational Cycle for Each PMO Coupling:

Step	Volume (ml)	Time (min)
DCM	1-2	2-5
Detritylation	1-2	5
Detritylation	1-2	5
Detritylation	1-2	5
Detritylation	1-2	5
Detritylation	1-2	5
DCM	1-2	2-5
Neutralization	1-2	2-5
Neutralization	1-2	2-5
Neutralization	1-2	2-5
Neutralization	1-2	2-5
DCM	1-2	2-5
DCM	1-2	2-5
DCM	1-2	2-5
Coupling	1	>180*
DCM	1-2	2-5
Neutralization	1-2	2-5
Neutralization	1-2	2-5
DCM	1-2	2-5
DCM	1-2	2-5
DCM	1-2	2-5
DCM	1-2	2-5
*40° C. for 3 hours or room temperature for 12 hours.

Release from Resin and Deprotection:

To the resin-bound 16-mer (after de-tritylation) was added 1:3 (v/v) of 28% aqueous ammonia/ethanol (˜5 ml). The mixture was sealed and heated at 45° C. for 20 hours. After cooling to room temperature, the mixture was filtered and washed with methanol. The filtrate was concentrated and diafiltered against 15 mM triethylammonium (TEAA) buffer pH 7.0. The apparatus used was an Amicon Stirred Cell (50 mL) with an Ultracel 1 kDa UF membrane. The samples were diafiltered by dilution/concentration until the original solvent was reduced to 1% original concentration (approximately 5 cycles) and then subjected to reverse phase preparative HPLC purification.

Reverse Phase Preparative HPLC Method for PMO Purification:

HPLC column	XBridge Prep C8 OBD column,
	9 × 150 mm, 5 μm
Column temperature	ambient temperature
Flow rate	30.0 ml/min
Gradient	Time (min)	% A	% B
	Initial	85	15
	18	80	20
	20	0	100
Mobile phase	Solvent A: 15 mM Triethylammonium
	acetate (TEAA) buffer pH7 + 10% MeOH
	Solvent B: acetonitrile + 10% MeOH
Diluting solution	15 mM TEAA buffer
Run time	20 min
Detection	UV 260 nm
Retention time	Stereoisomer 1	13.98 min
	Stereoisomer 2	14.03 min

LC/MS Method for Quality Assessment of PMOs:

HPLC column	Waters BEH C18 Oligo 2.1 × 50 mm
	130 Angstrom 1.7 um
Column temperature	45° C.
Flow rate	0.3 mL/min
Gradient	Time (min)	% A	% B
	Initial	95	5
	2	95	5
	20	50	50
	24	50	50
	24.1	95	5
	30	95	5
Mobile phase	Solvent A: 50 mM Ammonium acetate
	Solvent B: Acetonitrile/Methanol 1/1 v/v with
	50 mM Ammonium acetate
Run time	30 min
Injection volume	25 μL Diluent: water or 10 mM
	Triethylamine acetate
Detection	UV 260 nm
MS/Ionization mode	Synapt G2/Electrospray Positive Mode
Cone	30 V/4 V/2.8 kV
voltage/Extraction
Source Temp./	100° C./4 eV (low energy) 40-70 eV (high
Collision energies/MS	energy/MSE mode/Deconvolution and Deisotoping
function/Analysis	using Waters MSe Viewer Software
Retention time	Stereoisomer 1	10.83 min
	Stereoisomer 2	10.86 min

Materials and Conditions for Melting Temperature (Tm) Measurement

complimentary  5’-UUCCUUGAUGUUGGAG-3’
RNA            (SEQ ID NO. 1)
(16-mer)       (IDT Integrated
               DNA Technologies)
Diluting       10 mM Sodium Phosphate,
buffer         100 mM NaCl,
               0.1 mM EDTA,
               pH 7.0
               (adjusted with
               phosphoric acid)
Thermal        Shimadzu 2700 UV-Vis
Melt           Spectrophotometer
Apparatus      equipped with the
               Shimadzu S-1700
               Temperature Module
Vacuum         Labconco Centrivap
Centrifugation Concentrator
Concentrator   Model 7810015
Stock          8 μM in 250 μL buffer
solutions      of each sample and
               complimentary RNA
               were prepared using
               the Dilution buffer
               from samples
               concentrated and
               dried by vacuum
               centrifugation
Procedure      Each sample was then
               mixed with an
               equivalent volume
               of 8 pM complimentary RNA
               The mixtures were heated
               to 95° C. and then
               cooled to 25° C. for
               annealment prior to
               the Tm measurement.
               Tm analysis (UV 260 nm)
               was conducted from
               25° C. to 105° C. at
               0.5° C./min
               (with the temperature
               returning to starting
               conditions after
               each run) and then
               repeated under
               the same conditions.
               Tm Analysis software
               (Shimadzu) was used
               to calculate
               the Tm using the
               “averaging” function.

Summary for Thermal Melt Characterization of Complexes of Stereochemically Distinct PMOs with Complimentary RNAs:

	LC/MS purity (area %)	Tm (° C.)
Stereoisomer 1	97.6	62.8
Stereoisomer 2	94.2	57.2

Melting points for Stereoisomers 1 and 2 are shown in FIG. 7. Based on the different melting points, one may conclude that separate amounts of substantially pure stereoisomers have been prepared.

VI. Example of Stereospecific Synthesis and Absolute Stereochemical Assignment of Stereopure PMO Dinucleotide Compound 100 (5′-TA2-3′)

Late-eluting active A monomer (A₂; 200 mg, 0.277 mmol, 1 eq) was dissolved in a mixture of acetonitrile (2.0 ml) and DIPEA (0.12 ml, 0.69 mmol, 2.5 eq). T-morpholine-NH (1; 146 mg, 0.305 mmol, 1.1 eq) was then added and resultant suspension was sonicated for a few minutes until a clear solution was obtained. The reaction mixture was stirred at room temperature overnight. Upon complete reaction monitored by LC/MS, the mixture was concentrated and subjected to column chromatography (3% methanol in DCM, Biotage SnapUltra 10 g SiO₂). Clean product fractions were combined and concentrated under vacuum to give the fully protected stereopure 5′-TA-3′ dinucleotide 2 as a white solid (240 mg, 0.206 mmol, 74% yield).

To the fully protected dinucleotide 2 (500 mg, 0.429 mmol) in 25 ml flask was added 2,2,2-trifluoroethanol (TFE; 4.0 ml) and acetic acid (1.0 ml) at room temperature. The resultant mixture was stirred at room temperature and monitored by LC/MS. After 30 minutes, the reaction was quenched with saturated aqueous NaHCO₃ and DCM. The two layers were separated and the aqueous layer was back extracted. All organic layers were combined, washed with half-saturated brine, dried over anhydrous Na₂SO₄, filtered and concentrated to give crude product as white foam. The crude product was purified by column chromatography (20% MeOH in acetone, Biotage Snap Ultra 25 g SiO₂ cartridge) to give the partially protected dinucleotide 3 as a glassy solid (300 mg, 0.325 mmol, 76% yield).

The partially protected dinucleotide 3 (250 mg, 0.271 mmol) was dissolved in a mixture of methanol (12.5 ml) and THF (12.5 mL) and treated with 1 M NaOH (10.8 ml) at room temperature. After stirring at room temperature for 22 h (progress monitored by LC/MS), the mixture was neutralized with 1 M HCl (10.8 mL) to adjust pH at 8 and then concentrated under vacuum to dryness. The residue was dissolved in water (5 mL) and washed with EtOAc (5 mL). The aqueous layer was concentrated under vacuum to dryness to give crude product as white solid (480 mg). The crude product was purified by size-exclusion chromatography (Sephadex® LH-20, MeOH/water 4:1) to give the fully deprotected dinucleotide Compound 100 as white solid (137 mg, 0.236 mmol, 87% yield).

A drop of Compound 100 aqueous solution (200 mg/ml) was sealed in a well with pure water for one day to grow single crystals. X-ray structure of the single crystal confirmed absolute configuration of the phosphorous linkage as S. This X-ray structure is shown in an ORTEP plot in FIG. 8. ORTEP plots of separate fragments are shown in FIG. 9A and FIG. 9B. X-ray data was collected as reported below.

Data Collection

A single crystal of Compound 100 (C₂₂H₃₃N₁₀O₇P) was mounted on a glass fiber. All measurements were made on a diffractometer using graphite monochromated Cu—Kα radiation.

Cell constants and an orientation matrix for data collection, obtained from a least-squares refinement using the setting angles of 36473 carefully centered reflections in the range 7.75<2θ<147.10° corresponded to a C-centered monoclinic cell with dimensions:

a=33.3523(2) Å

b=13.80020(11) Å β=96.8075(6)°

c=14.19956(10) Å

V=6489.53(8) ų

For Z=4 and F.W.=580.54, the calculated density is 0.594 g/cm³. Based on the reflection conditions of:

hkl:h+k=2n

packing considerations, a statistical analysis of intensity distribution, and the successful solution and refinement of the structure, the space group was determined to be:

• • C2 (#5)

The data were collected at a temperature of 23±1° C. using the ω-2θ scan technique to a maximum 2θ value of 147.7°. Omega scans of several intense reflections, made prior to data collection, had an average width at half-height of 0.00° with a take-off angle of 6.0°. Scans of (0.00+0.00 tan θ)° were made at a speed of 0.0°/min (in ω).

Data Reduction

50795 reflections were collected, where 12008 were unique (Rint=0.0453). Data were collected and processed using CrysAlisPro (Rigaku Oxford Diffraction). (CrysAlisPro: Data Collection and Processing Software, Rigaku Corporation (2015). Tokyo 196-8666, Japan). No decay correction was applied.

The linear absorption coefficient, μ, for Cu—Kα radiation is 6.011 cm⁻¹. An empirical absorption correction was applied that resulted in transmission factors ranging from 0.341 to 1.000. The data were corrected for Lorentz and polarization effects.

Structure Solution and Refinement

The structure was solved by direct methods (SHELXT Version 2014/5: Sheldrick, G. M. (2014). Acta Cryst. A70, C1437) and expanded using Fourier techniques. The non-hydrogen atoms were refined anisotropically. Hydrogen atoms were refined using the riding model. The final cycle of full-matrix least-squares refinement (using Least Squares function minimized: (SHELXL Version 2014/7); Σw(F_o²−F_c²)² where w=Least Squares weights) on F² was based on 12008 observed reflections and 849 variable parameters and converged (largest parameter shift was 0.00 times its esd) with unweighted and weighted agreement factors of:

R1=Σ∥Fo∥−|Fc∥/Σ|Fo|=0.0522

wR2=[Σ(w(Fo²−Fc²)²/Σw(Fo²)²]^1/2=0.1632

The goodness of fit was 1.45. Goodness of fit is defined as: [Σw(Fo2−Fc2)2/(No−Nv)]^1/2, where: No=number of observations and Nv=number of variables.

Unit weights were used. The maximum and minimum peaks on the final difference Fourier map corresponded to 1.79 and −0.69 e⁻/ų, respectively. The final Flack parameter was 0.029(7), indicating that the structure is inversion-twin. (Parsons, S. and Flack, H. (2004), Acta Cryst. A60, s61; Flack, H. D. and Bernardinelli (2000), J. Appl. Cryst. 33, 114-1148).

Neutral atom scattering factors were taken from International Tables for Crystallography (IT), Vol. C, Table 6.1.1.4. (International Tables for Crystallography, Vol. C (1992). Ed. A. J. C. Wilson, Kluwer Academic Publishers, Dordrecht, Netherlands, Table 6.1.1.4, pp. 572). Anomalous dispersion effects were included in Fcalc (Ibers, J. A. & Hamilton, W. C.; Acta Crystallogr., 17, 781 (1964)); the values for Δf′ and Δf″ were those of Creagh and McAuley. (Creagh, D. C. & McAuley, W. J.; “International Tables for Crystallography”, Vol C, (A. J. C. Wilson, ed.), Kluwer Academic Publishers, Boston, Table 4.2.6.8, pages 219-222 (1992)). The values for the mass attenuation coefficients are those of Creagh and Hubbell. (Creagh, D. C. & Hubbell, J. H.; “International Tables for Crystallography”, Vol C, (A. J. C. Wilson, ed.), Kluwer Academic Publishers, Boston, Table 4.2.4.3, pages 200-206 (1992)). All calculations were performed using the CrystalStructure crystallographic software package except for refinement, which was performed using SHELXL Version 2014/7. (CrystalStructure 4.2: Crystal Structure Analysis Package, Rigaku Corporation (2000-2015). Tokyo 196-8666, Japan; SHELXL Version 2014/7: Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122).

Crystal data, intensity measurements, and structure solution and refinement were as shown below:

A. Crystal Data

Empirical Formula             C22H33N10O7P
Formula Weight                580.54
Crystal Color, Habit          nONE, nONE
Crystal Dimensions            not described
Crystal System                monoclinic
Lattice Type                  C-centered
No. of Reflections Used for Unit
Cell Determination (2θ range) 36473 ( 7.7 - 147.1° )
Omega Scan Peak Width
at Half-height                0.00°
Lattice Parameters            a = 33.3523(2) Å
                              b = 13.80020(11) Å
                              c = 14.19956(10) Å
                              β = 96.8075(6) °
                              V = 6489.53(8) Å3
Space Group                   C2 (#5)
Z value                       4
Dealc                         0.594 g/cm3
F000                          1224.00
μ(CuKα)                       6.011 cm−1

B. Intensity Measurements

Diffractometer
Radiation                    CuKα (λ = 1.54187 Å)
                             graphite monochromated
Take-off Angle               2.8°
Detector Aperture            2.0-2.5 mm horizontal
                             2.0 mm vertical
Crystal to Detector Distance 21 mm
Temperature                  23.0° C.
Scan Type                    ω-2θ
Scan Rate                    0.0°/min (in ω) (up to 0 scans)
Scan Width                   (0.00 + 0.00 tan θ)°
2θmax                        147.7°
No. of Reflections Measured  Total: 50795
                             Unique: 12008 (Rint = 0.0453)
                             Parsons quotients (Flack × parameter): 4813
Corrections                  Lorentz-polarization
                             Absorption
                             (trans. factors: 0.341-1.000)

C. Structure Solution and Refinement

Structure Solution               Direct Methods (SHELXT
                                 Version 2014/5)
Refinement                       Full-matrix least-squares on F2
Function Minimized               Σ w (Fo2 − Fc2)2
Least Squares Weights            w = 1/[ σ2(Fo2) + (0.1000 · P)2 +
                                 0.0000 · P ]
                                 where P = (Max(Fo2, 0) + 2Fc2)/3
2θmax cutoff                     147.70
Anomalous Dispersion             All non-hydrogen atoms
No. Observations (All reflections) 12008
No. Variables                    849
Reflection/Parameter Ratio       14.14
Residuals: R1 (I > 2.00σ(I))     0.0522
Residuals: R (All reflections)   0.0534
Residuals: wR2 (All reflections) 0.1632
Goodness of Fit Indicator        1.450
Flack parameter                  0.029(7)
(Parsons' quotients = 4813)
Max Shift/Error in Final Cycle   0.001
Maximum peak in Final Diff. Map  1.79 e−/Å3
Minimum peak in Final Diff Map   −0.69 e−/Å3

[¹H-NMR Data for Compound 100]

¹H NMR (400 MHz, D20) δ 8.25 (s, 1H), 8.15 (s, 1H), 7.40 (s, 1H), 5.85 (d, 1H), 5.45 (d, 1H), 4.25 (m, 2H), 4.05 (m, 1H), 3.85 (m, 1H), 3.6 (m, 2H), 3.4 (m, 4H), 2.90 (m, 4H), 2.60 (d, 6H), 1.8 (s, 3H).

All documents mentioned in this application are incorporated by reference herein. If there is any discrepancy between the incorporated document and this document, then this document controls.

Claims

1-3. (canceled)

4. A method for preparing a stereochemically pure oligonucleotide, comprising reacting substantially diastereomerically pure compounds selected from the group consisting of the compound of Formula 20, the compound of Formula 21, the compound of Formula 22, the compound of Formula 23, the compound of Formula 24, the compound of Formula 25, the compound of Formula 26, the compound of Formula 27, the compound of Formula 28, the compound of Formula 29, the compound of Formula 30, and the compound of Formula 31, Compound Formula # 20 21 22 23 24 25 26 27 28 29 30 31

wherein R1 and R2 may be the same or different, and are selected from the group consisting of —H, optionally substituted C1-C3 alkyl, optionally substituted phenyl, optionally substituted naphthyl, or, with the nitrogen to which they are attached, form an optionally substituted heterocycle, which may be, for example, pyrrolidine, piperazine, and morpholine;

wherein R3 is selected from the group consisting of trityl (Tr), which may be substituted trityl, including but not limited to such as MMTr (p-methoxyphenyldiphenylmethyl); optionally substituted benzyl, 4-methoxybenzyl (PMB, MPM), 3,4-dimethoxybenzyl, diphenylmethyl (Dpm), 4-methoxybenzyl, and sulfonyl;

R4, R5, and R6 are selected from the group consisting of —H, —C(O)R7, and —C(O)OR7, where R7 is C1-C6 alkyl, benzyl, 2,2,2-trichloroethyl, and aryl;

R9 is selected from the group consisting of optionally substituted alkyl, cyanoethyl, acyl, carbonate, carbamate, optionally substituted benzyl, 4-pivaloyloxy benzyl, and silyl, and enantiomers thereof.

5. A method for preparing a substantially diastereomerically pure oligomer, comprising:

selecting a substantially stereochemically pure activated monomer; and

synthesizing a substantially diastereomerically pure oligomer from the selected substantially stereochemically pure activated monomer.

6. The method of claim 5, wherein the oligomer is an oligonucleotide comprising chiral phosphorous linkages.

7. The method of claim 5, further comprising:

separating a diastereomeric mixture of activated monomers into two substantially stereochemically pure monomers prior to the step of selecting a substantially stereochemically pure activated monomer.

8. The method of claim 5, wherein said substantially diastereomerically pure oligomer is at least 90% diastereomerically pure.

9. The method of claim 8, wherein said substantially diastereomerically pure oligomer is at least 95% diastereomerically pure.

10. The method of claim 9, wherein said substantially diastereomerically pure oligomer is at least 99% diastereomerically pure.

11. The method of claim 10, wherein said substantially diastereomerically pure oligomer is 100% diastereomerically pure.

12. A method for preparing a substantially diastereomerically pure phosphorodiamidate oligomer, comprising:

selecting a substantially stereochemically pure phosphoramidochloridate monomers; and

synthesizing a substantially diastereomerically pure phosphorodiamidate oligomer from the selected substantially stereochemically pure phosphoramidochloridate monomer.

13. The method of claim 12, further comprising separating a diastereomeric mixture of phosphoramidochloridates into two substantially stereochemically pure phosphoramidochloridate monomers prior to the step of selecting a substantially stereochemically pure phosphoramidochloridate monomer.

14. The method of claim 13, wherein the separation of the diastereomeric mixture occurs by at least one member of the group consisting of chromatography and crystallization.

15. The method of claim 12, wherein the phorphorodiamidate oligomer is a phosphorodiamidate morpholino oligomer.

16-18. (canceled)

19. A substantially diastereomerically pure oligomer made by the method of claim 4.

20. A substantially diastereomerically pure oligomer made by the method of claim 5.

21. A substantially diastereomerically pure oligomer made by the method of claim 6.

22. A substantially diastereomerically pure oligomer made by the method of claim 7.

23. A substantially diastereomerically pure oligomer made by the method of claim 8.

24. A substantially diastereomerically pure oligomer made by the method of claim 9.

25. A substantially diastereomerically pure oligomer made by the method of claim 10.

26. A substantially diastereomerically pure oligomer made by the method of claim 11.

27. A pharmaceutical composition comprising a substantially diastereomerically pure oligomer of claim 19, or a pharmaceutically acceptable salt thereof.