Modulators of beta catenin and uses thereof

Abstract

Provided are compounds of the Formula I: or pharmaceutically acceptable salts thereof, which are useful for the modulation of beta catenin condensates and in the treatment of a variety of conditions or diseases associated therewith.

Description

139849-00420MODULATORS OF BETA CATENIN AND USES THEREOFRELATED APPLICATIONS

[0001] This application claims priority to U. S. Provisional Application No. 63 / 722,839, filed on November 20, 2024. The entire contents of the foregoing application are expressly incorporated herein by reference.BACKGROUND

[0002] Biomolecular condensates are ubiquitous spatiotemporal organizers of biology, compartmentalizing and integrating a wide variety of regulatory pathways within cells. See Banani, S. F. et al. Nat Rev Mol Cell Bio 18, 285-298 (2017); and Hyman, A. A. et al. Annu Rev Cell Dev Bi 30, 39-58 (2014). Aberrant condensates, or condensatopathies, act as central nodes of dysfunction in disease, representing a new class of targets for drug discovery. See Alberti, S. et al. Nat Rev Mol Cell Bio 22, 196-213 (2021); Boija, A. et al. Cancer Cell 39, 174-192 (2021); Mitrea, D. M. et al. Nat Rev Drug Discov 1-22 (2022); Martin, E. W. et al. J. Mol. Biol. 168380 (2023); and Patel, A. et al. Frontiers Mol Biosci 9, 1007744 (2022). This new perspective expands the target space and enables new strategies for pursuing targets historically considered ‘undruggable’; these strategies include but are not limited to modifying the condensates these targets associate to, or targeting structural states that are selectively adopted by the ‘undruggable’ target inside the condensate. See Mitrea, D. etaL Nat Rev Drug Discov 1-22 (2022). Due to their integrative role, dysfunction of condensates leads to complex defects in multiple biological processes, explaining the root cause of complex diseases, such as cancer and neurodegeneration. This central role in pathophysiology also opens opportunities to discover broad-acting drugs that are active across large patient populations with a shared condensatopathy but of diverse genetic background.

[0003] Beta catenin is a validated anti -neoplastic target, known to be a driver of overproliferation and aberrant transcriptional programming in a broad spectrum of cancers, including, but not limited to colorectal, breast, skin and pancreatic cancer. See Liu, J. et al. Signal Transduct Target Ther. (2022); and Zhang, Y. et al. J Hematol Oncol 13, 165 (2020). The cancer-driving activity of beta catenin is attributed to its constitutively active transcriptional promoting function, which results from several mutations and other aberrations along the dysregulated Wnt-pathway. Transcriptionally active beta catenin drives the expression of dozens of genes including NOTUM, MYC, AXIN2 and LEF1. See Nusse, R. etaL Nature 519, 163 (2015) and Herbst, A. et al. BMC Genomics 15, 74 (2014). Thus,1ME1\58440953. vl139849-00420what is needed is novel small molecules that modulate beta catenin’s aberrant transcriptional activation and cell proliferation through its sequestration into nuclear condensates.SUMMARY

[0004] Provided herein are compounds having the Formula I:R2R4\-S\ / R1X / / \R3N / / X0(I);and pharmaceutically acceptable salts and compositions thereof, wherein R1, R2, R3, R4, and X are as described herein. In one aspect, the described compounds of Formula I and pharmaceutically acceptable salts thereof modulate beta catenin (e.g., sequester beta catenin in nuclear condensates), and are useful in a variety of therapeutic applications such as, for example, in treating cancer. See for example the cancer cell-line derived xenograft study and related data shown in the exemplification section below.

[0005] Pharmaceutical compositions comprising the described compounds and pharmaceutically acceptable salts of the described compounds, as well as methods for their preparation are also included.BRIEF DESCRIPTION OF THE DRAWINGS

[0006] Figure 1 shows the beta catenin condensate modulation in DLD-1 cells treated with Example 1 or DMSO.

[0007] Figure 2 shows tumor volumes for mice treated with Example 1 and mice provided vehicle.

[0008] Figure 3 shows the gene expression changes in DLD-1 cells treated with Example 1 or DMSO.DETAILED DESCRIPTION1. General Description of Compounds

[0009] In a first embodiment, provided herein are compounds having the Formula I:2ME1\58440953. vl139849-00420R20or a pharmaceutically acceptable salt thereof, wherein:R1is hydrogen, (Ci-C4)alkyl, or (Ci-C4)alkylene[OP(O)(OH)2];R2is aryl, heteroaryl, heterocyclyl, or cycloalkyl, each of which are optionally substituted with 1 to 3 groups selected from R1A;R3is hydrogen, (Ci-C4)alkyl, halo, or (Ci-C4)alkylene(Ci-C4alkoxy);or R2and R3are taken together to form Cscycloalkyl substituted with phenyl;X is -OR6or -NR7R8;R4is (Ci-C4)alkyl, (Ci-C4)alkyl, halo(Ci-C4)alkyl, or heterocyclyl when X is -NR7R8, or R4is hydrogen, (Ci-C4)alkyl, halo(Ci-C4)alkyl, or heterocyclyl when X is -OR6;or R2and R4are taken together to form heterocyclyl;R6is cycloalkyl, heterocyclyl, (Ci-C4)alkylene(Ci-C4alkoxy), (Ci-C4)alkylene[aryl], (Ci-C4)alkylene[heteroaryl], or (Ci-C4)alkylene[cycloalkyl], wherein the aryl is substituted with 1 to 3 groups selected from R2Aand the heteroaryl is optionally substituted with 1 to 3 groups selected from R2A;R7is H;R8is cycloalkyl, heterocyclyl, (Ci-C4)alkylene(Ci-C4alkoxy), (Ci-C4)alkylene[aryl], (Ci-C4)alkylene[heteroaryl], or (Ci-C4)alkylene[cycloalkyl], wherein the cycloalkyl is optionally substituted with 1 to 3 groups selected from R2A;or R7and R8are taken together to form heterocyclyl or heteroaryl, each of which is optionally substituted with 1 to 3 groups selected from R2A;each R1Ais independently selected from halo, cyano, (Ci-C4)alkyl, hydroxy(Ci-C4)alkyl, hydroxy[halo(Ci-C4)alkyl], cyano(Ci-C4)alkyl, halo(Ci-C4)alkyl, (Ci-C4)alkoxy, deuterated(Ci-C4)alkoxy, (Ci-C4)alkoxyO(Ci-C4)alkyl, (Ci-C4)alkoxyO[deuterated(Ci-C4)alkyl], halo(Ci-C4)alkoxy, (Ci-C4)alkoxyO[halo(Ci-C4)alkyl], oxo, hydroxy, -O[hydroxy(Ci-C4)alkyl], -Ofcycloalkyl], -Ofheterocyclyl], -Ofaryl], -Ofheteroaryl], (Ci-C4)alkylene[cycloalkyl], (Ci-C4)alkylene[aryl], (Ci-C4)alkylene[heterocyclyl], (Ci-C4)alkylene[heteroaryl], -O(Ci-C4)alkylene[NRaRb], -O(Ci-C4)alkylene[NRaC(O)Rb], -O(Ci-C4)alkylene[cycloalkyl], -O(Ci-C4)alkylene[aryl], -O(Ci-C4)alkylene[heterocyclyl], -O(Ci-C4)alkylene[heteroaryl], cycloalkyl, heterocyclyl, aryl, heteroaryl, (Ci-C4)alkylene(Ci-3ME1\58440953. vl139849-00420C4)alkoxy, (Ci-C4)alkylene[deuterated(Ci-C4)alkoxy], (Ci-C4)alkylene[halo(Ci-C4)alkoxy], (Ci-C4)alkoxyO[cycloalkyl], (Ci-C4)alkoxyO[heterocyclyl], (Ci-C4)alkoxyO [heteroaryl], (Ci-C4)alkoxyO[phenyl], -C(O)[heterocyclyl], -SRa, -S(O)Ra, -SO2Ra, -S(O)(NRa)Rb, -NRbSO2Rb, -SO2NRa, -C(O)Ra, -C(O)ORa, -C(O)NRaRb, -NRaC(O)Rb, -NRaC(O)NRb, -NRaRb, -NH(Ci-C4)alkylene[heterocyclyl], and (Ci-C4)alkyleneNRaRb, where each occurrence of cycloalkyl, heterocyclyl, aryl, and heteroaryl alone, or as part of another group, is optionally substituted with 1 to 3 groups selected from halo, oxo, (Ci-C4)alkyl, halo(Ci-C4)alkyl, hydroxy(Ci-C4)alkyl, (Ci-C4)alkoxy, halo(Ci-C4)alkoxy, hydroxy, -NH2, -NH(Ci-C4)alkyl, -N((Ci-C4)alkyl)2, cycloalkyl, heterocyclyl, aryl, heteroaryl, and CN;each R2Ais independently selected from halo, (Ci-C4)alkyl, halo(Ci-C4)alkyl, hydroxy(Ci-C4)alkyl, deuterated(Ci-C4)alkyl, (Ci-C4)alkoxy, halo(Ci-C4)alkoxy, deuterated(Ci-C4)alkoxy, (Ci-C4)alkylene(Ci-C4)alkoxy, (Ci-C4)alkylene[deuterated(Ci-C4)alkoxy], (Ci-C4)alkylene[halo(Ci-C4)alkoxy], oxo, -Ofcycloalkyl], CN, hydroxy, S(O)(Ci-C4)alkyl, -S(O)2(Ci-C4)alkyl, hydroxy, cycloalkyl, heterocyclyl, aryl, heteroaryl, (Ci-C4)alkylene[cycloalkyl], (Ci-C4)alkylene[aryl], (Ci-C4)alkylene[heterocyclyl], (Ci-C4)alkylene[heteroaryl], -C(O)Ral, -C(O)ORal, -C(O)NRalRbl, -NRalC(O)Rbl, -NRalC(O)NRbl, wherein said heterocyclyl, aryl, heteroaryl, and cycloalkyl are each optionally substituted with 1 to 3 groups selected from halo, (Ci-C4)alkyl, halo(Ci-C4)alkyl, (Ci-C4)alkoxy, halo(Ci-C4)alkoxy, and CN;each Ra, Ral, Rb, and Rblis each independently selected from hydrogen, (Ci-C4)alkyl, halo(Ci-C4)alkyl, (Ci-C4)alkylene(Ci-C4)alkoxy, (Ci-C4)alkyleneNH2, (Ci-C4)alkyleneNH((Ci-C4alkyl), (Ci-C4)alkyleneN((Ci-C4alkyl)2, cycloalkyl, and heterocyclyl, wherein the cycloalkyl and heterocyclyl are each optionally substituted with (Ci-C4)alkyl, hydroxy, or hydroxy (Ci-C4)alkyl.2. Definitions

[0010] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure pertains. The terminology used in the description is for describing particular embodiments only and is not intended to be limiting of the disclosure.

[0011] As used in the structure herein a hyphen (-) or squiggly line “ “ indicates the point of attachment of the particular depicted structure or substituent group to the appropriate atom(s) in the remainder of the molecule.4ME1\58440953. vl139849-00420

[0012] The articles “a” and “an” as used herein and in the appended claims are used herein to refer to one or to more than one (e.g., to at least one) of the grammatical object of the article unless the context clearly indicates otherwise. By way of example, “an element” means one element or more than one element.

[0013] The term “alkyl,” when used alone or as part of a substituent group, refers to a straight- or branched-chain hydrocarbon group having from 1 to 12 carbon atoms (“C1-C12”), for example 1 to 6 carbons atoms (“Ci-Ce”), or 1 to 4 carbons atoms (“C1-C4”) in the group. Examples of alkyl groups include methyl (Ci), ethyl (C2), propyl (C3) (e.g., n-propyl, isopropyl), butyl (C4) (e.g., n-butyl, tert-butyl, sec-butyl, iso-butyl), pentyl (C5) (e.g., n-pentyl, 3-pentyl, amyl, neopentyl, 3-methyl-2-butanyl, tertiary amyl), hexyl (Ce) (e.g., n-hexyl), heptyl (C7) (e.g., n-heptyl), octyl (Cs) (e.g., n-octyl), and the like. In some embodiments, the alkyl group is a Ci-Cealkyl; in other embodiments, it is a Ci-C4alkyl; and in other embodiments, it is a Ci-Csalkyl.

[0014] As used herein, the term “alkenyl” refers to a straight- or branched-chain group having from 2 to 12 carbon atoms (“C2-C12”) in the group, wherein the group includes at least one carbon-carbon double bond. Examples of alkenyl groups include vinyl (-CH=CH2;C2alkenyl), allyl (-CH2-CH=CH2; Csalkenyl), propenyl (-CH=CHCH3; Csalkenyl), isopropenyl (-C(CH3)=CH2; Csalkenyl), butenyl (-CE^CElCEhCEE; C4alkenyl), sec-butenyl (-C(CH3)=CHCH3; C4alkenyl), iso-butenyl (-CH=C(CH3)2; C4alkenyl), 2-butenyl (-CH2CH=CHCH3; C4alkyl), pentenyl (-CE^CHCEECEECEE; Csalkenyl), and the like.

[0015] When a range of carbon atoms is used herein, for example, Ci-Ce, all ranges, as well as individual numbers of carbon atoms are encompassed. For example, “C1-C3” includes Cn C3, C1-C2, C2-C3, Ci, C2, and C3.

[0016] The term “cycloalkyl” when used alone or as part of a substituent group refers to cyclic-containing, saturated or partially unsaturated hydrocarbon groups having from 3 to 10 carbon atoms (“C3-C10”), for example from 3 to 7 carbon atoms (“C3-C7”). Examples of cycloalkyl groups include cyclopropyl (C3), cyclobutyl (C4), cyclopentyl (C5), cyclohexyl (Ce), cycloheptyl (C7), and the like. In some embodiments, the cycloalkyl group is a C3-4cycloalkyl; in other embodiments, it is a Cs-Cecycloalkyl; and in other embodiments, it is C3-Cscycloalkyl.

[0017] The term “alkylene” refers to a straight- or branched-chain group having from 2 to 12 carbon atoms (“C2-C12”) in the group which is further substituted by a separate group. Examples of alkylene include (Ci-C4)alkylene[heterocyclyl], which is a Ci-C4alkyl substituted with a heterocyclyl, (Ci-C4)alkylene[aryl], which is a Ci-C4alkyl substituted with 5ME1\58440953. vl139849-00420an aryl, (Ci-C4)alkylene[cycloalkyl], which is a Ci-C4alkyl substituted with a cycloalkyl, and (Ci-C4)alkylene[heteroaryl], which is a Ci-C4alkyl substituted with a heteroaryl.

[0018] The term “halo” or “halogen,” as used by itself or as part of another group refers to a fluorine, chlorine, bromine, or iodine atom.

[0019] As used herein, the term “haloalkyl” and “haloalkenyl” refer to an alkyl or alkenyl group, respectively, wherein one or more of the hydrogen atoms has been replaced with one or more halogen atoms which may be the same or different.

[0020] The term “alkoxy” as used by itself or as part of another group refers to an oxygen radical attached to an alkyl group by a single bond. Examples of alkoxyl groups include methoxy (OCH3), ethoxy (OCH2CH3), propoxy (e.g., -OnPr, -O'Pr), or butoxy (e.g., -OnBu, -O'Bu, -OsBu, -O’Bu), and the like. In other embodiments, the alkoxy group is a Ci-ealkoxy. In further embodiments, the alkoxy group is a Ci-4alkoxy. In further embodiments, the alkoxy group is a Ci-3alkoxy.

[0021] As used herein, the term “haloalkoxy” refers to an alkoxy group wherein one or more of the hydrogen atoms has been replaced with one or more halogen atoms which may be the same or different.

[0022] A “deuterated” alkyl or alkoxy group means that one or more hydrogen atoms is replaced with deuterium. The deuterium enrichment at any one of the sites where hydrogen has been replaced by deuterium is at least 50%, 75%, 85%, 90%, 95%, 98% or 99%.Deuterium enrichment is a mole percent and is obtained by dividing the number of deuterium atoms at all sites of enrichment with the number of hydrogen plus deuterium atoms at all of the sites of enrichment. For example, a compound with two deuterated methyl groups has a 98.0% enrichment when 98.0% of the hydrogen atoms on the two methyl groups have been replaced with deuterium.

[0023] The term “aryl” used alone or as part of a larger moiety refers to, unless otherwise specified, a 6- or 10-membered aromatic hydrocarbon ring. An aryl group may be mono- or bi-cyclic, e.g.,. phenyl or naphthyl.

[0024] The term “heteroaryl” used alone or as part of a larger moiety refers to, unless otherwise specified, a 5- to 12-membered aromatic radical containing 1-4 heteroatoms selected from N, O, and S. A heteroaryl group may be mono- or bi-cyclic. Monocyclic heteroaryl includes, for example, thienyl, furanyl, pyrrolyl, imidazolyl, pyrazolyl, triazolyl, tetrazolyl, oxazolyl, isoxazolyl, triazinyl, tetrazinyl, oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, etc. Bi-cyclic heteroaryls include groups in which a monocyclic heteroaryl ring is fused to one or more aryl or heteroaryl rings.6ME1\58440953. vl139849-00420Nonlimiting examples include indolyl, imidazopyridinyl, benzooxazolyl, benzooxodi azolyl, indazolyl, benzimidazolyl, benzthiazolyl, quinolyl, quinazolinyl, quinoxalinyl, pyrrolopyridinyl, pyrrolopyrimidinyl, pyrazolopyridinyl, thienopyridinyl, thienopyrimidinyl, indolizinyl, purinyl, naphthyridinyl, and pteridinyl. It will be understood that when specified, optional substituents on a heteroaryl group may be present on any substitutable position.

[0025] The term “heterocyclyl” means, unless otherwise specified, a 5- to 12-membered saturated or partially unsaturated heterocyclic ring containing 1 to 4 heteroatoms independently selected from N, O, and S. It can be monocyclic, bicyclic (e.g., a bridged, fused, or spiro bicyclic ring), or tricyclic. A heterocyclyl ring can be attached to its pendant group at any heteroatom or carbon atom that results in a stable structure. Examples of such saturated or partially unsaturated heterocyclic radicals include, without limitation, tetrahydrofuranyl, tetrahydrothienyl, terahydropyranyl, pyrrolidinyl, pyridinonyl, pyrrolidonyl, piperidinyl, oxazolidinyl, piperazinyl, dioxanyl, dioxolanyl, morpholinyl, dihydrofuranyl, dihydropyranyl, dihydropyridinyl, tetrahydropyridinyl, dihydropyrimidinyl, oxetanyl, azetidinyl and tetrahydropyrimidinyl. A heterocyclyl group may be mono- or bicyclic. The term “heterocyclyl” also includes, e.g., unsaturated heterocyclic radicals fused to another unsaturated heterocyclic radical or aryl or heteroaryl ring, such as for example, tetrahydronaphthyridine, indolinone, dihydropyrrolotriazole, imidazopyrimidine, quinolinone, dioxaspirodecane. It will also be understood that when specified, optional substituents on a heterocyclyl group may be present on any substitutable position.

[0026] The term “spiro” refers to two rings that shares one ring atom (e.g., carbon).

[0027] The term “fused” refers to two rings that share two adjacent ring atoms with one another.

[0028] The term “bridged” refers to two rings that share three ring atoms with one another.

[0029] The term “optionally substituted,” as used herein to describe a chemical moiety defined herein, means that the moiety may, but is not required to be, substituted with one or more suitable functional groups or other substituents as provided herein.

[0030] As used herein, the term “oxo” refers to a “=O” functional group.

[0031] As used herein, the term “substituted” means that an atom or group of atoms has replaced hydrogen as the substituent attached to another group.

[0032] The term “about” when used in combination with a numeric value or range of values means the value or range of values may deviate to an extent deemed reasonable to one of ordinary skill in the art.7ME1\58440953. vl139849-00420

[0033] Compounds described herein can comprise one or more asymmetric centers, and thus can exist in various stereoisomeric forms, e.g., enantiomers and / or diastereomers. For example, the compounds described herein can be in the form of an individual enantiomer, diastereomer or geometric isomer, or can be in the form of a mixture of stereoisomers, including racemic mixtures and mixtures enriched in one or more stereoisomer. Isomers can be isolated from mixtures by methods known to those skilled in the art, including supercritical fluid chromatography (SFC), chiral high-pressure liquid chromatography (HPLC) and the formation and crystallization of chiral salts; or preferred isomers can be prepared by asymmetric syntheses. See, for example, Jacques et al., Enantiomers, Racemates and Resolutions (Wiley Interscience, New York, 1981); Wilen et al., Tetrahedron 33:2725 (1977); Eliel, E. L. Stereochemistry of Carbon Compounds (McGraw-Hill, NY, 1962); and Wilen, S. H. Tables of Resolving Agents and Optical Resolutions p. 268 (E. L. Eliel, Ed., Univ, of Notre Dame Press, Notre Dame, IN 1972).

[0034] Exemplary compounds of the disclosure including a chiral center may be depicted herein as having particular stereochemistries, but for which absolute stereochemistry has not been obtained. Absolute configurations can be obtained using methods known in the art.

[0035] As used herein, the term “stereoisomers” refers to compounds which have identical chemical constitution and connectivity but differ with regard to the arrangement of the atoms or groups in space, e.g., enantiomers or diastereomers.

[0036] As discussed in more detail below, the enantiomers of certain compounds were resolved. Unless otherwise noted, the enantiomer which showed a greater potency in the DLD-1 cell viability and immunofluorescence assays was arbitrarly assigned the “R” stereochemistry, and the less potent enantiomer was arbitrarly assigned the “S” stereochemistry. The absolute configuration of the enantiomers can be verified by means known to those in the art such as by NMR and / or X-ray crystallography. Nonetheless, when the stereochemical configuration at a chiral center in a compound having one or more chiral centers is depicted by its chemical name (e.g., where the configuration is indicated in the chemical name by “R” or “S”) or structure (e.g., the configuration is indicated by dashed or wedge bonds), the enrichment of the indicated configuration relative to the opposite configuration is greater than 50%, 60%, 70%, 80%, 90%, 99% or 99.9%, preferably greater than 90%. “Enrichment of the indicated configuration relative to the opposite configuration” is a mole percent and is determined by dividing the number of compounds with the indicated stereochemical configuration at the chiral center(s) by the total number of all of the compounds with the same or opposite stereochemical configuration in a mixture.8ME1\58440953. vl139849-00420

[0037] When a disclosed compound is named or depicted by structure without indicating stereochemistry, it is understood that the name or the structure encompasses one of the possible stereoisomers or geometric isomers free of the others, or a mixture of the encompassed stereoisomers or geometric isomers.

[0038] It will be understood that certain compounds disclosed herein may exist in tautomeric forms. Such forms are included as part of the present disclosure. Thus, when a compound herein is represented by a structural formula or designated by a chemical name herein, all tautomeric forms which may exist for the compound are encompassed by the structural formula.

[0039] When the compounds described herein contain olefinic double bonds or other centers of geometric asymmetry, and unless specified otherwise, it is intended that they include both E and Z geometric isomers.

[0040] The terms “subject” and “patient” may be used interchangeably, and means a mammal in need of treatment, e.g., companion animals (e.g., dogs, cats, and the like), farm animals (e.g., cows, pigs, horses, sheep, goats and the like) and laboratory animals (e.g., rats, mice, guinea pigs and the like). Typically, the subject is a human in need of treatment.

[0041] The term “inhibit,” “inhibition” or “inhibiting” includes a decrease in the baseline activity of a biological activity or process.

[0042] As used herein, the terms “treatment,” “treat,” and “treating” refer to reversing, alleviating, delaying the onset of, or inhibiting the progress of a disease or disorder, or one or more symptoms thereof, as described herein. In some aspects, treatment may be administered after one or more symptoms have developed, z.e., therapeutic treatment. In other aspects, treatment may be administered in the absence of symptoms. For example, treatment may be administered to a susceptible individual prior to the onset of symptoms (e.g., in light of a history of symptoms and / or in light of exposure to a particular organism, or other susceptibility factors), z.e., prophylactic treatment. Treatment may also be continued after symptoms have resolved, for example to delay their recurrence.

[0043] The term “pharmaceutically acceptable carrier” refers to a non-toxic 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 described herein include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, serum proteins, such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine 9ME1\58440953. vl139849-00420sulfate, 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-polyoxypropylene-block polymers, polyethylene glycol and wool fat.

[0044] For use in medicines, the salts of the compounds described herein refer to non-toxic “pharmaceutically acceptable salts.” Pharmaceutically acceptable salt forms include pharmaceutically acceptable acidic / anionic or basic / cationic salts. Suitable pharmaceutically acceptable acid addition salts of the compounds described herein include e.g., salts of inorganic acids (such as hydrochloric acid, hydrobromic, phosphoric, nitric, and sulfuric acids) and of organic acids (such as, acetic acid, benzenesulfonic, benzoic, methanesulfonic, and p-toluenesulfonic acids). Compounds of the present teachings with acidic groups such as carboxylic acids can form pharmaceutically acceptable salts with pharmaceutically acceptable base(s). Suitable pharmaceutically acceptable basic salts include e.g., ammonium salts, alkali metal salts (such as sodium and potassium salts) and alkaline earth metal salts (such as magnesium and calcium salts). Compounds with a quaternary ammonium group also contain a counteranion such as chloride, bromide, iodide, acetate, perchlorate and the like. Other examples of such salts include hydrochlorides, hydrobromides, sulfates, methanesulfonates, nitrates, benzoates and salts with amino acids such as glutamic acid.

[0045] In some embodiments, the pharmaceutically acceptable salt of a compound described herein is a mono or di-sodium salt e.g., when R1is (Ci-C4)alkylene[OP(O)(OH)2].

[0046] “Pharmaceutically acceptable” means approved or approvable by a regulatory agency of the Federal or a state government or the corresponding agency in a country other than the United States, or that is listed in the U. S. Pharmacopoeia or other generally recognized pharmacopoeia for use in animals, e.g., in humans.

[0047] The term “effective amount” or “therapeutically effective amount” refers to an amount of a compound described herein that is sufficient to achieve the desired therapeutic effect (such as treatment of a condition recited herein) under the conditions of administration.

[0048] The use of any and all examples, or exemplary language (e.g., “such as” and “e.g.”) provided herein, is intended to better illustrate the disclosure and is not a limitation on the scope of the disclosure unless otherwise claimed. Phrases such as “in one aspect”, “in one embodiment”, “in another aspect”, “in another embodiment”, “in embodiments”, and the like should not be construed as indicating that such elements occur or exist in isolation or that such elements are not shared by other aspects or embodiments of the disclosure. Rather, it should be understood that all aspects and embodiments may be freely combined with any and 10ME1\58440953. vl139849-00420all other aspects and embodiments of the disclosure as described herein. No language in the specification should be construed as indicating that any non-claimed element is essential to the practice of the disclosure.3. Compounds

[0049] As part of a second embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, R1is hydrogen or (Ci-C4)alkylene[OP(O)(OH)2], and wherein the remaining variables are as described above for Formula I. Alternatively, as part of the second embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, R1is hydrogen, and wherein the remaining variables are as described above for Formula I.

[0050] As part of a third embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, R3is hydrogen, -CH3, or -CH2OCH3, and wherein the remaining variables are as described above for Formula I or the second embodiment. Alternatively, as part of the third embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, R3is hydrogen, and wherein the remaining variables are as described above for Formula I or the second embodiment.

[0051] As part of a fourth embodiment, for the compounds of Formula I, or apharmaceutically acceptable salt thereof, R4is -CH3, -CF3, -CH2F, -CHF2, -OCH3, or and wherein the remaining variables are as described above for Formula I or the second or third embodiment. Alternatively, as part of the fourth embodiment, for the compounds ofFormula I, or a pharmaceutically acceptable salt thereof, R4is -CH3 'vrvv', and wherein the remaining variables are as described above for Formula I or the second or third embodiment.

[0052] As part of a fifth embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, X is O and R4is hydrogen, and wherein the remaining variables are as described above for Formula I or the second or third embodiment.

[0053] As part of a sixth embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, R2is aryl, heteroaryl, or heterocyclyl, each of which are optionally substituted with 1 to 3 groups selected from R1A, and wherein the remaining variables are as described above for Formula I or any one of the second to fifth embodiments. Alternatively, as part of the sixth embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, R2is phenyl, pyridinyl, pyrimidyl, pyrazinyl,11ME1\58440953. vl139849-00420benzimidazolyl, pyrazolyl, or dihydrobenzooxazolyl, each of which is optionally substituted with 1 to 3 groups selected from R1A, and wherein the remaining variables are as described above for Formula I or any one of the second to fifth embodiments. Alternatively, as part of the sixth embodiment, for the compounds of Formula I, or a pharmaceutically acceptable saltthereof, R2is:or, each of which is optionally substituted with 1 to 3 groups selected from R1A, and wherein the remaining variables are as described above for Formula I or any one of the second to fifth embodiments. Alternatively, as part of the sixth embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, R2is:and wherein the remaining variables are as described above for Formula I or any one of the second to fifth embodiments.

[0054] As part of a seventh embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, each R1Ais independently halo, (Ci-C4)alkyl, halo(Ci-C4)alkyl, hydroxy(Ci-C4)alkyl, (Ci-C4)alkyleneNRaRb, cyano, hydroxy, (Ci-C4)alkoxy, deuterated(Ci-C4)alkoxy, halo(Ci-C4)alkoxy, -O[hydroxy(Ci-C4)alkyl], (Ci-C4)alkoxyO(Ci-C4)alkyl, -O(Ci-C4)alkylene[NRaRb], -O(Ci-C4)alkylene[NRaC(O)Rb], -O [cycloalkyl], -O[heterocyclyl], -O(Ci-C4)alkylene[heterocyclyl], -NRaRb, -NRaC(O)Rb, -SRa, -S(O)(NRa)Rb, -C(O)NRaRb, or heterocyclyl, wherein the heterocyclyl is optionally substituted with hydroxy or hydroxy(Ci-C4)alkyl, and wherein the remaining variables are as described above for Formula I or any one of the second to sixth embodiments.12ME1\58440953. vl139849-00420

[0055] As part of an eighth embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, Raand Rbare each independently hydrogen, (Ci-C4)alkyl, (Ci-C4)alkylene(Ci-C4)alkoxy, (Ci-C4)alkyleneNH2, or heterocyclyl, and wherein the remaining variables are as described above for Formula I or any one of the second to seventh embodiments.

[0056] As part of a ninth embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, each R1Ais independently -F, -Cl, -CH3, -CF3, -CH2OH, -CH2CH2CH2NH2, CN, hydroxy, -OCH3, -OCD3, -OCHF2, -OCF3, -OCH2CH3, -OCH(CH3)2, -OCH2CH2OH, -OCH2CH2OCH3, -OCH2CH2NH2, -OCH2CH2N(CH3)2, -OCH2CH2CH2NH2, -OCH2CH2CH2NHC(O)CH3, -OCH2CH2CH2CH2NH2, -OCH2CH2CH2CH2N(CH3)2, -NH2, -N(CH3), -N(CH3)CH2CH2OCH3, -NHCH2CH2OCH3, -NHCH2CH2CH2NH2, -NHCH2CH2CH2CH2NH2, -NHC(O)CH3, -SCH2CH2CH2NH2, -above for Formula I or any one of the second to eighth embodiments.

[0057] As part of a tenth embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, X is -OR6, and wherein the remaining variables are as described above for Formula I or any one of the second to ninth embodiments.

[0058] As part of an eleventh embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, R6is (Ci-C4)alkylene(Ci-C4alkoxy), (Ci-C4)alkylene[aryl], or (Ci-C4)alkylene[heteroaryl], wherein the aryl is substituted by R2A, and the heteroaryl is pyridinyl, oxazolyl, pyrazolyl, imidazolyl, triazolyl, or oxadiazolyl, each of which is optionally substituted by R2A, and wherein the remaining variables are as described above for Formula I or any one of the second to tenth embodiments. Alternatively, as part of the eleventh embodiment, for the compounds of Formula I, or a pharmaceutically acceptable R2Asalt thereof, R6is -CH2CH2OCH3, -CH2CH2CH2OCH3,13ME1\58440953. vl139849-00420R2Aor and wherein the remaining variables are as described above for Formula I or any one of the second to tenth embodiments.

[0059] As part of a twelfth embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, each R2Ais independently (Ci-C4)alkyl, halo(Ci-C4)alkyl, or (Ci-C4)alkoxy, and wherein the remaining variables are as described above for Formula I or any one of the second to eleventh embodiments. Alternatively, as part of the twelfth embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, each R2Ais independently -CH3, -CF3, -OCH3, and wherein the remaining variables are as described above for Formula I or any one of the second to eleventh embodiments.

[0060] As part of a thirteenth embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, X is -NR7R8, and wherein the remaining variables are as described above for Formula I or any one of the second to ninth embodiments.

[0061] As part of a fourteenth embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, R7is H and R8is cyclobutyl, oxetanyl, (Ci-C4)alkylene[aryl], or (Ci-C4)alkylene[heteroaryl], wherein the heteroaryl is oxazolyl, and wherein the cyclobutyl is optionally substituted by R2A, and wherein the remaining variables are as described above for Formula I or any one of the second to ninth or thirteenth embodiments. Alternatively, as part of the fourteenth embodiment, for the compounds ofFormula I, or a pharmaceutically acceptable salt thereof, R7is H and R8is:or, wherein the cyclobutyl is optionally substituted by 1 R2A, and wherein the cyclobutyl is optionally substituted by R2A, and wherein the remaining variables are as described above for Formula I or any one of the second to ninth or thirteenth embodiments. Alternatively, as part of the fourteenth embodiment, for the compounds ofFormula I, or a pharmaceutically acceptable salt thereof, R7is H and R8is:and wherein the remaining variables are as described 14ME1\58440953. vl139849-00420above for Formula I or any one of the second to ninth or thirteenth embodiments.Alternatively, as part of the fourteenth embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, R7and R8are taken together to form heterocyclyl optionally substituted with 1 or 3 R2A, and wherein the remaining variables are as described above for Formula I or any one of the second to ninth or thirteenth embodiments.Alternatively, as part of the fourteenth embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, R7and R8are taken together to form azetidinyl, pyrrolidinyl, azabicyclohexanyl, azaspiroheptanyl, oxaazaspiroheptanyl, oxaazaspirooctanyl, or oxadiazaspirononanyl, each of which is optionally substituted with 1 or 2 R2A, and wherein the remaining variables are as described above for Formula I or any one of the second to ninth or thirteenth embodiments. Alternatively, as part of the fourteenth embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof,optionally substituted with 1 or 2 R2A, and wherein the remaining variables are as described above for Formula I or any one of the second to ninth or thirteenth embodiments.Alternatively, as part of the fourteenth embodiment, for the compounds of Formula I, or apharmaceutically acceptable salt thereof, R and R are taken together to form: 4«-N^v>,and wherein the remaining variables are as described above for Formula I or any one of the second to ninth or thirteenth embodiments.

[0062] As part of a fifteenth embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, each R2Ais independently halo, (Ci-C4)alkyl, halo(Ci-C4)alkyl, (Ci-C4)alkylene(Ci-C4)alkoxy, (Ci-C4)alkylene[deuterated(Ci-C4)alkoxy], (Ci-C4)alkylene[halo(Ci-C4)alkoxy], hydroxy, (Ci-C4)alkoxy, halo(Ci-C4)alkoxy, deuterated(Ci-C4)alkoxy, -Ofcycloalkyl], cyano, -S(O)2(Ci-C4)alkyl, aryl, or heteroaryl, wherein the heteroaryl is optionally substituted with (Ci-C4)alkyl or (Ci-C4)alkoxy, and 15ME1\58440953. vl139849-00420wherein the remaining variables are as described above for Formula I or any one of the second to ninth, thirteenth, or fourteenth embodiments. Alternatively, as part of the fifteenth embodiment, for the compounds of Formula I, or a pharmaceutically acceptable salt thereof, each R2Aindependently is -F, -CH3, -CHF2, -CF3, -CF2CH3, -CH2OCH3, -CH2OCD3, -CH(CH3)OCH3, -C(CH3)2OCH3, -CH2OCF3, hydroxy, -OCH3, -OCD3, -OCHF2,NN, and wherein the remaining variables are as described above for Formula I or any one of the second to ninth, thirteenth, or fourteenth embodiments.

[0063] As part of a sixteenth embodiment, the compounds of Formula I have the structural Formula II:X I1I AN)H-X0(ii);or a pharmaceutically acceptable salt thereof, wherein:one of X1or X2is N, and the other is CH;n is 1 or 2;each R1Ais independently halo, (Ci-C4)alkyl, halo(Ci-C4)alkyl, (Ci-C4)alkoxy, deuterated(Ci-C4)alkoxy, halo(Ci-C4)alkoxy, or -Ofcycloalkyl];X is -OR6;R6is (Ci-C3)alkylene[heteroaryl], wherein the heteroaryl is optionally substituted with 1 to 3 groups selected from R2A, and wherein the remaining variables are as described above for Formula I.

[0064] As part of a seventeenth embodiment, for the compounds of Formula II, or a pharmaceutically acceptable salt thereof, X1is N and X2is CH, and wherein the remaining variables are as described above for Formula II.

[0065] As part of an eighteenth embodiment, for the compounds of Formula I or II, or a pharmaceutically acceptable salt thereof, each R1Ais independently -Cl, -CH3, -CF3, -OCH3, -16ME1\58440953. vl139849-00420OCH2CH3, -OCH(CH3)2, -O-cyclopropyl, -OCHF2, -OCF3, or -OCD3, and wherein the remaining variables are as described above for Formula I or II or the sixteenth or seventeenth embodiment. Alternatively, as part of the eighteenth embodiment, for the compounds of Formula I or II, or a pharmaceutically acceptable salt thereof, each R1Ais independently (Ci-C4)alkoxy, and wherein the remaining variables are as described above for Formula I or II or the sixteenth or seventeenth embodiment.

[0066] As part of a nineteenth embodiment, for the compounds of Formula I or II, or a pharmaceutically acceptable salt thereof, n is 1, and wherein the remaining variables are as described above for Formula I or II or any one of the sixteenth to eighteenth embodiments.

[0067] As part of a twentieth embodiment, for the compounds of Formula I or II, or a pharmaceutically acceptable salt thereof, R6is (Ci-C3)alkylene[5- to 6-membered heteroaryl], wherein the 5- to 6-membered heteroaryl is optionally substituted with 1 to 3 groups selected from R2A, and wherein the remaining variables are as described above for Formula I or II or any one of the sixteenth to nineteenth embodiments. Alternatively, as part of the twentieth embodiment, for the compounds of Formula I or II, or a pharmaceutically acceptable salt thereof, R6is (Ci-C3)alkylene[oxazolyl], wherein the oxazolyl is optionally substituted with 1 to 3 groups selected from R2A, and wherein the remaining variables are as described above for Formula I or II or any one of the sixteenth to nineteenth embodiments.

[0068] As part of a twenty -first embodiment, for the compounds of Formula I or II, or a pharmaceutically acceptable salt thereof, each R2Ais independently (Ci-C4)alkyl or halo(Ci-C4)alkyl, and wherein the remaining variables are as described above for Formula I or II or any one of the sixteenth to twentieth embodiments.

[0069] As part of a twenty-second embodiment, for the compounds of Formula I or II, or a pharmaceutically acceptable salt thereof, R6is -CH2[oxazole-2-yl], and wherein the remaining variables are as described above for Formula I or II or any one of the sixteenth to twenty-first embodiments.

[0070] As part of a twenty-third embodiment, the compounds of Formula I or II have the structural Formula III:S<r17ME1\58440953. vl139849-00420or a pharmaceutically acceptable salt thereof, and wherein the remaining variables are as described above for Formula I or II or any one of the sixteenth to twenty-second embodiments.

[0071] As part of a twenty-fourth embodiment, the compounds of Formula I, II, or III have the structural Formula Illa:R1Av|l / >-NHN ^-XO (Illa);or a pharmaceutically acceptable salt thereof, and wherein the remaining variables are as described above for Formula I, II, or III or any one of the sixteenth to twenty -third embodiments.

[0072] As part of a twenty -fifth embodiment, the for the compounds of Formula I, II, III, or Illa, or a pharmaceutically acceptable salt thereof, R1Ais -OCH3, and wherein the remaining variables are as described above for Formula I, II, III, or Illa, or any one of the sixteenth to twenty -fourth embodiments.

[0073] As part of the twenty-sixth embodiment, the compounds of Formula I is any one of Examples 1 to 164, or a pharmaceutically acceptable salt thereof.

[0074] Additional compounds are described and exemplified herein, and are included in the present disclosure. Pharmaceutically acceptable salts thereof as well as the neutral forms of such compounds are included.4. Uses, Formulation and Administration

[0075] The compounds and compositions described herein are generally useful for modulating the activity of beta catenin. In some aspects, the compounds, pharmaceutical acceptable salts, and pharmaceutical compositions described herein sequester beta catenin in nuclear condensates. In some aspects, the compounds, pharmaceutical acceptable salts, and pharmaceutical compositions described herein modulate beta catenin condensates.

[0076] In some aspects, the compounds and pharmaceutical compositions described herein are useful in treating a disease or condition associated with beta catenin function. Thus, provided herein are methods of treating a disease or condition associated with beta catenin function, comprising administering to a subject in need thereof, a therapeutically effective amount of a compound described herein, or a pharmaceutically acceptable salt thereof, or a 18ME1\58440953. vl139849-00420pharmaceutical composition comprising a disclosed compound or pharmaceutically acceptable salt thereof. In some aspects, the compounds and pharmaceutical compositions described herein are useful in treating a disease or condition associated with the modulation of beta catenin condensates. Thus, provided herein are methods of treating a disease or condition associated with the modulation of beta catenin condensates, comprising administering to a subject in need thereof, a therapeutically effective amount of a compound described herein, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition comprising a disclosed compound or pharmaceutically acceptable salt thereof.

[0077] Also provided is the use of a compound described herein, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition comprising a disclosed compound or pharmaceutically acceptable salt thereof, for the manufacture of a medicament for treating a disease or condition associated with beta catenin function. Also provided is a compound described herein, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition comprising a disclosed compound or pharmaceutically acceptable salt thereof, for use in treating a disease or condition associated with beta catenin. Also provided is the use of a compound described herein, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition comprising a disclosed compound or pharmaceutically acceptable salt thereof, for the manufacture of a medicament for treating a disease or condition associated with the modulation of beta catenin condensates. Also provided is a compound described herein, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition comprising a disclosed compound or pharmaceutically acceptable salt thereof, for use in treating a disease or condition associated with the modulation of beta catenin condensates.

[0078] In one aspect, the disease or condition associated with beta catenin or the modulation of beta catenin condensates is cancer. In embodiments, the cancer is bladder cancer, breast cancer, colorectal cancer, endometrial cancer, gastric cancer, head and neck cancer, leukemia, liver cancer, lung cancer, ovarian cancer, pancreatic cancer, or a solid tumor. In embodiments, the breast cancer is triple negative breast cancer. In embodiments, the leukemia is chronic lymphocytic leukemia or acute myeloid leukemia. In embodiments, the lung cancer is non-small cell lung cancer.

[0079] In some aspects, the compounds, pharmaceutical acceptable salts, and pharmaceutical compositions described herein modulate the function of beta catenin. In some aspects, modulating beta catenin comprises modulating beta catenin partitioning into condensates. In some aspects, modulating beta catenin comprises modulating transcription of 19ME1\58440953. vl139849-00420beta catenin-dependent genes. In some aspects, modulating beta catenin comprises modulating beta catenin association with chromatin. In some aspects, modulating beta catenin comprises modulating beta catenin interaction network. In some aspects, modulating beta catenin comprises modulating beta catenin posttranscriptional modification status. In some aspects, modulating beta catenin comprises modulating direct and indirect regulators of beta catenin and the WNT pathway. In some aspects, modulating beta catenin comprises modulating the cell cycle.

[0080] In certain aspects, a pharmaceutical composition described herein is formulated for administration to a patient in need of such composition. Pharmaceutical compositions described herein may be administered orally, parenterally, by inhalation spray, topically, rectally, nasally, buccally, vaginally or via an implanted reservoir. 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 some embodiments, the compositions are administered orally, intraperitoneally or intravenously. Sterile injectable forms of the pharmaceutical compositions described herein 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.

[0081] In some aspects, the pharmaceutical compositions are administered orally.

[0082] A specific dosage and treatment regimen for any particular patient will depend upon a variety of factors, including the activity of the specific compound employed, the age, body weight, general health, sex, diet, time of administration, rate of excretion, drug combination, and the judgment of the treating physician and the severity of the particular disease being treated. The amount of a compound described herein in the composition will also depend upon the particular compound in the pharmaceutical composition.EXEMPLIFICATION

[0083] While there is described herein a number of embodiments, it is apparent that the basic examples may be altered to provide other embodiments that utilize the compounds and methods of this invention. Therefore, it will be appreciated that the scope of this invention is to be defined by the appended claims rather than by the specific embodiments that have been represented by way of example.

[0084] The contents of all references (including literature references, issued patents, published patent applications, and co-pending patent applications) cited throughout this 20ME1\58440953. vl139849-00420application are hereby expressly incorporated herein in their entireties by reference. Unless otherwise defined, all technical and scientific terms used herein are accorded the meaning commonly known to one with ordinary skill in the art.

[0085] Intermediate synthesis

[0086] l-( 6-(Trifluoromethoxy)pyridin-3-yl)ethan-l-one

[0087] Step 1

[0088] Pd(PPh3)2Ch (1.02 g, 1.45 mmol) was added to a solution of tributyl(l- ethoxyvinyl)stannane (7.84 g, 21.7 mmol) and 5-bromo-2-(trifluoromethoxy)pyridine (3.50 g, 14.5 mmol) in DMF (30 mL). The resulting mixture was stirred at 100 °C for 16 h. Saturated aqueous potassium fluoride solution (40 mL) was added and the mixture was extracted into EtOAc (3 x 40 mL). The combined organic extracts were washed with brine (2 x 20 mL), dried over anhydrous sodium sulfate and concentrated in vacuo to afford 5 -(1 -ethoxy vinyl)-2- (trifluoromethoxy)pyridine (3 g, crude) as a yellow oil.

[0089] Step 2

[0090] Aqueous hydrochloric acid (2.0 M, 32.2 mL, 64.2 mmol) was added to a solution of 5-(l-ethoxyvinyl)-2-(trifluoromethoxy)pyridine (3 g crude from step 1) in THF (30 mL) and the resulting mixture was stirred at 20 °C for 2 h. Saturated aqueous sodium bicarbonate solution (100 mL) was added and the mixture was extracted into EtOAc (2 * 50 mL). The combined organic extracts were dried over anhydrous sodium sulfate and concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 1:5) afforded l-(6-(trifluoromethoxy)pyridin-3-yl)ethan-l-one (2.60 g, 88% over two steps) as a yellow oil; ES-MS [M+H]+: 206.2.

[0091] The following intermediate was prepared in an analogous manner. All intermediates are commercially available unless noted.IntermediatesName Structure ES-MS [M+H]+requiring synthesis21ME1\58440953. vl139849-00420

[0093] Diethyl (bromodifluoromethyl)phosphonate (50.2 g, 188 mmol) was added to a solution of 5-bromopyrimidin-2-ol (25.0 g, 143 mmol) and potassium fluoride (25.0 g, 430 mmol) in acetonitrile (250 mL). The reaction mixture was stirred at 25 °C for 12 h, then diluted with water (500 mL) and extracted into EtOAc (2 x 500 mL). The combined organic extracts were washed with brine (500 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by flash column chromatography on silica (THF: PE, 0:1 to 1:4) afforded 5-bromo-2-(difluoromethoxy)pyrimidine (6.50 g, 28.9 mmol) as a yellow oil; ES-MS [M+H]+: 227.0.

[0094] l-( 6-(Methoxy-d3)pyridin-3-yl)ethan-l-oneO O

[0095] Iodomethane-d3 (15.9 g, 109 mmol) was added to a solution of l-(6- hydroxypyridin-3-yl)ethan-l-one (10.0 g, 72.9 mmol) and silver oxide (33.8 g, 146 mmol) in acetonitrile (100 mL). The resulting mixture was stirred at 80 °C for 2 h, then filtered and concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 1:4) afforded l-(6-(methoxy-d3)pyridin-3-yl)ethan-l-one (4.20 g, 37%) as a white solid; ES-MS [M+H]+: 155.3.

[0096] l-( 6-Methoxy-5-(trifluoromethyl)pyridin-3-yl)ethan-l-one

[0097] Step 1o o22ME1\58440953. vl139849-00420

[0098] Methoxy(methyl)amine hydrochloride (2.51 g, 25.8 mmol) was added to a solution of 6-methoxy-5-(trifluoromethyl)nicotinic acid (3.80 g, 17.2 mmol) and HATU (9.80 g, 25.8 mmol) in DMF (30 mL). The reaction mixture was stirred at 25 °C for 1 h, then diluted with water (100 mL) and extracted into EtOAc (3 x 100 mL). The combined organic extracts were washed with brine (2 x 200 mL), dried over anhydrous sodium sulfate and concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 35:65) afforded N,6-dimethoxy-N-methyl-5-(trifluoromethyl)nicotinamide (5.60 g, 81%) as a yellow oil; ES-MS [M+H]+: 265.0.

[0099] Step 2o o

[0100] Methylmagnesium bromide (3.0 M in THF, 10.6 mL, 31.8 mmol) was added to a solution of N,6-dimethoxy-N-methyl-5-(trifluoromethyl)nicotinamide (5.60 g, 21.2 mmol) in THF (100 mL) at 0 °C. The reaction mixture was stirred at 0 °C for 1 h, then quenched by addition of saturated aqueous ammonium chloride solution (100 mL) and extracted into EtOAc (3 x 100 mL). The combined organic extracts were dried over anhydrous sodium sulfate and concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 1:4) afforded l-(6-methoxy-5-(trifluoromethyl)pyridin-3-yl)ethan-l-one (4.0 g, 84%) as a white solid; ES-MS [M+H]+: 220.0.

[0101] The following intermediate was prepared in an analogous manner:Name Structure Starting materials 'll NMRStep 1: oxetane-3- 8H(400 MHZ; CDC13); 7.75 carboxylic acid(4-chlorophenyl)(oxetan-3 - (2H, d, J 8.5 Hz), 7.48 (2H,ti n Step 2: 4- yl)methanone d, J 8.5 Hz), 5.05-4.93 (4H,0 chlorophenylmagnesiumm), 4.72-4.52 (1H, m) bromide

[0102] l-( 6-Methoxy-4-methylpyridin-3-yl)ethan-l-one

[0103] Step 123ME1\58440953. vl139849-00420

[0104] Pd(PPh3)2C12 (625 mg, 0.89 mmol) was added to a solution of 5-bromo-2-methoxy-4-methylpyridine (9.00 g, 44.5 mmol), butyl vinyl ether (5.80 g, 57.9 mmol) and potassium carbonate (18.5 g, 133.6 mmol) in DMF (100 mL) and water (5 mL). The resulting mixture was stirred at 100 °C for 12 h. Water (150 mL) was added and the mixture was extracted into EtOAc (3 x 50 mL). The combined organic extracts were washed with brine (50 mL), dried over anhydrous sodium sulfate and concentrated in vacuo to afford 5-(l-butoxyvinyl)-2-methoxy-4-methylpyridine (9.20 g, crude) as a yellow oil.

[0105] Step 2MeO^N MeO^N■ VY

[0106] Aqueous hydrochloric acid (3.0 M, 50.0 mL, 150 mmol) was added to a solution of 5-(l-butoxyvinyl)-2-methoxy-4-methylpyridine (9.20 g crude from step 1) in THF (50 mL) and the resulting mixture was stirred at 25 °C for 2 h. Saturated aqueous sodium carbonate solution (100 mL) was added and the mixture was extracted into EtOAc (3 x 50 mL). The combined organic extracts were dried over anhydrous sodium sulfate and concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 10:1) afforded l-(6-methoxy-4-methylpyridin-3-yl)ethan-l-one (3.70 g, 54% over two steps) as a yellow solid; 5H (400 MHZ; CDC13); 8.66 (1H, s), 6.59 (1H, s), 3.98 (3H, s), 2.58 (3H, s), 2.55 (3H, s).

[0107] (4-(Trifluoromethyl)oxazol-2-yl)methanol

[0108] Borane tetrahydrofuran complex (1.0 M in THF, 3.31 mL, 3.31 mmol) was added to a solution of 4-(trifluoromethyl)oxazole-2-carboxylic acid (200 mg, 1.10 mmol) in THF (2 mL) at 0 °C and the resulting mixture was stirred at 25 °C for 16 h. Water (2 mL) was added at 0 °C and the mixture was extracted into EtOAc (3 x 10 mL). The combined organic extracts were washed with brine (10 mL), dried over anhydrous sodium sulfate and concentrated in vacuo to afford (4-(trifluoromethyl)oxazol-2-yl)methanol (130 mg, 70%) as a white solid; 5H (400 MHZ; CDCI3); 8.00 (1H, m), 4.81 (2H, m).

[0109] l-(Oxazol-2-yl)propan-l-ol24ME1\58440953. vl139849-004200EtONHO0-3

[0110] Ethylmagnesium bromide (3.0 in Et2O, 13.2 mL, 39.6 mmol) was added dropwise to a solution of ethyl oxazole-2-carboxylate (2.00 g, 14.2 mmol) and titanium(IV) isopropoxide (5.86 mL, 19.8 mmol) in THF (90 mL) at 0 °C. The resulting mixture was stirred at 25 °C for 16 h. Water (30 mL) was added and precipitates were removed by filtration. The filtrate was extracted into EtOAc (3 x 40 mL). The combined organic extracts were washed with brine (40 mL), dried over anhydrous sodium sulfate and concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 1:0) afforded l-(oxazol-2-yl)propan-l-ol (370 mg, 2.91 mmol) as an orange oil; 5H (400 MHz; DMSO-d6) 8.02 (1H, s), 7.14 (1H, s), 5.64 (1H, m), 4.51 (1H, m), 1.86-1.69 (2H, m), 0.84 (3H, m).

[0111] (l-( (2-(Trimethylsilyl)ethoxy)methyl)-lH-l, 2, 4-triazol-3-yl)methanol

[0112] Step 1

[0113] A solution of ethyl 1H-1, 2, 4-triazole-3 -carboxylate (1.00 g, 7.09 mmol) in DMF (25 mL) was added dropwise to a suspension of sodium hydride (60% dispersion in oil, 340 mg, 8.50 mmol) in DMF (9 mL) at 0 °C and the resulting mixture was stirred at this temperature for 30 min. 2-(Trimethylsilyl)ethoxymethyl chloride (1.30 g, 7.79 mmol) was added at 0 °C and the reaction mixture was stirred at 25 °C for 1 h. Saturated aqueous ammonium chloride solution (50 mL) was added at 0 °C and the mixture was extracted into EtOAc (3 x 25 mL). The combined organic extracts were washed with brine (80 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 1:4) afforded ethyl l-((2-(trimethylsilyl)ethoxy)methyl)-lH-l,2,4-triazole-3-carboxylate as a colorless oil; 5H(400 MHz; CDC13); 8.01 (1H, s), 5.91 (2H, s), 4.49 (2H, m), 3.71-3.60 (2H, m), 1.45 (3H, m), 0.95-0.89 (2H, m), -0.03 (9H, s).

[0114] Step 2oN HOEtON'NSEMN'NSEM25ME1\58440953. vl139849-00420

[0115] Lithium borohydride (2.0 M in THF, 3.32 mL, 6.64 mmol) was added to a solution of ethyl l-((2-(trimethylsilyl)ethoxy)methyl)-lH-l,2,4-triazole-3-carboxylate (300 mg, 1.11 mmol) in THF (8 mL) at 0 °C and the resulting mixture was stirred at 20 °C for 2 h. Saturated aqueous ammonium chloride solution (50 mL) was added at 0 °C and the mixture was extracted into EtOAc (3 x 25 mL). The combined organic extracts were washed with brine (30 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo to afford (l-((2-(trimethylsilyl)ethoxy)methyl)-lH-l,2,4-triazol-3-yl)methanol as a colorless oil; 5H- (400 MHz; CDC13); 7.83 (1H, s), 5.56 (2H, s), 4.85 (2H, s), 3.64-3.58 (2H, m), 0.95-0.85 (2H, m), -0.03 (9H, s).

[0116] 3-(Azetidin-l-yl)-4-chlorobenzaldehyde

[0117] Azetidine hydrochloride (1.28 g, 13.7 mmol) was added to a mixture of 3-bromo- 4-chlorobenzaldehyde (2.00 g, 9.11 mmol), cesium carbonate (8.91 g, 27.3 mmol), Pd2(dba)s and BINAP (1.13 g, 1.82 mmol) in toluene (40 mL). The reaction mixture was stirred at 80 °C for 12 h, then diluted with water (20 mL) and extracted into EtOAc (2 x 20 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 1:10) afforded 3-(azetidin-l-yl)-4-chlorobenzaldehyde (1.40 g, 74%) as a yellow oil; ES-MS [M+H]+: 196.2.

[0118] The following intermediate was prepared in an analogous manner:Name Structure Starting material ES-MS [M+H]+Cbzbenzyl 4-(2-chloro-5- 0N benzyl piperazine- 1- formylphenyl)piperazine- 1 - 359.1carboxylatecarboxylate0

[0119] l-(4-( (T disopropylsilyl)oxy)phenyl)ethan-l-one26ME1\58440953. vl139849-00420

[0120] Triisopropyl silyl chloride (7.79 g, 40.4 mmol) was add to a solution of l-(4-hydroxyphenyl)ethan-l-one (5.00 g, 36.7 mmol) and imidazole (5.50 g, 80.8 mmol) in di chloromethane (50 mL). The reaction mixture was stirred at 25 °C for 3 h, then diluted with water (500 mL) and extracted into EtOAc (2 x 300 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 1:19) afforded l-(4-((triisopropylsilyl)oxy)phenyl)ethan-l-one (10.2 g, 95%) as a white solid; 5H (400 MHz; DMSO-d6) 7.95-7.83 (2H, m), 7.01-6.85 (2H, m), 2.50 (3H, s), 1.29-1.23 (3H, m), 1.05 (18H, d, J 7.3 Hz).

[0121] l-(4-chloro-3-((2-methoxyethyl)(methyl)amino)phenyl)ethan-l-one

[0122] Step 1

[0123] 2 -Methoxy -N-methylethan-1 -amine (6.33 g, 71.0 mmol) was added to a solution of l-(3-fluoro-4-nitrophenyl)ethan-l-one (10.0 g, 54.6 mmol) and potassium carbonate (22.6 g, 164 mmol) in acetonitrile (100 mL). The resulting mixture was stirred at 80 °C for 2 h, then filtered and concentrated in vacuo to afford l-(3-((2-methoxyethyl)(methyl)amino)-4-nitrophenyl)ethan-l-one (10.0 g, crude) as a brown oil; ES-MS [M+H]+: 253.2.

[0124] Step 2

[0125] Iron (5.98 g, 107 mmol) and ammonium chloride (5.73 g, 107 mmol) were added to a solution of l-(3-((2-methoxyethyl)(methyl)amino)-4-nitrophenyl)ethan-l-one (10.0 g, crude from Step 1) in ethanol (100 mL) and water (20 mL). The reaction mixture was stirred at 80 °C for 2 h, then filtered and concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 1:1) afforded l-(4-amino-3-((2-methoxyethyl)(methyl)amino)phenyl)ethan-l-one (7.00 g, 88%) as a yellow solid; 5H (40027ME1\58440953. vl139849-00420MHz; DMSO-d6) 7.54-7.45 (2H, m), 6.65 (1H, d, J8.3 Hz), 5.83 (2H, s), 3.47 (2H, m), 3.29 (3H, s), 2.88 (2H, m), 2.65 (3H, s), 2.40 (3H, s).

[0126] Step 3

[0127] Tert-Butyl nitrite (2.09 g, 20.2 mmol) and copper(I) chloride (2.18 g, 16.2 mmol) were added to a solution of l-(4-amino-3-((2-methoxyethyl)(methyl)amino)phenyl)ethan-l- one (3.0 g, 13.5 mmol) in acetonitrile (20 mL). The reaction mixture was stirred at 65 °C for 2 h, then quenched with saturated aqueous ammonium chloride solution (20 mL) and extracted into EtOAc (2 x 20 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 1:2) afforded l-(4-chloro-3-((2- methoxyethyl)(methyl)amino)phenyl)ethan-l-one (1.20 g, 37%) as a yellow oil; ES-MS [M+H]+: 242.2.

[0128] The following intermediate was prepared in an analogous manner:

[0129] 2-(Azetidin-3-yl)benzo[d]oxazole TFA salt

[0130] Step 1

[0131] EDC (1.67 g, 8.72 mmol) was added to a solution of l-(tert- butoxycarbonyl)azetidine-3-carboxylic acid (1.29 g, 6.39 mmol), 2-bromoaniline (1.00 g, 5.81 mmol), DIPEA (3.04 mL, 17.4 mmol) and DMAP (71 mg, 0.58 mmol) in28ME1\58440953. vl139849-00420di chloromethane (10 mL). The reaction mixture was stirred at 25 °C for 2 h, then diluted with water (10 mL) and extracted into di chloromethane (3 x 10 mL). The combined organic extracts were washed with brine (30 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 3:7) afforded tert-butyl 3 -((2-bromophenyl)carbamoyl)azetidine-l -carboxylate (600 mg, 28%) as a yellow solid; 5H (400 MHz; DMSO-d6) 9.65 (1H, s), 7.66 (1H, d, J 7.9 Hz), 7.57 (1H, br d, J7.7 Hz), 7.42-7.34 (1H, m), 7.21-7.10 (1H, m), 4.09-3.88 (4H, m), 3.62-3.52 (1H, m), 1.39 (9H, s).

[0132] Step 2

[0133] 1,10-Phenanthroline (50 mg, 0.28 mmol) was added to a mixture of copper(I) iodide (26 mg, 0.14 mmol), cesium carbonate (917 mg, 2.82 mmol) and tert-butyl 3-((2-bromophenyl)carbamoyl)azetidine-l -carboxylate (500 mg, 1.41 mmol) inDMF (10 mL). The reaction mixture was stirred at 110 °C for 2 h, then diluted with water (20 mL) and extracted into EtOAc (3 x 10 mL). The combined organic extracts were washed with brine (30 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 3:7) afforded tert-butyl 3-(benzo[d]oxazol-2-yl)azetidine-l -carboxylate (200 mg, 51%) as a yellow oil; 5H (400 MHz; DMSO-d6) 7.77-7.68 (2H, m), 7.44-7.33 (2H, m), 4.29 (2H, br s), 4.22-4.09 (3H, m), 1.40 (9H, s).

[0134] Step 3

[0135] TFA (0.30 mL, 4.04 mmol) was added to a solution of tert-butyl 3-(benzo[d]oxazol-2-yl)azetidine-l -carboxylate (150 mg, 0.55 mmol) in dichloromethane (0.5 mL). The reaction mixture was stirred at 20 °C for 1 h, then concentrated in vacuo to afford 2-(azetidin-3-yl)benzo[d]oxazole TFA salt (200 mg, 0.49 mmol) as a yellow oil; 5H (400 MHz; DMSO-d6) 7.82-7.63 (2H, m), 7.44-7.29 (2H, m), 4.18 (1H, m), 3.99-3.73 (4H, m).

[0136] 3-Methoxy-3-(methoxymethyl)azetidine29ME1\58440953. vl139849-00420

[0137] Step 1BocN"''\ BocN'"\V— V-OH - ► V-A-OMe^OH OMe

[0138] Sodium hydride (60% dispersion in oil, 30 mg, 0.75 mmol) was added to a solution of tert-butyl 3 -hydroxy-3 -(hydroxymethyl)azetidine-l -carboxylate (50 mg, 0.25 mmol) in THF (1 mL) at 0 °C. The mixture was stirred at 25 °C for 30 min, then iodomethane (48 pL, 0.77 mmol) was added and stirring was continued at 25 °C for another 1 h. Saturated aqueous ammonium chloride solution (20 mL) was added and the mixture was extracted into EtOAc (3 x 20 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo to afford tert-butyl 3 -m ethoxy-3 -(methoxymethyl)azetidine-l -carboxylate (57 mg, crude) as a yellow oil; 5H (400 MHz;CDC13) 3.92 (2H, d, J9.4 Hz), 3.79 (2H, d, J9.4 Hz), 3.59 (2H, s), 3.43 (3H, s), 3.33 (3H, s), 1.45 (9H, s).

[0139] Step 2BocN-"\ HN-"\V-A— OMe - ► V-A“OMe' — OMe ' — OMe

[0140] TFA (0.20 mL, 2.69 mmol) was added to a solution of tert-butyl 3-methoxy-3-(methoxymethyl)azetidine-l -carboxylate (56 mg, crude) in dichloromethane (0.5 mL). The reaction mixture was stirred at 25 °C for 1 h, then diluted with water (50 mL) and extracted into EtOAc (2 x 50 mL). The combined organic extracts were concentrated in vacuo to afford 3-methoxy-3-(methoxymethyl)azetidine (30 mg, crude) as a yellow oil.

[0141] The following intermediates were prepared in an analogous manner:'ll NMRofStep 1Name Structureproducttert-butyl 3-((methoxy- d3 )methy l)azetidine- 1 - carboxylate; 8H(4003-((methoxy-HN— 1 TFA salt MHz; CDCI3) 4.03-3.94 d3)methyl)azetidine TFA salt* V-OCD3 (2H, m), 3.70-3.60 (2H, m), 3.51 (2H, d, J 6.8Hz), 2.80-2.69 (1H, m),1.50-1.41 (9H, m)30ME1\58440953. vl139849-00420tert-butyl 3 -(methoxy - d3)azetidine-l- carboxylate: 8H(4003 -(methoxy -d3)azetidine TFA TFA salt MHz; DMSO-d6) 4.16- salt* 4.08 (1H, m), 4.01-3.93OCD3(2H, m), 3.63 (2H, brd,J 5.9 Hz), 1.37 (9H, s)3 -fluoro-3 -((methoxy - TFA salt- d3)methyl)azetidine TFA salt*^OCD3* Aqueous workup replaced with concentration in vacuo in final step to afford TFA salt

[0142] 6-Methoxy-3-azabicyclo[ 3.1.0 Jhexane HCl salt

[0143] Step 1

[0144] Sodium hydride (60% dispersion in oil, 161 mg, 4.02 mmol) was added to a solution tert-butyl 6-hydroxy-3-azabicyclo[3.1.0]hexane-3 -carboxylate (400 mg, 2.01 mmol) in THF (4 mL) at 0 °C. The mixture was stirred at 0 °C for 30 min, then iodomethane (187 pL, 3.01 mmol) was added and stirring was continued at 25 °C for another 16 h. Saturated aqueous ammonium chloride solution (10 mL) was added at 0 °C and the mixture was extracted into EtOAc (3 x 10 mL). The combined organic extracts were washed with brine (10 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 7:13) afforded tert-butyl 6-methoxy-3-azabicyclo[3.1.0]hexane-3-carboxylate (230 mg, 54%) as a colorless oil; 5H (400 MHz; CDC13) 3.59-3.48 (2H, m), 3.42-3.36 (2H, m), 3.35 (3H, s), 2.94 (1H, s), 1.70-1.66 (2H, m), 1.44 (9H, s).

[0145] Step 231ME1\58440953. vl139849-00420OMe OMeHCI salt

[0146] HCI (2M in dioxane, 2.3 mL, 4.6 mmol) was added to tert-butyl 6-methoxy-3-azabicyclo[3.1.0]hexane-3-carboxylate (230 mg, 1.08 mmol). The reaction mixture was stirred at 25 °C for 2 h, then concentrated in vacuo to afford 6-methoxy-3-azabicyclo[3.1.0]hexane HCI salt (160 mg, crude) as a light pink solid; 5H (400 MHz;DMSO-d6) 9.61 (1H, br d, J2.8 Hz), 9.31 (1H, br s), 3.33 (1H, s), 3.22 (7H, s), 1.86 (2H, s).

[0147] 2-(3-Methylazetidin-3-yl)oxazole TFA salt

[0148] Step 1

[0149] BOP-CI (12.8 g, 50.2 mmol) was added to a solution of l-(tert-butoxycarbonyl)-3-methylazetidine-3 -carboxylic acid (9.00 g, 41.8 mmol), methyl L-serinate hydrochloride (7.81 g, 50.2 mmol) and triethylamine (17.5 mL, 125 mmol) in dichloromethane (150 mL). The reaction mixture was stirred at 25 °C for 2 h, then diluted with water (30 mL) and extracted into EtOAc (3 x 30 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 1:0) afforded tert-butyl (5)-3 -((3 -hydroxy- 1 -methoxy- 1-oxopropan-2-yl)carbamoyl)-3 -methylazetidine- 1 -carboxylate (5.30 g, 40%) as a yellow oil; ES-MS [M-'Bu+H]: 261.0.

[0150] Step 2

[0151] Bis(2-methoxyethyl)aminosulfur trifluoride (2.85 g, 12.9 mmol) was added to a solution of tert-butyl (5)-3 -((3 -hydroxy- 1 -methoxy- 1 -oxopropan-2-yl)carbam oyl)-3-methylazetidine-1 -carboxylate (3.70 g, 11.7 mmol) in di chloromethane (70 mL) at -20 °C. The reaction mixture was stirred at 0 °C for 4 h, then diluted with water (30 mL) and extracted into EtOAc (3 x 50 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by flash column chromatography32ME1\58440953. vl139849-00420on silica (EtOAc: PE, 0:1 to 1:3) afforded methyl 2-(l-(tert-butoxycarbonyl)-3-methylazetidin-3-yl)oxazole-4-carboxylate (1.40 g, 4.72 mmol) as a white solid; 5H (400 MHz; CDC13) 8.21 (1H, s), 4.44-4.33 (2H, m), 3.93 (3H, s), 3.90-3.84 (2H, m), 1.76 (3H, s), 1.45 (9H, s).

[0152] Step 3

[0153] Lithium hydroxide (566 mg, 23.6 mmol) was added to a solution of methyl 2-(l-(tert-butoxycarbonyl)-3-methylazetidin-3-yl)oxazole-4-carboxylate (1.40 g, 4.72 mmol) in THF (15 mL) and water (5 mL). The reaction mixture was stirred at 25 °C for 2 h, then concentrated in vacuo. Water (20 mL) was added and the pH adjusted to ~5 by addition of 1.0 M HCl(aq). The mixture was extracted into EtOAc (3 x 20 mL) and the combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo to afford 2-(l-(tert-butoxycarbonyl)-3-methylazetidin-3-yl)oxazole-4-carboxylic acid (1.20 g, 90%) as a white solid; ES-MS [M-'Bu+H]: 227.1.

[0154] Step 4

[0155] Silver carbonate (488 mg, 1.77 mmol) was added to a solution of 2-(l-(tert-butoxycarbonyl)-3 -methylazeti din-3 -yl)oxazole-4-carboxylic acid (250 mg, 0.89 mmol) and acetic acid (10 pL, 0.18 mmol) in DMSO (10 mL). The reaction mixture was stirred at 140 °C for 4 h, then filtered and washed with EtOAc. The filtrate was diluted with water (40 mL) and extracted into EtOAc (3 x 40 mL). The combined organic extracts were washed with brine (2 x 40 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 1:3) afforded tertbutyl 3 -methyl-3-(oxazol-2-yl)azetidine-l -carboxylate (70 mg, 29%) as a yellow oil; ES-MS [M-'Bu+H]: 183.1.

[0156] Step 5TFA salt33ME1\58440953. vl139849-00420

[0157] TFA (0.11 mL, 1.47 mmol) was added to a solution of tert-butyl 3-methyl-3-(oxazol-2-yl)azetidine-l -carboxylate (70 mg, 0.29 mmol) in di chloromethane (3 mL). The reaction mixture was stirred at 25 °C for 2 h, then concentrated in vacuo to afford 2-(3-methylazeti din-3 -yl)oxazole TFA salt (70 mg, crude).

[0158] Benzyl 8-oxa-2, 5-diazaspiro[ 3.5 ]nonane-5-carboxylate

[0159] Step 1. HN %BOCNXo> — BOONX )

[0160] Benzyl chloroformate (329 mg, 1.93 mmol) was added to a solution of tert-butyl 8-oxa-2,5-diazaspiro[3.5]nonane-2-carboxylate (400 mg, 1.75 mmol) and pyridine (0.21 mL, 2.63 mmol) in dichloromethane (5 mL). The reaction mixture was stirred at 20 °C for 2 h, then diluted with water (5 mL) and extracted into EtOAc (2 x 5 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo.Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 1:3) afforded 5-benzyl 2-(tert-butyl) 8-oxa-2,5-diazaspiro[3.5]nonane-2,5-di carboxylate (400 mg, 63%) as a colorless oil; ES-MS [M+H]+: 363.2.

[0161] Step 2Cbz Cbz°°oO

[0162] TFA (1 mL) was added to a solution of 5-benzyl 2-(tert-butyl) 8-oxa-2,5-diazaspiro[3.5]nonane-2,5-dicarboxylate (350 mg, 0.97 mmol) in di chloromethane (2 mL). The reaction mixture was stirred at 20 °C for 2 h, then diluted with saturated aqueous sodium bicarbonate solution (10 mL) and extracted into dichloromethane (2 x 5 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo to afford benzyl 8-oxa-2,5-diazaspiro[3.5]nonane-5-carboxylate (350 mg, crude) as a colorless oil.

[0163] l-(Azetidin-3-yl)ethan-l-one TFA salt

[0164] TFA (0.10 mL, 1.35 mmol) was added to a solution of tert-butyl 3-acetylazetidine-1 -carboxylate (200 mg, 1.00 mmol) in di chloromethane (0.1 mL). The34ME1\58440953. vl139849-00420reaction mixture was stirred at 25 °C for 2 h, then concentrated in vacuo to afford l-(azetidin-3-yl)ethan-l-one TFA salt (100 mg, crude) as a yellow oil.

[0165] l-(4-Chloro-3-( ( triisopropylsilyl)oxy)phenyl)ethan-l-one

[0166] Step 1

[0167] Triisopropyl silyl chloride (9.17 g, 47.6 mmol) was add to a solution of 2-chloro-5-iodophenol (11.0 g, 43.2 mmol) and imidazole (6.47 g, 95.1 mmol) in dichloromethane (10 mL). The reaction mixture was stirred at 25 °C for 3 h, then diluted with water (100 mL) and extracted into EtOAc (3 x 60 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 1:4) afforded (2-chloro-5-iodophenoxy)triisopropylsilane (16.0 g, 90%) as a white solid; 5H (400 MHz; DMSO-d6) 7.27-7.21 (1H, m), 7.17-7.11 (2H, m), 1.26-1.14 (3H, m), 0.98 (18H, d, J 7.5 Hz).

[0168] Step 2

[0169] Isopropylmagnesium chloride lithium chloride complex (1.3 M solution in THF) was added to a solution of (2-chloro-5-iodophenoxy)triisopropylsilane (29.0 g, 70.6 mmol) and N-methoxy-N-methylacetamide (8.74 g, 84.7 mmol) in THF (300 mL) at 0 °C. The reaction mixture was stirred at this temperature for 5 h, then quenched by addition of saturated aqueous ammonium chloride solution (200 mL). Water (100 mL) was added and the mixture was extracted into EtOAc (3 x 100 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 1:19) afforded 1 -(4-chl oro-3 -((triisopropylsilyl)oxy)phenyl)ethan-l-one (20.2 g, 88%) as a white solid; 5H (400 MHz; DMSO-d6) 7.59 (2H, d, J0.7 Hz), 7.44 (1H, s), 2.55 (3H, s), 1.36-1.26 (3H, m), 1.08 (18H, d, J 7.5 Hz).

[0170] Phenyl (5-(l -(4-(oxetan-3-ylcarbamoyl )phenyl)ethyl) thiazol-2-yl)carbamate

[0171] Step 135ME1\58440953. vl139849-00420

[0172] Lithium hydroxide (2.0 M, 3 mL, 6 mmol) was added to a solution of methyl 4-(l-(2-aminothiazol-5-yl)ethyl)benzoate* (1.00 g, 3.81 mmol) in methanol (8 mL) and the resulting mixture was stirred at 20 °C for 12 h. The mixture was adjusted to pH 7 using hydrochloric acid, then diluted with water (50 mL) and extracted into EtOAc (3 x 100 mL). The combined organic extracts were washed with brine (50 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo to afford 4-(l-(2-aminothiazol-5-yl)ethyl)benzoic acid (1.00 g, crude); ES-MS [M+H]+: 249.1. *Prepared from methyl 4-acetylbenzoate using procedure C, Steps 1 and 2

[0173] Step 2

[0174] A mixture of 4-(l-(2-aminothiazol-5-yl)ethyl)benzoic acid (0.90 g, 3.62 mmol), oxetan-3 -amine (450 mg, 6.16 mmol), HATU (2.07 g, 5.44 mmol) and DIPEA (1.80 mL, 10.3 mmol) in DMF (10 mL) was stirred at 20 °C for 2 h, then concentrated in vacuo and purified by preparative HPLC (column: Welch Ultimate XB C18, 20-40 pm; solvent: acetonitrile: water; gradient: 3:7— >1:1) to afford 4-(l-(2-aminothiazol-5-yl)ethyl)-N-(oxetan-3-yl)benzamide (0.70 g, 60%) as a yellow solid; ES-MS [M+H]+: 304.1.

[0175] Step 336ME1\58440953. vl139849-00420

[0176] Phenyl (5-(l-(4-(oxetan-3-ylcarbamoyl)phenyl)ethyl)thiazol-2-yl)carbamate was prepared from 4-(l-(2-aminothiazol-5-yl)ethyl)-N-(oxetan-3-yl)benzamide according to procedure C, Step 3; ES-MS [M+H]+: 424.2.

[0177] Phenyl (5-(l-( 6-(oxetan-3-ylcarbamoyl )pyridin-3-yl)ethyl)thiazol-2-yl)carbamate

[0178] Step 1

[0179] Tri ethyl silane (18.0 mL, 113 mmol) was added to a solution of tert-butyl (5-(l-(6-chloropyridin-3-yl)-l-hydroxyethyl)thiazol-2-yl)carbamate* (4.0 g, 11.2 mmol) and TFA (8.5 mL, 114 mmol) in DCE (50 mL) and the resulting mixture was stirred at 60 °C for 12 h, then concentrated in vacuo. Water (100 mL) then saturated aqueous sodium bicarbonate solution were added until the pH was ~7. The reaction mixture was extracted into dichloromethane (3 x 100 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 1:1) afforded 5-(l-(6-chloropyridin-3-yl)vinyl)thiazol-2-amine (2.10 g, 75%) as a yellow solid; ES-MS [M+H]+: 238.0. *Prepared from l-(6-chloropyri din-3 -yl)ethan-l -one using procedure B, Step 1

[0180] Step 2

[0181] A mixture of 5-(l-(6-chloropyridin-3-yl)vinyl)thiazol-2-amine (2.50 g, 10.5 mmol), oxetan-3 -amine (2.50 g, 34.2 mmol), Pd(dppf)Cl2 (1.00 g, 1.37 mmol) and tri ethylamine (5.00 mL, 35.9 mmol) in DMF was stirred under carbon monoxide at 80 °C for 12 h. The reaction mixture was diluted with brine (150 mL), extracted into EtOAc (3 x 150 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by preparative HPLC (column: Welch Ultimate XB C18, 20-40 pm; solvent: acetonitrile: water; gradient: 3:7— >1:1) afforded 5-(l-(2-aminothiazol-5-yl)vinyl)-N-(oxetan-3-yl)picolinamide (0.80 g, 18%) as a yellow solid; ES-MS [M+H]+: 303.2.

[0182] Steps 3 and 437ME1\58440953. vl139849-00420

[0183] Phenyl (5-(l-(6-(oxetan-3-ylcarbamoyl)pyridin-3-yl)ethyl)thiazol-2-yl)carbamate was prepared from 5-(l-(2-aminothiazol-5-yl)vinyl)-N-(oxetan-3-yl)picolinamide according to procedure A, Steps 3 and 4; ES-MS [M+H]+: 425.1.

[0184] 3-(4-(l -(2-Aminothiazol-5-yl)ethyl)phenyl)oxetan-3-ol

[0185] Step 1

[0186] 2,4-Dimethoxybenzaldehyde (2.30 g, 13.8 mmol) and acetic acid (1 mL, 17.5 mmol) were added to a solution of 5-(l-(4-bromophenyl)ethyl)thiazol-2-amine* (1.00 g, 3.53 mmol) in methanol (10 mL) at 0 °C. The reaction mixture was stirred at this temperature for 30 min, then sodium cyanoborohydride (450 mg, 7.16 mmol) was added and stirring was continued at 25 °C for another 12 h. The mixture was diluted with water (20 mL) and extracted into EtOAc (3 x 20 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 2:3 to 1:1) afforded 5-(l-(4-bromophenyl)ethyl)-N-(2,4-dimethoxybenzyl)thiazol-2-amine (800 mg, 51%) as a yellow oil; ES-MS [M+H]+: 435.0. *Prepared from l-(4-bromophenyl)ethan-l-one using procedure C, steps 1 and 2

[0187] Step 2

[0188] n-BuLi (2.5 M in THF, 1.00 mL, 2.50 mmol) was added dropwise to a solution of 5-(l-(4-bromophenyl)ethyl)-N-(2,4-dimethoxybenzyl)thiazol-2-amine (200 mg, 0.46 mmol) in THF (3 mL) at -60 °C and the resulting mixture was stirred at this temperature for 1 h. A38ME1\58440953. vl139849-00420solution of oxetan-3-one (70 mg, 0.97 mmol) in THF (2 mL) was added and stirring was continued at -60 °C for 1 h. The reaction mixture was quenched with saturated aqueous ammonium chloride solution (20 mL) and extracted into EtOAc (3 x 50 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 9:1 to 1:0) afforded 3-(4-(l-(2-((2,4-dimethoxybenzyl)amino)thiazol-5-yl)ethyl)phenyl)oxetan-3-ol (85 mg, 43%) as a yellow oil; ES-MS [M+H]+: 427.2.

[0189] Step 3

[0190] A solution of 3-(4-(l-(2-((2,4-dimethoxybenzyl)amino)thiazol-5-yl)ethyl)phenyl)oxetan-3-ol (85, 0.20 mmol) in TFA (1 mL) was stirred at 25 °C for 12 h. Saturated aqueous sodium bicarbonate solution (20 mL) was added and the mixture was extracted into EtOAc (2 x 20 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo to afford 3-(4-(l-(2-aminothiazol-5-yl)ethyl)phenyl)oxetan-3-ol (50 mg, crude); ES-MS [M+H]+: 277.2.

[0191] Synthetic procedure A

[0192] Example 1: Oxazol-2-ylmethyl (R)-(5-( 1 -( 6-methoxypyridin-3-yl)ethyl)thiazol-2-y I) carbamate

[0193] Example 2: Oxazol-2-ylmethyl (S)-(5-(l-(6-methoxypyridin-3-yl)ethyl)thiazol-2-y I) carbamate

[0194] Step 1MeONHBocNHBoc

[0195] LDA (1.0 M in THF, 494.4 mL, 494 mmol) was added to a solution of tert-butyl thiazol-2-ylcarbamate (45.0 g, 225 mmol) in THF (900 mL) at -20 °C and stirred for 30 min at this temperature. A solution of l-(6-methoxypyridin-3-yl)ethan-l-one (40.8 g, 270 mmol) in THF (800 mL) was added slowly and stirring was continued at -20 °C for 1 h. The reaction mixture was quenched by addition of saturated aqueous ammonium chloride solution39ME1\58440953. vl139849-00420(500 mL) at 0 °C. Water was added (500 mL) and the mixture was extracted into EtOAc (3 x 300 mL). The combined organic extracts were washed with brine (500 mL), dried over anhydrous sodium sulfate and concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 1:0) afforded tert-butyl (5-(l-hydroxy-l-(6-methoxypyridin-3-yl)ethyl)thiazol-2-yl)carbamate (55.0 g, 69%) as a white solid; ES-MS [M+H]+: 352.1.

[0196] Step 2

[0197] TFA (150 mL, 2.02 mol) was added to a solution of tert-butyl (5 -(1 -hydroxy- 1 -(6-methoxypyridin-3-yl)ethyl)thiazol-2-yl)carbamate (55.0 g, 157 mmol) in DCE (450 mL) and the resulting mixture was stirred at 80 °C for 6 h. Saturated aqueous sodium carbonate solution was then slowly added until the pH was ~8. Water (500 mL) was added and the mixture was extracted into EtOAc (3 x 1 L). The combined organic extracts were washed with brine (3 L), dried over anhydrous sodium sulfate and concentrated in vacuo. Trituration with EtOAc afforded tert-butyl (5-(l-(6-methoxypyridin-3-yl)vinyl)thiazol-2-yl)carbamate (36.0 g, 99%) as a white solid; ES-MS [M+H]+: 234.0.

[0198] Step 3MeO MeO

[0199] 10% Pd(OH)2 / C (3.20 g) was added to a solution of 5-(l-(6-methoxypyridin-3-yl)vinyl)thiazol-2-amine (32.0 g, 137 mmol) in methanol (600 mL). The resulting mixture was stirred under hydrogen (50 PSI) at 70 °C for 24 h, filtered through a pad of Celite eluting with methanol (30 mL), then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 7:3) afforded 5-(l-(6-methoxypyridin-3-yl)ethyl)thiazol-2-amine (12.5 g, 38%) as a yellow solid; ES-MS [M+H]+: 236.1.

[0200] Step 440ME1\58440953. vl139849-00420

[0201] Phenyl chloroformate (7.44 mL, 58.4 mmol) was added to a solution of 5-(l-(6-methoxypyridin-3-yl)ethyl)thiazol-2-amine (12.5 g, 53.1 mmol) and pyridine (6.43 mL, 79.7 mmol) in THF (120 mL) at 0 °C. The resulting mixture was stirred at 20 °C for 1 h, then concentrated in vacuo. Trituration with acetonitrile:water (1:2) afforded phenyl (5-(l-(6-methoxypyridin-3-yl)ethyl)thiazol-2-yl)carbamate (17.0 g, 90%) as a white solid; ES-MS [M+H]+: 356.1.

[0202] Step 5

[0203] Sodium hydride (60% dispersion in oil, 3.83 g, 95.7 mmol) was added to a solution of oxazol-2-ylmethanol (9.48 g, 95.7 mmol) in THF (170 mL) at 0 °C. The resulting mixture was stirred 0 °C for 30 min and then a solution of phenyl (5-(l-(6-methoxypyridin-3-yl)ethyl)thiazol-2-yl)carbamate (17.0 g, 47.8 mmol) in THF (100 mL) was added. The reaction mixture was stirred at 20 °C for 12 h, then poured into saturated aqueous ammonium chloride solution (50 mL). The mixture was extracted into EtOAc (3 x 100 mL) and the combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Trituration with EtOAc afforded oxazol-2-ylmethyl (5-(l-(6-methoxypyridin-3-yl)ethyl)thiazol-2-yl)carbamate (14.7 g, 85%) as a white solid; ES-MS [M+H]+: 361.1.

[0204] Step 6Example 2

[0205] Oxazol-2-ylmethyl (5-(l-(6-methoxypyridin-3-yl)ethyl)thiazol-2-yl)carbamate (14.7 g) was purified by preparative SFC (column: CHIRALCEL® OX-10 / SFC 50x250mm,41ME1\58440953. vl139849-0042010 micron; CCh EtOH (0.1% NH4OH) 60:40) to afford oxazol-2-ylmethyl (7?)-(5-(l -(6-methoxypyridin-3-yl)ethyl)thiazol-2-yl)carbamate (6.17 g, 42%, Example 1) as a white solid; 5H (400 MHz; DMSO-d6) 11.89 (1H, br s), 8.15 (1H, s), 8.10 (1H, d, J2.4 Hz), 7.59 (1H, m), 7.25 (1H, s), 7.16 (1H, s), 6.77 (1H, d, J8.4 Hz), 5.27 (2H, s), 4.31 (1H, m), 3.82 (3H, s), 1.59 (3H, d, J6.8 Hz); ES-MS [M+H]+: 361.1; [a]D20-27.2 (c 0.47, DMSO) and oxazol-2-ylmethyl (5)-(5-(l-(6-methoxypyridin-3-yl)ethyl)thiazol-2-yl)carbamate (6.50 g, 44%, Example 2) as a white solid; 5H (400 MHz; DMSO-d6) 11.89 (1H, br s), 8.15 (1H, s), 8.10 (1H, d, J2.4 Hz), 7.59 (1H, m), 7.25 (1H, s), 7.16 (1H, s), 6.77 (1H, d, J 8.4 Hz), 5.27 (2H, s), 4.31 (1H, m), 3.82 (3H, s), 1.59 (3H, d, J6.8 Hz); ES-MS [M+H]+: 361.1; [a]D20+27.1 (c 0.48, DMSO). The absolute stereochemistry of Example 1 was verified by X-ray>crystallography.ZIZ>°

[0206] Other examples prepared using synthetic procedure A are shown in the following table. All intermediates are commercially available unless noted (see ‘Intermediate synthesis’ section).Intermediates ES-MSEx. No. Name Structure [OC]D20requiring synthesis [M+H]+oxazol-2- ylmethyl (R)- (5-(l-(6- -23.1 (c (difluorometho3 n / a 397.1 0.31, xy )py ridin-3 - DMSO) yl)ethyl)thiazo1-2- yl)carbamateoxazol-2- ylmethyl (£)- (5-(l-(6- F3CO\ l-(6- +19.1 (c (trifluorometh (trifluoromethoxy)p4 O 415.1 0.33, oxy )py ridin-3 - \ — \ JL I y ridin-3 -y l)ethan- 1 - / s'%' V 'Y°\ DMSO) yl)ethyl)thiazo one1-2- yl)carbamateoxazol-2- F3COXl-(6- ylmethyl (R)- -19.2 (c (trifluoromethoxy)p5 (5-(l-(6- 415.1\ — c ji K 0.33, y ridin-3 -y l)ethan- 1 - (trifluorometh DMSO)H0 oneoxy )py ridin-3-42ME1\58440953. vl139849-00420yl)ethyl)thiazo1-2- yl)carbamateoxazol-2- ylmethyl (S)- (5-(l-(6- D3COl-(6-(methoxy- +28.9 (c (methoxy- 6 / T~N O d3)pyridin-3- 364.1 0.33, d3)pyridin-3- \ — e if n _yl)ethan-l-one DMSO) yl)ethyl)thiazoHo1-2- yl)carbamateoxazol-2- ylmethyl (R)- (5-(l-(6- D3COl-(6-(methoxy- -30.1 (c (methoxy- 7 \d3 \ — e if O If _ d3)pyridin-3- 364.1 0.33, )pyridin-3- yl)ethan-l-one DMSO) yl)ethyl)thiazoHo1-2- yl)carbamate

[0207] Alternative, asymmetric synthesis of Example 1: Oxazol-2-ylmethyl (R)-(5-(l-(6-methoxypyridin-3-yl)ethyl)thiazol-2-yl)carbamate

[0208] Step 1

[0209] A mixture of potassium tert-butoxide (222 g, 1.98 mol) and methyl 2-(diethoxyphosphoryl)acetate (417 g, 1.98 mol) in THF (3 L) was stirred at 25 °C for l h. 1-(6-methoxypyridin-3-yl)ethan-l-one (150 g, 992 mmol) was then added and stirring was continued at 25 °C for an additional 12 h. Water (2 L) was added and the mixture was extracted into MTBE (3 x 1 L). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo to afford methyl (E)-3-(6-methoxypyri din-3 -yl)but-2-enoate (200 g, 55%) as a yellow solid; ES-MS [M+H]+: 208.1.

[0210] Step 2MeO^\

[00211] 1O1O43ME1\58440953. vl139849-00420

[0212] Sodium hydroxide (138 mg, 3.47 mol) was added to a solution of methyl (E)-3-(6-methoxypyridin-3-yl)but-2-enoate (240 g, 1.16 mol) in water (1.25 L) and ethanol (1.25 L). The reaction mixture was stirred at 25 °C for 12 h then concentrated in vacuo to remove ethanol and extracted into MTBE (3 x 1 L). The aqueous phase was separated and HCl(aq) (2.0 M) was added to adjust the pH to 5-6. The precipitate was filtered, then triturated with MTBE (1.25 mL, 25 °C, 12 h) to afford (£)-3-(6-methoxypyri din-3 -yl)but-2-enoic acid (95.0 g, 42%) as a white solid; 5H (400 MHz; DMSO-d6) 8.38 (1H, d, J2.40 Hz), 7.93 (1H, dd, J 8.6, 2.6 Hz), 6.84 (1H, d, J 8.6 Hz), 6.12 (1H, d, J 1.2 Hz), 3.88 (3H, s), 2.47 (3H, s).

[0213] Step 3MeO^?^ MeO^^N<5jjL^^5^OSiMe(OMe)2

[00214] 1O =

[0215] Methyldimethoxysilane (286 g, 2.69 mol) was added to a mixture of copper(II) acetate (1.30 g, 7.16 mmol), l,2-bis((2R,5R)-2,5-diphenylphospholan-l-yl)ethane (3.90 g, 7.70 mmol) and (E)-3-(6-methoxypyri din-3 -yl)but-2-enoic acid (130 g, 672 mmol) in toluene (1.5 L). The resulting mixture was stirred at 40 °C for 16 h, then concentrated in vacuo to afford (5,£)-5-(4-((dimethoxy(methyl)silyl)oxy)but-3-en-2-yl)-2-methoxypyridine (190 g, crude) as a yellow oil; ES-MS [M+H]+: 284.3.

[0216] Step 4N^J^^^^OSiMe(OMe)2-

[0217]

[0218] Water (200 mL) and ammonium fluoride (74.5 g, 2.01 mol) were added to a solution of (5,£)-5-(4-((dimethoxy(methyl)silyl)oxy)but-3-en-2-yl)-2-methoxypyridine (190 g, 670 mmol) in THF (1.8 L) at 0 °C. The mixture was stirred at 0-10 °C for 1 h, then diluted with water (I L) and extracted into EtOAc (2 x 1 L). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 1:15 to 1:5) afforded (5)-3-(6-methoxypyri din-3 -yl)butanal (90.3 g, 74%) as a yellow oil; ES-MS [M+H]+: 180.3.

[0219] Step 5

[0220] 44ME1\58440953. vl139849-00420

[0221] NCS (116 g, 870 mmol) was added to a solution of (5)-3-(6-methoxypyri din-3 -yl)butanal (130 g, 725 mmol) and DL-proline (16.7 g, 145 mmol) in dichloromethane (1.3 L) at 0 °C. The mixture was stirred at 25 °C for 4 h, then diluted with water (1 L) and extracted into dichloromethane (2 x IL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 1:10 to 1:1) afforded (3 A)-2-chl oro-3 -(6-methoxypyri din-3 -yl)butanal (120 g, 77%) as a yellow oil; ES-MS [M+H]+: 214.2.

[0222] Step 6

[00223] = =

[0224] Thiourea (85.5 g, 1.12 mol) was added to a solution of (3A)-2-chloro-3-(6-methoxypyri din-3 -yl)butanal (120 g, 561 mmol) in ethanol (1.2 L). The reaction mixture was stirred at 85 °C for 12 h, then cooled to 25 °C, adjusted to pH ~8 with ammonium hydroxide, filtered and concentrated in vacuo. Water (1 L) was added and the mixture was extracted into EtOAc (2 x 2 L). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 1:10 to 1:1) afforded (A)-5-(l-(6-methoxypyridin-3-yl)ethyl)thiazol-2-amine (56.0 g, 40%) as a yellow solid; ES-MS [M+H]+: 236.2.

[0225] Step 7

[00226] O

[0227] CDI (54.0 g, 333 mmol) was added in portions to a solution of oxazol-2-ylmethanol (30.0 g, 302 mmol) in THF (300 mL) at 0 °C. The reaction mixture was stirred at 25 °C for 2 h, then diluted with water (500 mL) and extracted into (EtOAc (2 x 500 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo to afford oxazol-2-ylmethyl IH-imidazole-l -carboxylate (58.0 g, crude) as a yellow oil.

[0228] Step 845ME1\58440953. vl139849-00420MeO

[0229]

[0230] Cesium carbonate (283 g, 869 mmol) was added to a solution of (7?)-5-( 1 -(6-methoxypyridin-3-yl)ethyl)thiazol-2-amine (47.0 g, 199 mmol) and oxazol-2-ylmethyl 1H-imidazole-1 -carboxylate (Step 7, 56.0 g, 289 mmol) in DMF (500 mL). The reaction mixture was stirred at 40 °C for 3 h, then cooled to 25 °C, diluted with water (I L) and extracted into di chloromethane (2 x 500 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Trituration with MTBE (200 mL, 25 °C, 2 h) and purification by preparative SFC (column: CHIRALPAK® AD 30x250mm, 10 micron; Phase A: CO2, Phase B: 1:1 acetonitrile: [EtOH (0.1% ammonium hydroxide)]; Isocratic elution: B: A 60:40) afforded oxazol-2-ylmethyl (7?)-(5-(l-(6-methoxypyridin-3-yl)ethyl)thiazol-2-yl)carbamate (39.0 g, 37%) as a white solid; 5H (400 MHz; DMSO-d6) 11.89 (1H, br s), 8.15 (1H, s), 8.10 (1H, d, J2.4 Hz), 7.59 (1H, m), 7.25 (1H, s), 7.16 (1H, s), 6.77 (1H, d, J8.4 Hz), 5.27 (2H, s), 4.31 (1H, m), 3.82 (3H, s), 1.59 (3H, d, J6.8 Hz); [a]D20-29.4 (c 0.52, DMSO).

[0231] Synthetic procedure B

[0232] Example 8: Oxazol-2-ylmethyl (R)-(5-(l -(6-isopropoxypyridin-3-yl)ethyl)thiazol- 2 -y I) carbamate

[0233] Example 9: Oxazol-2-ylmethyl (S)-(5-(l-(6-isopropoxypyridin-3-yl)ethyl)thiazol-2 -y I) carbamate

[0234] Step 1s NHBoc rNQHsS NHBoc

[0235] n-BuLi (2.5 M in THF, 11.0 mL, 27.5 mmol) was added dropwise to a solution of tert-butyl thiazol-2-ylcarbamate (2.50 g, 12.5 mmol) in THF (20 mL) at -60 °C and the resulting mixture was stirred at this temperature for 1 h. A solution of l-(6-isopropoxypyridin-3-yl)ethan-l-one (2.24 g, 12.5 mmol) in THF (10 mL) was added and stirring was continued at -60 °C for 2 h. The reaction mixture was quenched with saturated aqueous ammonium chloride solution (50 mL) and extracted into EtOAc (3 x 50 mL). The 46ME1\58440953. vl139849-00420combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 2:3) afforded tert-butyl (5-(l-hydroxy-l-(6-isopropoxypyridin-3-yl)ethyl)thiazol-2-yl)carbamate (2.00 g, 40%) as a white solid; ES-MS [M+H]+: 380.2.

[0236] Step 2

[0237] TFA (7 mL, 94.2 mmol) was added to a solution of tert-butyl (5-(l-hydroxy-l-(6-isopropoxypyridin-3-yl)ethyl)thiazol-2-yl)carbamate (2.00 g, 5.27 mmol) in DCE (20 mL) and the resulting mixture was stirred at 80 °C for 2 h. Water (50 mL) then solid sodium carbonate were added until the pH was ~8. The mixture was extracted into EtOAc (3 x 60 mL). The combined organic extracts were washed with brine (2 x 100 mL), dried over anhydrous sodium sulfate and concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 2:3) afforded 5-(l-(6-isopropoxypyridin-3-yl)vinyl)thiazol-2-amine (1.20 g, 86%) as a white solid; ES-MS [M+H]+: 262.2.

[0238] Step 3

[0239] 10% Pd / C (200 mg) was added to a solution of 5-(l-(6-isopropoxypyridin-3-yl)vinyl)thiazol-2-amine (1.00 g, 3.83 mmol) in methanol (20 mL) and the resulting mixture was stirred under hydrogen (50 PSI) at 60 °C for 12 h. The mixture was filtered through celite and concentrated in vacuo to afford 5-(l-(6-isopropoxypyridin-3-yl)ethyl)thiazol-2-amine (300 mg, 29%) as a white solid; ES-MS [M+H]+: 264.2.

[0240] Step 447ME1\58440953. vl139849-00420Example 9

[0241] CDI (924 mg, 5.70 mmol) was added to a solution of oxazol-2-ylmethanol (564 mg, 5.70 mmol) in THF (10 mL) and the resulting mixture was stirred at 60 °C for 4 h. The mixture was then transferred to a solution of 5-(l-(6-isopropoxypyridin-3-yl)ethyl)thiazol-2-amine (300 mg, 1.14 mmol), triethylamine (0.79 mL, 5.70 mmol) and DMAP (28 mg, 0.23 mmol) in THF (5 mL) at 20 °C and stirred at 60 °C for 12 h. Water (30 mL) was added and the mixture was extracted into EtOAc (3 x 30 mL). The combined organic extracts were washed with brine (2 x 20 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Trituration with methanol and further purification by preparative SFC (column:CHIRALPAK® IG-10 / SFC 50x250mm, 10 micron; CO2: [1 / 1 acetonitrile / isopropanol (0.1% NH4OH)] 60:40 afforded oxazol-2-ylmethyl (A)-(5-(l-(6-isopropoxypyridin-3-yl)ethyl)thiazol-2-yl)carbamate (46 mg, 17%, Example 8) as a white solid; 5H (400 MHz; DMSO-d6) 11.90 (1H, br s), 8.15 (1H, d, J 0.9 Hz), 8.07 (1H, d, J= 2.4 Hz), 7.56 (1H, m), 7.25 (1H, d, J0.7 Hz), 7.16 (1H, d, J 1.0 Hz), 6.68 (1H, d, J 8.7 Hz), 5.27 (2H, s), 5.20 (1H, m), 4.29 (1H, m), 1.58 (3H, d, J7.1 Hz), 1.26 (6H, d, J6.1 Hz); ES-MS [M+H]+: 389.2; [a]D20-25.3 (c 0.28, DMSO) and oxazol-2-ylmethyl (5)-(5-(l-(6-isopropoxypyridin-3-yl)ethyl)thiazol-2-yl)carbamate (68 mg, 25%, Example 9) as a white solid; 5H (400 MHz; DMSO-d6) 11.90 (1H, br s), 8.15 (1H, d, J 0.9 Hz), 8.07 (1H, d, J= 2.4 Hz), 7.56 (1H, m), 7.25 (1H, d, J0.7 Hz), 7.16 (1H, d, J 1.0 Hz), 6.68 (1H, d, J 8.7 Hz), 5.27 (2H, s), 5.20 (1H, m), 4.29 (1H, m), 1.58 (3H, d, J7.1 Hz), 1.26 (6H, d, J6.1 Hz); ES-MS [M+H]+: 389.2; [a]D20+26.0 (c 0.38, DMSO).

[0242] Other examples prepared using synthetic procedure B are shown in the following table. All intermediates are commercially available unless noted (see ‘Intermediate synthesis’ section).48ME1\58440953. vl139849-00420ESChiral SFC Ex. Intermediates MSName Structure analytical method* No. requiring synthesis [M+H]+ and retention time oxazol-2- ylmethyl(7?)-(5-(l- Column: Lux 3 uni Cellulose-2, LC Column (2- MeO 250 x 4.6 mm; Phase A: methoxyp CO2, Phase B: EtOH 10 yrimidin- 0 n / a 362.1 (0.05% DEA);5- / S^N^0^<0\ Gradient elution: B: A from 30% to 60% yl)ethyl)thiazol-2- RT 1.50 min yl)carbamateoxazol-2- ylmethyl(7?)-(5-(l- (6- Column: CHIRALPAK®IG-34.6x50mm, 3 methoxy- MeO micron; Phase A: CO2, 5-N\\ l-(6-methoxy-5- Phase B: EtOH (0.05%F3C^\ / 11 (trifluoro ^=< Z~~N 0 (trifluoromethyl)pyri 429.1 DEA); methyl)py din-3 -y l)ethan- 1 -one Gradient elution: B: A from 20% to 60% ridin-3- yl)ethyl)th RT 1.34 min iazol-2- yl)carbamateoxazol-2- ylmethyl(S)-(5-(l- Column: CHIRALPAK®IG-34.6x50mm, 3 (6- MeO micron; Phase A: CO2, methoxy- l-(6-methoxy-5- Phase B: EtOH (0.05%F3C— \ / 12 5- (trifluoromethyl)pyri 429.1 DEA);(trifluoro din-3 -y l)ethan- 1 -one Gradient elution: B: AHfrom 20% to 60% methyl)pyridin-3- RT 1.67 min yl)ethyl)thiazol-2-49ME1\58440953. vl139849-00420yl)carbamateoxazol-2- ylmethyl Column: CHIRALPAK® (7?)-(5-(l- IG-34.6x50mm, 3EtO(6- micron; Phase A: CO2, ethoxypyr Phase B: IPA / [MeCN 13 v) « 0 n / a 375.1 (0.05% DEA)] 50 / 50;idin-3- Isocratic elution: B: A yl)ethyl)th 50:50 iazol-2- yl)carbam RT0.89 min ateoxazol-2- ylmethyl Column: CHIRALPAK® (S)-(5-(l- IG-34.6x50mm, 3EtO(6- micron; Phase A: CO2, ethoxypyr Phase B: IPA / [MeCN 14 V} 0 n / a 375.0 (0.05% DEA)] 50 / 50;idin-3- Isocratic elution: B: A yl)ethyl)thHO 50:50 iazol-2- yl)carbam RT 1.58 min ateoxazol-2- ylmethyl(7?)-(5-(l- Column: CHIRALPAK® (6- IG-34.6x50mm, 3 methoxy- MeO micron; Phase A: CO2, 2- ky Phase B: EtOH (0.05% 15 \=< rf-N 0 n / a 375.1 DEA)]; methylpyr Isocratic elution: B: A idin-3-HSJ 50:50 yl)ethyl)thiazol-2- RT0.92 min yl)carbamateoxazol-2- Column: CHIRALPAK® ylmethyl MeO IG-34.6x50mm, 3 (S)-(5-(l- ky micron; Phase A: CO2, 16 \=< #" N 0 n / a 375.2 Phase B: EtOH (0.05% (6- DEA)]; methoxy- KVVYOHSJ Isocratic elution: B: A 2- 50:5050ME1\58440953. vl139849-00420methylpyridin-3- RT 1.77 min yl)ethyl)thiazol-2- yl)carbamateoxazol-2- ylmethyl(7?)-(5-(l- (6- Column: CHIRALPAK® methoxy- MeO AD-3 4.6x50mm, 3 l-(6-methoxy-4- 4- micron; Phase A: CO2, 17 methy Ipy ridin-3 - 375.1 Phase B: EtOH (0.05% methylpyr \ < '1 11yl)ethan-l-one DEA)]; Isocratic elution: idin-3- B: A 50:50 yl)ethyl)thiazol-2- RT0.77 min yl)carbamateoxazol-2- ylmethyl(S)-(5-(l- Column: CHIRALPAK® (6- AD-3 4.6x50mm, 3 methoxy- MeOl-(6-methoxy-4- micron; Phase A: CO2, 4- Phase B: EtOH (0.05% 18 methy Ipy ridin-3 - 375.1methylpyr y- x 'i ii DEA)]; Isocratic elution:yl)ethan-l-oneidin-3- B: A 50:50 yl)ethyl)th RT 1.52 min iazol-2- yl)carbamateoxazol-2- ylmethyl(5-(6- XX?chloro- 2,3- \019 AfVyo n / a 378.0 n / a dihydrobeHTz>nzofuran- N-A3- alternate reduction conditions used:yl)thiazol- Mg (5 eq), MeOH, 0 to 25 °C, 16 h2-51ME1\58440953. vl139849-00420yl)carbam

[0243] *Flow rate: 3mL / min; Detector: PDA; Column temperature: 35 °C; Back pressure: 100 Bar

[0244] Synthetic procedure C

[0245] Example 20: Oxazol-2-ylmethyl (R)-(5-(l-(4-chlorophenyl)ethyl)thiazol-2-y I) carbamate

[0246] Example 21: Oxazol-2-ylmethyl (S)-(5-(l-(4-chlorophenyl)ethyl)thiazol-2-y I) carbamate

[0247] Step 1N IIQHS NHBOC

[0248] n-BuLi (2.5 M in THF, 49.9 mL, 125 mmol) was added dropwise to a solution of tert-butyl thiazol-2-ylcarbamate (2.50 g, 12.5 mmol) in THF (20 mL) at -60 °C and the resulting mixture was stirred at this temperature for 30 min. A solution of l-(4-chlorophenyl)ethan-l-one (9.71 mL, 74.9 mmol) in THF (100 mL) was added and stirring was continued at -60 °C for 4 h. The reaction mixture was quenched with saturated aqueous ammonium chloride solution (200 mL) and extracted into EtOAc (3 x 200 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 3:7) afforded tert-butyl (5-(l-(4-chlorophenyl)-l-hydroxyethyl)thiazol-2-yl)carbamate (30.6 g, 86%) as a white solid; ES-MS [M+H]+: 355.0.

[0249] Step 2N IINHBoc s

[0250] Triethylsilane (54.0 mL, 338 mmol) was added to a solution of tert-butyl (5-(l-(4-chlorophenyl)-l -hydroxy ethyl)thiazol-2-yl)carbamate (30.0 g, 84.5 mmol) in TFA (200 mL) and the resulting mixture was stirred at 60 °C for 2 h, then concentrated in vacuo. Water (100 mL) then saturated aqueous sodium bicarbonate solution were added until the pH was ~7. The reaction mixture was extracted into EtOAc (3 x 100 mL). The combined organic extracts52ME1\58440953. vl139849-00420were dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 7:3) afforded 5-(l-(4-chlorophenyl)ethyl)thiazol-2-amine (10.6 g, 52%) as a white solid; ES-MS [M+H]+: 238.9.

[0251] Step 3

[0252] A solution of phenyl chloroformate (1.58 mL, 12.6 mmol) in THF (2 mL) was added to a solution of 5-(l-(4-chlorophenyl)ethyl)thiazol-2-amine (2.00 g, 8.38 mmol) and pyridine (2.03 mL, 25.1 mmol) in THF (20 mL) at 0 °C. The resulting mixture was stirred at 25 °C for 2 h. Water (20 mL) was added and the mixture was extracted into EtOAc (3 x 20 mL). The combined organic extracts were washed with brine (20 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Trituration with EtOAc:water 9:1 afforded phenyl (5-(l-(4-chlorophenyl)ethyl)thiazol-2-yl)carbamate (2.70 g, 7.52 mmol) as an off-white solid; ES-MS [M+H]+: 359.1.

[0253] Step 4Example 21

[0254] Sodium hydride (60% dispersion in oil, 134 mg, 3.34 mmol) was added to a solution of oxazol-2-ylmethanol (414 mg, 4.18 mmol) in THF (10 mL) at 0 °C. The resulting mixture was stirred 0 °C for 30 min and then phenyl (5-(l-(4-chlorophenyl)ethyl)thiazol-2-yl)carbamate (1.00 g, 2.79 mmol) was added. The reaction mixture was stirred at 0 °C for 3 h, then poured into saturated aqueous ammonium chloride solution (50 mL). The mixture was extracted into EtOAc (3 x 100 mL) and the combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on53ME1\58440953. vl139849-00420silica (EtOAc: PE, 0:1 to 4:1), followed by purification by preparative HPLC (column:Waters™ XBridge BEH C18 OBD Prep Column, 130A, 10 pm, 50 mm X 150 mm; acetonitrile: [water (0.1% ammonium carbonate)]; gradient: 35:65— >65:35), followed by further purification by preparative SFC (column: CHIRALPAK® IG-10 / SFC 50x250mm, 10 micron; CChdsopropanol (0.1%NH4OH) 40:60) afforded oxazol-2-ylmethyl (7?)-(5-(l -(4-chlorophenyl)ethyl)thiazol-2-yl)carbamate (170 mg, 17% Example 20) as an off-white solid; 5H (400 MHZ; DMSO-d6) 12.12-11.66 (1H, m), 8.15 (1H, s), 7.39-7.35 (2H, m), 7.33-7.29 (2H, m), 7.25 (1H, s), 7.17 (1H, s), 5.27 (2H, s), 4.36-4.31 (1H, m), 1.58 (3H, d, J 7.20 Hz); ES-MS [M+H]+: 364.1; [a]o20-2.87 (c 0.25, acetonitrile) and oxazol-2-ylmethyl (5)-(5-(l-(4-chlorophenyl)ethyl)thiazol-2-yl)carbamate (173 mg, 17%, Example 21) as an off-white solid; 5H (400 MHZ; DMSO-d6) 12.12-11.66 (1H, m), 8.15 (1H, s), 7.39-7.35 (2H, m), 7.33-7.29 (2H, m), 7.25 (1H, s), 7.17 (1H, s), 5.27 (2H, s), 4.36-4.31 (1H, m), 1.58 (3H, d, J 7.20 Hz); ES-MS [M+H]+: 364.1; [a]o20+2.41 (c 0.25, acetonitrile). The absolute stereochemistry of Example 20 was verified by X-ray crystallography.

[0255] Other examples prepared using synthetic procedure C are shown in the following table. All intermediates are commercially available unless noted (see ‘Intermediate synthesis’ section).Chiral SFCanalytica Ex. Intermediates ES-MS 1 Name StructureNo. requiring synthesis [M+H]+method* and retention time 3- methoxybenzyl (5-(l- ci(4- 22 chlorophen '==< ^~-N O n / a 403.1 n / a yl)ethyl)thi / V^N HXo^yOMeazol-2- yl)carbamate54ME1\58440953. vl139849-00420(4- methyloxazol-2- yl)methyl Cl(5-(l-(4- 23 / ZN 0n / a 378.1 n / a chlorophenyl)ethyl)thiHazol-2- yl)carbamate(4- LL?(trifluorom Oethyl)oxazo1-2- yl)methyl o (4- 24 (5-(l-(4- ZX (trifluoromethyl)oxa 432.0 n / a chlorophen zol-2-yl)methanolyl)ethyl)thiazol-2- oJ XJyl)carbamateColumn: CHIRALPAK® IG-3 4.6x50mm, 3 micron; oxazol-2- Phase A: ylmethylCO2, Phase (7?)-(5-(l- Cl(4- B: chlorophen O IPA / [MeCN 20 n / a 364.0 yl)ethyl)thi (0.05% azol-2- DEA)] yl)carbamahSA 50 / 50;te Isocratic elution: B: A 40:60 RT0.94 min Cl Column: oxazol-2- CHIRALPA ylmethyl o K® IG-3 21 \=< O n / a 364.0(S)-(5-(l- 4.6x50mm,AAA A o 3 micron; (4-HSA Phase A:55ME1\58440953. vl139849-00420chlorophen CO2, Phase yl)ethyl)thi B:IPA / [MeCN azol-2- (0.05% yl)carbama DEA)] te 50 / 50;Isocratic elution: B: A 40:60 orr RT 1.54 min l-benzyl-3- Cl(5-(l-(4- ^Z=IZchlorophen O25 > O° n / a 372.1yA O n / a yl)ethyl)thi A A / S N N Y^Aazol-2-H HL Jyl)urea L z1-(oxazol- 2-yl)propyl(5-(l-(4- chlorophen l-(oxazol-2- 26 392.0 n / a yl)ethyl)thi yl)propan-l-olazol-2- yl)carbamate(2H- 1,2,3 - triazol-2- yl)methyl Cl(5-(l-(4- 27 chlorophen / 'N 0 n / a 364.1 n / a yl)ethyl)thiazol-2-Hyl)carbamate(1H- pyrazol-1-Cl\yl)methyl28 (5-(l-(4- \=< yf-N 0 n / a 363.1 n / a y-< jl uchlorophen / S ^N O NASyl)ethyl)thiHiWazol-2-56ME1\58440953. vl139849-00420yl)carbamate(3-methyl- 1,2,4- oxadiazol- Cl5-yl)methyl(5-(l-(4- o29 n / a 379.1 n / a chlorophenyl)ethyl)thi H n °~N ''azol-2- yl)carbamateColumn: CHIRALCoxazol-2- EL® OX-3 ylmethyl 4.6x50mm, (7?)-(5-(l- 3 micron;MeO Phase A: (5- CO2, Phase methoxypy B: EtOH 30 n / a 361.1ridin-2- (0.05% yl)ethyl)thi DEA);HSA Isocratic azol-2- elution: B: A yl)carbama 40:60 teRT 1.32 min Column: CHIRALCoxazol-2- ClEL® OX-3 ylmethyl 4.6x50mm,N=\ / " N O(7?)-(5-(l- \ — e _ 3 micron;Phase A: (5-HSA CO2, Phase chloropyra Step 2 furnished the dihydrothiazole: (£)- B: EtOH 31 n / a 366.1zin-2 - (0.05%5 -( 1 -(5 -chloropyrazin-2-y l)ethy lidene)- yl)ethyl)thi DEA);4,5-dihydrothiazol-2-amine. An additional Isocratic azol-2- isomerization step was used to provide the elution: B: A yl)carbama terminal thiazole: DBU (2 eq), CH2O2, 25 40:60 te °C, 16 hRT 1.27 min57ME1\58440953. vl139849-00420Cl(1H- pyrazol-5- #-N Oyy i Ayl)methyl / S^N'^O'^X\(5-(l-(4- » HU32 chlorophen Step 4 used THP-protected starting n / a 363.0 n / a yl)ethyl)thi material: ( 1 -(tetrahydro-2H-pyran-2-yl)- azol-2- lH-pyrazol-5-yl)methanol.yl)carbama A subsequent THP-removal step providedte the final compound:4 M HC1 in dioxane, CH2C12, 25 °C. 1 hCl(1H-1,2,4- A=Z > C~N Otriazol-3- y ry A A MS'^NH><O^^N'Nyl NnH)methylMN= / (l-((2- (5-(l-(4- Step 4 used SEM-protected starting (trimethylsilyl)ethox33 chlorophen material: (l-((2- y)methy 1)-1H- 1,2,4- 364.1 n / a yl)ethyl)thi (trimethylsilyl)ethoxy)methyl)- 1H- 1,2,4- triazol-3- azol-2- triazol-3 -yl)methanol. yl)methanolyl)carbama A subsequent SEM-removal step providedte the final compound:TFA, CH2C12, 25 °C.

[0256] *Flow rate: 3mL / min; Detector: PDA; Column temperature: 35 °C; Back pressure: 100 Bar

[0257] Synthetic procedure D

[0258] Example 34: Pyridin-2-ylmethyl (5-(l-(4-chlorophenyl)ethyl)thiazol-2-yl) carbamate

[0259] CDI (17.0 g, 105 mmol) was added to a solution of 2-pyridylmethanol (11.4 g, 105 mmol) in THF (50 mL) and the resulting mixture was stirred at 60 °C for 6 h. The mixture was then transferred to a solution of 5-(l-(4-chlorophenyl)ethyl)thiazol-2-amine* (5 g, 20.94 mmol), triethylamine (14.6 mL, 105 mmol) and DMAP (256 mg, 2.09 mmol) in58ME1\58440953. vl139849-00420THF (50 mL) at 25 °C and stirred at 60 °C for 12 h. Water (50 mL) was added and the mixture was extracted into EtOAc (3 x 60 mL). The combined organic extracts were washed with brine (2 x 100 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by preparative HPLC (column: Welch Ultimate XB-SiO2, 10pm, 50><250mm; hexane: ethanol; gradient: 99:1— >85:15) afforded pyridin-2-ylmethyl (5-(l-(4-chlorophenyl)ethyl)thiazol-2-yl)carbamate (7.77 g, 48%) as a white solid; 5H (400 MHz; DMSO-d6) 11.79 (1H, s), 8.54 (1H, m), 7.82 (1H, s), 7.42-7.28 (6H, m), 7.17 (1H, s), 5.24 (2H, s), 4.33 (1H, m), 1.57 (3H, s); ES-MS [M+H]+: 374.0.

[0260] *Prepared according to Synthetic Procedure C, Steps 1 and 2c / A

[0261] Other examples prepared using synthetic procedure D are shown in the following r r rtable. All intermediates are commercially availab o o ole unless noted (see ‘Intermediate synthesis’ section). ZI ZI ZIK<?z==W L Intermediates ES-MS Ex. No. Name Structurerequiring synthesis [M+H]+oxazol-2- ylmethyl (5-(2- ^ 101(dimethy lamin35 n / a 359.1 o)benzyl)thiazol-2- yl)carbamateoxazol-2- ylmethyl (5-(2- (pyrrolidin-1- 36 n / a 385.2 yl)benzyl)thiazol-2- yl)carbamateoxazol-2- ylmethyl (5-(2- 37 morpholinoben n / a 401.1 zyl)thiazol-2- yl)carbamate2-fluorobenzyl Cl(5-(l-(4- 38 chlorophenyl)e \=< O n / a 391.0>-x JL Athyl)thiazol-2-HL JIyl)carbamate59ME1\58440953. vl139849-00420(3- fluoropyridin- 2-yl)methyl (5- 39 (l-(4- n / a 392.1 chlorophenyl)ethyl)thiazol-2- yl)carbamateoxazol-2- oylmethyl (5-(l- Clcr(4-chloro-3- N= — C #40 \ yf'N O n / a 389.0 cyanophenyl)e \ jlX c / thyl)thiazol-2- ^z=HS7yl)carbamate IZooxazol-2- >°ZT oylmethyl (5-(l- X( -ClLo cz48chlorophenyl)- 41 O n / a 400.02,2- difluoroethyl)t LL?hiazol-2- yl)carbamateoxazol-2- ylmethyl (5-(l- (4-Clchlorophenyl)- 42 \ O n / a 382.02-p> — \ X X__ / S'^N^K0^><0\fluoroethyl)thihH N "-# / / azol-2- yl)carbamateoxazol-2- ylmethyl (5-(l- (4- 43 (trifluorometh n / a 398.0 yl)phenyl)ethyl)thiazol-2- yl)carbamate60ME1\58440953. vl139849-00420oxazol-2- Fylmethyl (5-(l- (4- O44 n / a 348.2 fluorophenyl)ethyl)thiazol-2-Hyl)carbamateoxazol-2- ylmethyl (5-(l- MeO,OMe(3,4,5- z _MeO— 4.45 trimethoxyphe n / a 420.1 nyl)ethyl)thiazHMol-2- C / ) / zyl)carbamate Z I ooxazol-2- zr oylmethyl (5-(4- cichloro-3- MeO— 4 / )46 n / a 380.0 methoxybenzyl)thiazol-2- yl)carbamate o(1,3,4- oxadiazol-2- yl)methyl (5- 47 (l-(4- n / a 365.0 chlorophenyl)ethyl)thiazol-2- yl)carbamatel-(oxazol-2- yl)ethyl (5-(l-Cl\(4- kA48 \=< / " N O | n / a 378.0 chlorophenyl)e ) — \ JL JIthyl)thiazol-2-Hoyl)carbamateoxazol-2- ylmethyl (5-(l- (4- 49 acetamidophen n / a 387.1 yl)ethyl)thiazo1-2- yl)carbamate61ME1\58440953. vl139849-004202- methoxy ethyl Cl(5-(l-(4- 50 o n / a 341.1 chlorophenyl)ethyl)thiazol-2- / 'SANAJ""-0"’Hyl)carbamate3- methoxypropyl Cl(5-(l-(4- 51 O n / a 355.1 chlorophenyl)e yx. Ji x / S ^N O ^^ OMethyl)thiazol-2- Hyl)carbamateoxazol-2- ylmethyl (5- MeO((6- methoxypyridi52 n / a 347.1 n-3- Hz! Jyl)methyl)thiaHozol-2- yl)carbamateoxazol-2- ylmethyl (5-(3- Cl(azetidin-l-yl)- 3 -(azetidin- 1 -y l)-4 - 53 4- O-w0405.1 chlorobenzaldehyde chlorobenzyl)tHOhiazol-2- yl)carbamateH_Noxazol-2- u >=\ylmethyl (5-(l-x— \ / -N 0(1H- ) — \ JL i / s^N' \y'^x°\benzo[d]imidaHo54 n / a 370.1 zol-5- Step 1 used Boc-protected startingyl)ethyl)thiazo material: tert-butyl 5-acetyl-lH- 1-2- benzo [d]imidazole- 1 -carboxylate.yl)carbamate The Boe group was cleaved in Step2.62ME1\58440953. vl139849-00420( 1 -methyl- 1H- imidazol-2- Clyl)methyl (5- o55 (l-(4- 0 n / a 377.1 chlorophenyl)e / V.-Vykthyl)thiazol-2-HMeN— Vyl)carbamateoxazol-2- Cloylmethyl (5-(7- O56 chlorochroman0n / a 392.1 -4-yl)thiazol- °V7^ COSMANA0-VNXJ2-yl)carbamate ^z=IZoxazol-2- TZ Foylmethyl (5- >° oZT o57 (chroman-4- n / a 358.1Jyl)thiazol-2- L zyl)carbamateoxazol-2- ylmethyl (5-(l- o(2- methoxypyridi MeO— < / O58 n / a 361.1 n-4- yl)ethyl)thiazohSJ1-2- yl)carbamateoxazol-2- ylmethyl (5- ((4- (4- chlorophenyl)(59 chlorophenyl)(oxeta 406.1 oxetan-3- n-3 -y l)methanone yl)methyl)thiazol-2- yl)carbamateoxazol-2- ylmethyl (5-(7- chloroisochro60 n / a 392.1 man-4 - yl)thiazol-2- yl)carbamate63ME1\58440953. vl139849-00420oxazol-2- ylmethyl (5 -(8- 61 chlorochroman n / a 391.9 -4-yl)thiazol- 2-yl)carbamateoxazol-2- ylmethyl (5-(l- (6- oMeO— \ / methoxypyridi62 n / a 361.1 n-2- yl)ethyl)thiazoH1-2- yl)carbamate >zzzoxazol-2- oylmethyl (5-(l- ^N.(1 -methyl- 1H- MeN^=< 063 pyrazol-4- n / a 334.1 yl)ethyl)thiazoHSJ1-2- yl)carbamateoxazol-2- ylmethyl (R)- R(5-(l-(2- y-oF l-(2- (difluorometho(difluoromethoxy)p64 xy)pyrimidin- M Z~N 0 398.0 y rimidin-5 -y l)ethan- 5-Ho 1-one yl)ethyl)thiazo[a]D20-4.0 (c 0.12, DMSO)1-2- yl)carbamateCl\oxazol-2- #-N Oylmethyl (R)- X — # jl(5-(l-(6-HSJ1chloropyridin- RT 1.47 min65 n / a 365.03- Column: CHIRALPAK® AD-34.6x50mm, 3yl)ethyl)thiazomicron; Phase A: CO2, Phase B: 1 / 11-2- IPA / [EtOH (0.05% DEA)]; Isocratic elution:yl)carbamate B: A 40:60; Flow rate: 3mL / min; Detector:PDA; Column temperature: 35 °C; Backpressure: 100 Bar64ME1\58440953. vl139849-00420Cloxazol-2- \ Oylmethyl (S)- < 1 JI o(5-(l-(6-HJIJ’chloropyridin- RT 1.84 min66 n / a 365.03- Column: CHIRALPAK® AD-34.6x50mm, 3yl)ethyl)thiazomicron; Phase A: CO2, Phase B: 1 / 11-2- IPA / [EtOH (0.05% DEA)]; Isocratic elution:yl)carbamate B: A 40:60; Flow rate: 3mL / min; Detector:PDA; Column temperature: 35 °C; Backpressure: 100 Baroxazol-2- ylmethyl (S)- MeO(5-(l-(5- methoxypyrazi67Ny-O? n / a 362.1 n-2- yl)ethyl)thiazoHV1-2- [OC]D20+48.3 (c 0.19, methanol)yl)carbamateoxazol-2- ylmethyl (R)- MeO(5-(l-(5- methoxypyrazi68N=< X!1 U n / a 362.1 n-2- / S-^N^O^rf0®yl)ethyl)thiazo1-2- [a]D20 —45.2 (c 0.19, methanol)yl)carbamate / A-NH2\=< / ~-N O' — e if jf _oxazol-2- ylmethyl (5-(2-Ho69 aminobcnzyljt Step 1 used 2-nitrobenzaldehyde. n / a 331.0 hiazol-2- A final nitro -reduction step providedyl)carbamate the final compound:Fe (5 eq), NH4C1 (5 eq), EtOH, H2O60 °C, 2 h65ME1\58440953. vl139849-00420HO\=\ #-N Ooxazol-2- \ — e if jf..Iylmethyl (5-(l-HSJ l-(4- (4- (70 Step 1 used TIPS-protected starting (triisopropylsilyl)o 346.0 hydroxyphenyl material: l-(4- xy )pheny l)ethan- 1 - )ethyl)thiazol- ((triisopropylsilyl)oxy)phenyl)ethan- one2-yl)carbamate 1-one. A final TIPS-removal stepprovided the title compound:LiOAc (2 eq), DMF, 40 °C, 12 h.F3C\Ooxazol-2- N=\ J~N Oylmethyl (5-(l-HNJ(5- (trifluorometh Step 2 furnished the dihydrothiazole:71 (£)-5 -( 1 n / a 399.0 yl)pyridin-2- -(5 -(trifhioromethy l)py ridin- yl)ethyl)thiazo 2-yl)ethylidene)-4,5-dihydrothiazol- 1-2- 2-amine. An additionalyl)carbamate isomerization step was used toprovide the terminal thiazole: DBU(3 eq), CH2CI2, 20 °C, 12 hH2N^~ / 0oxazol-2- ylmethyl (5- ((3-(3- Step 1 used 2-oxo-2,3- aminopropyl)- dihy drobenzo [d] oxazole-5 - 2-oxo-2,3- carbaldehyde. The product of Step 272dihydrobenzo[ was alkylated with Boc-protected n / a 430.1 d]oxazol-5- amine: tert-butyl (3- yl)methyl)thia bromopropyl)carbamate (1.2 eq),zol-2- K2CO3 (3 eq), DMF, 25 °C, 12 h. Ayl)carbamate final Boc-removal step provided thetitle compound: 4 M HC1 in dioxane,CH2CI2, 25 °C, 2 h.66ME1\58440953. vl139849-00420F3C\oxazol-2- M °ylmethyl (5-(l-HO(6- Step 2 furnished the dihydrothiazole:(trifluorometh73 oxazol-2-ylmethyl (E)-(5-(l-(6- n / a 399.0 yl)pyridin-3- (trifluoromethy l)py ridin-3 - yl)ethyl)thiazo yl)ethylidene)-4,5-dihydrothiazol-2- 1-2- yl)carbamate. An additionalyl)carbamate isomerization step was used toprovide the terminal thiazole: DBU(3 eq), DCE, 25 °C, 12 hCloxazol-2-N=K #'~N °ylmethyl (5-(l-HSJ(5- chloropyridin- Step 2 furnished the dihydrothiazole:74 365.12 oxazol-2-ylmethyl (E)-(5-(l-(5- n / a - yl)ethyl)thiazo chloropyridin-2-yl)ethylidene)-4,5- 1-2- dihydrothiazol-2-yl)carbamate. Anyl)carbamate additional isomerization step wasused to provide the thiazole: DBU (3eq), DCE, 25 °C, 12 hoxazol-2- Clylmethyl (5-(4- 75 chlorobcnzyljt n / a 350.0 hiazol-2- yl)carbamateHSJClHN' Foxazol-2- ylmethyl (5-(4-HM benzyl 4-(2-chloro- chloro-3- Step 1 used Cbz-protected starting 5- 76 (piperazin-1- 434.1 material: benzyl 4-(2-chloro-5- formylphenyl)pipera yl)benzyl)thiazformylphenyl)piperazine- 1 - zine- 1 -carboxylate ol-2- carboxylate. A final Cbz-removalyl)carbamatestep provided the title compound: 6M HO in dioxane, 60 °C, 2 h.67ME1\58440953. vl139849-00420D3COoxazol-2- \\ Z^N O\ — \ JL Aylmethyl (5-(l- / S'^N'^O'X^YO\(6-(methoxy- l-(6-(methoxy- Step 2 furnished the terminal alkene:77 d3)pyridin-3- d3)py ridin-3 - 364.05 -( 1 -(6-(methoxy-d3 )py ridin-3 - yl)ethyl)thiazo yl)ethan-l-one yl)vinyl)thiazol-2 -amine. A1-2- subsequent hydrogenation wasyl)carbamaterequired to reduce the double bond:10% Pd / C, H2, MeOH, 50 °C, 12 h.MeO^ _Cl\oxazol-2- / N^-Noylmethyl (5-(l- m W(4-chloro-3-Hol-(4-chloro-3-((2- ((2- Step 2 furnished the terminal alkene:methoxyethyl)(meth78 methoxyethyl) 5-(l-(4-chloro-3-((2- 451.1 yl)amino)phenyl)eth (methyl)amino methoxyethyl)(methyl)amino)phenylan- 1 -one )phenyl)ethyl)t )vinyl)thiazol-2 -amine. A subsequenthiazol-2- hydrogenation was required toyl)carbamate reduce the double bond: Pt / C, H2(50 PSI), MeOH, 60 °C, 12 h.ClOoxazol-2- / sylmethyl (5-(l-Ho(4-chloro-3- Step 2 furnished the terminal alkene: l-(4-chloro-3- 79 morpholinophe 5-(l-(4-chloro-3- morpholinophenyl)e 449.1 nyl)ethyl)thiaz morpholinophenyl)vinyl)thiazol-2- than- 1 -one ol-2- amine. A subsequent hydrogenationyl)carbamate was required to reduce the doublebond: Pt / C, H2(50 PSI), MeOH,60 °C, 12 h.oxazol-2- Clylmethyl (5-(l- (4- \ zT-N Ochlorophenyl)- / — \ K I80 F3CSN ' > n / a 418.02,2,2-HNJtrifluorocthyl)t Step 2 removed the Boc group buthiazol-2- not the hydroxyl. An additionalyl)carbamate dihydroxylation step was required:68ME1\58440953. vl139849-00420iodine (1.5 eq), hypophosphorousacid (8 eq), AcOH, 100 °C, 16 h.°~7--2 Z' N oHN- / oxazol-2- O, Step 1 used l-(4- ylmethyl (5-(l- bromophenyl)ethan-l-one. An(4-(oxetan-3- additional final step was required to81 n / a 386.1 yl)phenyl)ethy convert the bromide to the oxetane:l)thiazol-2- 4,4,5,5-tetramethyl-2-(oxetan-3-yl)- yl)carbamate 1,3,2-dioxaborolane IZ (2 eq), (4,4'- dtbbpy)NiC12 (0.0 >°5 eq),o(Ir[dF(CF3)ppy]2(dtbpy))PF6(0.01eq), L omorpholine (1.5 eq), DMF, 25 °C,16 hoxazol-2- ylmethyl (5-(l- (4-(3- 3-(4-(l-(2- hydroxyoxetan aminothiazol-5- 82 402.1 -3- yl)ethyl)phenyl)oxet yl)phenyl)ethy an-3-oll)thiazol-2- yl)carbamate

[0262] Synthetic procedure E

[0263] Example 83: Oxazol-2-ylmethyl (R)-(5-(l -(6-cyclopropoxypyridin-3-yl) e thy I) thiazol -2-yl) carbamate

[0264] Example 84: Oxazol-2-ylmethyl (S)-(5-(l-(6-cyclopropoxypyridin-3-yl) e thy I) thiazol -2-yl) carbamate

[0265] Step 1

[0266] Cyclopropanol (10.0 g, 172 mmol) was added to a mixture of potassium tert-butoxide (19.2 g, 171 mmol) and 2-fluoro-5 -iodopyridine (20.0 g, 89.7 mmol) in THF (20069ME1\58440953. vl139849-00420mL). The reaction mixture was stirred at 80 °C for 3 h, then filtered and concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 1:19) afforded 2-cy cl opropoxy-5 -iodopyridine (13.0 g, 42%) as a yellow oil; ES-MS [M+H]+: 262.0.

[0267] Step 2

[0268] Palladium(II) acetate (870 mg, 3.88 mmol) was added to a mixture of (E)-but-2-en-l-ol (1.85 g, 25.6 mmol), TBAB (6.17 g, 19.2 mmol), sodium bicarbonate (3.26 g, 38.8 mmol) and 2-cyclopropoxy-5-iodopyridine (5.00 g, 19.2 mmol) in DMF (100 mL). The reaction mixture was stirred at 40 °C for 12 h, then diluted with brine (120 mL) and extracted into EtOAc (2 x 100 mL). The combined organic extracts were dried over anhydrous sodium sulfate and concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 3:7) afforded 3-(6-cyclopropoxypyridin-3-yl)butanal (2.40 g, 61%) as a yellow oil; ES-MS [M+H]+: 206.2.

[0269] Step 3

[0270] Aqueous hydrobromic acid solution (1.6 g, 5.93 mmol) and bromine (0.30 mL, 5.82 mmol) were added to a solution of 3-(6-cyclopropoxypyridin-3-yl)butanal (1.00 g, 4.87 mmol) in dichloromethane (5 mL) at 0 °C. The reaction mixture was stirred at this temperature for 1 h, then diluted with water (20 mL) and extracted into dichloromethane (3 30 mL). The combined organic extracts were dried over anhydrous sodium sulfate and concentrated in vacuo to afford 2-bromo-3-(6-cyclopropoxypyridin-3-yl)butanal (330 mg, crude) as a yellow oil; ES-MS [M+H]+: 284.0.

[0271] Step 4

[0272] Thiourea (280 mg, 3.68 mmol) was added to a solution of 2-bromo-3-(6-cyclopropoxypyridin-3-yl)butanal (330 mg, 1.16 mmol) in ethanol (5 mL). The reaction mixture was stirred at 90 °C for 12 h, then concentrated in vacuo and purified by flash column chromatography on silica (EtOAc: PE, 0:1 to 1:1) to afford 5-(l-(6-70ME1\58440953. vl139849-00420cyclopropoxypyridin-3-yl)ethyl)thiazol-2-amine (210 mg, 62%) as a yellow solid; ES-MS [M+H]+: 262.1.

[0273] Step 5Example 84

[0274] CDI (590 mg, 3.64 mmol) was added to a solution of oxazol-2-ylmethanol (360 mg, 3.63 mmol) in THF (10 mL) and the resulting mixture was stirred at 60 °C for 4 h. 5-(l-(6-Cyclopropoxypyridin-3-yl)ethyl)thiazol-2-amine (190 mg, 0.73 mmol), triethylamine (0.79 mL, 2.17 mmol) and DMAP (20 mg, 0.16 mmol) were then added and stirring was continued at 60 °C for 12 h. Acetic acid was added until the pH was ~6 and the mixture was filtered. The filtrate was concentrated in vacuo, then purified by preparative HPLC (column: Welch Xtimate Cl 8, 5 pm, 25x150mm; gradient: acetonitrile: [water (0.1% formic acid)]; gradient: 70:30^40:60) and preparative SFC (column: CHIRALCEL® OX-10 / SFC 50x250mm, 10 micron; CC>2:ethanol (0.1% NH4OH) 60:40) to afford oxazol-2-ylmethyl (R)-(5-(l-(6-cyclopropoxypyridin-3-yl)ethyl)thiazol-2-yl)carbamate (37 mg, 13%, Example 83) as a white solid; Retention time: 1.24; 6H (400 MHz; DMSO-d6) 11.98-11.75 (1H, m), 8.19-8.10 (2H, m), 7.66-7.57 (1H, m), 7.29-7.14 (2H, m), 6.81 (1H, d, J8.6 Hz), 5.27 (2H, s), 4.38-4.28 (1H, m), 4.20-4.12 (1H, m), 1.64-1.54 (3H, m), 0.77-0.70 (2H, m), 0.68-0.61 (2H, m); ES-MS [M+H]+: 387.1 and oxazol-2-ylmethyl (5)-(5-(l-(6-cyclopropoxypyridin-3-yl)ethyl)thiazol-2-yl)carbamate (37 mg, 13%, Example 84) as a white solid; Retention time: 0.99; 5H (400 MHZ; DMSO-d6) 11.98-11.75 (1H, m), 8.19-8.10 (2H, m), 7.66-7.57 (1H, m), 7.29-7.14 (2H, m), 6.81 (1H, d, J 8.6 Hz), 5.27 (2H, s), 4.38-4.28 (1H, m), 4.20-4.12 (1H, m), 1.64-1.54 (3H, m), 0.77-0.70 (2H, m), 0.68-0.61 (2H, m); ES-MS [M+H]+: 387.1.

[0275] Example 85 was also prepared using synthetic procedure E:71ME1\58440953. vl139849-00420ES-MS Ex. No. Name Structure Starting material[M+H]+oxazol-2- Clylmethyl (5-(l- (4-chloro-2- \=\ #-N O 2-bromo-5- 85 ) - \ 1 I 388.9 cyanophenyl)e / S^N' V'YA chlorobenzonitrilethyl)thiazol-2- yl)carbamate No step 1

[0276] Synthetic procedure F

[0277] Example 86: N-(5-( 1 -( 4-Chlorophenyl)ethyl)thiazol-2-yl)-3-phenylazetidine-l-carboxamide

[0278] 3 -Phenylazetidine hydrochloride (57 mg, 0.33 mmol) was added to a solution of phenyl (5-(l-(4-chlorophenyl)ethyl)thiazol-2-yl)carbamate* (100 mg, 0.28 mmol) and triethylamine (0.19 mmol, 1.39 mmol) in dichloromethane (2 mL). The reaction mixture was stirred at 25 °C for 12 h. The precipitate was filtered and triturated (acetonitrile: water 1:1, 1 mL) to afford N-(5-(l-(4-chlorophenyl)ethyl)thiazol-2-yl)-3-phenylazetidine-l-carboxamide (49 mg, 44%) as a white solid; 5H (400 MHz; DMSO-d6) 10.86 (1H, br s), 7.40-7.33 (6H, m), 7.33-7.24 (3H, m), 7.11 (1H, s), 4.38 (2H, m), 4.31 (1H, m), 3.98-3.91 (2H, m), 3.88-3.79 (1H, m), 1.58 (3H, d, JIA Hz). ES-MS [M+H]+: 398.2.

[0279] *Prepared according to Synthetic Procedure C, Steps 1-3

[0280] Other examples prepared using synthetic procedure F are shown in the following table. All intermediates are commercially available unless noted (see ‘Intermediate synthesis’ section).Intermediates ES-MS Ex. No. Name Structurerequiring synthesis [M+H]+72ME1\58440953. vl139849-00420N-(5-(l-(4- chlorophenyl)e Clthyl)thiazol-2- 87 yi)-3- \=\ rf-N 0 n / a 338.1X Xhydroxyazetidi / S^N^N'AH V-J<ne-1- OHcarboxamideN-(5-(l-(4- chlorophenyl)e Clthyl)thiazol-2- O88 yi)-3- \=X #-N O n / a 352.1VX X Xmethoxyazetid / S"^N N"\Hine-1- OMecarboxamideN-(5-(l-(4- chlorophenyl)e Clthyl)thiazol-2- 89 yl)-l-oxa-6- \=< 0 n / a 364.0Xx Xazaspiro[3.3]h / S^N N-^\eptane-6-HO'3carboxamideN-(5-(l-(4- Clchlorophenyl)e XXthyl)thiazol-2- / ^N 090 389.0 yl)-3-(oxazol- yx x x n / a2-yl)azetidine-H vX,ox1 -carboxamideN-(5-(l-(4- chlorophenyl)eCl\thyl)thiazol-2- 91 yl)-2-oxa-6- o n / a 364.1y-x x xazaspiro[3.3]h / S^N NXH tAxeptane-6- V-0carboxamideN-(5-(l-(4-Cl\chlorophenyl)e92 thyl)thiazol-2- \=\ O \— / n / a 398.1 yl)-2- yx JL x / phenylazetidin H v_>73ME1\58440953. vl139849-00420e-1- carboxamideN-(5-(l-(4- Clchlorophenyl)ethyl)thiazol-2- \=< rf-N 093 < A A n / a 388.1 yl)-3-(furan-2- / S^N N-"\yl)azetidine-l-HcarboxamideN-(5-(l-(4- Clchlorophenyl)ethyl)thiazol-2- zr-N O94 YA A A n / a 399.2 yl)-3-(pyridin- / S-"^N N" AH4-yl)azetidine- 1 -carboxamide3- (benzo[d]oxazCl\ol-2-yl)-N-(5- 2-(azetidin-3- (l-(4- 095 A A / S^N N^ yl)benzo [d]oxazole 439.2 chlorophenyl)e \HVA_N TFA salt thyl)thiazol-2- yl)azetidine-l- carboxamideN-(5-(l-(4- chlorophenyl)ethyl)thiazol-2-Cl\yl)-3- 96 Z^N o n / a 420.0 ((trifluorometh \ JI Koxy)methyl)azHUA^, OCF3etidine-1- carboxamidel-(5-(l-(4- chlorophenyl)eCl\ / Athyl)thiazol-2- 97 n / a 363.0 yl)-3-(oxazol- 2- ylmethyl)urea74ME1\58440953. vl139849-00420N-(5-(l-(4- chlorophenyl)e Clthyl)thiazol-2- o98 yi)-3- / r~N O n / a 366.0yy(methoxymeth / s^N A N-nHVA^OMeyl)azetidine-l- carboxamideN-(5-(l-(4- chlorophenyl)e Clthyl)thiazol-2- o\=< / ^N O99 yl)-6-oxa-2- A A n / a 378.1 azaspiro[3.4]o / SHctane-2- ^0carboxamideN-(5-(l-(4- chlorophenyl)e Clthyl)thiazol-2- O\=< O100 yl)-3-(l- < X A n / a 380.1 methoxy ethyl)HlA AMeazetidine- 1- carboxamideN-(5-(l-(4- chlorophenyl)ethyl)thiazol-2- Clyl)-3 -metho xy- O101 \=< ^~N O n / a 366.13-; — \ A X / S-^N N-Amethylazetidin H V-VOMee-1- carboxamideN-(5-(l-(4-Cl\chlorophenyl)eOthyl)thiazol-2- \=< O102 A A n / a 399.0 yl)-3-(pyridin- / S N N-^\H2-yl)azetidine- kJ1 -carboxamideCl\N-(5-(l-(4- chlorophenyl)e Z'N O103 A A n / a 399.1 thyl)thiazol-2- / S^N N-AH \Ayl)-3-(pyridin- IUN75ME1\58440953. vl139849-004203-yl)azetidine- 1 -carboxamideN-(5-(l-(4- chlorophenyl)ethyl)thiazol-2- Clyl)-3- O104 (methoxymeth \=< O n / a 380.0C A Ayl)-3- / S^N N-^\HmethylazetidinxOMee-1- carboxamideN-(5-(l-(4- chlorophenyl)e Clthyl)thiazol-2- O105 yl)-3-fluoro-3- \==< Z^N O\ X X n / a 384.1 (methoxymeth / S N N^\H '" VAyl)azetidine-l- F OMecarboxamidel-(5-(l-(4- chlorophenyl)e Clthyl)thiazol-2- XA106 z^N O 1 —.cOMe n / a 366.1 yl)-3-(trans-3- ) — <( X K 7 / 7methoxy cyclo H Hbutyl)ureal-(5-(l-(4- chlorophenyl)eCl\thyl)thiazol-2- XA107 Z^N O 1 — ^OMe n / a 366.1 yl)-3-(cis-3- > — \ JL A JATmethoxy cyclo H Hbutyl)ureaN-(5-(l-(4- chlorophenyl)ethyl)thiazol-2-Cl\3 -metho xy -3- yl)-3 -metho xy- 108 x=< ^~N O (methoxymethyl)aze 396.13- A A / S^N N- / (methoxymeth H V— V-OMe tidine^OMeyl)azetidine-l- carboxamide76ME1\58440953. vl139849-00420N-(5-(l-(4- chlorophenyl)e Clthyl)thiazol-2- OAN O109 yi)-3- n / a 400.2 (methylsulfony1 sElN. ol)azetidine-l- 0carboxamide(lR,5S,6s)-N- (5-(l-(4- chlorophenyl)e Clthyl)thiazol-2- o 6-methoxy-3- \=< A~N O110 yl)-6-methoxy- azabicyclo[3.1.0]he 378.03-HL_ / \ xane HO salt azabicyclo[3.1. H0]hexane-3- carboxamideN-(5-(l-(4- chlorophenyl)ethyl)thiazol-2-Cl\yl)-3-hydroxy- o111 \=< O n / a 383.13- yX i / S^N A N^\(methoxymethH^-" VAOHOMeyl)azetidine-l- carboxamideN-(5-(l-(4- chlorophenyl)eCl\thyl)thiazol-2- Oyl)-3-(3- \=< Z'N 0112 X A n / a 404.0 methyl- 1,2,4- / S^N N-^\Hoxadiazol-5- o-r?yl)azetidine-l- carboxamideN-(5-(l-(4- chlorophenyl)eCl\thyl)thiazol-2- o113 yl)-3-hydroxy- n / a 415.0x x3-(pyridin-2- I S^N N^\H / yl)azetidine-l- carboxamide77ME1\58440953. vl139849-00420N-(5-(l-(4- chlorophenyl)e Clthyl)thiazol-2- yl)-3-(3- Z^N 0114 y / y A A n / a 429.0 methoxypyridiH Ak / Nn-2- T jyl)azetidine-l- MeO'x^^carboxamidel-(5-(l-(4- Clchlorophenyl)e115 thyl)thiazol-2- n / a 338.1 yl)-3-(oxetan- yy x A X / 3-yl)urea H HN-(5-(l-(4- chlorophenyl)ethyl)thiazol-2- Cl3-((methoxy- yi)-3- 116 A=Z 0 d3 )methy l)azetidine 369.1((methoxy- / S^N N" A TFA salt d3)methyl)azet H V-V^. OCD3idine-1- carboxamideN-(5-(l-(4- chlorophenyl)eCl\thyl)thiazol-2- 117 yi)-3- n / a 388.0^yy A A(difluorometho / S^N N-^\ IH \Axy)azetidine-l- 0 FcarboxamideN-(5-(l-(4- chlorophenyl)ethyl)thiazol-2-Cl\yl)-3-(2- \=\ yf-N 0118 A A n / a 394.1 methoxypropa / S^N N-^H \Ax / )Men-2- yl)azetidine-l- carboxamide78ME1\58440953. vl139849-00420N-(5-(l-(4- chlorophenyl)e Clthyl)thiazol-2- 3 -(metho xy- 119 yi)-3- X=\ rf-N O d3)azetidine TFA 355.0\ < X X(methoxy- / S N NXH saltOCDd3)azetidine-l-3carboxamideN-(5-(l-(4- chlorophenyl)e Clthyl)thiazol-2- 120 \=Z / T~N oyi)-3,3- \ ( X X n / a 358.1 difluoroazetidi / S^N NXHne-1- FcarboxamideN-(5-(l-(4- Clchlorophenyl)ethyl)thiazol-2-zrN o121 yi)-3,3- 372.0A A n / a / S^N N \difluoropyrroliHdine-1- carboxamideN-(5-(l-(4- chlorophenyl)eCl\thyl)thiazol-2- o\=< 0 122 347.0 n / a yi)-3- / S^N NA cyanoazetidine H-1- carboxamideN-(5-(l-(4- chlorophenyl)eCl\thyl)thiazol-2- 123 336.0 n / a yi)-3- Vx X X methylazetidin / S^N NXH t-X. e-1- carboxamideN-(5-(l-(4-Cl\chlorophenyl)eOZ^N O 124 378.0 thyl)thiazol-2- n / a\ x x / A yi)-3- H \_X X-XOcyclopropoxya79ME1\58440953. vl139849-00420zetidine-1- carboxamideN-(5-(l-(4- Clchlorophenyl)e125 thyl)thiazol-2- ZT-N 0 n / a 322.1 yl)azetidine-l- y-A A A / S^N NAcarboxamide HN-(5-(l-(4- chlorophenyl)eClthyl)thiazol-2- 3-fluoro-3- yl)-3-fluoro-3- O ((methoxy- 126 \=\ Z^N 0 387.1((methoxy- \-\ X XI S N NA d3 )methy l)azetidineHd3)methyl)azet F OCD3TFA salt idine-1- carboxamideN-(5-(l-(4- chlorophenyl)e Clthyl)thiazol-2- oZ^N 0127 yi)-3- n / a 372.0 / S^N(difluoromethyHl)azetidine-l- FcarboxamideN-(5-(l-(4- chlorophenyl)eCl\thyl)thiazol-2- 128 yi)-3- n / a 390.0 (trifluorometh / S'^N N'AHyl)azetidine-l- ^^CF3carboxamideN-(5-(l-(4- chlorophenyl)ethyl)thiazol-2-C|yl)-6-methoxy- o129 1 n / a 392.22- azaspiro[3.3]hH^^OMeeptane-2- carboxamide80ME1\58440953. vl139849-00420N-(5-(l-(4- chlorophenyl)e Clthyl)thiazol-2- 2-(3 -methylazetidin- O130 yl)-3-methyl- \==\ zr-N 0\ A 3-yl)oxazole TFA 403.1 3-(oxazol-2- / S N N-"\ saltHJyl)azetidine-l- \ l\rcarboxamideClO \=< / ^N OVAN-(5-(l-(4- A AHPss vAchlorophenyl)ethyl)thiazol-2- benzyl 8-oxa-2,5- 131 yl)-8-oxa-2,5- Cbz-protected starting material was diazaspiro [3,5]nona 393.1 diazaspiro[3.5] used: benzyl 8-oxa-2,5- ne-5 -carboxylate nonane-2- diazaspiro [3.5] nonane -5 - carboxamide carboxylate. A subsequent Cbz- removal step provided the titlecompound: 6 M HO in dioxane,60 °C, 2 h.ClN-(5-(l-(4- chlorophenyl)e AA0thyl)thiazol-2- benzyl 8-oxa-2,5- yl)-5-methyl- 132 diazaspiro [3,5]nona 407.18-oxa-2,5- Ar ne-5 -carboxylate diazaspiro[3.5]Prepared by methylation of Examplenonane-2- 131 using formaldehyde, NaBH3CN,carboxamideMeOH, 60 °CClAAN-(5-(l-(4- \=\ A-N Ochlorophenyl)e H l A / s" Athyl)thiazol-2-H133 yl)-5-oxa-2,8- n / a 393.1 diazaspiro[3.5] Boc-protected starting material wasnonane-2- used: tert-butyl 5-oxa-2,8- carboxamide diazaspiro[3.5]nonane-8- carboxylate. A subsequent Boc- removal step provided the title81ME1\58440953. vl139849-00420compound: 3 eq TFA, CH₂Cl₂,20 °C, 2 h.N-(5-(l-(4- Clchlorophenyl)ethyl)thiazol-2- / "N0y- < 11 uyl)-8-methyl- 134Hn / a 407.15-oxa-2,8- diazaspiro[3.5] Prepared by methylation of Examplenonane-2- 133 using formaldehyde, NaBH3CN,carboxamide AcOH, MeOH, 40 °CClN-(5-(l-(4- Ochlorophenyl)e\ ( if jnthyl)thiazol-2- l-(azetidin-3- / S^N NAH VA / 135 yl)-3-(l,l- yl)ethan-l-one TFA 386.1 difluoroethy TFl)a saltAn additional final difluorinationzetidine-1- step provided the title compound: 9carboxamideeq DAST, DCE, 0^20 °C, 2 h.3-fluoro-3- (methoxymethyl)-N-(5-(l-(4- phenyl (5-(l-(4- 0HN(oxetan-3- (oxetan-3- \=< Z~~N 0 136 ylcarbamoyl)phenyl 449.2 ylcarbamoyl)pJL A / s'A tr: henyl)ethyl)thi )ethyl)thiazol-2-H'A~\F OMe azol-2- yl)carbamate yl)azetidine-l- carboxamide5-(l-(2-(3- fluoro-3- (methoxymethphenyl (5-(l-(6- yl)azetidine-l- Q j HN-\ (oxetan-3- carboxamido)t137 ylcarbamoyl)pyridin 450.2 hiazol-5- y / X I -3 -y l)ethy l)thiazol- yl)ethyl)-N-H2-yl)carbamate F OMe(oxetan-3- yl)picolinamide

[0281] Synthetic procedure G82ME1\58440953. vl139849-00420

[0282] Example 138: Oxazol-2-ylmethyl (5-(3-(4-aminobutoxy)benzyl)thiazol-2-y I) carbamate

[0283] Step 1

[0284] Triisopropyl silyl chloride (26.1 g, 135 mmol) was added dropwise to a solution of 3 -hydroxybenzaldehyde (15 g, 123 mmol) and imidazole (18.4 g, 270 mmol) at 0 °C. The reaction mixture was stirred at 0 °C for 30 min then at 25 °C for 90 min. The mixture was diluted with water (150 mL), then extracted into EtOAc (3 x 150 mL). The combined organic extracts were washed with brine (150 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by flash column chromatography on silica (EtOAc: PE, 0:1 to 1:19) afforded 3-((triisopropylsilyl)oxy)benzaldehyde (32.0 g, 94%) as a light yellow oil; ES-MS [M+H]+279.1

[0285] Step 2

[0286] n-BuLi (2.5 M in THF, 74.9 mL, 150 mmol) was added dropwise to a solution of tert-butyl thiazol-2-ylcarbamate (15.0 g, 74.9 mmol) in THF (150 mL) at -60 °C and the resulting mixture was stirred at this temperature for 30 min. A solution of 3-((triisopropylsilyl)oxy)benzaldehyde (27.1 g, 97.4 mmol) in THF (50 mL) was added and stirring was continued at -60 °C for 2 h. The reaction mixture was quenched with saturated aqueous ammonium chloride solution (100 mL) and extracted into EtOAc (2 x 100 mL). The combined organic extracts were washed with brine (100 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 3:7) afforded tert-butyl (5-(hydroxy(3-((triisopropylsilyl)oxy)phenyl)methyl)thiazol-2-yl)carbamate (21.0 g, 58%) as a yellow oil; ES-MS [M+H]+: 479.2.

[0287] Step 3

[0288] TFA (60.5 mL, 815 mmol) was added to a solution of tert-butyl (5 -(hydroxy (3- ((triisopropylsilyl)oxy)phenyl)methyl)thiazol-2-yl)carbamate (15.6 g, 32.6 mmol) and83ME1\58440953. vl139849-00420tri ethyl silane (26.0 mL, 163 mmol) in dichloromethane (150 mL) The resulting mixture was stirred at 25 °C for 2.5 h, then adjusted to pH 8 with saturated aqueous sodium bicarbonate solution and extracted into dichloromethane (2 x 100 mL). The combined organic extracts were washed with brine (100 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 3:7) afforded 5-(3-((triisopropylsilyl)oxy)benzyl)thiazol-2-amine (9.50 g, 80%) as a yellow oil; ES-MS [M+H]+: 363.2.

[0289] Step 4

[0290] A mixture of 5-(3-((triisopropylsilyl)oxy)benzyl)thiazol-2-amine (5.00 g, 13.8 mmol) in TFA (35 mL) was stirred at 60 °C for 3 h, then adjusted to pH 8 with saturated aqueous sodium bicarbonate solution and extracted into EtOAc (2 x 50 mL). The combined organic extracts were washed with brine (100 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 7:3) afforded 3-((2-aminothiazol-5-yl)methyl)phenol (2.50 g, 12.1 mmol) as a yellow solid; ESMS [M+H]+: 207.0.

[0291] Step 5BocHN

[0292] A solution of DIAD (1.47 g, 7.27 mmol) in THF (5 mL) was added to a mixture of 3-((2-aminothiazol-5-yl)methyl)phenol (1.00 g, 4.85 mmol), tert-butyl (4-hydroxybutyl)carbamate (1.38 g, 7.27 mmol) and triphenylphosphine (1.91 g, 7.27 mmol) in THF (20 mL) at 0 °C. The reaction mixture was stirred at 25 °C for 12 h, then concentrated in vacuo and purified by flash column chromatography (EtOAc: PE, 0:1 to 7:3) to afford tertbutyl (4-(3-((2-aminothiazol-5-yl)methyl)phenoxy)butyl)carbamate (2.40 g, 66%) as a yellow oil; ES-MS [M+H]+: 378.1.

[0293] Step 684ME1\58440953. vl139849-00420BocHN BocHNH

[0294] Phenyl chloroformate (0.60 mL, 4.82 mmol) was added to a solution of tert-butyl (4-(3-((2-aminothiazol-5-yl)methyl)phenoxy)butyl)carbamate (2.40 g, 3.21 mmol) and triethylamine (0.89 mL, 6.42 mmol) in THF (25 mL) at 0 °C. The resulting mixture was stirred at 25 °C for 2 h, then diluted with water (15 mL) and extracted into EtOAc (2 x 15 mL). The combined organic extracts were washed with brine (15 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 3:7) afforded tert-butyl (4-(3-((2-((phenoxycarbonyl)amino)thiazol-5-yl)methyl)phenoxy)butyl)carbamate (1.1 g, 62%) as a white solid; ES-MS [M+H]+: 498.2.

[0295] Step 7BocHN BocHNH

[0296] Sodium hydride (60% dispersion in oil, 97 mg, 2.43 mmol) was added to a solution of oxazol-2-ylmethanol (241 mg, 2.43 mmol) in THF (3 mL) at 0 °C. The resulting mixture was stirred 0 °C for 30 min and then a solution of tert-butyl (4-(3-((2-((phenoxycarbonyl)amino)thiazol-5-yl)methyl)phenoxy)butyl)carbamate (1.10 g, 2.21 mmol) in THF (10 mL) was added. The reaction mixture was stirred at 20 °C for 12 h, then poured into saturated aqueous ammonium chloride solution (10 mL). The mixture was extracted into EtOAc (2 x 10 mL) and the combined organic extracts were washed with brine (10 mL) dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 4:1) afforded tert-butyl (4-(3-((2-(((oxazol-2-ylmethoxy)carbonyl)amino)thiazol-5-yl)methyl)phenoxy)butyl)carbamate (870 mg, 1.32 mmol) as a white solid; ES-MS [M+H]+: 503.2.

[0297] Step 8BocHN85ME1\58440953. vl139849-00420

[0298] Hydrochloric acid (4.0 M in dioxane, 5 mL, 20 mmol) was added to tert-butyl (4-(3-((2-(((oxazol-2-ylmethoxy)carbonyl)amino)thiazol-5-yl)methyl)phenoxy)butyl)carbamate (470 mg, 0.94 mmol). The reaction mixture was stirred at 25 °C for 1 h, then concentrated in vacuo and purified by preparative HPLC (column: Waters™ XB ridge BEH Cl 8 OBD Prep Column, 130A, 10 pm, 50 mm X 150 mm; acetonitrile: [water (0.1% ammonium carbonate)]; gradient: 1:4— >2:3) to afford oxazol-2-ylmethyl (5-(3-(4-aminobutoxy)benzyl)thiazol-2-yl)carbamate (32 mg, 7%) as a white solid; 5H (400 MHz; CD3OD) 7.94 (1H, s), 7.23-7.17X I M NJ(2H, m), 7.06 (1H, s), 6.85-6.75 z z (3H, m), 5.29 (2H, s), 4.02 (2H, s), 3.98 (2H, m), 2.83-2.71 (2H, m), 1.85-1.77 (2H, m), 1.73^-1.6 04 (2H, m); ES-MS [M+H]+: 403.1.7

[0299] Other examples prepared using synthetic procedure G are shown in the following table. All intermediates are commercially available unless noted (see ‘Intermediate synthesis’ section). >z>zIZ IZIntermediates ES-MS Ex. No. Name Structure 0 0requiring synthesis [M+H] J+J.oxazol-2- L 0ylmethyl (5-(3- (3- 139 aminopropoxy n / a 389.1 )benzyl)thiazol-2- yl)carbamateoxazol-2- ylmethyl (5-(3- (2- 140 n / a 375.2 aminoethoxy)benzyl)thiazol- 2-yl)carbamateoxazol-2- Me2Nylmethyl (5-(3- 4~N O(4- nVo'Y.141 (dimethy laminhM n / a 431.1 o)butoxy)benz Prepared by methylation of Exampleyl)thiazol-2- 140 using formaldehyde,yl)carbamate NaBH3OAc, AcOH, MeOH, 25 °Coxazol-2- Me2NCl\ _l-(4-chloro-3- 142 ylmethyl (5-(l- \ / T-N O 451.2 ((triisopropylsilyl)o(4-chloro-3-(2-HM86ME1\58440953. vl139849-00420(dimethy lamin Step 1 omitted. Step 2 used l-(4- xy )pheny l)ethan- 1 - o)ethoxy)phen chloro-3- one yl)ethyl)thiazo ((triisopropylsilyl)oxy)phenyl)ethan- 1-2- 1-one. Additional finalyl)carbamate demethylation step in analogy toExample 141.oxazol-2- ylmethyl (5-(4- chloro-3- X z143 (piperidin-4- n / a 449.1 yloxy)benzyl)t L - hiazol-2- yl)carbamate5*) GJoxazol-2- IZ TZylmethyl (5-(3- >° o O(azetidin-3- J144 ylmethoxy)-4- L o n / a 435.1 chlorobcnzyljthiazol-2- yl)carbamateoxazol-2- MeOylmethyl (5-(3- ''O-4 #(2- 145 methoxyethoxHM n / a 390.2 y)benzyl)thiaz Step 5 used 2-methoxyethan-l-ol.ol-2- No Boe removal stepyl)carbamateoxazol-2- ylmethyl (5-(4- Meo^ _Cl\=\o4 #chloro-3-(2- ^~N o146 methoxyethoxHn / a 424.1 y)benzyl)thiazStep 5 used 2-methoxyethan-l-ol.ol-2- No Boe removal stepyl)carbamateoxazol-2- MeOCl\ylmethyl (5-(l- \ — (( Z^N 0 H147 (4-chloro-3-(2-Ho n / a 438.0 methoxyethoxStep 5 used 2-methoxyethan-l-ol.y)phenyl)ethylNo Boe removal step87ME1\58440953. vl139849-00420)thiazol-2- yl)carbamateCl\ _— < #~N ooxazol-2- \ — v n ij / ylmethyl (5-(l-HV(4-chloro-3-(2- Step 5 used TBS-protected starting l-(4-chloro-3- ((triisopropylsilyl)o148 hydroxyethoxy material: 2-((tert- 424.0 xy )pheny l)ethan- 1 - )phenyl)ethyl)t buty Idimethy lsilyl)oxy )ethan- 1 -ol.hiazo In the final step, modified conditions one l-2- yl)carbamate removed the TBS group to providethe title compound: 2 M HCl indioxane, CH2CI2, 25 °C, 1 h.oxazol-2- HO^ _C\ IZylmethyl (5-(4- chloro-3-(2- \ / T~N 0 0\ 1 11149 hydroxyethoxy n / a 410.0HJiJ)benzyl)thiazolPrepared in analogous manner to-2- Example 148yl)carbamateoxazol-2- ylmethyl (5-(3- (3- H2N-\CL>\aminopropoxy150 0 n / a 423.1)-4- chlorobenzyl)thiazol-2- yl)carbamateoxazol-2- ylmethyl (5-(3- (3- acetamidoprop V— \ \ Zr~N || 0 y151 n / a 465.1 oxy)-4- chlorobenzyl)t Prepared by acylation of Examplehiazol-2- 150 using AC2O, 25 °C, 1 h.yl)carbamateOxazol-2- ylmethyl (5-(3- 152 n / a 415.2 (piperidin-4- yloxy)benzyl)t88ME1\58440953. vl139849-00420hiazol-2- yl)carbamate

[0300] Synthetic procedure H

[0301] Example 153: Oxazol-2-ylmethyl (5-(4-chloro-3-((2-methoxyethyl)amino)benzyl)thiazol-2-yl)carbamate

[0302] Step 1O2N-A JS NHBocS NHBoc

[0303] n-BuLi (2.5 M in THF, 74.9 mL, 187 mmol) was added dropwise to a solution of tert-butyl thiazol-2-ylcarbamate (15.0 g, 74.9 mmol) in THF (150 mL) at -60 °C and the resulting mixture was stirred at this temperature for 30 min. A solution of 4-chloro-3-nitrobenzaldehyde (20.9 g, 112 mmol) in THF (75 mL) was added and stirring was continued at -60 °C for 2 h. The reaction mixture was quenched with saturated aqueous ammonium chloride solution (200 mL) and extracted into EtOAc (3 x 300 mL). The combined organic extracts were washed with brine (300 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 2:3) afforded tert-butyl (5-((4-chloro-3-nitrophenyl)(hydroxy)methyl)thiazol-2-yl)carbamate (2.00 g, 40%) as a white solid; 5H (400 MHz; DMSO-d6) 11.38 (1H, br s), 8.07 (1H, d, J 1.6 Hz), 7.81-7.65 (2H, m), 7.21 (1H, s), 6.54 (1H, d, J 4.4 Hz), 6.05 (1H, d, J 4.4 Hz), 1.44 (9H, s).

[0304] Step 2s s NH2

[0305] TFA (100 mL, 1.35 mmol) was added to a solution of tert-butyl (5-((4-chloro-3-nitrophenyl)(hydroxy)methyl)thiazol-2-yl)carbamate (20.0 g, 51.8 mmol) and triethylsilane (82.8 mL, 518 mmol) in dichloromethane (220 mL) The resulting mixture was stirred at 25 °C for 16 h, then adjusted to pH 7 with saturated aqueous sodium bicarbonate solution and extracted into EtOAc (3 x 400 mL). The combined organic extracts were washed with brine (400 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 1:0) afforded 5-(4-chloro-3-nitrobenzyl)thiazol-89ME1\58440953. vl139849-004202-amine (5.20 g, 37%) as a yellow solid; 5H (400 MHz; DMSO-d6) 7.93 (1H, d, J 2.0 Hz), 7.70 (1H, d, J 8.4 Hz), 7.56 (1H, m), 6.79 (2H, s), 6.76 (1H, s), 4.02 (2H, s).

[0306] Step 3

[0307] A solution of phenyl chloroformate (3.63 mL, 28.9 mmol) in THF (10 mL) was added to a solution of 5-(4-chloro-3-nitrobenzyl)thiazol-2-amine (5.20 g, 19.3 mmol) and pyridine (4.67 mL, 57.8 mmol) in THF (52 mL) at 0 °C. The resulting mixture was stirred at 25 °C for 2 h, then diluted with water (50 mL) and extracted into EtOAc (3 x 50 mL). The combined organic extracts were washed with brine (50 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 1:0) afforded phenyl (5-(4-chloro-3-nitrobenzyl)thiazol-2-yl)carbamate (7.00 g, 93%) as a light yellow solid; ES-MS [M+H]+: 390.0.

[0308] Step 4

[0309] Sodium hydride (60% dispersion in oil, 1.44 g, 35.9 mmol) was added to a solution of oxazol-2-ylmethanol (2.67 g, 26.9 mmol) in THF (70 mL) at 0 °C. The resulting mixture was stirred 0 °C for 30 min and then a solution of phenyl (5-(4-chloro-3-nitrobenzyl)thiazol-2-yl)carbamate (17.0 g, 47.8 mmol) in THF (30 mL) was added. The reaction mixture was stirred at 25 °C for 16 h, then quenched by addition of saturated aqueous ammonium chloride solution (50 mL) at 0 °C. The mixture was extracted into EtOAc (3 x 70 mL) and the combined organic extracts were washed with brine (50 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 1:0) afforded oxazol-2-ylmethyl (5-(4-chloro-3-nitrobenzyl)thiazol-2-yl)carbamate (2.30 g, 5.83 mmol) as a yellow solid; ES-MS [M+H]+: 395.0.

[0310] Step 590ME1\58440953. vl139849-00420

[0311] Iron (974 mg, 17.5 mmol) and ammonium chloride (1.56 g, 29.1 mmol) were added to a solution of oxazol-2-ylmethyl (5-(4-chloro-3-nitrobenzyl)thiazol-2-yl)carbamate (2.30 g, 5.83 mmol) in ethanol (46 mL) and water (8 mL). The reaction mixture was stirred at 60 °C for 3 h, then filtered and concentrated in vacuo. Water (30 mL) was added and the mixture was extracted into EtOAc (3 x 30 mL). The combined organic extracts were washed with brine (30 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo.Trituration with EtOAc: PE (1:5, 10 mL)afforded oxazol-2-ylmethyl (5-(3-amino-4-chlorobenzyl)thiazol-2-yl)carbamate (1.30 g, 61%) as a yellow solid; ES-MS [M+H]+: 365.0.

[0312] Step 6

[0313] Acetic acid (16 pL, 0.27 mmol) was added to a solution of 2-methoxyacetaldehyde (81 mg, 1.10 mmol) and oxazol-2-ylmethyl (5-(3-amino-4-chlorobenzyl)thiazol-2-yl)carbamate (100 mg, 0.27 mmol) in methanol (10 mL). The reaction mixture was stirred at 25 °C for 16 h, then sodium cyanoborohydride (34 mg, 0.55 mmol) was added and stirring was continued for at the same temperature for 2 h. The mixture was concentrated in vacuo, diluted with water (15 mL) and extracted into EtOAc (3 x 15 mL).The combined organic extracts were washed with brine (15 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by preparative HPLC (column: Phenomenex Luna 10 pm C18 150 x 25 mm; acetonitrile: [water (0.1% formic acid)]; gradient: 41:59— >71:29) afforded oxazol-2-ylmethyl (5-(4-chloro-3-((2-methoxyethyl)amino)benzyl)thiazol-2-yl)carbamate (52 mg, 45%) as an off-white solid; 5H (400 MHz; DMSO-d6) 11.87 (1H, br s), 8.15 (1H, s), 7.25 (1H, s), 7.19-7.14 (2H, m), 6.67 (1H, d, J 1.6 Hz), 6.47 (1H, m), 5.28 (2H, s), 5.14 (1H, m), 3.97 (2H, s), 3.50 (2H, m), 3.30-3.25 (5H, m); ES-MS [M+H]+: 423.0.91ME1\58440953. vl139849-00420

[0314] Other examples prepared using synthetic procedure H are shown in the following table. All starting materials are commercially available.ES-MSEx. No. Name Structure[M+H]+oxazol-2- ylmethyl (5-(l- (4-chloro-3- MeO^ _Cl\=\((2- HN-4 #154 / T~N O 437.1 methoxy ethyl)amino)phenyl)HMethyl)thiazol- 2-yl)carbamateH2N-^CI>=\oxazol-2-HNA x—? \ #~N Oylmethyl (5-(3-HM((3- Boc-protected starting material wasaminopropyl)a155 used: tert-butyl (3- 422.0mino)-4- oxopropyl)carbamate. A subsequentchlorobenzyl)tBoc-removal step provided the titlehiazol-2- compound: 2 M HCl in dioxane,yl)carbamate25 °C, 1 h.H2Noxazol-2- HN-4 # 0ylmethyl (5-(3-hM((4- Boc-protected starting material was156 aminobutyl)am used: tert-butyl 2-hydroxy-l- 402.3 ino)benzyl)thia pyrrolidinecarboxylate. Azol-2- subsequent Boc-removal stepyl)carbamate provided the title compound: TFA(23 eq), CH2C12, 20 °C, 1 h.

[0315] Example 157: Oxazol-2-ylmethyl (7-phenyl-4,5,6,7-tetrahydrobenzo[d]thiazol-2-yl) carbamate

[0316] Step 192ME1\58440953. vl139849-00420

[0317] A solution of 2-amino-5,6-dihydrobenzo[d]thiazol-7(4H)-one (3.00 g, 17.9 mmol) in acetic anhydride (30 mL) was stirred at 80 °C for 2 h. The precipitate was collected by filtration and washed with THF (3 x 3 mL) to afford 2-amino-5,6-dihydrobenzo[d]thiazol-7(4H)-one (3.40 g, 91%) as a white solid; ES-MS [M+H]+: 211.2.

[0318] Step 2O N O HO U U S^NH

[0319] Phenylmagnesium bromide (3.0 M in THF, 7.61 mL, 22.8 mmol) was added to a solution of N-(7-oxo-4,5,6,7-tetrahydrobenzo[d]thiazol-2-yl)acetamide (2.40 g, 11.4 mmol) in THF (48 mL) at 0 °C. The reaction mixture was stirred at 25 °C for 2 h, then quenched by addition of saturated aqueous ammonium chloride solution (30 mL) and extracted into EtOAc (3 x 30 mL). The combined organic extracts were washed with brine (30 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 19:1) afforded N-(7-hydroxy-7-phenyl-4, 5,6,7-tetrahydrobenzo[d]thiazol-2-yl)acetamide (2.00 g, 61%) as a light yellow solid; ES-MS [M+H]+: 289.1.

[0320] Step 3f'N O L~N OHO X A X AS^hL S^lsFH H

[0321] 10% Pd / C (450 mg, 0.42 mmol) was added to a solution of N-(7-hydroxy-7-phenyl-4,5,6,7-tetrahydrobenzo[d]thiazol-2-yl)acetamide (1.50 g, 5.20 mmol) in methanol (50 mL) and TFA (5 mL). The reaction mixture was stirred under hydrogen (15 PSI) at 25 °C for 2 h, then filtered and concentrated in vacuo. Water (20 mL) was added and the mixture was extracted into EtOAc (3 x 20 mL). The combined organic extracts were washed with brine (20 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 7:3) to afford N-(7-phenyl-4, 5,6,7-tetrahydrobenzo[d]thiazol-2-yl)acetamide (750 mg, 53%) as a light yellow solid; ES-MS [M+H]+: 273.1.

[0322] Step 493ME1\58440953. vl139849-00420

[0323] Hydrochloric acid (6.0 M in water, 1.38 mL, 8.28 mmol) was added to a solution of N-(7-phenyl-4,5,6,7-tetrahydrobenzo[d]thiazol-2-yl)acetamide (750 mg, 2.75 mmol) in ethanol (7.5 mL). The reaction mixture was stirred at 80 °C for 16 h, then concentrated in vacuo, diluted with water (15 mL) and washed with EtOAc (15 mL). The aqueous phase was adjusted to pH 7 with saturated aqueous sodium bicarbonate and extracted into EtOAc (3 x 15 mL). The combined organic extracts were washed with brine (15 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo to afford 7-phenyl-4, 5,6,7-tetrahydrobenzo[d]thiazol-2-amine (500 mg, 79%) as a yellow solid; ES-MS [M+H]+: 231.2.

[0324]

[0325] CDI (352 mg, 2.17 mmol) was added to a solution of oxazol-2-ylmethanol (215 mg, 2.17 mmol) in THF (2 mL) and the resulting mixture was stirred at 60 °C for 4 h. The mixture was then transferred to a solution of 7-phenyl-4,5,6,7-tetrahydrobenzo[d]thiazol-2-amine (100 mg, 0.43 mmol), triethylamine (0.30 mL, 2.17 mmol) and DMAP (5 mg, 0.04 mmol) in THF (2 mL) at 20 °C and stirred at 60 °C for 16 h. The mixture was cooled to 25 °C and the precipitate was filtered. Trituration with methanol: EtO Ac (5:1, 5 mL) afforded oxazol-2-ylmethyl (7-phenyl-4,5,6,7-tetrahydrobenzo[d]thiazol-2-yl)carbamate (78 mg, 50%) as an off-white solid; 5H (400 MHz; DMSO-d6) 11.84 (1H, br s), 8.15 (1H, d, JO.8 Hz), 7.35-7.15 (6H, m), 5.32-5.17 (2H, m), 4.17-4.03 (1H, m), 2.70-2.55 (2H, m), 2.18-2.04 (1H, m), 1.95-1.81 (1H, m), 1.79-1.67 (2H, m); ES-MS [M+H]+: 356.1.

[0326] Example 158: Oxazol-2-ylmethyl (6-phenyl-5,6-dihydro-4H-cyclopenta[d]thiazol-2 -y I) carbamate

[0327] Step 194ME1\58440953. vl139849-00420

[0328] Bromine (1.06 mL, 20.6 mmol) was added to a solution of 3-phenylcyclopentan-l-one (3.00 g, 18.7 mmol) and thiourea (1.57 g, 20.6 mmol) in acetic acid (30 mL). The reaction mixture was stirred at 100 °C for 12 h, then basified to pH ~8 with saturated aqueous sodium bicarbonate solution and extracted into EtOAc (3 x 20 mL). The combined organic extracts were washed with brine (60 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 1:1) to afford 6-phenyl-5,6-dihydro-4H-cyclopenta[d]thiazol-2-amine (400 mg, 4%) as a yellow solid; ES-MS [M+H]+: 217.1.

[0329] Step 23s NH2s N OH

[0330] CDI (337 mg, 2.08 mmol) was added to a solution of oxazol-2-ylmethanol (206 mg, 2.08 mmol) in THF (4 mL) and the resulting mixture was stirred at 60 °C for 4 h. The mixture was then transferred to a solution of 6-phenyl-5,6-dihydro-4H-cyclopenta[d]thiazol-2-amine (200 mg, 0.42 mmol), triethylamine (0.29 mL, 2.08 mmol) and DMAP (5 mg, 0.04 mmol) in THF (2 mL) at 20 °C and stirred at 60 °C for 12 h. The reaction mixture was diluted with water (6 mL) and extracted into EtOAc (3 x 3 mL). The combined organic extracts were washed with brine (9 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by preparative HPLC (column: Phenomenex Luna 10 pm Cl 8 150 x 25 mm; acetonitrile: [water (0.1% formic acid)]; gradient: 42:58^72:28) afforded oxazol-2-ylmethyl (6-phenyl-5,6-dihydro-4H-cyclopenta[d]thiazol-2-yl)carbamate (28 mg, 20%) as a white solid; ES-MS [M+H]+: 342.1.

[0331] Example 159: Oxazol-2-ylmethyl (5-(3-((3-aminopropyl)thio)-4-chlorobenzyl) thiazol-2-yl) carbamate

[0332] Step 1s NHBoc

[0333] n-BuLi (2.5 M in THF, 45.0 mL, 112.5 mmol) was added dropwise to a solution of tert-butyl thiazol-2-ylcarbamate (10.0 g, 49.9 mmol) in THF (150 mL) at -65 °C and the resulting mixture was stirred at this temperature for 1 h. 3-Bromo-4-chlorobenzaldehyde (12.1 g, 55.1 mmol) in THF (10 mL) was added and stirring was continued at -65 °C for 1 h.95ME1\58440953. vl139849-00420The reaction mixture was quenched with saturated aqueous ammonium chloride solution (200 mL) and extracted into EtOAc (3 x 300 mL). The combined organic extracts were washed with brine (3 x 200 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 1:1) afforded tert-butyl (5-((3-bromo-4-chlorophenyl)(hydroxy)methyl)thiazol-2-yl)carbamate (14.0 g, 62%) as a white solid; ES-MS [M+H]+: 421.0.

[0334] Step 2

[0335] Tri ethyl silane (9.62 mL, 60.2 mmol) was added to a solution of tert-butyl (5-((3-bromo-4-chlorophenyl)(hydroxy)methyl)thiazol-2-yl)carbamate (5.00 g, 11.9 mmol) and TFA (12 mL, 162 mmol) in dichloromethane (36 mL). The resulting mixture was stirred at 25 °C for 4 h, then quenched by addition of saturated aqueous sodium bicarbonate solution (200 mL) and extracted into EtOAc (3 x 300 mL). The combined organic extracts were washed with brine (3 x 200 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 1:1) afforded 5-(3-bromo-4-chlorobenzyl)thiazol-2-amine (2.40 g, 60%) as a yellow oil; ES-MS [M+H]+: 305.0.

[0336] Step 3

[0337] A mixture of 5-(3-bromo-4-chlorobenzyl)thiazol-2-amine (1.00 g, 3.29 mmol), 2-ethylhexyl 3-mercaptopropanoate (1.00 g, 4.58 mmol), XantPhos Pd G4 (320 mg, 0.33 mmol and triethylamine (1.50 mL, 10.8 mmol) in dioxane (15 mL) was stirred at 100 °C for 12 h. The reaction mixture was filtered, concentrated in vacuo and purified by flash column chromatography on silica (EtOAc: PE, 0:1 to 3:2) to afford 2-ethylhexyl 3-((5-((2-aminothiazol-5-yl)methyl)-2-chlorophenyl)thio)propanoate (1.30 g, 81%) as a yellow oil; ES-MS [M+H]+: 441.2.

[0338] Step 496ME1\58440953. vl139849-00420

[0339] CDI (370 mg, 2.28 mmol) was added to a solution of oxazol-2-ylmethanol (220 mg, 2.22 mmol) in THF (5 mL) and the resulting mixture was stirred at 60 °C for 4 h. 2-Ethylhexyl 3-((5-((2-aminothiazol-5-yl)methyl)-2-chlorophenyl)thio)propanoate (200 mg, 0.45 mmol), triethylamine (0.30 mL, 2.16 mmol) and DMAP (10 mg, 0.08 mmol) were then added at 20 °C and stirring was continued at 60 °C for 12 h. The reaction mixture was concentrated in vacuo and purified by flash column chromatography on silica (EtOAc: PE, 0:1 to 1:1) to afford 2-ethylhexyl 3-((2-chloro-5-((2-(((oxazol-2-ylmethoxy)carbonyl)amino)thiazol-5-yl)methyl)phenyl)thio)propanoate (120 mg, 44%) as a yellow oil; ES-MS [M+H]+: 566.3.

[0340] Step 5

[0341] Sodium ethoxide (0.30 g, 0.88 mmol) was added to a solution of 2-ethylhexyl 3-((2-chloro-5-((2-(((oxazol-2-ylmethoxy)carbonyl)amino)thiazol-5-yl)methyl)phenyl)thio)propanoate (120 mg, 0.21 mmol) in ethanol (1 mL) at 0 °C. The reaction mixture was stirred at 25 °C for 1 h and then tert-butyl (3-bromopropyl)carbamate (60 mg, 0.25 mmol) was added and stirring continued at this temperature for another 2 h. Water (20 mL) was added and the mixture was extracted into EtOAc (3 x 30 mL). The combined organic extracts were washed with brine (3 x 20 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo to afford oxazol-2-ylmethyl (5 -(3 -((3 -((tertbutoxy carbonyl)amino)propyl)thio)-4-chlorobenzyl)thiazol -2 -yl)carbamate (100 mg, crude) as a yellow gum; ES-MS [M+H]+: 540.2.

[0342] Step 697ME1\58440953. vl139849-00420

[0343] Hydrochloric acid (2.0 M in dioxane, 0.50 mL, 1 mmol) was added to a solution of oxazol-2-ylmethyl (5-(3-((3-((tert-butoxycarbonyl)amino)propyl)thio)-4-chlorobenzyl)thiazol-2-yl)carbamate (80 mg, 0.15 mmol) in dioxane (1 mL). The reaction mixture was stirred at 25 °C for 12 h, then concentrated in vacuo and purified by preparative HPLC (column: Phenomenex Luna 10 pm C18 150 x 25 mm; acetonitrile: [water (0.1% formic acid)]; gradient: 12:88^42:58) to afford oxazol-2-ylmethyl (5-(3-((3-aminopropyl)thio)-4-chlorobenzyl)thiazol-2-yl)carbamate (10 mg, 14%) as a white solid; 5H (400 MHz; DMSO-d6) 8.17-8.14 (1H, m), 7.42-7.37 (1H, m), 7.35-7.29 (1H, m), 7.26-7.24 (1H, m), 7.22-7.15 (1H, m), 7.10-7.03 (1H, m), 5.29-5.23 (2H, m), 4.10-4.04 (2H, m), 3.10-3.03 (2H, m), 2.92-2.80 (2H, m), 1.89-1.76 (2H, m); ES-MS [M+H]+: 439.1.

[0344] Example 160: Oxazol-2-ylmethyl (5-(3-(3-aminopropylsulfonimidoyl)-4-chlorobenzyl) thiazol-2-yl) carbamate

[0345] Step 1

[0346] Ammonium carbonate (41 mg, 0.52 mmol) and (di acetoxy iodo)benzene (81 mg, 0.25 mmol) were added to a solution of oxazol-2-ylmethyl (5-(3-((3-((tert-butoxycarbonyl)amino)propyl)thio)-4-chlorobenzyl)thiazol-2-yl)carbamate* (50 mg, 0.09 mmol) in methanol (1 mL). The reaction mixture was stirred at 25 °C for 12 h, then concentrated in vacuo to afford oxazol-2-ylmethyl (5 -(3 -(3 -((tertbutoxy carbonyl)amino)propylsulfonimidoyl)-4-chlorobenzyl)thiazol-2-yl)carbamate (50 mg, crude); ES-MS [M+H]+: 570.3. *see Step 5 of Example 159

[0348] Hydrochloric acid (2.0 M in dioxane, 0.20 mL, 0.40 mmol) was added to a solution of oxazol-2-ylmethyl (5-(3-(3-((tert-butoxycarbonyl)amino)propylsulfonimidoyl)-4-chlorobenzyl)thiazol-2-yl)carbamate (40 mg, 0.070 mmol) in methanol (1 mL). The reaction mixture was stirred at 25 °C for 2 h, then concentrated in vacuo and purified by preparative HPLC (column: Phenomenex Luna 10 pm C18 150 x 25 mm; acetonitrile: [water (0.1%98ME1\58440953. vl139849-00420formic acid)]; gradient: 34:66^64:36) to afford oxazol-2-ylmethyl (5-(3-(3-aminopropylsulfonimidoyl)-4-chlorobenzyl)thiazol-2-yl)carbamate (8 mg, 24%) as a white solid; 5H (400 MHz; DMSO-d6) 8.40-8.30 (1H, m), 8.06 (1H, d, J0.7 Hz), 7.91 (1H, d, J 2.0 Hz), 7.63-7.57 (1H, m), 7.54 (1H, br d, J2.1 Hz), 7.20 (2H, d, J3.5 Hz), 5.24 (2H, s), 4.14 (2H, s), 3.44 (2H, m), 2.85 (2H, m), 1.90 - 1.75 (2H, m); ES-MS [M+H]+: 470.1.

[0349] Example 161: Oxazol-2-ylmethyl (5-(4-chlorobenzyl)-4-(methoxymethyl)thiazol-2-y I) carbamate

[0350] Step 1ci

[0351] LDA (2.0 M in THF, 30.0 mL, 60.0 mmol) was added to a solution of tert-butyl (5-bromothiazol-2-yl)carbamate (45.0 g, 225 mmol) in THF (50 mL) at -70 °C and the resulting mixture was stirred for 30 min at this temperature. 4-Chlorobenzaldehyde (8.31 g, 59.1 mmol) was then added at -70 °C and stirring was continued at 25 °C for 2 h. The reaction mixture was quenched by addition of saturated aqueous ammonium chloride solution (200 mL) at 0 °C and extracted into EtOAc (3 x 200 mL). The combined organic extracts were dried over anhydrous sodium sulfate and concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 1: 10 to 1:1), followed by purification by preparative HPLC (column: Phenomenex Luna 15 pm C18 150 x 40 mm; acetonitrile: [water (0.1% formic acid)]; gradient: 60:40^90: 10) afforded tert-butyl (4-bromo-5-((4-chlorophenyl)(hydroxy)methyl)thiazol-2-yl)carbamate (2.00 g, 27%) as an off-white solid; 5H (400 MHz; CDC13) 7.45-7.39 (2H, m), 7.37-7.30 (2H, m), 6.06 (1H, s), 2.01 (1H, s), 1.52 (9H, s).

[0352] Step 2Cl Cl

[0353] Tri ethyl silane (1.00 mL, 6.26 mmol) was added to a solution of tert-butyl (4-bromo-5-((4-chlorophenyl)(hydroxy)methyl)thiazol-2-yl)carbamate (200 mg, 0.48 mmol) in TFA (2 mL) and dichloromethane (2 mL). The reaction mixture was stirred at 25 °C for 1 h, then diluted with water (50 mL) and extracted into EtOAc (3 x 100 mL). The combined99ME1\58440953. vl139849-00420organic extracts were washed with brine (50 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 1:4) afforded 4-bromo-5-(4-chlorobenzyl)thiazol-2-amine (140 mg, 85%) as a colorless oil; ESMS [M+H]+: 305.1.

[0354] Step 3

[0355] Di-tert-butyl dicarbonate (719 mg, 3.29 mmol) was added to a solution of 4-bromo-5-(4-chlorobenzyl)thiazol-2-amine (500 mg, 1.65 mmol), DMAP (20 mg, 0.16 mmol) and DIPEA (0.86 mL, 4.94 mmol) in dichloromethane (5 mL). The reaction mixture was stirred at 25 °C for 2 h, then diluted with water (50 mL) and extracted into EtOAc (3 x 50 mL). The combined organics were washed with brine (50 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 0:1 to 1:4) afforded di-tert-butyl (4-bromo-5-(4-chlorobenzyl)thiazol-2-yl)iminodicarbonate (350 mg, 42%) as a white solid; ES-MS [M+H]+: 505.1.

[0356] Step 4Ct Cl\K\KOMeQB\ — Q (A '"' X JLS^N(BOC)2S^N(BOC)2

[0357] Potassium (Methoxymethyl)trifluoroborate (450 mg, 2.96 mmol) was added to a mixture of di-tert-butyl (4-bromo-5-(4-chlorobenzyl)thiazol-2-yl)iminodicarbonate (300 mg, 0.60 mmol), Pd(dppf)Ch (60 mg, 0.08 mmol), sodium carbonate (180 mg, 1.70 mmol) and water (0.6 mL) in dioxane (3 mL). The reaction mixture was stirred at 80 °C for 3 h, then concentrated in vacuo and purified by flash column chromatography on silica (EtOAc: PE, 0:1 to 1:4) to afford di-tert-butyl (5-(4-chlorobenzyl)-4-(methoxymethyl)thiazol-2-yl)iminodicarbonate (160 mg, 36%) as a yellow oil; ES-MS [M-Boc+H]+: 369.0.

[0358] Step 5100ME1\58440953. vl139849-00420

[0359] Hydrochloric acid (2.0 M, 2 mL, 4.00 mmol) was added to di-tert-butyl (5-(4-chlorobenzyl)-4-(methoxymethyl)thiazol-2-yl)iminodicarbonate (150 mg, 0.32 mmol) and the resulting mixture was stirred at 60 °C for 12 h, then concentrated in vacuo to afford 5-(4-chlorobenzyl)-4-(methoxymethyl)thiazol-2-amine HC1 salt (80 mg, crude) as a yellow oil; ES-MS [M+H]+: 269.1.

[0360] Step 6

[0361] CDI (240 mg, 1.48 mmol) was added to a solution of 5-(4-chlorobenzyl)-4-(methoxymethyl)thiazol-2-amine HC1 salt (80 mg, 0.30 mmol) in THF (2 mL) at 0 °C and the resulting mixture was stirred at 60 °C for 1 h. Oxazol-2-ylmethanol (140 mg, 1.41 mmol), triethylamine (0.20 mL, 1.44 mmol) and DMAP (10 mg, 0.08 mmol) were then added at 20 °C and stirring was continued at 60 °C for 2 h. The reaction mixture was diluted with water (50 mL) and extracted into EtOAc (3 x 50 mL). The combined organic extracts were washed with brine (3 x 50 mL), dried over anhydrous sodium sulfate and concentrated in vacuo. Purification by preparative HPLC (column: Phenomenex Luna 10 pm Cl 8 150 x 25 mm; acetonitrile: [water (0.1% formic acid)]; gradient: 38:62^68:32) afforded oxazol-2-ylmethyl (5-(4-chlorobenzyl)-4-(methoxymethyl)thiazol-2-yl)carbamate (13 mg, 11%) as a white solid; 5H (400 MHz; CD3OD) 7.94 (1H, s), 7.33-7.27 (2H, m), 7.26-7.19 (3H, m), 5.30 (2H, s), 4.42 (2H, s), 4.11 (2H, s), 3.35 (3H, s); ES-MS [M+H]+: 394.1.

[0362] Example 162: Oxazol-2-ylmethyl (5-((4-chlorophenyl)(methoxy)methyl)thiazol-2-y I) carbamate

[0363] Step 1ci

[0364] n-BuLi (2.5 M in THF, 10.0 mL, 25.0 mmol) was added dropwise to a solution of tert-butyl thiazol-2-ylcarbamate (2.00 g, 9.99 mmol) in THF (20 mL) at -60 °C and the resulting mixture was stirred at this temperature for 1 h. 4-Chlorobenzaldehyde (2.20 g, 15.7 mmol) was then added and stirring was continued at -60 °C for 1 h. The reaction mixture was quenched with saturated aqueous ammonium chloride solution (50 mL) and extracted101ME1\58440953. vl139849-00420into EtOAc (3 x 50 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Flash column chromatography on silica (EtOAc: PE, 3:7 to 1:1) afforded tert-butyl (5-((4-chlorophenyl)(hydroxy)methyl)thiazol-2-yl)carbamate (2.20 g, 65%) as a white solid; ES-MS [M+H]+: 341.0.

[0365] Step 2

[0366] TFA (1.50 mL, 20.2 mmol) was added to a solution of tert-butyl (5-((4-chlorophenyl)(hydroxy)methyl)thiazol-2-yl)carbamate (300 mg, 0.88 mmol) indi chloromethane (1.5 mL) and the resulting mixture was stirred at 25 °C for 1 h. Methanol (1.50 mL, 37.1 mmol) was added and stirring was continued at 25 °C for another 1 h.Concentration in vacuo afforded 5-((4-chlorophenyl)(methoxy)methyl)thiazol-2-amine TFA salt (200 mg, crude) as a yellow oil; ES-MS [M+H]+: 255.1.

[0367]

[0368] CDI (190 mg, 1.17 mmol) was added to a solution of oxazol-2-ylmethanol (120 mg, 1.21 mmol) in THF (2 mL) at 25 °C and the resulting mixture was stirred at 60 °C for 2 h. 5-((4-Chlorophenyl)(methoxy)methyl)thiazol-2-amine (100 mg, 0.39 mmol), triethylamine (0.18 mL, 1.28 mmol) and DMAP (10 mg, 0.08 mmol) were then added at 20 °C and stirring was continued at 60 °C for 12 h. The reaction mixture was concentrated in vacuo.Purification by preparative HPLC (column: Phenomenex Luna 10 pm C18 150 x 25 mm; acetonitrile: [water (0.1% formic acid)]; gradient: 4:6^7:3) afforded oxazol-2-ylmethyl (5-((4-chlorophenyl)(methoxy)methyl)thiazol-2-yl)carbamate (19 mg, 13%) as a white solid; 5H (400 MHz; DMSO-d6) 12.28-11.75 (1H, m), 8.15 (1H, d, J0.6 Hz), 7.46-7.42 (2H, m), 7.41-7.37 (2H, m), 7.26 (2H, d, J 5.9 Hz), 5.60 (1H, s), 5.28 (2H, s), 3.27 (3H, s); ES-MS [M+H]+: 380.1.

[0369] Example 163: Sodium (R)-((5-(l-(4-chlorophenyl)ethyl)thiazol-2-yl)((oxazol-2-ylmethoxy)carbonyl)amino)methyl phosphate

[0370] Step 1102ME1\58440953. vl139849-00420

[0371] Di-tert-butyl chloromethyl phosphate (500 mg, 1.93 mmol) was added to a mixture of Example 20 (350 mg, 0.83 mmol), potassium iodide (50 mg, 0.30 mmol) and potassium carbonate (400 mg, 2.89 mmol) in DMF (10 mL). The resulting mixture was stirred at 60 °C for 4 h. Water (20 mL) was added and the mixture was extracted into EtOAc (3 x 20 mL). The combined organic extracts were dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by lash column chromatography on silica (EtOAc: PE, 0:1 to 1:3) afforded a mixture of oxazol-2-ylmethyl (A)-(5-(l-(4-chlorophenyl)ethyl)thiazol-2-yl)(((di-tert-butoxyphosphoryl)oxy)methyl)carbamate (150 mg, 19%); ES-MS [M+H]+: 586.2; and oxazol-2-ylmethyl (((tert-butoxy(hydroxy)phosphoryl)oxy)methyl)(5-((A)-l-(4-chlorophenyl)ethyl)thiazol-2-yl)carbamate (180 mg, 25%); ES-MS [M+H]+: 530.2.

[0372] Step 2t-BuO-P=OOH103ME1\58440953. vl139849-00420

[0373] Hydrochloric acid (2.0 M in dioxane, 8 mL, 16 mmol) was added to the two products from Step 1 and the resulting mixture was stirred at 20 °C for 2 h, then concentrated in vacuo. Purification by preparative HPLC (column: Waters™ XBridge, 25 mm X 150 mm, 10 pM; acetonitrile: [water (0.1% ammonium bicarbonate)]; gradient: 1:4— >2:3) afforded oxazol-2-ylmethyl (A)-(5-(l-(4-chlorophenyl)ethyl)thiazol-2-yl)((phosphonooxy)methyl)carbamate (40 mg, 14%) as a white solid; 5H (400 MHz; CD3OD) 7.94 (1H, d, JO.8 Hz), 7.33-7.25 (4H, m), 7.20 (2H, d, J0.9 Hz), 5.88 (2H, d, J7.6 Hz), 5.42 (2H, s), 4.32 (1H, m), 1.66 (3H, d, J 7.1 Hz).

[0374] Step 3N O fN O A A S N O A"O HO-P=OOH

[0375] A solution of oxazol-2-ylmethyl (R)-(5-(l-(4-chlorophenyl)ethyl)thiazol-2-yl)((phosphonooxy)methyl)carbamate (40 mg, 0.044 mmol) in water (10 mL) was filtered through Dowex 50W X8 Ion Exchange Resin (sodium form, 100-200 mesh, strongly acidic, 500 mg). The filtrate was lyophilized to afford sodium (A)-((5-(l-(4-chlorophenyl)ethyl)thiazol-2-yl)((oxazol-2-ylmethoxy)carbonyl)amino)methyl phosphate (14 mg, 31%) as a white solid; 5H (400 MHz; D2O) 7.90 (1H, s), 7.41-7.37 (2H, m), 7.33 (3H, d, J 8.6 Hz), 7.22 (1H, s), 5.77 (2H, br d, J 8.3 Hz), 5.45 (2H, s), 4.43-4.36 (1H, m), 1.67 (3H, d, J 7.1 Hz); ES-MS [M+H]+: 474.1.

[0376] Example 164: Oxazol-2-ylmethyl (5-(4-chlorobenzyl)-4-methylthiazol-2-yl)carbamate

[0377] Step 1BrAiiA s

[0378] 2,4,6-Trimethyl-l,3,5,2,4,6-trioxatriborinane (720 mg, 2.87 mmol) was added to a mixture of di-tert-butyl (4-bromo-5-(4-chlorobenzyl)thiazol-2-yl)iminodicarbonate (see Example 161, 200 mg, 0.40 mmol), Pd(dppf)C12 (40 mg, 0.05 mmol), sodium carbonate (120 mg, 1.13 mmol) and water (0.3 mL) in dioxane (1.5 mL). The reaction mixture was stirred at 80 °C for 12 h, then concentrated in vacuo and purified by flash column chromatography on 104ME1\58440953. vl139849-00420silica (EtOAc: PE, 0:1 to 1:4) to afford tert-butyl (5-(4-chlorobenzyl)-4-methylthiazol-2-yl)carbamate (130 mg, 97%) as a yellow oil; ES-MS [M+H]+: 339.1.

[0379] Step 2

[0380] Hydrochloric acid (2.0 M, 2 mL, 4.00 mmol) was added to tert-butyl (5-(4-chlorobenzyl)-4-methylthiazol-2-yl)carbamate (130 mg, 0.38 mmol) and the resulting mixture was stirred at 60 °C for 12 h, then concentrated in vacuo to afford 5-(4-chlorobenzyl)-4-methylthiazol-2-amine HC1 salt (80 mg, crude) as a yellow oil; ES-MS [M+H]+: 239.1.

[0381] Step 3

[0382] CDI (340 mg, 2.10 mmol) was added to a solution of 5-(4-chlorobenzyl)-4-methylthiazol-2-amine HC1 salt (100 mg, 0.42 mmol) in THF (2 mL) at 0 °C and the resulting mixture was stirred at 60 °C for 1 h. Oxazol-2-ylmethanol (210 mg, 2.12 mmol), triethylamine (0.29 mL, 2.08 mmol) and DMAP (10 mg, 0.08 mmol) were then added at 20 °C and stirring was continued at 60 °C for 12 h. The reaction mixture was diluted with water (50 mL) and extracted into EtOAc (3 x 50 mL). The combined organic extracts were washed with brine (3 x 50 mL), dried over anhydrous sodium sulfate and concentrated in vacuo. Purification by preparative HPLC (column: Phenomenex Luna 10 pm C18 150 x 25 mm; acetonitrile: [water (0.1% formic acid)]; gradient: 45:55^65:35) afforded oxazol-2-ylmethyl (5-(4-chlorobenzyl)-4-methylthiazol-2-yl)carbamate (10 mg, 7%) as an off-white gum; 6H (400 MHz; DMSO-d6) 12.00-11.51 (1H, m), 8.15 (1H, s), 7.36 (2H, d, J 8.4 Hz), 7.25 (1H, s), 7.23 (2H, d, J 8.4 Hz), 5.26 (2H, s), 3.99 (2H, s), 2.19 (3H, s); ES-MS [M+H]+: 364.1.

[0383] Biological Assays

[0384] DLD-1 Cell Viability Assay

[0385] Compound cytotoxicity in DLD-1 human colorectal adenocarcinoma cells (ATCC CCL-221) was gauged using the CellTiter Gio 2.0 Luminescent Cell Viability Assay (Promega). DLD-1 cells maintained in growth medium (RPMI, 10% FBS, 1% P / S) were105ME1\58440953. vl139849-00420seeded into 1536-well black clear bottom plates (Coming 3836) at a density of 400 cells / 5 pL / well (0.08X10A6cells / mL) and incubated overnight in a 5% CO2 incubator at 37°C.Compounds in 10 point 1:3 serial dilution in DMSO (provided by compound management in 384-well Low Dead Volume Echo certified plates, Labcyte LP-0200) were stamped (15 nL) onto 1536-well plates containing DLD-1 cells (at about 30-40% cell density) for a final compound concentration ranging from 30 pM to 1.5 nM. 30 pM (final concentration) of Toxoflavin served as a low control while DMSO only served as a high control in these experiments. The final DMSO concentration in the assay plate is 0.3%. Each sample was tested in triplicate.

[0386] 72 hours post compound introduction, 5 pL of CellTiter Gio 2.0 at room temperature is added to the cells in media using a multidrop combi and incubated for 30 minutes at room temperature. Luminescence from the samples is recorded with a Clariostar Plus plate reader and all data is normalized to the average of DMSO treated group and expressed as the percentage of control. IC50 values based on curve classification for each compound were calculated from the concentration response curves (percentage inhibition) using Dotmatics data management software.

[0387] Immunofluorescence Nuclear Condensate Assay

[0388] An immunofluorescence (IF) assay was used to measure the sequestration of beta catenin into nuclear condensates. DLD-1 cells (ATCC CCL-221) were maintained in growth medium RPMI 1640 (ATCC modification) (Thermo, A1049101) supplemented with 10% fetal bovine serum (VWR, 89510-196). Twenty -four hours prior to compound treatment, cells were seeded into 1536-well black clear bottom plates (Greiner, GR 789866) at a density of 600 cells / 5 pL / well and incubated overnight in a 5% CO2 incubator at 37 °C for 24 hours. Compounds in 10 point 1:3 serial dilution in DMSO in 384-well Low Dead Volume Echo certified plates (Labcyte, LP-0200) were stamped (15 nL) onto 1536-well plates containing DLD-1 cells for a final compound concentration ranging from 30 pM to 1.5 nM. NCB-0846 (30 pM) (Selleck, S8392) served as a high control while DMSO served as a low control in these experiments. The final DMSO concentration in the assay plate is 0.3%. Each sample was tested in triplicate.

[0389] Twenty -four hours after compound treatment, cells were fixed with the addition of 2 pL of 12% formaldehyde (Sigma, 1.04003) at room temperature for 15 minutes, permeabilized in 0.1% Triton X-100 (Sigma, 93443) in PBS for 15 minutes, blocked in 0.2% gelatin from cold water fish (Sigma, G7765) in PBS for 1 hour, and then stained with a 1:1000 dilution of the phospho beta catenin antibody (Invitrogen, 703638) in 0.2% gelatin 106ME1\58440953. vl139849-00420overnight at 4 °C followed by incubation with a 1: 10000 dilution of Hoechst (Thermo, H3570) and with a 1:1000 dilution of secondary antibody (Thermo, Al 1070) for 1 hour at room temperature. Plates were then imaged (Opera Phenix, Perkin Elmer), and analyzed with the Harmony software quantitating the fraction of cells with bright phospho beta catenin depots (see Figure 1). The data was normalized to the high (NCB-0846, 30 pM) and low (DMSO) controls. ECso values based on curve classification for each compound were calculated from the concentration response curves (percentage response) using Dotmatics data management software.

[0390] The data from the viability IC50 and immunofluorescence (IF) EC50 values are shown in the table below:Ex. No. DLD-1 Cell Viability IC50 DLD-1 IF ECso1 A A2 C C3 A A4 C C5 A A6 B C7 A A8 A A9 C C10 B B11 B B12 A B13 A B14 C B15 A A16 B C17 B A18 B B19 B B20 A A21 C C22 A B23 B B24 C C25 A B26 C C27 C C28 c C29 B C30 A A31 A A32 C C107ME1\58440953. vl139849-0042033 C C 34 B B 35 B B 36 C C 37 B B 38 B C 39 B B 40 B B 41 C C 42 B C 43 A A 44 A A 45 B B 46 B B 47 C C 48 C C 49 B B 50 B B 51 B B 52 B B 53 A A 54 B B 55 C C 56 B C 57 C C 58 A B 59 C C 60 C C 61 c C 62 B B 63 B B 64 A A 65 A A 66 C C 67 C C 68 A A 69 C D 70 A A 71 B B 72 C C 73 A A 74 B B 75 C C 76 B B 77 A A 78 B B 79 B B80 B C108ME1\58440953. vl139849-0042081 A nd 82 B B 83 B B 84 D D 85 A A 86 A A 87 C C 88 B B 89 C C 90 A A 91 C C 92 B B 93 A A 94 B B 95 B C 96 B B 97 A A 98 A A 99 C C 100 A B 101 B B 102 B B 103 C C 104 B B 105 A A 106 A A 107 A A 108 A A 109 C C 110 B B 111 C C 112 C C 113 C C 114 B B 115 B C 116 A A 117 A A 118 B B 119 A A 120 C C 121 C C 122 c c 123 B B 124 A A 125 C C 126 B B 127 B B128 B B109ME1\58440953. vl139849-00420129 A A 130 A A 131 C C 132 C C 133 c c 134 B B 135 B B 136 C C 137 C D 138 B B 139 B B 140 C C 141 C C 142 B B 143 C D 144 C D 145 B B 146 C C 147 B B 148 A A 149 A B 150 B B 151 B B 152 C C 153 B B 154 B B 155 B B 156 B B 157 C C 158 B B 159 C D 160 C D 161 C D 162 B B 163 A A164 C CA: IC50 orECso <0.1 |iMB: IC50 or EC50 >0.1 and <1 |1MC: IC50 or EC50 >1 and <10 |iMD: IC50 orEC5o >10 |iMnd: not determined

[0391] Mouse Pharmacokinetic Study110ME1\58440953. vl139849-00420

[0392] Example 1 was formulated in DMSO: PEG400: water (1:4:5) for IV dosing and Cremophor® RH 40: 20% HP-P-CD (1:19) for PO dosing. Three female BALB / c mice were dosed IV (1 mg / kg) and serial bleed time-points were taken at 0 min, 5 min, 15 min, 30 min, 1 h, 2 h, 4 h, 8 h and 24 h. Ten female BALB / c mice were dosed PO (10 mg / kg) and bleeds were taken at 0 min, 30 min, 1 h, 2 h, 4 h, 8 h and 24 h across the group (maximum two samples per mouse). Samples were prepared by protein precipitation with acetonitrile and analyzed by quantitative LC / MS using a AB API 5500 LC / MS / MS. PK parameters were estimated by non-compartmental model using WinNonlin 8.3. The PK data for Example 1 is shown in the table below:Route of administration Dose Parameter ValueTl / 2 2.96 hCmax 4.45 pMPO 10 mg / kgAUClast 12.3 h*pMF% >99%32.4ClIV 1 mg / kg mL / min / kgVss 1.34 L / kg

[0393] Colorectal Cancer Cell-Line Derived Xenograft Study

[0394] HCT-116 cells (ATCC CCL-247) were cultured in McCoy’s %A media until sufficient cell numbers for implantation into mice were obtained. Cells were harvested and inoculated (5×106in 100 pL in McCoy's 5a medium) subcutaneously into the right flank of nude mice and tumor growth was monitored by caliper measurement. When tumors reached -70-100 mm3, mice were randomized into treatment groups (5 groups, n=10 / group) and treatment was initiated. Example 1, formulated in Cremophor® RH 40: 20% HP-P-CD (1:19) for PO dosing, was administered as follows: Vehicle; Example l-50mg / kg QD. Tumor volume measurements were captured twice weekly using digital calipers and the data is represented as the mean group tumor volume + / - S. E. M. Figure 2 shows the tumor volumes for mice treated with Example 1 and mice provided with vehicle.

[0395] qPCR Assay

[0396] Gene expression of beta catenin target genes was measured by duplexed Real-Time quantitative Polymerase Chain Reaction (RT- qPCR) in DLD-1 human colorectal adenocarcinoma cells (ATCC CCL-221). DLD-1 cells maintained in growth medium (RPMI ATCC formulation, 10% FBS) were seeded in 384-well black clear bottom plates (Revvity, Phenoplate) at a density of 2000 cells / 40 pL / well (5.0×104cells / mL) and incubated overnight at 37°C with 5% CO2. The example compound diluted in DMSO at the indicated concentrations was added to the cells. The final DMSO concentration in each well was 0.1%.111ME1\58440953. vl139849-0042024 hours after compound addition, cells were washed once with lx Phosphate Buffered Saline (PBS) and lysed using 30 pL of cell lysis buffer (ThermoFisher #4391851C). Cell lysis occurs over an 8-minute period at room temperature while shaking the plate on a platform shaker. After cell lysis, 3 pL of stop solution (ThermoFisher #4391851C) was added. 4 pL of cell lysate was then transferred to 384-well qPCR-compatible plates (ThermoFisher #4483285). qPCR Master Mix (ThermoFisher #A15299) containing target and housekeeping TaqMan probes is then dispensed, and each reaction was assembled according to the manufacturer’s instructions. Transcript abundance was measured by qPCR using a Quantstudio 7 Flex thermocycler. Each sample was tested in duplicate across 4 beta catenin target genes: Axin2 (ThermoFisher Hs00610344_m1), Lef1 (ThermoFisher Hs01547250_m1), Myc (ThermoFisher Hs00153408_m1), and Notum (ThermoFisher Hs00394510_m1). The housekeeping control gene, RNase P, was duplexed with one target gene per well. Quantification was performed by calculating the AACt and relative quantification (2-ΔΔCt) values. Figure 3 shows the gene expression changes in DLD-1 cells treated with Example 1 or DMSO.112ME1\58440953. vl

Claims

139849-00420CLAIMSWhat is claimed is:

1. A compound having the structural Formula I:or a pharmaceutically acceptable salt thereof, wherein:R1is hydrogen, (Ci-C4)alkyl, or (Ci-C4)alkylene[OP(O)(OH)2];R2is aryl, heteroaryl, heterocyclyl, or cycloalkyl, each of which are optionally substituted with 1 to 3 groups selected from R1A;R3is hydrogen, (Ci-C4)alkyl, halo, or (Ci-C4)alkylene(Ci-C4alkoxy);or R2and R3are taken together to form Cscycloalkyl substituted with phenyl;X is -OR6or -NR7R8;R4is (Ci-C4)alkyl, (Ci-C4)alkyl, halo(Ci-C4)alkyl, or heterocyclyl when X is -NR7R8, or R4is hydrogen, (Ci-C4)alkyl, halo(Ci-C4)alkyl, or heterocyclyl when X is -OR6;or R2and R4are taken together to form heterocyclyl;R6is cycloalkyl, heterocyclyl, (Ci-C4)alkylene(Ci-C4alkoxy), (Ci-C4)alkylene[aryl], (Ci-C4)alkylene[heteroaryl], or (Ci-C4)alkylene[cycloalkyl], wherein the aryl is substituted with 1 to 3 groups selected from R2Aand the heteroaryl is optionally substituted with 1 to 3 groups selected from R2A;R7is H;R8is cycloalkyl, heterocyclyl, (Ci-C4)alkylene(Ci-C4alkoxy), (Ci-C4)alkylene[aryl], (Ci-C4)alkylene[heteroaryl], or (Ci-C4)alkylene[cycloalkyl], wherein the cycloalkyl is optionally substituted with 1 to 3 groups selected from R2A;or R7and R8are taken together to form heterocyclyl or heteroaryl, each of which is optionally substituted with 1 to 3 groups selected from R2A;each R1Ais independently selected from halo, cyano, (Ci-C4)alkyl, hydroxy(Ci-C4)alkyl, hydroxy[halo(Ci-C4)alkyl], cyano(Ci-C4)alkyl, halo(Ci-C4)alkyl, (Ci-C4)alkoxy, deuterated(Ci-C4)alkoxy, (Ci-C4)alkoxyO(Ci-C4)alkyl, (Ci-C4)alkoxyO[deuterated(Ci-C4)alkyl], halo(Ci-C4)alkoxy, (Ci-C4)alkoxyO[halo(Ci-C4)alkyl], oxo, hydroxy, -O[hydroxy(Ci-C4)alkyl], -Ofcycloalkyl], -Ofheterocyclyl], -Ofaryl], -Ofheteroaryl], (Ci-113ME1\58440953. vl139849-00420C4)alkylene[cycloalkyl], (Ci-C4)alkylene[aryl], (Ci-C4)alkylene[heterocyclyl], (Ci-C4)alkylene[heteroaryl], -O(Ci-C4)alkylene[NRaRb], -O(Ci-C4)alkylene[NRaC(O)Rb], -O(Ci-C4)alkylene[cycloalkyl], -0(Ci-C4)alkylene[aryl], -O(Ci-C4)alkylene[heterocyclyl], -O(Ci-C4)alkylene[heteroaryl], cycloalkyl, heterocyclyl, aryl, heteroaryl, (Ci-C4)alkylene(Ci-C4)alkoxy, (Ci-C4)alkylene[deuterated(Ci-C4)alkoxy], (Ci-C4)alkylene[halo(Ci-C4)alkoxy], (Ci-C4)alkoxyO[cycloalkyl], (Ci-C4)alkoxyO[heterocyclyl], (Ci-C4)alkoxyO [heteroaryl], (Ci-C4)alkoxyO[phenyl], -C(O)[heterocyclyl], -SRa, -S(O)Ra, -SO2Ra, -S(O)(NRa)Rb, -NRbSO2Rb, -SO2NRa, -C(O)Ra, -C(O)ORa, -C(O)NRaRb, -NRaC(O)Rb, -NRaC(O)NRb, -NRaRb, -NH(Ci-C4)alkylene[heterocyclyl], and (Ci-C4)alkyleneNRaRb, where each occurrence of cycloalkyl, heterocyclyl, aryl, and heteroaryl alone, or as part of another group, is optionally substituted with 1 to 3 groups selected from halo, oxo, (Ci-C4)alkyl, halo(Ci-C4)alkyl, hydroxy(Ci-C4)alkyl, (Ci-C4)alkoxy, halo(Ci-C4)alkoxy, hydroxy, -NH2, -NH(Ci-C4)alkyl, -N((Ci-C4)alkyl)2, cycloalkyl, heterocyclyl, aryl, heteroaryl, and CN;each R2Ais independently selected from halo, (Ci-C4)alkyl, halo(Ci-C4)alkyl, hydroxy(Ci-C4)alkyl, deuterated(Ci-C4)alkyl, (Ci-C4)alkoxy, halo(Ci-C4)alkoxy, deuterated(Ci-C4)alkoxy, (Ci-C4)alkylene(Ci-C4)alkoxy, (Ci-C4)alkylene[deuterated(Ci-C4)alkoxy], (Ci-C4)alkylene[halo(Ci-C4)alkoxy], oxo, -Ofcycloalkyl], CN, hydroxy, S(O)(Ci-C4)alkyl, -S(O)2(Ci-C4)alkyl, hydroxy, cycloalkyl, heterocyclyl, aryl, heteroaryl, (Ci-C4)alkylene[cycloalkyl], (Ci-C4)alkylene[aryl], (Ci-C4)alkylene[heterocyclyl], (Ci-C4)alkylene[heteroaryl], -C(O)Ral, -C(O)ORal, -C(O)NRalRbl, -NRalC(O)Rbl, -NRalC(O)NRbl, wherein said heterocyclyl, aryl, heteroaryl, and cycloalkyl are each optionally substituted with 1 to 3 groups selected from halo, (Ci-C4)alkyl, halo(Ci-C4)alkyl, (Ci-C4)alkoxy, halo(Ci-C4)alkoxy, and CN;each Ra, Ral, Rb, and Rblis each independently selected from hydrogen, (Ci-C4)alkyl, halo(Ci-C4)alkyl, (Ci-C4)alkylene(Ci-C4)alkoxy, (Ci-C4)alkyleneNH2, (Ci-C4)alkyleneNH((Ci-C4alkyl), (Ci-C4)alkyleneN((Ci-C4alkyl)2, cycloalkyl, and heterocyclyl, wherein the cycloalkyl and heterocyclyl are each optionally substituted with (Ci-C4)alkyl, hydroxy, or hydroxy (Ci-C4)alkyl.

2. The compound of Claim 1, or a pharmaceutically acceptable salt thereof, wherein R1is hydrogen or (Ci-C4)alkylene[OP(O)(OH)2],3. The compound of Claim 1 or 2, or a pharmaceutically acceptable salt thereof, wherein R1is hydrogen.114ME1\58440953. vl139849-004204. The compound of any one of Claims 1 to 3, or a pharmaceutically acceptable salt thereof, wherein R3is hydrogen, -CH3, or -CH2OCH3.

5. The compound of any one of Claims 1 to 4, or a pharmaceutically acceptable salt thereof, wherein R3is hydrogen.

6. The compound of any one of Claims 1 to 5, or a pharmaceutically acceptable saltthereof, wherein R4is -CH3, -CF3, -CH2F, -CHF2, -OCH3, or7. The compound of any one of Claims 1 to 6, or a pharmaceutically acceptable salt thereof, wherein R4is -CH3.

8. The compound of any one of Claims 1 to 5, or a pharmaceutically acceptable salt thereof, wherein X is O and R4is hydrogen.

9. The compound of any one of Claims 1 to 8, or a pharmaceutically acceptable salt thereof, wherein R2is aryl, heteroaryl, or heterocyclyl, each of which are optionally substituted with 1 to 3 groups selected from R1A.

10. The compound of any one of Claims 1 to 9, or a pharmaceutically acceptable salt thereof, wherein R2is phenyl, pyridinyl, pyrimidyl, pyrazinyl, benzimidazolyl, pyrazolyl, or dihydrobenzooxazolyl, each of which is optionally substituted with 1 to 3 groups selected from R1A.

11. The compound of any one of Claims 1 to 10, or a pharmaceutically acceptable salt3 groups selected from R1A.115ME1\58440953. vl139849-0042012. The compound of any one of Claims 1 to 11, or a pharmaceutically acceptable salt13. The compound of any one of Claims 1 to 12, or a pharmaceutically acceptable salt thereof, wherein each R1Ais independently halo, (Ci-C4)alkyl, halo(Ci-C4)alkyl, hydroxy(Ci- C4)alkyl, (Ci-C4)alkyleneNRaRb, cyano, hydroxy, (Ci-C4)alkoxy, deuterated(Ci-C4)alkoxy, halo(Ci-C4)alkoxy, -O[hydroxy(Ci-C4)alkyl], (Ci-C4)alkoxyO(Ci-C4)alkyl, -O(Ci- C4)alkylene[NRaRb], -O(Ci-C4)alkylene[NRaC(O)Rb], -O[cycloalkyl], -O[heterocyclyl], - O(Ci-C4)alkylene[heterocyclyl], -NRaRb, -NRaC(O)Rb, -SRa, -S(O)(NRa)Rb, -C(O)NRaRb, or heterocyclyl, wherein the heterocyclyl is optionally substituted with hydroxy or hydroxy(Ci- C4)alkyl.

14. The compound of any one of Claims 1 to 13, or a pharmaceutically acceptable salt thereof, wherein Raand Rbare each independently hydrogen, (Ci-C4)alkyl, (Ci- C4)alkylene(Ci-C4)alkoxy, (Ci-C4)alkyleneNH2, or heterocyclyl.

15. The compound of any one of Claims 1 to 14, or a pharmaceutically acceptable salt thereof, wherein each R1Ais independently -F, -Cl, -CH3, -CF3, -CH2OH, -CH2CH2CH2NH2, CN, hydroxy, -OCH3, -OCD3, -OCHF2, -OCF3, -OCH2CH3, -OCH(CH3)2, -OCH2CH2OH, - OCH2CH2OCH3, -OCH2CH2NH2, -OCH2CH2N(CH3)2, -OCH2CH2CH2NH2, - OCH2CH2CH2NHC(O)CH3, -OCH2CH2CH2CH2NH2, -OCH2CH2CH2CH2N(CH3)2, -NH2, -116ME1\58440953. vl139849-00420N(CH3), -N(CH3)CH2CH2OCH3, -NHCH2CH2OCH3, -NHCH2CH2CH2NH2, - NHCH2CH2CH2CH2NH2, -NHC(O)CH3, -SCH2CH2CH2NH2, -S(O)(NH)CH2CH2CH2NH2,16. The compound of any one of Claims 1 to 15, or a pharmaceutically acceptable salt thereof, wherein X is -OR6.

17. The compound of any one of Claims 1 to 16, or a pharmaceutically acceptable salt thereof, wherein R6is (Ci-C4)alkylene(Ci-C4alkoxy), (Ci-C4)alkylene[aryl], or (Ci-C4)alkylene[heteroaryl], wherein the aryl is substituted by R2A, and the heteroaryl is pyridinyl, oxazolyl, pyrazolyl, imidazolyl, triazolyl, or oxadiazolyl, each of which is optionally substituted by R2A.

18. The compound of any one of Claims 1 to 17, or a pharmaceutically acceptable salt19. The compound of any one of Claims 1 to 18, or a pharmaceutically acceptable salt thereof, wherein each R2Ais independently (Ci-C4)alkyl, halo(Ci-C4)alkyl, or (Ci-C4)alkoxy.117ME1\58440953. vl139849-0042020. The compound of any one of Claims 1 to 20, or a pharmaceutically acceptable salt thereof, wherein each R2Ais independently -CH3, -CF3, -OCH3.

21. The compound of any one of Claims 1 to 15, or a pharmaceutically acceptable salt thereof, wherein X is -NR7R8.

22. The compound of any one of Claims 1 to 15 or 21, or a pharmaceutically acceptable salt thereof, wherein R7is H and R8is cyclobutyl, oxetanyl, (Ci-C4)alkylene[aryl], or (Ci-C4)alkylene[heteroaryl], wherein the heteroaryl is oxazolyl, and wherein the cyclobutyl is optionally substituted by R2A.

23. The compound of any one of Claims 1 to 15, 21, or 22, or a pharmaceuticallyacceptable salt thereof, wherein R7is H and R8is: / O.,1,, wherein the cyclobutyl is optionally substituted by 1 R2A.

24. The compound of any one of Claims 1 to 15 or 21 to 23, or a pharmaceuticallyacceptable salt thereof, wherein R7is H and R8is:

25. The compound of any one of Claims 1 to 15 or 21, or a pharmaceutically acceptable salt thereof, wherein R7and R8are taken together to form heterocyclyl optionally substituted with 1 or 3 R2A.

26. The compound of any one of Claims 1 to 15, 21, or 25, or a pharmaceutically acceptable salt thereof, wherein R7and R8are taken together to form azetidinyl, pyrrolidinyl, azabicyclohexanyl, azaspiroheptanyl, oxaazaspiroheptanyl, oxaazaspirooctanyl, or oxadiazaspirononanyl, each of which is optionally substituted with 1 or 2 R2A.118ME1\58440953. vl139849-0042027. The compound of any one of Claims 1 to 15, 21, 25, or 26, or a pharmaceuticallyacceptable salt thereof, wherein R7and R8are taken together to form: fo 5 fN05NH, each of which is optionally substituted with 1 or 2 R2A.

28. The compound of any one of Claims 1 to 15, 21, or 25 to 27, or a pharmaceutically acceptable salt thereof, wherein R7and R8are taken together to form: ‘N >■N0>—r2A29. The compound of any one of Claims 1 to 15 or 21 to 28, or a pharmaceutically acceptable salt thereof, wherein each R2Ais independently halo, (Ci-C4)alkyl, halo(Ci-C4)alkyl, (Ci-C4)alkylene(Ci-C4)alkoxy, (Ci-C4)alkylene[deuterated(Ci-C4)alkoxy], (Ci-C4)alkylene[halo(Ci-C4)alkoxy], hydroxy, (Ci-C4)alkoxy, halo(Ci-C4)alkoxy, deuterated(Ci-C4)alkoxy, -Ofcycloalkyl], cyano, -S(O)2(Ci-C4)alkyl, aryl, or heteroaryl, wherein the heteroaryl is optionally substituted with (Ci-C4)alkyl or (Ci-C4)alkoxy.

30. The compound of any one of Claims 1 to 15 or 21 to 29, or a pharmaceutically acceptable salt thereof, wherein each R2Aindependently is -F, -CH3, -CHF2, -CF3, -CF2CH3, -CH2OCH3, -CH2OCD3, -CH(CH3)OCH3, -C(CH3)2OCH3, -CH2OCF3, hydroxy, -OCH3, -OCD3, -OCHF2,, cyano, -S(O2)CH3, phenyl,119ME1\58440953. vl139849-0042031. The compound of Claim 1, having the structural Formula II:or a pharmaceutically acceptable salt thereof, wherein:one of X1or X2is N, and the other is CH;n is 1 or 2;each R1Ais independently halo, (Ci-C4)alkyl, halo(Ci-C4)alkyl, (Ci-C4)alkoxy, deuterated(Ci-C4)alkoxy, halo(Ci-C4)alkoxy, or -Ofcycloalkyl];X is -OR6;R6is (Ci-C3)alkylene[heteroaryl], wherein the heteroaryl is optionally substituted with 1 to 3 groups selected from R2A.

32. The compound of Claim 31, or a pharmaceutically acceptable salt thereof, wherein X1is N and X2is CH.

33. The compound of Claim 31 or 32, or a pharmaceutically acceptable salt thereof, wherein each R1Ais independently -Cl, -CH3, -CF3, -OCH3, -OCH2CH3, -OCH(CH)2, -O-cyclopropyl, -OCHF2, -OCF3, or -OCD3.

34. The compound of Claim 31 or 32, or a pharmaceutically acceptable salt thereof, wherein each R1Ais independently (Ci-C4)alkoxy.

35. The compound of any one of Claims 31 to 34, or a pharmaceutically acceptable salt thereof, wherein n is 1.

36. The compound of any one of Claims 31 to 35, or a pharmaceutically acceptable salt thereof, wherein R6is (Ci-C3)alkylene[5- to 6-membered heteroaryl], wherein the 5- to 6-membered heteroaryl is optionally substituted with 1 to 3 groups selected from R2A.120ME1\58440953. vl139849-0042037. The compound of any one of Claims 31 to 36, or a pharmaceutically acceptable salt thereof, wherein R6is (Ci-C3)alkylene[oxazolyl], wherein the oxazolyl is optionally substituted with 1 to 3 groups selected from R2A.

38. The compound of any one of Claims 31 to 37, or a pharmaceutically acceptable salt thereof, wherein each R2Ais independently (Ci-C4)alkyl or halo(Ci-C4)alkyl.

39. The compound of any one of Claims 31 to 37, or a pharmaceutically acceptable salt thereof, wherein R6is -CH2[oxazole-2-yl],40. The compound of any one of Claims 31 to 39, having the structural Formula III:R1As.o^Xor a pharmaceutically acceptable salt thereof.

41. The compound of any one of Claims 31 to 40, having the structural Formula Illa:R1Aor a pharmaceutically acceptable salt thereof.42 The compound of any one of Claims 31 to 41, or a pharmaceutically acceptable salt thereof, wherein R1Ais -OCH3.

43. The compound of Claim 1, wherein the compound is selected from any one of Examples 1 to 164, or a pharmaceutically acceptable salt thereof.121ME1\58440953. vl139849-0042044. A pharmaceutical composition comprising a compound according to any one of Claims 1 to 43, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

45. A method of treating a disease or condition responsive to the modulation of beta catenin condensates, the method comprising administering to a subject in need an effective amount of a compound according to any one of Claims 1 to 43, or a pharmaceutically acceptable salt thereof, or the pharmaceutical composition of Claim 44.

46. The method of Claim 45, wherein the disease or condition is cancer.

47. The method of Claim 46, wherein the cancer is bladder cancer, breast cancer, colorectal cancer, endometrial cancer, gastric cancer, head and neck cancer, leukemia, liver cancer, lung cancer, ovarian cancer, pancreatic cancer, or a solid tumor.

48. The method of Claim 47, wherein the breast cancer is triple negative breast cancer, the leukemia is chronic lymphocytic leukemia or acute myeloid leukemia, and the lung cancer is non-small cell lung cancer.122ME1\58440953. vl

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