NZ737090B2 - Processes for making compounds useful as inhibitors of ATR kinase - Google Patents

Abstract

The present disclosure relates to processes and intermediates for preparing compounds useful as inhibitors of ATR kinase, such as aminopyrazine-isoxazole derivatives and related molecules. The present disclosure also relates to compounds useful as inhibitors of ATR protein kinase. The disclosure relates to pharmaceutically acceptable compositions comprising the compounds; methods of treating of various diseases, disorders, and conditions using the compounds; processes for preparing the compounds; intermediates for the preparation of the compounds; and solid forms of the compounds. The compounds have formula (I) or (II) wherein the variables are as defined herein. ates to pharmaceutically acceptable compositions comprising the compounds; methods of treating of various diseases, disorders, and conditions using the compounds; processes for preparing the compounds; intermediates for the preparation of the compounds; and solid forms of the compounds. The compounds have formula (I) or (II) wherein the variables are as defined herein.

Description

S FORM NO. 5 Our ref: SGR 238158NZPR NEW ZEALAND PATENTS ACT 1953 COMPLETE SPECIFICATION A DIVISIONAL PATENT APPLICATION FILED OUT OF NZ 719122 PROCESSES FOR MAKING COMPOUNDS USEFUL AS INHIBITORS OF ATR KINASE We, Vertex Pharmaceuticals Incorporated of 50 rn Avenue, Boston, 02210, Massachusetts, United States of America hereby declare the invention, for which we pray that a patent may be granted to us and the method by which it is to be performed, to be particularly described in and by the following statement: [followed by page 1a] VPI/11-127 WO PROCESSES FOR MAKING COMPOUNDS USEFUL AS INHIBITORS OF ATR KINASE BACKGROUND OF THE INVENTION ATR (“ATM and Rad3 related”) kinase is a protein kinase involved in cellular responses to DNA damage. ATR kinase acts with ATM (“ataxia telangiectasia mutated”) kinase and many other ns to regulate a cell’s response to DNA damage, commonly referred to as the DNA Damage Response (“DDR”). The DDR stimulates DNA repair, promotes survival and stalls cell cycle progression by activating cell cycle checkpoints, which provide time for repair.

Without the DDR, cells are much more sensitive to DNA damage and readily die from DNA lesions induced by endogenous cellular processes such as DNA replication or exogenous DNA damaging agents commonly used in cancer therapy.

Healthy cells can rely on a host of different proteins for DNA repair including the DDR kinase ATR. In some cases these proteins can compensate for one another by activating functionally redundant DNA repair processes. On the contrary, many cancer cells harbour defects in some of their DNA repair processes, such as ATM signaling, and ore y a greater reliance on their remaining intact DNA repair proteins which include ATR.

In addition, many cancer cells express ted oncogenes or lack key tumour suppressors, and this can make these cancer cells prone to ulated phases of DNA replication which in turn cause DNA damage. ATR has been implicated as a critical ent of the DDR in response to disrupted DNA replication. As a result, these cancer cells are more dependent on ATR activity for survival than y cells. Accordingly, ATR inhibitors may be useful for cancer treatment, either used alone or in combination with DNA ng , because they shut down a DNA repair mechanism that is more important for cellular survival in many cancer cells than in healthy normal cells.

In fact, disruption of ATR function (e.g. by gene deletion) has been shown to promote cancer cell death both in the absence and presence of DNA damaging . This suggests that ATR inhibitors may be effective both as single agents and as potent sensitizers to radiotherapy or genotoxic chemotherapy. wed by page 2) 103831200_1.docx:JX:ewa PCT/U82012/058127 For all of these reasons, there is a need for the pment of potent and selective ATR tors for the treatment of cancer, either as single agents or as combination therapies with radiotherapy or genotoxic chemotherapy. Furthermore, it would be desirable to have a synthetic route to ATR inhibitors that is amenable to large—scale synthesis and improves upon currently known s.

ATR peptide can be expressed and isolated using a variety of methods known in the literature (sgg e. g., Kacmaz et al, PNAS 99: 10, pp6673-6678, May 14, 2002; see al_so Kumagai et a1. gel; 124, pp943-955, March 10, 2006; Unsal—Kacmaz et al. Molecular and Cellular Biology, Feb 2004, 1300; and Hall—Jackson et a1. Oncogene 1999, 18, 67076713).

DESCRIPTION OF THE FIGURES FIGURE 1a: XRPD Compound I—2 free base FIGURE 2a: TGA Compound I-2 free base FIGURE 3a: DSC Compound 1-2 free base FIGURE 43: ORTEP plot ofthe asymmetric unit of the Compound 1-2 free form single crystal structure FIGURE 1b:XRPD Compound 1-2 0 HCl FIGURE 2b: TGA Compound 1-2 ° HCl FIGURE 3b: DSC Compound I—2 ' HCl FIGURE 4b: ORTEP plot of the asymmetric unit of the Compound 1—2 ° HCl anhydrous structure.

FIGURE 10: XRPD nd 1—2 - 2HC1 FIGURE 2c: TGA Compound 1—2 ° 2HC1 FIGURE 30: DSC Compound I—2 ° 2HC1 FIGURE 1d: XRPD Compound 1—2 - HCl monohydrate FIGURE 2d: TGA Compound 1—2 ° HCl monohydrate FIGURE 3d: DSC Compound I-2 ° HCl monohydrate FIGURE 1e: XRPD Compound I—2 - HCl * 21-120 FIGURE 2e: TGA Compound 1—2 ° HCl - 2H20 FIGURE 3e: DSC Compound I-2 - HCI ° 2H20 FIGURE 4a: Solid State Compound I—l free base FIGURE 4b: Solid State 13CNMR of Compound I-l - HCl W0 2013f049726 PCT/U52012/058127 SUMMARY OF THE INVENTION The present invention relates to processes and intermediates for preparing compounds useful as inhibitors of ATR kinase, such as aminopyrazine-isoxazole derivatives and related molecules. Aminopyrazine—isoxazole derivatives are useful as ATR inhibitors and are also useful for preparing ATR inhibitors. The present invention also relates to solid forms of ATR inhibitors as well as ated ATR inhibitors.

One aspect of the invention provides a process for preparing a nd of formula 1: NH o’N 3 \\ / WN’R NO +3 H YN J1 sing preparing a compound of formula 4: HO-N\ / ”NR3 —l=/ FI’G from a compound of formula 3: Rl—O /—y\N'RS R2_O Lit] '56 under suitable oxime ion conditions.

Another aspect ses preparing a compound of formula 4: HO"N\ / WN’R3 ’J FI’G from a compound of formula 3: / WNIRB R2_O -|:/ [56 under suitable oxime formation conditions.

PCT/U82012/058127 Another aspect of the present invention comprises a compound of formula II: R4 R33 0\ R3b 0// R30 R1 2 R1 0 R1 0 or a pharmaceutically acceptable salt thereof,wherein each R1“, Rlb, R”, R2, R33, R3b, R3“, R4, R5, R6, R7, R8, R93, R91), R10, R11, R12, and R13 is independently hydrogen or deuterium, andat least one of R”, R‘b, R”, R2, R3“, R3b, R32 R4, R5, R6, R7, R8, R93, R911 R10, R“, R”, and R13 is ium.

Yet r aspect of the invention es solid forms of a compound of formula 1-2: NH2 o—“l HN‘ 0:8CO Other s of the invention are set forth herein.

The present invention has several advantages over previously known methods.

First, the present process has fewer number of total synthetic steps compared with previously disclosed processes. Second, the present process has improved yields over previously disclosed processes. Third, the present process is effective for compounds wherein R3 is a wide range of groups, such as alkyl groups or a large, hindered moiety, such as a ring. Fourth, W0 2013IO49726 PCT/U52012/058127 the t process comprises intermediates which are more stable and have a longer shelf life. In certain embodiments, the non-acidic formation of the oxime group in the present process allows the preservation of acid-sensitive protecting groups such as Boc or CB2 during the course of the synthesis. In other embodiments, the process is more easily scaled up to larger quantities due to the elimination of chromatography as a purification step.

DETAILED DESCRIPTION OF THE INVENTION One aspect of the invention provides a process for making a compound of preparing a compound of formula 4: HO-—N R3 \ / ”N, -l=/ FI’G from a compound of formula 3: R1—o R3 / ”N, R2_O -|:/ I'l’G under suitable oxime formation conditions; wherein R1 is C1_6alkyl; R2 is C1_6alkyl; or R1 and R2, together With the oxygen atoms to which they are attached, form an optionally substituted 5 or 6 ed saturated heterocyclic ring having two oxygen atoms; R3 is hydrogen, C\1_6alkyl, or a 3—6 membered saturated or lly unsaturated heterocyclyl having 1-2 heteroatoms selected from the group consisting of oxygen, nitrogen, and sulfur; wherein the heterocyclyl is optionally substituted with l ence of halo or C1-3alky1; J'1 is halo, yl, or CMalkoxy; PG is a carbamatc ting group.

Another aspect es a process for preparing a compound of formula I: comprising the steps of: preparing a compound of formula 4: HO—N ,R3 \ / ”N from a compound of formula 3: under suitable oximc formation conditions; R1 is Cmalkyl; R2 is C1.6alky1; or R1 and R2, together with the oxygen atoms to which they are attached, form an Optionally tuted 5 or 6 membered saturated heterocyclic ring having two oxygen atoms; R3 is hydrogen, C~1_6alkyl, or a 3—6 membered saturated or partially unsaturated heterocyclyl having 1—2 heteroatoms selected from the group consisting of oxygen, nitrogen, and sulfur; wherein the cyclyl is optionally substituted with l occurrence of halo or C1_3alkyl; (J2)q R4 is ; Q is phenyl, pyridyl, or an N—alkylated pyridine; J‘ is 1-1, halo, CMalkyl, or C1.4a1koxy; 2012/058127 12 is halo; CN; phenyl; oxazolyl; or a C1.5aliphatic group n up to 2 methylene units are optionally replaced with 0, NR”, C(O), S, 8(0), or 8(0):; said C1.5aliphatic group is optionally substituted with 1~3 fluoro or CN; q is 0, 1, or 2; PG is a carbamate protecting group.

Another embodiment further comprises the step of protecting a compound of formula 2: R1-O ,R3 RZ-O ‘i— under suitable protection conditions to form the compound of a 3.

Another embodiment further comprises the step of reacting a compound of formula 1: R1-O / W0 with a suitable amine under suitable reductive amination conditions to form a compound of formula 2.

In some embodiments, the suitableamine is NHCH3. In other embodiments, the suitable amine IS .

Another embodiment further comprises the step of ng a compound of formula 4: under suitable isoxazole formation ions to form a compound of formula 5: r embodiment further comprises the step of ng a compound of formula 5 under suitable coupling conditions followed by suitable ection conditions to form a compound of formula I.

In some embodiments, PG is Boc or Cbz. In some embodiments, PG is Boc.

In other embodiments, R1 is ethyl and R2 ethyl.

In yet other embodiments, R3 is CH3 or é—C . 02):; In some embodiments, R4 is ; wherein Q is phenyl. In some embodiments, Q is substituted in the para position with J2, wherein q is 1.

In some embodiments, J1 is H or halo. In some embodiments, J1 is H. In other embodiments, J is halo.

In other embodiments, J2 is a C1_6aliphatic group wherein up to l methylene unit is optionally replaced with S(O)2. In some embodiments, J2 is ~S(O)2—(C1_5alkyl). In some embodiments, q is 1.

According to another embodiment, R1 is ethyl; R2 is ethyl; R3 is CH3 or $.00; PG is Boc or Cbz; J] is H; 02%.

R4 is wherein Q is phenyl; J2 is —S(O)2-CH(CH3)2; q is 1; PCT/U32012/058127 In some ments, R3 is CH3. In some embodiments, R3 is CH3. In yet E 0 another embodiments, R3 is CH3 or ‘C .

According to another embodiment, R1 is ethyl; R2 is ethyl; a s0 R” is ' PG is B00; 1‘ is H; (an 3X R4 is wherein Q is pyridyl; J2 is N q is 1; \ CH3 N CH3 In some ments, R_ 4 _ IS N Reactions Conditions In some embodiments, the suitable oxime formation conditions t of either a single step sequence or a two step sequence.

In some embodiments, the two step ce consists of first deprotecting the ketal group in the compound of formula 3 into an aldehyde under suitable deprotection conditions, and then g the oxime of formula 4 under suitable oxime formation conditions. In some embodiments, suitable deprotcction conditions comprise adding catalytic amounts of para—toluenesulfonic acid (pTSA), acetone, and water; and suitable oxime formation conditions comprise mixing together hydroxylamine, a catalytic amount of acid, a dehydrating agent, and an alcoholic t. In other embodiments, the acid is pTSA or HCl, the dehydrating agent is lar sieves or dimethoxyacetone, and the alcoholic solvent is methanol or ethanol.

In other embodiments, the single step sequence comprises adding NHzOH.HCl and a mixture of THF and water. In other embodiments, the sequence comprises adding PCT/USZ012/058127 NHzOHHCl with a mixture of 2-methyl ydrofuran and water optionally buffered with Na2804. In some embodiments, 1 equivalent of the compound of formula 3 is combined with a 1.1 equivalents ofNHZOHHCl in a 10:1 v/v mixture ofTHF and water. In some ments, 1 equivalent of the nd of formula 3 is combined with a 1.1 equivalents ofNHZOHHCI in a 10:1 v/v mixture of 2—methyl tetrahydrofuran and water optionally buffered with NaZSO4.

In other embodiments, the protection conditions are selected from the group consisting of o R—OCOCl, a le ry amine base, and a suitable solvent; n R is C1_5alkyl optionally substituted with phenyl; o R(C02)OR’, a suitable solvent, and optionally a tic amount of base, wherein R is and R’ are each independently C1.6alkyl optionally substituted with phenyl; 0 [RO(C=O)]20, a suitable base, and a suitable solvent.

In some embodiments, the le base is Et3N, diisopropylamine, and pyridine; and the suitable solvent is selected from a chlorinated solvent, an ether, or an aromatic hydrocarbon. In other embodiments, the suitable base is Eth, the suitable solvent is a chlorinated solvent selected from DCM. In yet other ments, the protection conditions comprise adding 1.20 equivalents of (Boe)20 and 1.02 lents of Eth in DCM. ing to another ment suitable coupling conditions comprise adding a suitable metal and a suitable base in a suitable solvent. In other embodiments, the suitable metal is Pd[P(tBu)3]2; the suitable solvent is a e of acetonitrile and water; and the suitable base is sodium carbonate. In yet other embodiments, the suitable coupling conditions se adding 0.1 equivalents of Pd[P(tBu)3]2; 1 equivalent of boronic acid or ester; and 2 equivalents of sodium carbonate in a 2:1 ratio v/v of acetonitrile/watcr at 60-70°C.

According to another embodiment, le deprotection conditions comprise combining the compound of formula Q with a suitable acid in a suitable solvent. In some embodiments, the suitable acid is selected from para-toluenesulfonic acid (pTSA), HC], TBAF, H3PO4, or TFA and the suitable solvent is selected from acetone, methanol, ethanol, CH2C12, EtOAc, THF, 2-MeTHF, dioxane, toluene, or diethylether.

According to another embodiment, suitable isoxazole-formation conditions consists of two steps, the first step comprising reacting the compound of a 4 under suitable chlorooxime formation conditions to form a chlorooxime intermediate; the second step comprising reacting the chlorooxime intermediate with acetylene under suitable cycloaddition ions to form a compound of formula 5.

According to another embodiment, suitable chlorooxime formation ions are selected from . N—chlorosuccinimide and suitable solvent or ' potassium peroxymonosulfate, HCl, and dioxane.

In some embodiments, the le solvent is selected from a nonprotic solvent, an ic arbon, or an alkyl acetate. According to another embodiment, the suitable chlorooximc formation conditions are 1.05 equivalents ofN—chlorosuccinimide in isopropylacetate at 40-50°C. ing to another embodiment, le cycloaddition conditions consist of a suitable base and a suitable solvent. In some embodiments, the suitable base is selected from pyridine, DIEA, TEA, t-BuONa, and K2C03 and the suitable solvent is selected from acetonitrile, tetrahydrofuran, 2—methyltetrahydrofuran, MTBE, EtOAc, i—PrOAc, DCM, toluene, DMF, and methanol. In other embodiments, the suitable base is selected-from Et3N and the suitable solvent is selected from DCM.

According to another embodiment, the second step comprises reacting 1 equivalent of acetylene with 1.2 equivalents of the chlorooxime intermediate and 1.3 equivalents ofRN in DCM at room temperature.

According to another embodiment, suitable isoxazoIe-formation conditions comprise combining the nd of formula 4 with an oxidant in a suitable solvent. In som embodiments, said oxidant is rifluoroacetoxy)iodo] benzene and said solvent is a 1:121 mixture of methanol, water, and dioxane.

Synthesis of Compounds I—2 and L3 One ment provides a process for preparing a compound of formula 1-2: NH2 0"‘{ HN\ SOziPr comprising one or more of the following steps: PCT/USZ012/058127 a) Reacting a nd of formula 1b: EC 3 0 EC H with methylamine under suitable ive amination conditions to form a compound of formula 2b: 2b . b) reacting a nd of formula 2b under suitable Boc protection conditions to form the compound of formula 3b: EtOJ\©\/{[300N\ 3b . c) reacting a compound of formula 3b under suitable oxime formation conditions to form the compound of formula 4-i: HOc|N [1300 d) reacting a compound of formula 4-i under suitable chlorooxime formation conditions to form the nd of formula 4—ii: 4-ii e) reacting the compound of formula 4—ii with a compound of formula 4—iii W0 2013I049726 PCTIU52012/058127 f) .reacting a compound of formula 4-iV with a compound of formula A—S—i: B(OH)2 A-S-i under suitable coupling conditions to form the compound of formula 5-i: Boos ’Boc 300‘ N 0 N SOZiPr g) ecting a compound of formula 5—i under suitable Boc deprotection conditions optionally followed by treatment under basic aqueous conditions to form a compound of formula 1-2.

Another embodiment provides a process for preparing a compound of formula 1-3: PCT/U82012/058127 SOgiPr comprising one or more of the following steps: a) Reacting a compound of formula A—l: EC 8 O HO H with tetrahydro-2H-pyran-4—amine under le reductive amination conditions to form a compound of formula A-2: EC 3 HN‘CO b) reacting a compound of formula A-2 under suitable Boc protection conditions to form the compound of formula A—3: ‘ Boc c) reacting a nd of a A—3 under suitable oxime formation conditions to form the compound of formula A-4: d) reacting a compound of formula A-4: W0 2013f049726 PCT/U82012/058127 N“$69 under suitable chlorooxime formation conditions to form the compound of formula Ai: HO\ O “*CgN‘BocN A—4-i e) reacting the compound of formula Ai with a compound of a A—4—ii: N(BOC)2 ‘5»: Aii under suitable cycloaddition conditions to form the compound of formula A-S: Boc\ / N \ W”N l N\Boc Br (j0 f) reacting a nd of formula A-S with a nd of formula A—5-i: i-PrOZS Ai under suitable coupling conditions to form the compound of formula A-6: PCT/U82012/058127 SOziPr g) deprotecting a compound of formula A-6 under suitable Boc deprotection conditions optionally followed by treatment under basic aqueous conditions to form a compound of a 1-3. le coupling conditions comprise ing a suitable palladium catalyst with a suitable base in a le solvent. Suitable palladium catalyst include, but are not limited to, Pd[P(tBU)3]2, Pd(dtbpf)C12, 3)2Clz, Pd(PCy3)2Clg and , Pd(dppf)C12, Pd(dppe)C12. Suitable solvents include, but are not limited to. toluene, MeCN, water, EtOH, IPA, 2—Me—THF, or IPAc. Suitable bases include, but are not limited to, K2CO3, Na2CO3, or K3PO4.

Suitable oxime formation conditions consist of either a single step sequence or a two step sequence. The two step sequence consists of first deprotecting the ketal group in the compound of formula A—3 into an aldehyde under suitable deprotection conditions, and then forming the oxime of formula A-4 under suitable oxime formation conditions.

The single step sequence comprises, for example, comprise mixing er hydroxylamine, an acid, an c solvent, and water. In some embodiments, NH20H.HC1 is added to a e of THF and water. In some embodiments, 1 equivalent of the compound of formula 3-A is combined with a 1.1 equivalents ofNHgOHHCl in a 10:1 v/v mixture of THF/water.

Suitable deprotection conditions comprise adding an acid, acetone, and water.

Suitable acids include pTSA or HCl, tsuitable organic solvents e chlorinated ts (e. g., dichloromethane (DCM), dichloroethane (DCE), CHZClz, and chloroform); an ether (e.g., THF, 2—MeTHF and dioxane); an aromatic hydrocarbons (e. g., toluene and xylenes, or other aprotic solvents.

PCT/U52012/058127 Suitable cycloaddition conditions comprise a suitable base (e.g., pyridine, DIEA, TEA, t-BuONa, or K2C03) and a suitable t (e.g., itrile, tetrahydrofuran, 2-methyltetrahydrofuran, MTBE, EtOAc, i-PrOAc, DCM, toluene, DMF, and methanol_.

Suitable chlorooxime formation conditions comprise adding HCl in dioxame to a solution of the oxime in the presence ofNOS in a suitable solvent ed from a nonprotie solvents (DCM, DCE, THF, and e), aromatic hydrocarbons (e.g. toluene, xylenes), and alkyl acetates (e.g., isopropyl acetate, ethyl acetate).

Suitable Boc deproteetion ions comprises adding a suitable Boc deproteeting agent (e. g, , HCl, TBAF, H3PO4, or TFA) and a suitable solvent (e.g., acetone, toluene, methanol, ethanol, l-propanol, panol, CHZCIZ, EtOAc, isopropyl acetate, tetrahydrofuran, 2~methyltetraydrofuran, dioxane, and diethylether). In some embodiments, the le Boc deprotection conditions comprises adding a suitable Boc deprotecting agent selected from HCl, TFA and a suitable solvent ed from acetone, toluene, isopropyl acetate, ydrofuran, or 2—methyltetraydrofuran.

Suitable Boc protection conditions include (Boc)20, a suitable base, and a suitable solvent. Suitable bases include, but are not limited to, Eth, diisopropylamine, and pyridine. Suitable solvents include, but are not limited to, chlorinated solvents (e. g., diehloromethane (DCM), dichloroethane (DCE), CHzClz, and chloroform); an ether (e. g., THF, 2-MeTHF and dioxane); an aromatic hydrocarbons (e.g., toluene and xylenes, or other aprotic solvents. In some ments, the suitable base is Eth, the suitable solvent is DCM, tetrahydrofuran or 2—methy1tetrahydrofuran. In certain ments, the protection conditions se adding 105 equivalents of (Boc)20 in 2~methyltetrahydrofi1ran or DCM.

Suitable reductive amination conditions comprise adding a reducing agent selected from NaBH4 NaBH4, NaBH3CN, or NaBI-I(OAC)3 in the presence of a solvent selected from diehloromethane (DCM), diehloroethane (DCE), an alcoholic solvent selected from ol, ethanol, 1~propanol, isopropanol, or a nonprotie solvent selected from dioxane, tetrahydrofuran, or 2—methyltetrahydrofuran and optionally a base selected from Eth or diisopropylethylamine. In some embodiments, the suitable reductive amination conditions comprise adding 1.2 equivalents ofNaBH4 s in the presence Et3N in MeOH.

Another aspect of the present invention provides a compound of Formula II: WO 49726 PCT/USZ012/058127 R4 R33 O§S R3b 0// R30 R13 R10 or a ceutically acceptable salt thereof, . 7 Whereln e3,011 R13, Rlb, Ric, R", R38, R31), R30, R4, R5, R6, R7, R8, R91, Rgb, R103, RIOb,( and R100 is ndently hydrogen or deuterium, and at least one of Rla’ Rib, Rlc’ R2, R33, R31»’ R3c, R4, R5, R6, R7, R8, R9“, Rm), RIOa’ R1015, and R10c is deuterium.

In some embodiments, R98 and R91) are the same. In other embodiments, R93 and R9b are deuterium, and R”, R“: R‘“, R2, R33, R3“, R3“, R4, R5, R6, R7, R8, R10, R' "d, R‘ “1 Rn“, Rm, R13“, Rm), R143, and R14b are deuterium or hydrogen. In yet another embodiment, Rga and R9b are deuterium, and R”, R“: R1“, R2, R3”: R3b, R32 R4, R5, R6, R7, R8, R‘”, 12““, R1”, R123, Rub, R133, Rm’, R14“, and R1419 are en.

In one embodiment, R9“, R91), R10“, Rum, and Rmc are the same. In another embodiment, Rga, Rgb, R103, Rmb, and Rmc are deuterium, and R1“, Rib, R1“, R2, R3“, R3b, Rh, R4, R5, R6, R7, and R8 are deuterium or hydrogen. In some embodiments, R9”, R9b, Rwa, Rmb, and R10: are deuterium, and R”, R“), R“, R2, R3a, R3b, R3°, R4, R5, R6, R7, and R8 are hydrogen.

In other embodiments, R10“, wa, and R10c are the same. In one embodiment, R103, Rmb, and R1°° are deuterium, and R“, Rm, R”, R2, R3“, R”, R3“, R4, R5, R6, R7, R8, R93, and R9b are deuterium or hydrogen. In yet another embodiment, R10“, Rmb, and Rloc are deuterium, and R13, R“), R”, R2, R33, R”, R“, R4, R5, R6, R7, R8, R9“, and Rgb are hydrogen.

In some embodiments, R”, Ru’, R”, R2, R38, R3b, and R3° are the same. In another embodiment R”, R”, R1“, R2, R3”, R3“, and R3c are deuterium, and R4, R5, R6, R7, R8, Rga, R9b, R103, R101”, and R10C are deuterium or hydrogen. In yet another embodiment, R”, R”, PCT/U52012/058127 R‘“, R2, R33, R3”, and R36 are deuterium, and R4, R5, R6, R7, R8, R9a, RQ", Rm”, Rm", and R10“ are deuterium.

In another ment, R6 is deuterium, and R13, Rlb, R“, R2, R3“, R33, R3°, R4, R5, R7, R8, R93, R9b, R103, Rlob, and R10c are deuterium or hydrogen. In yet another embodiment, R6 is deuterium, and R13, R”, R”, R2, R38, R“: R3“, R4, R5, R7, R8, R93, 119‘“, Rloa, RIOb, and R10c are hydrogen.

In other embodiments, R2 is ium, and R”, Rlb, R1“, R38, R3b, and R3°, R4, R5, R6, R7, R8, R9“, R913, R103, Km, and R10c are deuterium or hydrogen. In another embodiment, R2 is deuterium, and R18, R”, R”, R3“, R31”, and R3“, R4, R5, R6, R7, R8, R93, R91”, Rm", Rlob, and R10c are hydrogen.

In r embodiment, R7 is deuterium, and R18, R”, R”, R2, R33, RSb, R3°, R4, R5, R6, R8, R93, R91”, Rica, Rum, and R100 are deuterium or hydrogen. In other embodiments, R7 is deuterium, and R13, Rlb, R10, R2, R33, R”, R36, R4, 115,116, R8, R9“, Rgb, R103, R10”, R‘°° are hydrogen.

In yet another embodiment, R8 is deuterium, and R”, R”, R”, R2, R3“, R312 R3”, R4, R5, R6, R7, R93, Rgb, R108, Rmb, and R10c are deuterium or hydrogen. In another embodiment, R8 is deuterium, and R13, R“: R“, R2, R3“, R3b, R32 R4, R5, R6, R7, R9“, R9b, Rm“, R‘Ob, R10c are hydrogen.

In some embodiments, at least one of Rm“, Rmb, or R10C are the same. In another ment, at least one of R103, Rmb, or ch are deuterium, and R13, R”, R”, R2, R33, R“: R3”, R4, R5, R6, R7, R8, R93, and R9b are deuterium or hydrogen. In yet another embodiment, at least one of Rm”, Rm", or R10C are deuterium, and R”, R”, R”, R2, R3”, R3”, R3“, R4, R5, R6, R7, R8, R93, and R91) are hydrogen.

In some embodiments, at least two of R103, Rmb, or R10c are the same. In another embodiment, at least two of Rloa, R1011 or R10c are deuterium, and R”, R”, R”, R2, R“, R”, R3°, R4, R5, R6, R7, R8, R98, and R91) are ium or hydrogen. In yet another embodiment, at least two of R103, R”, or R“)c are deuterium, and R13, R”, R”, R2, R33, R”, RR, R4, R5, R6, R7, R8, R93, and R91) are hydrogen.

In another embodiment, R13, R”, RIC, R3“, RSb, and R3c are the same. In some embodiments, R18, R”, R”, R38, R3b, and R30 are ium, and R2, R4, R5, R6, R7, R8, R93, Rm’, Rloa, Rmb, and R10c are deuterium or hydrogen. In yet another embodiment, R”, R”, R”, R3“, R3“), and R3c is deuterium, and R2, R4, R5, R6, R7, R8, R9“, R917, R103, R‘“; and R‘°° are hydrogen.

W0 2013f049726 PCT/USZ012/058127 In yet another embodiment, R4 is deuterium, and R”, R1“, R1“, R2, R33, R3”, R3“, R5, R6, R7, R8, R98, R9b, R103, Rm, and R10c are deuterium or hydrogen. In other embodiments, R4 is deuterium, and R1“, Rlb, R”, R2, R38, R3b, Rh, R5, R6, R7, R8, R93, Rm’, R103, Rmb, and R100 are hydrogen.

In another embodiment, R5 is deuterium, and R13, R”, R”, R2, R38, R3b, R3“, R4, R6, R7, R8, R98, Rgb, R108, wa, and ch are deuterium or en. In yet r embodiment, R5 is deuterium, and R“, Rlb, R”, R2, 1132111311 R3“, R4, R6, R7, R8, R9“, R9b, R108, Rmb, and R10c are hydrogen.

In another embodiment, at least one of R98 or R9b are the same. In other embodiments, at least one of R9a or R9b are deuterium, and R13, R”, R”, R2, R3”, R3b, R3°, R4, R5, R6, R7, R8, R10”, Km”, and R10C are deuterium or en. In some embodiments, at least one of R9a and R9b are deuterium, and R”, R”, R”, R2, R33, R”, R3“, R4, R5, R6, R7, R8, R103, R“, R10c are hydrogen.

In one embodiment, R6, R9a and R9b are the same. In some embodiments, R6, R9“ and R9b are deuten'um, and R“: R“: R1“, R2, R3”, R3", R3“, R4, R5, R7, R8, R10“, R”, R‘““ are deuterium or hydrogen. In other ments, R6, R93 and Rgb are deuterium, and R”, R”, R“, R2, R33, R3b, R“, R4, R5, R7, R8, R10“, wa, and 11”“ are hydrogen.

In some embodiments, R2, Rm“, Rm", and R100 are the same. In another embodiment, R2, R10“, Rmb, and R10c are ium, and R1“, Rlb, R”, R“, R3b, R3°, R4, R5, R6, R2 R8, R93, and R9b are deuterium or hydrogen. In yet another embodiment, R2, R10“, Rmb, and R10: are deuterium, and R13, R“: R1“, R33, R3b, R3C, R“, R5, R6, R7, R8, R9“, and R9" are hydrogen.

In some embodiments, R7 and at least two of R103, Rlob, or R10c are the same. In another embodiment, R7 and at least two of Rwa, wa, or R10c are ium, and R1“, Rib, R”, R2, R3“, R”, R3“, R4, R5, R6, R8, R9“, and R91) are deuterium or hydrogen. In yet another embodiment, R7 and at least two of R103, Rmb, or R10c are deuterium, and R”, R"’, R”, R2, R33, R”, R3“, R4, R5, R6, R8, R98, and Rgb are hydrogen.

In some embodiments, R”, R”, R”, R2, R3“, R3b, R30, and at least one of Rm“, wa, or R10c are the same. In another embodiment, R”, R”, R”, R2, R3“, R3”, R32 and at least one of Rloa, wa, or R100 are deuterium, and R4, R5, R6, R7, R8, R93, and R9‘) are deuterium or en. In yet another embodiment, R”, R”, R”, R2, R3", RSb, R3“, and at least one of Rm", R10”, or R100 are deuterium, and R4, R5, R6, R7, R8, Rga, and R9b are hydrogen.

In some embodiments, R13, R”, R1“, R3“, R3b, R3”, and R5 are the same. In another embodiment, R13, Ru’, RIC, R33, R3b, R“, and R5 are deuterium, and R2, R4, R6, R7, R8, PCT/U32012/058127 R9”, R9b, Rm“, Rmh, and R100 are deuterium or hydrogen. In yet another embodiment, R”, R”, R“, R33, R”, R3°, and R5 are deuterium, and R2, R4, R6, R7, R8, Rg“, R91“, R103, Rm", and R1“ are hydrogen.

In other embodiments, R4 and R6 are the same. In another embodiment, R4 and R6 are deuterium, and R“: R”, R”, R2, R33, R3b, R32 R5, R7, R8, R93, 119", R103, Rmb, and R” are deuterium or hydrogen. In yet r embodiment, R4 and R6 are deuterium, and R13, Riba RIC, R2, R3a, R3b, R3°, R5, R7, R8, R93, R91), R102!) R101), and Rioe are hydrogen.

In one ment, R2, R5, R9“, and R9b are the same. In some embodiments, R2, R5, R93, and Rgb are deuterium, and R”, R”: R”, R33, R3b, R32 R4, R6, R7, R8, R103, Rm, and Rloc are deuterium or hydrogen. In another ment, R2, R5, R93, and R91) are deuterium, and R”, R“: R“, R3“, R3”, R3“, R4, R6, R7, R8, R103, R101: and R1°° are hydrogen.

In yet another embodiment, R”, R”, R1“, R2, R33, R”, R3“, R5, R6, R9“, R9211”, Rmb, and R10c are the same. In some embodiments, Rla, Rlb, R1“, R2, R38, R3b, R3°, R5, R6, R93, R9b, R103, Rm, and Rlo‘: are deuten'um, and R4, R7, and R8 are deuterium or hydrogen. In other embodiments, R”, R“, R‘“, R2, R3“, R”, R3“, R5, R6, 119“, 11%, Rm“, R‘Ob, and R'“ is deuterium, and R4, R7, and R8 are hydrogen.

In some embodiments, the les are as depicted in the compounds of the disclosure including compounds in the tables below.

TableI NH? 0"1 HN‘CQ NH? O’N\ HNx \ \ N \ N \ l | /N /N H 033:0 N /i\ 1—1 1-2 W0 49726 PCT/U82012/058127 SOziPr Table II NH2 O‘N\ HN‘ D N D NH \ NHz 0;\ 2 0'“ N \ HN+D D HN+D \\ I D N \ D N \ D / N | D I /N /N Oj:0 o=s=o 03:0 11—] 11-2 11—3 WMNH —N ””2 041‘ HN~ HN‘ NI \ \ /N NW“”2°"‘\' I | /N D /N O=S=O DOW 8:8 83 D 0 D D Y {0 11-4 II-S 11-6 NH2 0": HM\ NHZ 041' HN‘ NH2 o—Q HN\<D \ \ \ N \ N \ N \ D | l I /N D /N D /N 0% o\\ 0% 0981/ 0481/ o’rSY 11—7 11-8 11—9 WO 49726 PCT/U82012/058127 NH2 04: HN\ 11—12 l D D /N D o’zSY 11-15 NWINHz 04$ “N40 ms D 0 fit: D D 11—18 NHZ O’r‘i HN\ I D 11—20 11—21 II-22 W0 2013l049726 PCT/U82012/058127 Compounds of this invention include those described generally herein, and are r illustrated by the s, subclasses, and species disclosed herein. As used herein, the following definitions shall apply unless otherwise ted. For purposes of this invention, the chemical elements are fied in accordance with the Periodic Table of the Elements, CAS version, Handbook of Chemistry and Physics, 75th Ed. onally, general principles of organic chemistry are described in “Organic Chemistry”, Thomas Sorrell, University Science Books, Sausalito: 1999, and “March’s ed Organic Chemistry”, 5lh Ed., Ed.: Smith, MB. and March, J., John Wiley & Sons, New York: 2001, the entire ts of which are hereby incorporated by reference.

As described herein, a specified number range of atoms includes any integer n. For example, a group having from 1—4 atoms could have 1, 2, 3, or 4 atoms.

As described herein, compounds of the invention may optionally be substituted with one or more substituents, such as are illustrated generally herein, or as ified by particular classes, subclasses, and species of the invention. It will be appreciated that the phrase “optionally substituted” is used interchangeably with the phrase “substituted or unsubstituted.” In general, the term “substituted”, whether preceded by the term nally” or not, refers to the replacement of hydrogen radicals in a given structure with the radical of a specified substituent. Unless otherwise indicated, an optionally tuted group may have a substituent at each tutable position of the group, and when more than one position in any given structure may be substituted with more than one tuent selected from a specified group, the substituent may be either the same or different at every position.

Combinations of substituents envisioned by this invention are preferably those that result in the formation of stable or chemically feasible compounds.

Unless ise indicated, a substituent connected by a bond drawn from the center of a ring means that the substituent can be bonded to any position in the ring. In example i below, for instance, I1 can be bonded to any position on the pyridyl ring. For bicyclic rings, a bond drawn through both rings indicates that the substituent can be bonded from any position of the bicyclic ring. In example ii below, for instance, I1 can be bonded to the 5—membered ring (on the nitrogen atom, for instance), and to the 6—membered ring.

/ /NW' 1 _I_(J1)5 )0—5 \ §.<NJI\/ (J N H i ii PCT/U52012/058127 The term “stable”, as used herein, refers to compounds that are not substantially altered when subjected to conditions to allow for their production, detection, recovery, purification, and use for one or more of the purposes disclosed herein. In some embodiments, a stable compound or chemically feasible compound is one that is not substantially altered when kept at a temperature of 40°C or less, in the absence of moisture or other chemically reactive conditions, for at least a week. [0084} The term “aliphatic” or atic group”, as used herein, means a straight-chain (i.e., unbranched), branched, or cyclic, substituted or unsubstituted hydrocarbon chain that is completely saturated or that contains one or more units of ration that has a single point of attachment to the rest of the molecule.

Unless otherwise specified, aliphatic groups contain 1—20 aliphatic carbon atoms.

In some embodiments, aliphatic groups contain l-lO aliphatic carbon atoms. In other embodiments, tic groups contain 1-8 aliphatic carbon atoms. In still other embodiments, aliphatic groups contain 1-6 aliphatic carbon atoms, and in yet other ments aliphatic groups contain 1—4 tic carbon atoms. Aliphatic groups may be linear or branched, substituted or unsubstituted alkyl, alkenyl, or alkynyl groups. Specific examples include, but are not limited to, methyl, ethyl, isopropyl, n-propyl, tyl, vinyl, n-butenyl, ethynyl, and tert-butyl. Aliphatic groups may also be cyclic, or have a combination of linear or branched and cyclic groups. Examples of such types of aliphatic groups include, but are not d to cyclopropyl, cyclobutyl, entyl, cyclohexyl, cyclohexenyl, —CH2- cyclopropyl, CH2CH2CH(CH3)—cyclohexyl.

The term “cycloaliphatic” (or cycle” or “carbocyclyl”) refers to a monocyclic C3-C8 hydrocarbon or bicyclic C8-C12 hydrocarbon that is tely saturated or that ns one or more units of unsaturation, but which is not aromatic, that has a single point of ment to the rest of the molecule wherein any individual ring in said bicyclic ring system has 3—7 members. Examples of cycloaliphatic groups include, but are not limited to, lkyl and cycloalkenyl groups. Specific examples include, but are not limited to, cyclohexyl, cyclopropenyl, and cyclobutyl.

The term “heterocycle”, “heterocyclyl”, or “heterocyclic” as used herein means non-aromatic, monocyclic, bicyclic, or tricyclic ring systems in which one or more ring members are an independently selected heteroatom. In some embodiments, the “heterocycle”, “heterocyclyl”, or “heterocyclic” group has three to fourteen ring members in which one or more ring members is a heteroatom independently selected from oxygen, sulfur, nitrogen, or phosphorus, and each ring in the system contains 3 to 7 ring members.

Examples of heterocycles include, but are not limited to, 3—lH—benzimidazol—2— one, 3-(1-alkyl)-benzimidazol-Z-one, 2-tetrahydrofuranyl, 3-tetrahydrofuranyl, 2- tetrahydrothiophenyl, 3-tetrahydrothiophenyl, 2-morpholino, 3-morpholino, 4-morpholino, 2- thiomorpholino, 3-thiomorpholino, 4—thiomorpholino, l—pyrrolidinyl, 2—pyrrolidinyl, 3— pyrrolidinyl, l—tetrahydropiperazinyl, 2—tetrahydropiperazinyl, 3—tetrahydropiperazinyl, 1- pipcridinyl, 2-piperidinyl, 3-pipcridinyl, l—pyrazolinyl, zolinyl, 4-pyrazolinyl, 5— pyrazolinyl, l—piperidinyl, 2—piperidinyl, ridinyl, 4—piperidinyl, 2—thiazolidinyl, 3— thiazolidinyl, 4—thiazolidinyl, l~imidazolidinyl, 2—imidazolidinyl, 4—imidazolidinyl, 5— imidazolidinyl, indolinyl, ydroquinolinyl, tctrahydroisoquinolinyl, benzothiolane, ithiane, and 1,3 -dihydro-imidazol~2~one Cyclic groups, (e.g. cycloaliphatic and heterocycles), can be linearly fused, bridged, or spiroeyclic.

The term “heteroatom” means one or more of oxygen, , en, phosphorus, or silicon ding, any oxidized form of nitrogen, sulfur, phosphorus, or n; the quaternized form of any basic nitrogen or; a substitutable nitrogen of a heterocyclic ring, for example N (as in 3,4—dihydro—2H—pyrrolyl), NH (as in pyrrolidinyl) or NR+ (as in N-substituted pyrrolidinyl)).

The term "unsaturated", as used herein, means that a moiety has one or more units of unsaturation. As would be known by one of skill in the art, rated groups can be partially unsaturated or fully unsaturated. Examples of partially unsaturated groups include, but are not limited to, butene, cyclohexene, and tetrahydropyridine. Fully unsaturated groups can be aromatic, anti—aromatic, or non-aromatic. Examples of fully unsaturated groups include, but are not d to, phcnyl, cyclooctatctraene, pyridyl, thienyl, and l— pyridin—2(1H)—one.

The term “alkoxy”, or “thioalkyl”, as used , refers to an alkyl group, as previously defined, attached through an oxygen (“alkoxy”) or (“thioalkyl”) atom.

The terms “haloalkyl”, “haloalkenyl”, “haloaliphatic”, and “haloalkoxy” mean alkyl, alkenyl or alkoxy, as the case may be, substituted with one or more halogen atoms.

This term includes perfluorinated alkyl groups, such as -CF3 and —CF2CF3.

The terms “halogen”, “halo”, and “hal” mcan F, Cl, Br, or I.

The term “aryl” used alone or as part of a larger moiety as in “aralkyl”, “aralkoxy”, or “aryloxyalkyl”, refers to monocyclic, bicyclic, and tricyclic ring systems having a total of five to fourteen ring members, wherein at least one ring in the system is W0 20131049726 PCT/U82012/058127 aromatic and n each ring in the system contains 3 to 7 ring members. The term “aryl” may be used interchangeably with the term “aryl ring”.

The term “heteroaryl”, used alone or as part of a larger moiety as in “heteroaralkyl” or “heteroarylalkoxy”, refers to monocyclic, bicyclic, and tricyclic ring systems having a total of five to fourteen ring members, wherein at least one ring in the system is aromatic, at least one ring in the system contains one or more heteroatoms, and wherein each ring in the system contains 3 to 7 ring members. The term “heteroaryl” may be used interchangeably with the term “heteroaryl ring” or the term “heteroaromatic”. Examples of heteroaryl rings include, but are not limited to, 2-furanyl, 3—furanyl, N—imidazolyl, 2— imidazolyl, 4—imidazolyl, 5—imidazolyl, benzimidazolyl, 3—isoxazolyl, 4—isoxazolyl, 5— isoxazolyl, 2-oxazolyl, 4—oxazolyl, 5-oxazolyl, N—pyrrolyl, 2—pyrrolyl, olyl, 2—pyridyl, 3—pyridyl, dyl, 2-pyrimidinyl, 4—pyrimidinyl, 5—py1imidinyl, zinyl (e.g., 3- pyridazinyl), 2—thiazolyl, zolyl, S—thiazolyl, tetrazolyl (e.g., 5—tetrazolyl), triazolyl (e. g., zolyl and 5-triazolyl), 2—thienyl, 3—thienyl, benzofuiyl, benzothiophenyl, indolyl (e.g., 2— indolyl), pyrazolyl (e.g., 2-pyrazolyl), isothiazolyl, 1,2,3—oxadiazolyl, 1,2,5—oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,3—triazolyl, 1,2,3-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,5—thiadiazolyl, purinyl, pyrazinyl, 1,3,5-triazinyl, quinolinyl (e.g., 2-quinolinyl, 3-quinolinyl, olinyl), and isoquinolinyl (e.g., 1-isoquinolinyl, 3-isoquinolinyl, or 4-isoquinolinyl).

It shall be understood that the term oaryl” includes certain types of heteroaryl rings that exist in equilibrium between two different forms. More specifically, for e, species such hydropyridine and pyridinone (and likewise hydroxypyrimidine and pyrimidinone) are meant to be encompassed within the definition of “heteroaryl.” |\ |\ /N‘— NH OH O The term “protecting group” and “protective group” as used herein, are interchangeable and refer to an agent used to temporarily block one or more desired functional groups in a compound with multiple reactive sites. In certain embodiments, a ting group has one or more, or preferably all, of the ing characteristics: a) is added selectively to a functional group in good yield to give a protected substrate that is b) stable to reactions occurring at one or more of the other ve sites; and c) is selectively removable in good yield by reagents that do not attack the regenerated, deprotected functional group. As would be tood by one skilled in the art, in some cases, the reagents do not PCT/U82012/058127 attack other reactive groups in the compound. In other cases, the reagents may also react with other reactive groups in the compound. Examples of protecting groups are ed in Greene, T.W., Wuts, P. G in “Protective Groups in Organic Synthesis”, Third n, John Wiley & Sons, New York: 1999 (and other editions of the book), the entire contents of which are hereby incorporated by reference. The term “nitrogen protecting group”, as used , refers to an agent used to temporarily block one or more desired nitrogen reactive sites in a multifunctional compound. Preferred nitrogen ting groups also possess the teristics exemplified for a protecting group above, and certain exemplary nitrogen protecting groups are also detailed in Chapter 7 in Greene, T.W., Wuts, P. G in “Protective Groups in Organic Synthesis”, Third Edition, John Wiley & Sons, New York: 1999, the entire contents of which are hereby incorporated by reference.

In some embodiments, a methylene unit of an alkyl or tic chain is optionally replaced with another atom or group. Examples of such atoms or groups include, but are not limited to, nitrogen, oxygen, sulfur, -C(O)-, -C(=N—CN)—, )-, —C(=NOR)—, —SO—, and -SOz-. These atoms or groups can be combined to form larger groups. Examples of such larger groups include, but are not limited to, -OC(O)—, —C(O)CO-, —COz-, -C(O)NR—, —C(=N— CN), -NRCO-, ~NRC(O)O-, -SOzNR-, —NRSOz-, -NRC(O)NR-, -OC(O)NR-, and NR-, n R is, for example, H or C1-5aliphatie. It should be understood that these groups can be bonded to the methylene units of the aliphatic chain via single, , or triple bonds. An example of an al replacement (nitrogen atom in this case) that is bonded to the aliphatic chain via a double bond would be ~CH2CH=N—CH3. In some cases, especially on the terminal end, an optional replacement can be bonded to the aliphatic group via a triple bond. One example of this would be CHZCHZCHZCEN. It should be understood that in this situation, the terminal en is not bonded to another atom.

It should also be understood that, the term “methylene unit” can also refer to branched or substituted methylene units. For example, in an isopropyl moiety [—CH(CH3)2], a nitrogen atom (e.g. NR) replacing the first recited “methylene unit” would result in dimethylamine [-N(CH3)2]. In ces such as these, one of skill in the art would understand that the en atom will not have any additional atoms bonded to it, and the “R” from “NR” would be absent in this case.

Unless otherwise indicated, the optional replacements form a chemically stable compound. Optional replacements can occur both within the chain and/or at either end of the chain; i.e. both at the point of attachment and/or also at the terminal end. Two optional replacements can also be adjacent to each other within a chain so long as it results in a W0 2013.1049726 2012/058127 ally stable compound. For example, a C3 aliphatic can be optionally replaced by 2 nitrogen atoms to form —C—N—=-N. The optional replacements can also completely replace all of the carbon atoms in a chain. For example, a C3 aliphatic can be ally replaced by —NR-, —C(O)—, and -NR— to form —NRC(O)NR— (a urea).

Unless otherwise indicated, if the replacement occurs at the al end, the replacement atom is bound to a hydrogen atom on the terminal end. For example, if a methylene unit of —CH2CH2CH3 were optionally replaced with -O-, the resulting compound could be -OCH2CH3, H3, or -CH2CH20H. It should be tood that ifthe terminal atom does not contain any free valence electrons, then a hydrogen atom is not required at the terminal end (e. g., 2CH=O or ~CH2CH2CEN).

Unless otherwise indicated, structures ed herein are also meant to include all isomeric (e.g., enantiomeric, diastereomeric, geometric, conformational, and rotational) forms ofthe structure. For example, the R and S configurations for each asymmetric center, (Z) and (E) double bond isomers, and (Z) and (E) conformational s are included in this invention. As would be understood to one skilled in the art, a substituent can freely rotate around any rotatable bonds. For e, a substituent drawn as \ also represents Therefore, single stereochemical isomers as well as enantiomeric, diastereomeric, geometric, conformational, and rotational mixtures of the present compounds are within the scope of the invention.

Unless otherwise indicated, all tautomeric forms of the compounds of the invention are within the scope of the invention.

In the compounds of this invention any atom not specifically designated as a particular isotope is meant to represent any stable isotope of that atom. Unless otherwise stated, when a on is designated specifically as "H" or "hydrogen", the position is understood to have hydrogen at its natural abundance isotopic composition. Also unless ise stated, when a position is designated specifically as "D" or "deuterium", the position is understood to have deuterium at an abundance that is at least 3340 times r than the natural abundance of deuterium, which is 0.015% (i.e., at least 50.1% incorporation of deuterium).

WO 49726 PCT/USZ012/058127 "D" and "d" both refer to deuterium.

Additionally, unless otherwise ted, structures depicted herein are also meant to include compounds that differ only in the presence of one or more isotopically enriched atoms. For example, compounds having the present structures except for the replacement of hydrogen by ium or tritium, or the ement of a carbon by a 13C- or 14C—enriched carbon are within the scope of this invention. Such compounds are useful, for example, as analytical tools or probes in biological assays.

Processes Processes and compounds described herein are useful for producing ATR inhibitors that n an aminopyrazine-isoxazole core. The general synthetic procedures shown in schemes herein are useful for generating a wide array of chemical species which can be used in the manufacture of pharmaceutical compounds.

SCHEME A R1_O R1 0._ / \ \ SteP 1 o / \ (Ra SlepZ Rl-O ,R3 -|_—jt t N N ‘_» H _—> R2_O R2- ‘ :/ tion R -O2 IIDG Reductuve J1 amination J1 J1 1 2 g N 0’” ,R / (\E‘G‘ Step3 HO-N ,R3 Step4 \\ Step5 —* \ /l_)wI? ———> N \ "'— --—-—> Oxime PG lsoxazole J1 Suzuki formation J1 formation "\(N (when R4 is Br) 4 (1 or 2 steps) R4 Deprotection NH2 o—N 3 NH O’N 3 NH 0~N 3 \\ / ”NR 2 Step6 \\ / ”N’R 2 Step7 \\ N’R 1:) H —-———> hi \ H ————-——> H free base 1:) N' \ NI \ RfN KrN saItforma Iont' J1 J1 YN . acid formation J1 R4 R, R, I [—A 1-3 Step 1 The compound of formula I can be made according to the steps outlined in Scheme A. Step 1 depicts the use of a readily available aldehyde/ketal as a starting point for the preparation of compounds of formula 1, LA, and LB. ive amination n compound _1_ and a suitable primary amine, under conditions known to those skilled in the art leads to compound _2_ where a benzylamine motif has been installed. For example, imines can be formed by combining an amine and an aldehyde in a suitable solvent, such as dichloromethane (DCM), dichloroethane (DCE), an alcoholic solvent (e. g., methanol, ethanol), or a nonprotic solvent (e.g., dioxane or tetrahydrofuran . These imines can then be d by known reducing agents including, but not limited to, NaBH4, NaBH3CN, and NaBH(OAc)3 (sfl JOC 1996, 3849). In some embodiments, 1.05 equivalents of amine is combined with 1 equivalent of aldehyde in methanol. In other embodiments, 1.2 equivalents of amine is ed with 1 equivalent of aldehyde in methanol. This step is then followed by reduction with 0.6 to 1.4 (such as 1.2) equivalents ofNaBH4. In some cases, if an amine salt is used, base (e.g., Et3N or diisopropylethylamine) can also be added.

Step 2 depicts the protection of the benzylamine _1_ prepared above, using a carbamate—based protecting group, under suitable protection ions known to those skilled in the art. Various protecting groups, such as Cbz and Boo, can be used. Protection conditions include, but are not limited to the following: a) R-OCOCl, a suitable ry amine base, and a suitable solvent; wherein R is C1-6alkyl optionally substituted with phenyl; b) R(C02)OR’, a suitable t, and optionally a catalytic amount of base, wherein R is and R’ are each independently C1_5alkyl optionally substituted with ; c) [RO(C=O)]20, a suitable base, and a suitable solvent.

Examples of suitable bases include, but are not limited to, EN, diisopropylamine, and pyridine. Examples of suitable solvents include chlorinated ts (e.g., dichloromethane (DCM), dichloroethane (DCE), CHzClz, and chloroform), ethers (e. g., , 2-MeTHF, and dioxane), aromatic hydrocarbons (e.g., toluene, xylenes) and other aprotic solvents.

In some embodiments, tion can be done by reacting the benzylamine with (Boc)20 and Et3N in DCM. In some embodiments, 1.02 lents of (Boc)20 and 1.02 equivalents ofEth 1.02 are used. . In r embodiment, protection can be done by reacting the benzylamine with (Boc)20 in 2—MeTHF. In some embodiments, 1.05 equivalents of (Boc)20 are used.

Step 3 Step 3 shows how the ketal onal group in s is then converted into the oxime fl in a single step. This direct conversion from ketal to oxime is not ively described in the literature and it will be appreciated that this step could also be conducted in a 2012/058127 two-step sequence, transiting through the aldehyde after ection of the ketal using methodologies known to those skilled in the art.

Oxime formation conditions se mixing together hydroxylamine, acid, optionally a dehydrating agent, and an alcoholic solvent. In some embodiments, the acid is a catalytic amount. In some embodiments, the acid is pTSA or HCI, the dehydrating agent is molecular sieves or oxyacetonc, and the alcoholic solvent is methanol or ethanol. In some embodiments, the hydroxylamine hydrochloride is used in which case no additional acid is required. In other embodiments, the desired product is isolated via a biphasic work up and optionally precipitation or crystallization. If a biphasic work up is used, a dehydrating agent is not .

In another embodiment, the oxime formation conditions comprise of mixing together hydroxylamine, an acid, an organic solvent and water. Examples of suitable organic solvents include chlorinated ts (e.g., dichloromethane (DCM), dichloroethane (DCE), CH2C12, and chloroform), ethers (e.g., THF, 2—MeTHF and dioxane), aromatic arbons (e.g., toluene, xylenes) and other aprotic ts. In some embodiments, 1.5 equivalents of hydroxylamine hydrochloride are used, the organic solvent is 2-MeTHF and the water is buffered with NaZSO4. In another embodiment, 1.2 equivalents of hydroxylamine hydrochloride are used, the organic solvent is THF.

In some embodiments, le deprotection conditions comprise adding catalytic amounts of para—toluenesulfonic acid (pTSA), acetone, and water; and then forming the oxime using conditions known to one skilled in the art. In other embodiments, a single step sequence is used. In some embodiments, the single step sequence comprises adding NHZOHHCI and a mixture ofTHF and water. In some embodiments, 1 equivalent of the compound of formula 3 is combined with a 1.1 equivalents ofNHZOHHCI in a 10:1 v/V mixture of THF/water.

Step 4 Step 4 illustrates how the oxime fl is then transformed and engaged in a [3+2] cycloaddition to for the isoxazole Q. This transformation can be conducted in one pot but requires two distinct steps. The first step is an oxidation of the oxime onal group into a nitrone, or a similar intermediate with the same degree of ion, for example a chlorooxime. This ve species then reacts with an alkyne in a [3+2] cycloaddition to form the ole adduct.

W0 2013f049726 2012/058127 In some embodiments, the suitable isoxazole—formation conditions consists of two steps, the first step comprising reacting the compound of formula 4 under suitable chlorooxime ion conditions to form a chlorooxime intermediate; the second step comprising reacting the chlorooxime intermediate with acetylene under suitable cycloaddition conditions to form a compound of formula 5.

] In some embodiments, the chlorooxime formation conditions are selected from a) N—chlorosuccinimide and suitable solvent; b) ium peroxymonosulfate, HCl, and dioxane; and c) Sodium hypochlorite and a suitable solvent Examples of le ts include, but are not limited to, nonprotic solvents (e.g., DCM, DCE, THF, F, MTBE and dioxane), aromatic hydrocarbons (e.g. toluene, xylenes), and alkyl acetates (e. g., isopropyl acetate, ethyl acetate).

Isolation of the product can be achieved by adding an antisolvent to a solution of a compound of formula 5. Examples of suitable solvents for isolating the chlorooxime intermediate include mixtures of suitable solvents (EtOAc, IPAC) with hydrocarbons (e.g., hexanes, heptane, exane), or aromatic hydrocarbons (e.g., e, xylenes). In some embodiments, heptane is added to a solution of chlorooxime in IPAC.

Suitable cycloaddition conditions consist of combining the chlorooxime with acetylene with a suitable base and a suitable solvent. le solvents include protic solvents, aproptic solvents, polar solvents, and nonpolar ts. Examples of suitable solvent include, but are not limited to, itrile, tetrahydrofuran, 2—methy1tetrahydrofuran, MTBE, EtOAc, i—PrOAc, DCM, toluene, DMF, and methanol. le bases e, but are not d to, pyridine, DIEA, TEA, t—BuONa, and K2C03. In some embodiments, suitable cycloaddition conditions comprise adding 1.0 equivalents of chlorooxime, 1.0 equivalents of acetylene, 1.1 equivalents of Et3N in DCM.

Isolation of the t can be achieved by adding an antisolvent to a solution of a compound of formula 5. Examples of suitable solvents for isolating the chlorooxime include mixtures of suitable solvents (EtOAc, IPAC) with hydrocarbons (e.g., s, heptane, cyclohexane), or aromatic hydrocarbons (e.g., toluene, xylenes). In some embodiments, heptane is added to a solution of chlorooxime in IPAC.

Step 5 Step 5 depicts the final step(s) of the preparation of compounds of formula I.

When the R4 group is bromo, intermediate i can be subjected to a Suzuki cross—coupling W0 2013/049726 PCT/U82012/058127 with boronic acid or esters, under conditions known to those skilled in the art, to form compounds Where R4 an aryl, aryl or alternative moieties resulting from the metal- assisted coupling on. When intermediate Q is ly functionalised, a deprotection step can be carried out to remove the ting groups and generate the compounds of formula I.

Metal assisted coupling reactions are known in the art (se_e e.g., Org.Proc. Res.

Dev. 2010, 30-47). In some ments, suitable coupling conditions comprise adding 0.1 equivalents of Pd[P(tBu)3]2; 1 equivalent of boronic acid or ester; and 2 equivalents of sodium carbonate in a 2:1 ratio v/v of acetonitrile/water at 60—70°C. In other embodiments, suitable coupling conditions comprise adding 0010—0005 equivalents Pd(dtbpt)Clg, 1 equivalent of boronic acid or ester, and 2 lents of potassium carbonate in a 7:2 v/v of toluene and water at 70 °C The final t can treated with a metal scavenger a gel, fiinctionalized resins, charcoal) (sgge.g., Org. Proc. Res. Dev. 2005, 198-205). In some embodiments, the solution of the product is treated with Biotage MP—TMT resin.

The product can also be isolated by crystallization from an alcoholic solvent (e. g. methanol, ethanol, isopropanol). In some embodiments the solvent is ethanol. In other embodiments the solvent is isopropanol.

Deprotection of B00 groups is known in the art (see eg. Protecting Groups in Organic Synthesis, Greene and Wuts). In some embodiments, suitable ection conditions are hydrochloric acid in acetone at 35—45 °C. In other embodiments, suitable deprotection conditions are TFA in DCM.

Step 6 Step 6 illustrates how compounds of formula I are ted to compounds of formula I—A using a base under suitable conditions known to those skilled in the art. In some embodiments, isolation of the free-base form of compounds of formula I may be achieved by adding suitable base, such as NaOH to an alcoholic acidic solution of nds of formula Ito precipitate the product. $12.2 Step 7 illustrates how compounds of formula I—A are converted to nds of formula I-B using an acid under syuitable conditions known to those skilled in the art.

In some embodiments suitable ions involve adding aqueous HCl, to a suspension of compounds of formula LA in acetone at 35 °C then heating at 50 °C.

PCTIU82012/058127 SCHEME B: Formation of dl—boronate x W x O\,0 1) Base te 2) 020 Formation —————> ——————> O=S=O Scheme B shows a general synthetic method for the preparation of dl—boronate intermediates. A suitable 1-halo-(isopropylsulfonyl)benzene is treated with a base such as, but not limited to NaH, LiHMDS or KHMDS followed by quenching of the anion with deuterium source such as D20. The halogen is then transformed into a suitable te derivative via, for example, metal mediated cross—coupling catalyzed by, for instance, Pd(‘Bu3)2 or Pd(dppt)Clz-DCM.

SCHEME C: ion of d6-boronate x W x O\,0 1) Base Boronate 2) DECX Formation __—_.). 023:0 o=s=o | DWD 0:3:0 D D D D 3W3 D D Scheme C shows a general synthetic method for the preparation of d6-boronate intermediates. A suitable 1-halo-(methylsulfonyl)benzene is treated with a base such as, but not limited to NaH, LiHMDS or KHMDS followed by quenching of the anion with deuterium source such as D3CI. This reaction is repeated until the desired amount of deuterium has been incorporated into the molecule. The halogen is then transformed into a suitable boronate derivative via, for example, metal mediated coupling catalyzed by, for ce, Pd(tBu3)2 or Pd(dppf)C12-DCM.

PCT/U52012/058127 SCHEME D: Formation of d7-boronate Br Br Br W < 1 © © 0~ ,0 Boronate Alkylation 3 m O=S=O Formation SH “ ’ [3WD 0WD “————> 0-3—0 D D D D D D D D D D D D D D D D Scheme D shows a general synthetic method for the preparation of d7—boronate intermediates. 4—Bromobenzenethiol is treated with a base such as, but not limited to NaH, LiHMDS or KHMDS followed by quenching of the anion with deuterium source such as 1,1,1,2,3,3,3—heptadeuterio~2-iodo-propane. The sulfide is then ed to the corresponding sulfone using, for example, mCPBA or Oxone. The halogen is then transformed into a suitable boronate derivative via, for example, metal mediated cross-coupling catalyzed by, for instance, Pd(‘Bu3)2 or f)Clg-DCM.

SCHEME E: Formation of aryl ring ated boronate Br Br W W Br 0e9,0 0‘5,0 / ' / / ' ' ' DI +x +x Boronate TX splacernent \ Oxadauon \ Formation i}X ogenaflon @- \ __—'> D l I \ \ s o=s=o l; 323“ ”I, til, Br O‘BD O‘B,O ©X/ __-_ Emma.” / Deuterogenation / Formation +X ————> +5 \ \ 0:0 o=s=o o=s=o D D Scheme B shows a general synthetic method for the preparation of boronate intermediates where the aryl ring is substituted with a deuterium. A le l-iodo—4—bromo— aryl derivative is treated with a substituted thiol such as propane—Z-thiol under metal catalyzed ng conditions using a catalyst such as CuI. The sulfide is then oxidized to the corresponding sulfone using, for example, mCPBA or Oxone. The bromide is then transformed into a suitable boronate derivative via, for example, metal mediated cross- eoupling catalyzed by, for instance, 3)2 or Pd(dppf)C12-DCM. The remaining substituent is then converted into ium by, for instance, metal catalyzed halogen— deuterium exchange using a suitbale metal catalyst, such as Pd on C under an atmposhere of deuterium gas. In on, the l—bromo—(isopropylsulfonyl)benzene can be treated with a base such as, but not limited to NaH, LiHMDS or KHMDS followed by quenching of the anion with deuterium source such as D20. The bromide is then transformed into a suitable boronate tive via, for example, metal mediated cross-coupling catalyzed by, for instance, Pd(‘Bu3)2 or Pd(dppf)Clz-DCM. The remaining substituent is then converted into deuterium by, for instance, metal zed halogen-deuterium exchange using a le metal catalyst, such as Pd on C under an atmposhere of deuterium gas.

SCHEME F: Formation of aryl ring deuterated boronate Br Br B! W 0‘ ,0 . /-:-X /—;X 0‘3’0 \TX \ \ ~ I hon Oxldation Boronate ~ / _ _ _'x Deuterogenation ion \ SH [5&0 0:93;?) __:_D O=S=O DDDDD DDDDD 0=5=0 D D D D D D D 3 D g D D Scheme F shows another general synthetic method for the preparation of boronate ediates where the aryl ring is substituted with a deuterium. A substituted 4- bromobenzenethiol is d with a base such as, but not limited to NaH, LiHMDS or KHMDS followed by quenching of the anion with deuterium source such as 1,] ,1,2,3,3,3— heptadeuterio-2—i0donpropane. The sulfide is then oxidized to the corresponding sulfone using, for example, mCPBA or Oxone. The halogen is then ormed into a suitable boronatc derivative via, for example, metal mediated cross—coupling catalyzed by, for instance, Pd(tBu3)z or Pd(dppf)Clz'DCM. The remaining substituent is then converted into deuterium by, for instance, metal catalyzed halogen-deuterium exchange using a suitbale metal catalyst, such as Pd on C under an atmposhere of deuterium gas.

SCHEME G: Formation of aryl ring deuterated boronate Br Br Br / / / TX / . _._X .1.X 1)Base \ -—x_ Alkylatlon a I Oxidatlon l l —_).. \ \ _____.) \ __).JC_X_>2 D Formation O=S=O --—-———-> S 0=S=O SH D D [ l D D D D 0‘ ,O 0» ,0 / / —'X Deutamganation +0 \ \ O=S=O O=S=O D D D D DownD D D W0 2013f049726 PCT/U52012/058127 Scheme G shows another l tic method for the preparation of boronate intermediates where the aryl ring is substituted with a deuterium. A substituted 4- bromobenzenethiol is d with a base such as, but not limited to NaH, LiHMDS or KHMDS followed by quenching of the anion with for instance Mel. The sulfide is then ed to the corresponding sulfone using, for example, mCPBA or Oxone. The sulfone is treated with a base such as, but not limited to NaH, LiHMDS or KHMDS followed by quenching of the anion with deuterium source such as D3CI. This reaction is repeated until the desired amount of deuterium has been incorporated into the molecule. The halogen is then transformed into a suitable boronate derivative via, for example, metal ed cross— coupling catalyzed by, for instance, Pd(tBu3)2 or f)C12-DCM. The remaining substituent is then converted into deuterium by, for instance, metal catalyzed halogen- deuterium exchange using a suitbale metal catalyst, such as Pd on C under an atmposhere of ium gas.

SCHEME H: Formation of aryl ring deuterated oxime intermediates 3, L 0/ / O I 3' / I x] 1 o\ ernination Hydrolysis 7‘ 0\ Protection /\0 / ’ I O\M -‘—‘> 7‘ x | ‘/ 0 O X 0 X\ \ ' O k0 to L Hoductwe. ~ /\o / mm“ Aom M /\O Amination I __._._> 7\ o x o l \ D/ \ \/ D/ o o 0 300 O 0 /\o /\0 \ 0Y0 Oxlme Formatlon \ Y \ Protection I H ————————> I l I/ N R10 // N Rm 0// °11 D D RD- away?" RD- gnaw?" Figa Rwfi1 Scheme H shows a general synthetic method for the preparation of oxime intermediates where the aryl ring is substituted with a deuterium. The methyl group of an appropriately substituted methyl ALmethylbenzoate derivative can be converted into the corresponding dibromide under conditions such as AIBN catalyzed bromination with NBS.

This di-bromide is then hydrolysed to the corresponding aldehyde, for instance using AgN03 in acetone/water. Protection of the aldehyde as a suitable acetal, for instance the diethyl acetal and subsequent sion of the remaining substituent into deuterium by, for instance, metal catalyzed n-deuterium exchange using a suitable metal catalyst, such as Pd on C under an atmosphere of deuterium gas gives the deuterated ester intermediate. The ester W0 20131049726 PCT/U52012/058127 functionality can be reduced using reagents such as LiAlH4, NaBH4, NaBD4 or LiAlD4 to give corresponding aldehyde. This can be reacted under ive amination conditions using a suitable amine, such as methylamine or d3-methylamine using a reducing agent such as NaBH4 or NaBD4 to give the corresponding amine derivative. This can be protected with, for instance a Boc group and the acetal converted into the oxime using, for instance, ylamine hydrochloride in THF/water.

SCHEME 1: Formation of aryl ring deuterated oxime intermediates \ 0/ / ‘o I 3’ / I X] I o\ ation I Hydrolysis 7~ 0\ Protection / 0\ *—’ “'_’ \0 7» x ' O X ~/ O X‘ o\ 0 \O \O Deuterogenation~ \0 / - \o \ \ Amide FormationA ion- 0 \ BOG ———-—————> I —-———-—-——> I —> I _ 7~ 0\ // NH; D// NHZm D D 0 0 R9“ F19" \O \l/ \O \{/ H0~IN \o O \ 0Y0 tion \o o 0 O \ Oxime Formation \ I I I // NH D// N R10 D D// N¥R1° Rea R» R" R9531?" R!» R” at?" Scheme 1 shows another general synthetic method for the preparation of oxime ediates Where the aryl ring is substituted with a deuterium. The methyl group of an appropriately substituted methyl 4—methylbenzoate derivative can be converted into the corresponding dibromide under conditions such as AIBN catalyzed bromination with NBS.

This di—bromide is then hydrolysed to the corresponding aldehyde, for instance using AgNO3 in acetone/water. Protection of the de as a suitable acetal, for instance the dimethyl acetal and subsequent conversion of the remaining subtituent into deuterium by, for instance, metal catalyzed halogen-deuterium exchange using a suitable metal catalyst, such as Pd on C under an here of deuterium gas gives the deuterated ester intermediate. The ester functionality can be converted into the corresponding primary amide under standard conditions, such as heating with a solution of ammonia in methanol. The amide can be reduced to the corresponding amine using reagents not d to LiAlH4 or LiA1D4. This can be protected with, for instance a Bee group. The carbamate NH can be alkylated under basic conditions using for instance NaH, LiHMDS or KHMDS followed by quenching of the anion with deuterium source such Mel or D3CI. The acetal can be converted into the oxime using, for instance, hydroxylamine hydrochloride in THF/water.

SCHEME J: Formation of aryl ring deuterated oxime intermediates / 0’ / \O x/‘l o\ Byomlnatlnn 5’ I Hydrolysis 7,] o\ Protectlon \0 / o X 0 \o \ \ o o / \ Deuterogenalion \0 I Amide Fonnafion \0 I Reduction \0 \ I 22?:3: 7‘ O\ ——)- // NH; ——————->~ // NH: ————> D D D O 0 R8- Rab \o \O \i/ HoaN \I/ \0 \ O O I \ Oxlme Formation \ H Satcect‘mn \o I 10 I / "\KR ———> I // N a") 1/ N am D u D R9951?“ D 39' Rwfi‘ Fl“ R‘" Roam?" Scheme J shows another general synthetic method for the preparation of oxime intermediates where the aryl ring is substituted with a deuterium. The methyl group of an appropriately tuted methyl 4-methy1benzoate derivative can be converted into the corresponding dibromide under conditions such as AIBN catalyzed bromination with NBS.

This di—bromide is then hydrolysed to the corresponding aldehyde, for instance using AgN03 in acetone/water. tion of the de as a suitable , for instance the dimethyl acetal and subsequent conversion of the remaining substituent into deuterium by, for instance, metal catalyzed halogen-deuterium exchange using a suitable metal catalyst, such as Pd on C under an atmposhere of deuterium gas gives the deuterated ester intermediate. The ester functionality can be converted into the corresponding primary amide under standard conditions, such as heating with a on of ammonia in methanol. The amide can be reduced to the corresponding amine using reagents not limited to LiAlH4 or LiAlD4. This can be reacted under reductive amination conditions using a suitable amine, such as methylamine, d3 lamine, formaldehyde or d2-formaldehyde using a reducing agent such as NaBH4 or NaBD4 to give the corresponding amine tive. This can be protected with, for instance a Boc group. The acetal can be ted into the oxime using, for instance, hydroxylamine hydrochloride in THF/water.

PCT/U82012/058127 SCHEME K: Formation of aryl ring deuterated oxime intermediates an R9‘1 / / I o I / x o Bmmination Br \ ———-—> I Hydrolysis Deuterogenation 7‘ 0 X 7‘ o\ \ 0 X 0 o \4/ $333: \0 ° 0 Protection \ l Alkylafion /R5' R9"2 D// NH \an R93 R9” /R9‘ Rim?" Reduction Oxldalion II \ DY Oxlme Formatlon R9131?KR“) / / N R10 D/ / N H10 11 D K \K 11 R9“ Rah R15" Fl“ R“ R‘ Scheme K shows another general synthetic method for the preparation of oxime intermediates where the aryl ring is substituted with a deuterium. The methyl group of an appropriately substituted methyl 4-methylbenzoate derivative can be converted into the corresponding dibromide under conditions such as AIBN catalyzed bromination with NBS.

This di—bromide is then ysed to the corresponding de, for instance using AgN03 in acetone/water. tion of the aldehyde as a suitable acetal, for instance the dimethyl acetal and subsequent conversion of the remaining substituent into deuterium by, for instance, metal catalyzed halogen-deuterium exchange using a suitable metal catalyst, such as Pd on C under an atmosphere of deuterium gas gives the deuterated ester intermediate. This can be reacted under reductive amination conditions using a suitable amine, such as ammonium hydroxide using a ng agent such as NaBH4 or NaBD4 to give the corresponding amine tive. This can be ted with, for instance a Boc group and the carbamate NH alkylated under basic conditions using for instance NaH, LiHMDS or KHMDS followed by quenching of the anion with deuterium source such Mei or D3CI. The ester can be reduced to the corresponding alcohol using a suitable reducing agent such as LiBH4 or NaBH4. The alcohol can be oxidized to the aldehyde using regeants such as MnOz or Dess—Martin periodane. The acetal can be converted into the oxime using, for ce, aqueous hydroxylamine.

PCT/U52012/058127 SCHEME L: Formation of deuterated oxime intermediates r Lo Lo \4/ O ive BOC Aminafion /\O Protection /\O /\ H 0Y0 o ——> ——> N mo N R10 0 11 Han REDS?" Ran R9:Rl<1 Hot'N \i/ 0 O Oxime ion N R10 RSI: nab}: Scheme L shows a general synthetic method for the preparation of deuterated oxime intermediates. 4-(diethoxymethyl)benzaldehyde can be reacted under reductive amination conditions using a suitable amine, such as methylamine or d3 —methy1amine using a reducing agent such as NaBH4 or NaBD4 to give the corresponding amine derivative. This can be protected with, for instance a Boc group and the acetal converted into the oxime using, for instance, hydroxylamine hydrochloride in THF/water.

SCHEME M: Formation of deuterated oxime intermediates \0 \O \O \O \l/ \0 Amide Formation \0 Reduction \0 ggiiacllon \0 .—-—> ——* 0Y0 0\ NH, NH: ——> NH 0 o R9I Fl” R" Rob \0 \P Hos“ \k Alkylation \o 0Y0 Oxima Formation ’ ’ 0Y0 NXR“) NXRW R“ R“b R1?“ R“ nwmf‘" Scheme M shows another l synthetic method for the preparation of ated oxime intermediates. The ester functionality of methyl 4— hoxymethyl)benzoate can be converted into the corresponding primary amide under standard conditions, such as heating with a solution of ammonia in methanol. The amide can be reduced to the corresponding amine using reagents not limited to LiAlH4 or LiAlD4. This can be protected with, for instance a Boc group. The ate NH can be ted under basic conditions using for instance NaH, LiHMDS or KHMDS followed by quenching of the anion with deuterium source such Mel or D3CI. The acetal can be converted into the oxime using, for instance, hydroxylamine hydrochloride in THF/water.

PCT/USZ012/058127 SCHEME N: Formation of deuterated oxime intermediates \ \ o o \ \0 Amide Formation \0 Reduction \0 WEEK: 0\ ——‘> NH2 ——"‘> NH2 ————> o o R" fish O \O \i/ HO‘N \1/ \ I H Eggctlon \0 Oxime Formation NXRw 0Y0 0Y0 -——-~——> N R10 N R10 Fififl HWRi \l< \|< 11 R“ R3" R15“ R9: 3% R: Scheme N shows another general synthetic method for the ation of deuterated oxime intermediates. The ester functionality of methyl 4- (dimethoxymethyl)benzoate can be ted into the corresponding y amide under standard ions, such as heating with a solution of ammonia in methanol. The amide can be reduced to the corresponding amine using reagents not limited to LiAlH4 or LiAlD4. This can be reacted under reductive amination conditions using a suitable amine, such as methylaminc, d3-methylaminc, formaldehyde or dZ—formaldehyde using a reducing agent such as NaBH4 or NaBD4 to give the ponding amine tive. This can be protected with, for instance a Boc group. The acetal can be converted into the oxime using, for instance, hydroxylamine hydrochloride in THF/water.

SCHEME 0: Formation of deuterated oxime intermediates 0 \l/ o 4/ \0 Protection \0 0Y0 tlon \0 _..~._> ____._.> 0Y0 "“2 NH F19“ R9” NKRW R9: Rab R98 RWR1E“ \l/ (I) \l/ HoxN \l/ Reduction HO 0Y0 ion 0Y0 Oxime Formation "*9 a a 0Y0 N n10 N n10 N R‘” K5" w< .1 x R9. Rab R1 R93 R9°n1 Rea Room?“ Scheme 0 shows another general synthetic method for the preparation of deuterated oxime intermediates. A 4-substituted benzylmine can be protected with, for instance a Boc group. The carbamate NH can be alkylated under basic conditions using for ce NaH, LiHMDS or KHMDS followed by quenching of the anion with deuterium source such Mel or D3CI. The ester can be reduced to the corresponding alcohol using a suitable reducing agent such as LiBI-I4 or NaBH4. The alcohol can be oxidized to the aldehyde using regeants such as MnOz or Dess-Martin periodane. The acetal can be converted into the oxime using, for instance, aqueous hydroxylamine.

PCT/U82012/058127 SCHEME P: Formation of isoxazole derrivatives (306)2N NH2 NH, TMS (30cm ms / / Br / / H5 N \ N \ BOG N \ YN1 _E§._,Son ashlra KKNI Protection I 2 ms Rama]1;Suzukl .__._.___> /N —.——.> Br Br Br O=S=O R1u Rae HI I: 92 R32: R1: R3' [3+2] cycloaddlton HQIN \i/ HO‘IN \i/ 0Y0 Chlorination Cl 03/0 N am N aw “7 ”K511 "7 R3 R R‘ RB Re” R”*5“R1 0 NH; o—N HN 0 \ Rn (BOChN 04.: ‘4\N‘6H;:1 NWR12 \ I R9. R9” N \ RI2 /N R7 I 9" no /N R7 R R3 R5 Deprotectiun R5 ' " R. o=s=o 9‘“ “3° o=s=o R“ R2 R3” Rt: Ric R1: R33 nib R2 fish Rm FF“ Scheme P shows a general synthetic method for the preparation of deuterated pyrazine-isoxazole derrivatives. 3,5-Dibromopyrazin-2—amine is converted into the corresponding protected alkyne under rd Sonagashira conditions utilizing, for example, 3)4 and Cul as catalysts. The pyrazine NH; can then be protected as, for e the di~Boc derivative. Coupling of the pyrazine bromide with a te, for instance those outlined in Schemes l to 6 above, under rd Suzuki cross—coupling conditions ed by removal of the silyl protecting group give the desired alkyne intermediate. Oximes, such as those outline in Schems 7 to 14 above, can be converted into the corresponding chlorooximcs using, for instance, NCS. The alkyne and chlorooxime intermediates can undergo a [3+2] cycloaaditon to give corresponding isoxazole under standard conditions, for instance by the addition of Et3N. The Boc protecting groups can be removed under acicid conditions such as TFA in DCM or HCl in MeOH/DCM to give the deuterated pyrazine isoxale derrivatives.

W0 2013I049726 SCHEME Q: Formation of deuterated ole derrivatives O 0 NH2 o—N F30 10 \\ HN‘éan" FsckNH O"! N \ ‘(N‘éfifiu I Rae N \ File /N R7 R9” l R“ n8 /N W R9b tion R5 Haloganation ——-—-———> _—> O=S=O R13 Rae R1!) R2 R30 R” R3“ an R2 R38: . W R5 Deprotection Deuterogenalion —-——)> -—--~———>- o=s=o O=S=O R1: Rae Rib H2 R35 Rte R33 Scheme Q shows a general synthetic method for the preparation of deutcrated isoxazole derrivatives. The pyrazine NH; and benzylamineamine NH can be ted under standard conditions using trifluoroacetic anhydride. nation of the isoxazole ring with, for example NIS followed by removal of the trifluoroacetate protecting group under basic conditions provides the d halogenated interemdiates. The halogen can then converted into deuterium by, for instance, metal catalyzed halogen—deuterium exchange using a suitbale metal catalyst, such as Pd on C under an atmposhere of deuterium gas. iations The following abbreviations are used: ATP adenosine triphosphate Boc tert-butyl carbamate Cbz Carboxybenzyl DCM dichloromethane PCT/USZ012/058127 DMSO dimethyl sulfoxide Et3N triethylamine 2-MeTHF 2-methyltetrahydrofuran NMM N-Methyl morpholine DMAP 4-Dimethylaminopyridine TMS Trimethylsilyl MTBE methyl tertbutyl ether EtOAc ethyl acetate i—PrOAc isopropyl acetate IPAC isopropyl acetate DMF dimethylformamide DIEA diisopropylethylamine TEA triethylamine t—BuONa sodium teitbutoxide K2C03 potassium carbonate PG Protecting group pTSA para-toluenesulfonic acid TBAF n-butylammonium fluoride 1HNMR proton nuclear ic resonance HPLC high performance liquid tography LCMS liquid chromatography—mass spectrometry TLC thin layer chromatography Rt retention time SCHEMES AND EXAMPLES The compounds of the disclosure may be prepared in light of the specification using steps generally known to those of ordinary skill in the art. Those compounds may be analyzed by known methods, including but not limited to LCMS (liquid tography mass spectrometry) and NMR (nuclear magnetic resonance). The following generic schemes and examples illustrate how to prepare the compounds of the present disclosure. The examples are for the purpose of illustration only and are not to be construed as limiting the scope of the ion in any way. H—NMR spectra were recorded at 400 MHz using a Bruker DPX 400 instrument. Mass spec. samples were analyzed on a MicroMass Quattro Micro mass ometer ed in single MS mode with electrospray ionization. und I-lz £2 J o\ HN NU Method 1 Method 2 Method 3 JL J< ’ —> N 0 m cm A o/\ Ho \«GA o a, om 61 J< 0 i J< JOL 5; N O >L0 -N Q 0 N 0° Method4 Methods \ N~< 22 ..___, N H0, \ -—-—————> \ CI I 0 /N J< ° >qu‘; Q0 o N oo—N\ N~\< ‘6 NW"~90 N/ / Method6 \ N Method7 / ————> —> I or Method 63 / I or Method 73 N ‘N II N Compound I—1 Method 1: To a solution of tetrahydropyran-4—amine (100 g, 988.7 mmol) in MeOH (3.922 L) was added 4—(diethoxymethy1)benzaldehyde (196.1 g, 941.6 mmol) over 2 min at RT. The reaction mixture was stirred at RT for 80 min, until the aldimine formation was complete (as seen by NMR). NaBH4 (44.49 g, 1.176 mol) was carrefully added over 45 min, maintaining the temperature between 24 °C and 27 °C by mean of an ice bath. After 75 min at RT, the reaction has gone to tion. The reaction mixture was quenched with 1M NaOH (1 L).

The reaction mixture was partitioned between brine (2.5 L) and TBDME (4 L then 2 x 1 L).

The organic phase was washed with brine (500 mL) and concentrated in vacuo. The crude mixture was rediselved in DCM (2 L). The aqueous phase was ted, the organic phase was dried over MgSO4, filtered and concentrated in vacuo to give the title compound as a yellow oil (252.99 g, 91%).

W0 2013I049726 Method 2: A solution ofN-[[4-(diethoxymethyl)phenyl]methyl] tetrahydropyran~4-amine (252.99 g, 862.3 mmol) and Boo anhydride (191.9 g, 202.0 mL, 879.5 mmol) in DCM (2.530 L) was cooled down to 3.3 °C. Et3N (89.00 g, 122.6 mL, 879.5 mmol) was added over 4 min, keeping the internal temperature below 5 °C. The bath was removed 45 min after the end of the addition. And the reaction mixture was stirred at RT overnight. The reaction mixture was sequentially washed with 0.5 M citric acid (1 L), saturated NaHCO3 solution (1 L) and brine (1 L). The organic phase was dried (MgSO4), filtered and concentrated in vacuo to give a less oil (372.38 g, 110%). 1H NMR (400.0 MHz, DMSO); MS (ES+) Method 3: tert-butylN—[[4-(diethoxymethyl)phenyl]methyl]-N-tetrahydropyran—4—y1—carbamate (372.38 g, 946.3 mmol) was dissolved in THF (5 L) and water (500 mL). ylamine hydrochloride (72.34 g, 1.041 mol) was added in one portion and the reaction mixture was stirred overnight at RT. The reaction mixture was partitioned between DCM (5 L) and water.

The combined organic extract was washed with water (1L x 2). The organic phase was concentrated in vacuo to a volume of about 2L. The organic layer was dried over MgSO4, filtered and concentrated in vacuo to give a sticky less oil that crystallized on standing under vacuo. (334.42g, 106%). 1H NMR (400.0 MHz, CDC13); MS (ES+) Method 4: tert—butylN—[[4—[(E)—hydroxyiminomethyl]phenyl]methyl]-N-tetrahydropyran-4—yl— carbamate (334.13 g, 999.2 mmol) was dissolved in isopropyl acetate (3.0 L) (the e was warmed to 40 °C to allow all the solids to go into solution). rosuccinimide (140.1 g, 1.049 mol) was added portionwise over 5 min and the reaction mixture was heated to 55 °C (external block temperature). After 45 min at 55°C The reaction had gone to completion.

The reaction mixture was cooled down to RT. The solids were filtered off and rinsed with Isopropyl acetate (1 L). Combined organic extract was tially washed with water (1.5 L, 5 times) and brine, dried over MgSO4, filtered and trated in vacuo to give a s yellow oil (355.9 g; 96%). 1H NMR (400.0 MHz, CDC13); MS (ES+) Method 5: EN (76.97 g. 106.0 mL, 760.6 mmol) was added over 20 minutes to a solution of tert—butyl romo—3 -ethynyl-pyrazin—Z—yl)—N-tert-butoxycarb0nyl-carbamate (233.0 g, 585.1 mmol) and teit-butyl N-[[4-[(Z)-C-chloro-N-hydroxy-carbonimidoyl]phenyl]methyl]- N—tetrahydropyranyl-carbamate (269.8 g, 731.4 mmol) in DCM (2.330 L) at RT. During W0 2013f049726 addition of triethylamine, the exotherm was stabilised by cooling the mixture in an ice bath, then the reaction mixture was gradually warmed up to RT and the mixture was stirred at RT overnight. The on mixture was sequentially washed with water (1.5 L, 3 times) and brine. The organic extract was dried over MgSO4, filtered and partially concentrated in vacuo. Heptane (1.5L) was added and the concentration was continued yielding 547.63 g of a yellow—orange solid. ] 542.12 g was taken up into ~2 vol (1 L) of ethyl e. The mixture was heated to 74—75 °C internally and stirred until all the solid went into solution. e (3.2 L) was added slowly via on funnel to the hot solution keeping the internal temperature between 71 °C and 72 °C . At the end of the addition, the dark brown solution was seeded with some recrystallised product, and the reaction mixture was allowed to cool down to RT without any stirring to crystallise O/N. The solid was filtered off and rinsed with heptane (2 x 250 mL), then dried in vacuo to yield 307.38 g of the title product (72 %). %). 1H NMR (400.0 MHz, CDCl3); MS (ES+) Method 6: tert~butyl N—[[4-[5-[3-[bis(tert—butoxycarbonyl)amino]bromo-pyrazinyl] isoxazol—3-yl]phenyl]methyl]-N-tetrahydropyran-4—yl-carbamate (303 g, 414.7 mmol) and 2- methyl[4-(4,4,5,5-tetramethyl-l ,3,2-dioxaborolanyl)pyridyl] propanenitrile (112.9 g, 414.7 mmol) were suspended in MeCN (2 L) and H20 (1 L). Na2C03 (414.7 mL of 2 M, 8294 mmol) followed by Pd[P(tBu)3]2 (21.19 g, 41.47 mmol) were added and the reaction e was degassed with N2 for 1 h. The reaction mixture was placed under a nitrogen atmosphere and heated at 70 °C (block temperature) for 4 h (internal ature fluctuated between 60 °C and 61 °C). The reaction was cooled down to room temperature and stirred at RT overnight. The on mixture was ioned between EtOAc (2 L) and water (500 mL). The ed organic extract was washed with brine (500 mL), filtered through a short pad of celite and concentrated under reduced pressure to a volume of about 3 L. The solution was dried over MgSO4, filtered and partially concentrated in vacuo. iPrOH (1.5 L) was added and the solvent was removed in vacuo to yield the desired product as a light brown foam (405 400 g was taken up into ~5 vol (2 L) of iPrOH and the e was heated to 80 °C until all the solid went into solution. The dark brown solution was seeded, and the reaction mixture was allowed to slowly cool down to RT overnight. The solid was filtered off and rinsed with iPrOH (2 x 250 mL) and Petroleum ether (2x200 mL). The resulting solid was W0 2013/‘049726 PCT/U82012/058127 slurried in petroleum ether (2.5 L), filtered off and dried in vacuo. The resulting solid was dissolved in DCM (2.5 L) and stirred slowly for 1 h with 30 g of SPM32 ( 3-mercaptopropyl ethyl sulfide ). The silica was filtered through a pad of florisil and rinsed with DCM.

The procedure was repeated twice, then the DCM solution was concentrated in vacuo to give 23 8.02 g of a light yellow solid.

Method 7: tert—butyl N—[[4-[5-[3-[bis(tert—butoxycarbonyl)amino]~6—[2-(l—cyanomethyl— ethyl)—4—pyridyl]pyraziny1]isoxazol—3-yl]phenyl]methyl]~N—tetrahydropyran-4—yl— carbamate (238 g, 299.0 mmol) was ved in DCM (2.380 L). TFA (500 mL, 6.490 mol) was added at RT over 3 min, The reaction mixture was stirred at RT for 3.5 h. The on mixture was concentrated under reduced pressure then azeotroped with heptane ml).

The oil was then slurried in abs. EtOH (2.5 L) and filtered a . The solid was dissolved in mixture of ethanol (1.190 L) and water (1.190 L). potassium carbonate (124.0 g, 897.0 mmol) in water (357.0 mL) was added to the solution and the mixture was stirred at RT overnight.

The solid was filtered off, was washed with water (2.5 L), and dried at 50 °C in vacuo to give 108.82 g of the title compound (Compound 1—1) as a yellow powder. (73 %) Methods 6a and 7a Os ,0 B Method 6a BocxN,Bo%'N\NW / \N ON I ‘Boc .__.______.. 0 1. cat. Pd(dtbpf)Clz, PhCHa, aq. K2003 2, crystallization N , \ 1.TFA \ N \ N~Boc DCM I NH / N /“ 6 25°C -—-—————> (3 o 2. NaOH / O I 90% I \ CN Compound 1-] A e of utyl N-[[4—[5-[3-[bis(tert—butoxycarbonyl)amino]—6—bromo— pyrazin-Z-yl] isoxazolyl]pheny1]methyl]-N-tetrahydropyranyl-carbamate (110.0 g, 151 mmol), K2CO3 (41.6 g, 301 mmol), and 2-methy1—2-[4-(4,4,5,5-tetramethyl-1,3,2- dioxaborolan—2—y1)—2-pyridy1] propanenitrile (41.0 g, 151 mmol) in toluene (770 mL) and water (220 mL) is stirred and degassed with N2 for 30 min. at 20 °C. The catalyst Pd(dtbpf)Clz (1.96 g, 3.01 mmol) is added and the mixture is degassed for an additional 10 min. The mixture is heated at 70 CC until the on is complete. The mixture is cooled to ambient temperature, diluted with water (220 mL), and filtered through a bed of . The organic phase is concentrated to remove most of the solvent. The concentrate is diluted With i-PrOH (550 mL). The resultant sion is stirred for at least 1 h and then the solid is collected by filtration to afford a tan powder. The solid is dissolved in toluene (990 mL) and d with Biotage MP-TMT resin (18.6 g) for 2 h at ambient temperature. The resin is removed by filtration. The filtrate is concentrated then diluted with i-PrOH (550 mL) and then re—concentratd. Add i—PIOH (550 mL) and stir for 1 h at ambient temperature. Cool the suspension to 5 °C and collect the solid by filtration then dry to afford utyl N—[[4—[5-[3- [bis(tert-butoxycarbony1)amino]—6—[2—(1-cyano—1—methyl—ethyl)—4—pyridyl]pyrazin~2- yl]isoxazoly1]pheny1]methy1]-N-tetra'hydropyran—4-yl-carbamate (Compound 1-1) (81.9 g; 68%, yield, 98.7 area % purity by HPLC) as a cream-colored powder.

Form Chan 6 to Corn ound I-l-HCl-1.5 H20 ,N -N \ \ N \ N \ | N” /N 1MHC| l N” 0 /N ———-————> / o / (j; -1.5H20 o \ CN \N CN A suspension of tert—butyl N-[[4—[5-[3—[bis(tert-butoxycarbony1)amino]-6—[2-(1- cyanomethyl—ethyl)—4—pyridyl]pyrazin-2~yl]isoxazol—3 -yl]pheny1]methy1]—N- tetrahydropyrany1—carbamate (Compound 1-1) (36.0 g, 72.6 mmol) in CH3CN (720 mL) is stirred at ambient temperature (20 °C) in a flask equipped with mechanical stirring. A 1 M aqueous solution of HCl (72.6 mL; 72.6 mmol) is added. The suspension is stirred at ambient temperature for 20 h. The solid is collected by ion. The filter-cake is washed with CH3CN (3 x 50 mL) then dried under vacuum with high humidity for 2 h to afford Compound 1—1°HC1°1.5 H20 (30.6 g; 74%) yield, 98.8 area % purity by HPLC) as a yellow powder. .1H NMR (400 MHz, DMSO) 5 9.63 (d, J= 4.7 Hz, 2H), 9.05 (s, 1H), 8.69 (d, J = .2 Hz, 1H), 8.21 (s, 1H), 8.16 — 8.03 (m, 3H), 7.84 (t, J= 4.1 Hz, 3H), 7.34 (br s, 2H), 4.40 — 4.18 (m, 2H), 3.94 (dd, J: 11.2, 3.9 Hz, 2H), 3.32 (t, J: 11.2 Hz, 3H), 2.17 — 2.00 (m, 2H), 1.81 (s, 6H), 1.75 (dd, J= 12.1, 4.3 Hz, 2H).

Exam 1e 2: S nthesis of 3- - 4-iso r0 lsulfonvl hen l razin—Z—amine Com ound II-l ' (B0C)2N NH; NHZ TMS (BOC)2N ms I NJ§r3r ¢ // N \ 800 N \ Ki K7“! mp RNSonogashira Protection {KN 2)TMS Removal Br Br Br i H Hi W \o \o \o \o \ \ O O 0 Amide Formation 0 Reduction \0 ggidion \O Y K —-——————> ———————> o\ NH2 NH2 ——_——> NH D n D D 0 0 V vii viii 0 HOW“ H0\|N \ 0 0 ‘ O O Alkylation. O Y 7< Oxtme Formation. . O 0 OrOOXll'ne Y \'< cm Formation Y \'< N\ N\ N\ D D D D D D u fl O=< + ””2 0'N \ HN—N \ D N] \N D l D /N [3+2] cycloaddilon Deproteclion ~—-——-—> -——> 0=S=O xii II-l Step 1: 5-Bromo-3—((trimethylsilyl)ethynyl)pyrazinamine NHZ TMS (Trimethylsilyl)acetylene (1.845 g, 2.655 mL, 18.78 mmol) was added dropwise to a solution of bromopyrazin—2—amine (compound 1) (5 g, 19.77 mmol) in DMF (25 mL). Triethylamine (10.00 g, 13.77 mL, 98.85 mmol), copper(1) iodide (451.7 mg, 2.372 mmol) and Pd(PPh3)4 (1.142 g, 0.9885 mmol) were then added and the resulting solution stirred at RT for 30 s.The reaction e was diluted with EtOAc and water and the layers separated. The aqueous layer was extracted further with EtOAc and the combined organic layers washed with water, dried (MgSO4) and concentrated in vacuo. The residue was purified by column tography eluting with 15% EtOAc/Petroleum ether to give the product as a yellow solid (3.99 g, 75% Yield). 1H NMR (400.0 MHZ, DMSO) 3 0.30 (9H, s), 8.06 (II-I, 5); MS (ES+) 271.82.

Step 2: tert—Butyl N-tert-butoxycarbonyI-N-[S-br0m0((trimethylsilyl)ethyynyl) pyrazin-Z-yl]carbamate (BOC)2N TMS 5—Br0mo—3-(2-t1imethylsilylethynyl)pyrazin-2—amine (2.85 g, 10.55 mmol) was dissolved in DCM (89.06 mL) and treated with Boc anhydride (6.908 g, 7.272 mL, 31.65 mmol) followed by DMAP (128.9 mg, 1.055 mmol). The reaction was allowed to stir at ambient temperature for 2 hours. The mixture was then diluted with DCM and NaHC03 and the layers separated. The aqueous layer was extracted further with DCM, dried (MgSQ4), filtered and concentrated in vacuo. The resultant residue was purified by column chromatography g with dichloromethane to give the desired product as a colourless oil (4.95g, 99% Yield). 1H NMR (400.0 MHZ, DMSO) 5 0.27 (9H, s). 1.42 (18H, s), 8.50 (1H, ); MS (ES+) 472.09.

Step 3: tert-Butyl N—(3-ethynyl-5—(4—(isopropylsulfonyl)phenyl)pyrazin—2—yl)N- toxycarbonyl—carbamate utyl (BOC)2N O=S=O N— [5-Bromo(2-trimethylsi1ylethynyl)pyrazinyl]-N- toxycarbonylcarbamate (3 g, 6.3 77 mmol) and propylsulfonylphenyl)boronic acid (1.491 g, 6.536 mmol) were dissolved in MeCN/water (60/12 mL). K3PO4 (2.706 g, 12.75 mmol) was added and the reaction mixture was degassed with a flow of nitrogen (5 cycles).

Pd[P(tBu)3]2 (162.9 mg, 0.3188 mmol) was added and the resulting mixture was stirred at room temperature for 1h. The reaction mixture was poured y into a mixture of ethyl acetate (500 mL), water (90 mL) and 1% aqueous sodium metabisulphite at 4 °C, shaken well and the layer separated. The organic on was dried over MgSO4, filtered and the filtrate was treated with 3-mercaptopropyl ethyl sulphide on silica ol/g, 1 g), sorbed onto silica gel then purified by column chromatography on silica gel eluting with 30—40% EtOAc/petroleum ether. The solvents were concentrated in vacuo to leave the product as a yellow viscous oil that was triturated with petroleum ether to yield the product as beige crystals (1.95 g, 61% Yield); 1H NMR (400 MHz, DMSO) 5 1.20 (m, 6H), 1.39 (s, 18H), 3.50 (m, 1H), 5.01 (s, 1H), 8.03 (m, 2H), 8.46 (m, 2H) and 9.37 (s, IH).

Step 4: 4-(Dimethoxymethy1)benzamide A mixture of methyl 4—(dimethoxymethyl)benzoate (3.8 g, 18.08 mmol) and 7M NH3 in MeOH (30 mL of 7 M, 210.0 mmol) in a sealed tube was heated at 110 °C for 22 hours. A further portion of 7M NH3 in MeOH (20 mL of 7 M, 140.0 mmol) was added and the reaction heated at 135 °C for 23 hours. The on was cooled to ambient temperature and the solvent removed in vacuo. The residue was re—submitted to the reaction conditions (7M NH3 in MeOH (30 mL of 7 M, 210.0 mmol) at 115 °C) for a further 16 hours. The solvent was removed in vacuo and the residue tritruated from Et20. The resultant precipitate was isolated by filtration to give the sub—title compound as a white solid (590 mg, 17% yield).

The filtrate was purified by column tography (ISCO Companion, 40 g column, eluting with 0 to 100% EtOAc/Petroleum Ether to 10% tOAc, loaded in EtOAc/MeOH) to give a further protion of the sub-title product as a white solid (225 mg, 6% Yield). Total PCT/U52012/058127 isolated (815 mg, 23% Yield); 1H NMR (400 MHz, DMSO) 5 3.26 (s, 6H), 5.44 (s, 1H), 7.37 (s, 1H), 7.46 (d, J = 8.0 Hz, 2H), 7.84 - 7.91 (m, 2H) and 7.98 (s, 1H) ppm; MS (ES+) 196.0.

Steo 5: Dideuterio—[4-(dimethoxymethyl)phenyl]methanamine LiDH4 (12.52 mL of 1 M, 12.52 mmol) was added dropwise to a stirred solution of 4- (dimethoxymethyl)benzamide (815 mg, 4.175 mmol) in THF (20 mL) at 0 °C under an atmosphere of nitrogen. The reaction was heated at reflux for 16 hours then cooled to ambient temperature. The reaction was ed by the tial addition of D20 (1 mL), 15% NaOH in D20 (1 mL) and D20 (4 mL). The resultant solid was removed by filtration and washed with EtOAc. The filtrate was concentrated in vacuo and the residue dried by azeotropic distillation with toluene (x 3) to give the tle compound as a yellow oil (819 mg) that was used without further purification; 11-1 NMR (400 MHz, DMSO) 5 3.23 (3, 61-1), .36 (s, 1H) and 7.30 - 7.35 (m, 4H) ppm; MS (ES+) 167.0.

Step 6: tert-Butyl N-[dideuterio—[4-(dimethoxymethyl)phenyl]methyl]carbamate \o OYOKNH D D viii Eth (633.7 mg, 872.9 pL, 6.262 mmol) was added to a stirred suspension of dideuterio—[4-(dimethoxymethyl)pheny1]methanamine (765 mg, 4.175 mmol) in THF (15 mL) at 0 °C. The reaction was allowed to stir at this temperature for 30 minutes then Boczo (956.8 mg, 1.007 mL, 4.384 mmol) was added in portions. The reaction was d to warm to ambient temperature and stirred for 18 hours. The t was removed in vacuo and the residue was purified by column chromatography (ISCO Companion, 120 g column, eluting with 0 to 50% EtOAc/Petroleum Ether, loaded in DCM) to give the tle product as a colourless oil (1.04 g, 88% Yield); 1H NMR (400 MHz, DMSO) 6 1.40 (s, 9H), 3.23 (s, 6H), .36 (s, 1H), 7.24 (d, J = 8.2 Hz, 2H), 7.33 (d, J = 8.0 Hz, 2H) and 7.38 (s, 1H) ppm.

Step 7: tert-Butyl N-[dideuterio—[4-(dimethoxymethyl)phenyl]methyl]-N-methyl— carbamate \o 0Y07<N D D ‘ LiHMDS (1M in THF) (1.377 mL of l M, 1.377 mmol) was added dropwise to a sittred on of utyl N—[dideuterio-[4-(dimethoxymethyl)phenyl]methyl]carbamate (300 mg, 1.059 mmol) in THF (5 mL) at —78 °C. The solution was stirred at this temperature for 10 minutes then iodomethane (225.4 mg, 98.86 uL, 1.588 mmol) was added dropwise and the mixture allowed to warm to t temperature over 1 hour. The reaction was again cooled to ~78 °C and LiHMDS (1M in THF) (635.4 uL of 1 M, 0.6354 mmol) was added.

After 10 minutes iodomethane (105.2 mg, 46.14 uL, 0.7413 mmol) was added and the reaction allowed to warm to ambient temperature over 6 hours. The mixture was d with EtOAc and the organic layer washed with saturated aqueous NaHC03 (x 2), brine (x 1), dried (MgSO4) d and concentrated in vacuo. The residue was purified by column chromatography (ISCO Companion, 24 g column, eluting with 0 to 30% EtOAc/Petroleum Ether, loaded in DCM) to give the sub-title product as a colourless oil (200 mg, 63% Yield); 1H NMR (400 MHz, DMSO) 6 1.41 (d, J = 27.7 Hz, 9H), 2.76 (s, 3H), 3.24 (s, 6H), 5.37 (s, 1H), 7.23 (d, J = 7.9 Hz, 2H) and 7.37 (d, J = 8.0 Hz, 2H) ppm.

Step 8: tert—Butyl N—[dideuterio-[4-[hydroxyiminomethyl]phenyl]methyl]-N— (methyl)carbamate OYOKN D D Hydroxylamine hydrochloride (51.15 mg, 0.7361 mmol) was added to a d solution of utyl N-[dideuterio-[4-(dimethoxymethyl)phenyl]methyl]-N-methyl- carbamate (199 mg, 0.6692 mmol) in THF (10 mL)/water (1.000 mL) and the reaction allowed to stir at ambient temperature for 4 hours. The reaction was partitioned between DCM and brine and the layers separated. The aqueous layer was extracted with DCM (x 2) and the combined organic extracts washed with brine (x 1), dried (MgSO4), filtered and PCT/U52012/058127 concentrated in vacuo to give the sub—title compound as a white solid (180 mg, 100 % ; 1H NMR (400 MHz, DMSO) 8 1.41 (d, J = 24.6 Hz, 9H) 2.76 (s, 3H), 7.25 (d, J = 8.1 Hz, 2H), 7.58 (d, J = 8.0 Hz, 2H), 8.13 (s, 1H) and 11.20 (s, 1H) ppm; MS (ES+) 211.0 (M-Boc).

Step 9: tert-Butyl N-[[4-[chloro—N—hydroxy-carbonimidoyl]phenyl]-dideuterio-methyl]- N—methyl—carbamate D D tert—Butyl N~[dideuterio-[4-[hydroxyiminomethyl]phenyl]methyl]—N— (methyl)carbamate (178 mg, 0.6683 mmol) in DMF (2 mL) was treated with NCS (89.24 mg, 0.6683 mmol) and the reaction warmed to 65 °C for 1 hour. The on was cooled to ambient temperature and diluted with water. The mixture was extracted with EtOAc (x 2) and the combined organic extracts washed with brine (x 4), dried (MgSO4), filtered and concentrated in vacuo to give the sub-title compound as a white solid (188 mg, 94% Yield); 1H NMR (400 MHZ, DMSO) 8 1.42 (d, J = 24.7 Hz, 9H), 2.78 (s, 3H), 7.32 (d, J = 8.4 Hz, 2H), 7.78 (d, J = 8.2 Hz, 2H) and 12.36 (s, 1H) ppm.

Step 10: tert-Butyl N-[[4-[5—[3-[bis(tert-butoxycarbonyl)amin01—6-(4- isopropylsulfonylphenyl)pyrazin-2—yl]isoxazol—S-yl]phenyl]-dideuteri0-methyl]-N- -carbamate Oz< ‘6 (BOC)2NWW041 N\ ] Eth (36.31 mg, 50.01 uL, 0.3588 mmol) was added dropwise to a stirred solution of tert-butyl N-teit-butoxycarbonyl-N-[3 -ethyny1-5~(4- isopropylsulfonylphenyl)pyrazin—2—yl]carbamate (150 mg, 0.2990 mmol) and tert—Butyl N- [[4-[chloro—N-hydroxy-carbonimidoyl]phenyl]—dideuterio—methyl]~N~methyl-carbamate (89.93 mg, 0.2990 mmol) in ous THF (3 mL) and the reaction mixture heated at 65 °C for 3 hours. The reaction mixture was cooled to ambient temperature and diluted with EtOAc/brine. Water was added until the aqueous layer became clear and the layers were separated. The aqueous layer was extracted with EtOAc (x 1) and the combined organic ts were washed with brine (x 1), dried (MgSO4), filtered and concentrated in vacuo.

The e was purified by column chromatography (ISCO Companion, 40 g column, elueting with 0 to 30% EtOAc/Petroleum Ether, loaded in DCM) to give the sub-title product as a White solid (134 mg, 59% Yield); 1H NMR (400 MHZ, DMSO) 6 1.22 (d, J = 6.8 Hz, 6H) 1.32 (s, 18H), 1.43 (d, J = 23.1 Hz, 9H), 2.82 (s, 3H), 3.56 (pent, 1H), 7.43 (d, J = 8.3 Hz, 3H), 8.02 - 8.03 (m 3H), 8.06 — 8.11 (m, 2H), 8.62 — 8.67 (m, 2H) and 9.51 (s, 1H) ppm; MS (ES+) 666.2 (M-Boc).

Step 11: 3-[3-[4-[Dideuterio(methylamino)methyl]phenyl]isoxazol—S—ylj-S-(4- isopropylsulfonylphenyl)pyrazin—2-amine (compound II-l) II—l 3M HCl in MeOH (1.167 mL of 3 M, 3.500 mmol) was added to a stirred solution of tert-butyl N~[[4-[5—[3—[bis(tert—but0xycarbonyl)amino]—6-(4- isopropylsulfonylphenyl)pyrazin—2—y1]isoxazol~3-yl]phenyl]-dideuterio-methyl]—N—methyl— ate (134 mg, 0.1750 mmol) in DCM (5 mL) and the reaction heated at reflux for 16 hours. The reaction was cooled to ambient temperature and the resultant precipitate was isolated by filtration and dried under vacuum at 40 °C to give the di-HCl salt of the title compound as a yellow solid (58.8 mg, 62% Yield); 1H NMR (400 MHz, DMSO) 5 1.20 (d, J = 6.8 Hz, 6H), 2.60 (t, J = 5.4 Hz, 3H), 3.48 (hept, J = 6.8 Hz, 1H), 7.22 (br s, 2H), 7.69 — 7.75 (m, 2H), 7.85 (s, 1H), 7.92 - 7.99 (m, 2H), 8.08 — 8.15 (m, 2H) 8.37 - 8.42 (m, 2H), 8.97 (s, 1H) and 9.10 (d, J = 5.8 Hz, 2H) ppm; MS (ES+) 466.2.

D ‘N 0 0 D D \ \i/ I O\i/D \O Y K .

Alkylation O Oxime Formation qxume —_> Formation NH N O ———————> N 0 D o D D 701/ \i< a u 1)], W< viii xiii xiv A D 0 NH; 0" \ HN 6 D O=<N D \ D (BOC)2N o—N N \ 0 HOW \\ 3D I I D D NI \ D CI \1/D [3+2] cycloadditon /N Deprotection ——-—’ —————’- ”Y°j< O=S=O xv xvi “-2 Step 1: tert—Butyl euterio- [4-(dimethoxymethyl)phenyl] methyl] (trideuteriomethyl)carbamate ] LiHMDS (1M in THF) (1.181 mL of 1 M, 1.181 mmol) was added dropwise to a sittred solution of tert—butyl N—[dideuterio-[4—(dimethoxymethy1)phenyl]methyl]carbamate (300 mg, 1.059 mmol) in THF (5 mL) at ~78 °C. The solution was stirred at this temperature for 30 minutes then trideuterio(iodo)methane (198.0 mg, 84.98 uL, 1.366 mmol) was added dropwise and the mixture allowed to warm to ambient temperature over 21 hours. The reaction was again cooled to -78 °C and a further portion of LiHMDS (1M in THF) (635.4 pL of 1 M, 0.6354 mmol) was added. After 15 minutes more trideuterio(iodo)methane (76.75 mg, 32.94 pL, 0.5295 mmol) was added and the on allowed to warm to ambient temperature over 5 hours. The mixture was diluted with EtOAc and the organic layer washed with saturated aqueous NaHC03 (x 2), brine (x 1), dried (MgSO4) filtered and concentrated in vacuo. The residue was purified by column chromatography (ISCO Companion, 24 g column, eluting with 0 to 30% Petroleum Ether, loaded in DCM) to give the sub-title product as a colourless oil (213 mg, 67% Yield); 1H NMR (400 MHz, DMSO) 5 1.36 - 1.42 (m, 9H) 3.22 (s, 6H), 5.35 (s, 1H), 7.21 (d, J = 7.8 Hz, 2H) and 7.35 (d, J = 7.7 Hz, 2H) ppm.

PCT/U32012/058127 Step 2: utyl N—[dideuterio—[4-[hydroxyiminomethyl]phenyl]methyl]-N— uteriomethyl)carbamate D. D o 7< Hydroxylamine hydrochloride (53.95 mg, 0.7763 mmol) was added to a stirred solution of tert—butyl N—[dideuterio-[4-(dimethoxymethyl)phenyl]methyl]—N- (trideuteriomethyl)carbamate (212 mg, 0.7057 mmol) in THF (10 mL)/water (1.000 mL) and the reaction allowed to stir at ambient temperature for 22 hours. The on was partitioned between DCM and brine and the layers separated. The aqueous layer was extracted with DCM (x 2) and the combined organic extracts washed with brine (x 1), dried (MgSO4), filtered and concentrated in vacuo to give the sub—title nd as a white solid (190 mg, 100% Yield). ); 1H NMR (400 MHz, DMSO) 6 1.41 (d, J = 24.2 Hz, 9H) ), 7.25 (d, J = 8.1 Hz, 2H), 7.58 (d, J = 8.0 Hz, 2H), 8.13 (s, 1H) and 11.20 (s, 1H) ppm.

Step 3: tert-Butyl N-[[4-[chloro-N-hydroxy-carbonimidoyl]phenyl]-dideuterio-methyl]- N-(trideuteriomethyl)carbamate HO\N I D D a + N\n’OK D D tert—Butyl N—[dideuterio-[4-[hydroxyiminomethyl]phenyl]methyl]—N— (trideuteriomethy1)carbamate (190.0 mg, 0.7054 mmol) in DMF (2 mL) was treated with NCS (94.19 mg, 0.7054 mmol) and the reaction warmed to 65 °C for 1 hour. The reaction was cooled to ambient temperature and diluted with water. The mixture was ted with EtOAc (x 2) and the combined organic extracts washed with brine (x 4), dried (MgSO4), filtered and concentrated in vacuo to give the sub-title compound as a white solid (198 mg, 93% Yield); 1H NMR (400 MHZ, DMSO) 5 1.41 (d, J = 26.0 Hz, 9H), 7.32 (d, J = 8.3 Hz, 2H), 7.78 (d, J = 8.2 Hz, 2H) and 12.36 (s, 1H) ppm.

W0 2013f049726 PCT/U52012/058127 Step 4: tert-Butyl N—[ [4-[5-[3-[bis(tert-butoxycarbony1)amino](4- isopropylsulfonylphenyl)pyrazin—2-y1]isoxazol—S—yl]phenyl]-dideuterio—methyl]-N- (trideuteriomethyl)carbamate 0% D (Boc)2N O'N\ N40 \ D N \ D I D o=s=o EN (36.31 mg, 50.01 uL, 0.3588 mmol) was added dropwise to a stirred solution of tert-butyl N—tert—butoxycarbonyl-N-[3 —ethyny1-5—(4— isopropylsulfonylphenyl)pyrazin-2~y1]carbamate (150 mg, 0.2990 mmol) and tert—butyl N- [[4-[chloro-N—hydroxy—carbonimidoyl]phenyl]-dideuterio—methyl]—N- (trideuteriomethyl)carbamate (90.84 mg, 0.2990 mmol) in anhydrous THF (3 mL) and the reaction e heated at 65 °C for 3.5 hours. The reaction mixture was cooled to ambient temperature and diluted with EtOAc/brine. Water was added until the aqueous layer became clear and the layers were ted. The aqueous layer was extracted with EtOAc (x l) and the combined organic extracts were washed with brine (x 1), dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by column chromatography (ISCO Companion, 40 g column, ng with 0 to 35% EtOAc/Petroleum Ether, loaded in DCM) to give the sub—title product as a white solid (158 mg, 69% Yield); 1H NMR (400 MHz, DMSO) 8 1.22 (d, I = 6.8 Hz, 6H) ), 1.44 (d, J = 22.0 Hz, 9H), 3.56 (dt, J = 13.5, 6.7 Hz, 2H), 7.43 (d, J = 8.2 Hz, 3H), 8.02 (d, J = 6.9 Hz, 2H), 8.08 (d, J = 8.7 Hz, 2H), 8.65 (d, J = 8.8 Hz, 2H) and 9.51 (s, 1H) ppm; MS (ES+) 669.3 (M—Boc).

Step 5: 3—[3-[4-[dideuteri0-(trideuteriomethylamino)methyl]phenyl]isoxazol—S—yl]~5-(4- pylsulfonylphenyl)pyrazin—2-amine (compound 11-2) NH2 0"‘{ HN‘é o \ D N \ o i D o=s=o 11-2 3M HCl in MeOH (1.361 mL of 3 M, 4.084 mmol) was added to a d solution of utyl N-[[4—[5-[3—[bis(tert-butoxycarbonyl)amino]—6—(4- isopropylsulfonylphenyl)pyrazin—2—yl]isoxazol-3 ~yl]phenyl]-dideuterio-methyl]~N— (trideuteriomethyl)carbamate (157 mg, 0.2042 mmol) in DCM (5 mL) and the reaction heated at reflux for 16 hours. The reaction was cooled to ambient temperature and the resultant precipitate was isolated by filtration and dried under vacuum at 40 °C to give the di-HCl salt of the title compound as a yellow solid (72.5 mg, 66% Yield); 1H NMR (400 MHz, DMSO) 6 1.20 (d, J = 6.8 Hz, 6H), 3.48 (dq, J = 13.6, 6.7 Hz, 1H), 7.21 (s, 2H), 7.68 — 7.78 (m, 2H), 7.85 (s, 1H), 7.91 - 8.42 (m, 2H), 8.96 (s, 1H) and - 7.99 (m, 2H), 8.08 - 8.13 (m, 2H), 8.36 9.14 (s, 2H) ppm; MS (ES+) 469.1.

Exam 1e 4: S nthesis of 5- 4—iso r0 lsulfon l hen 1 3- 4- trideuteriometh lamino meth l hen lisoxazol-S- l razin-Z-amine iCompound 11-3) 0 o \OJKQ/NW 800 \o Reduction Protection midan/ Alkylaiion 0% D+\:/OOK xvii xviii xix m/\©\l:\1:;roD\‘/D HO‘N | D l D\T,D Oxidation NYOK Oxime Formation N 0 $333:ng o l< xx xxi xxii 3< D o ””2 0’N\ HN+D ECU»? D D (800>2N 0’” 0% \ n+0 NW, \ ’N “‘ D I . [3+2]cycloadditon / N ec’tion ————————> xxiii xxiv A II-3 O=S=O W0 2013f049726 PCT/U82012/058127 Step 1: Methyl 4-[(tert—butoxycarbonylamino)methyl]benzoate xviii Et3N (1.882 g, 2.592 mL, 18.60 mmol) was added to a stirred sion of methyl 4—(aminomethyl)benzoate (Hydrochloric Acid (1)) (1.5 g, 7.439 mmol) in THF (20 mL) at 0 °C. The reaction was allowed to stir at this te,perature for 30 minutes then B0020 (1.705 g, 1.795 mL, 7.811 mmol) was added in portions. The reaction was allowed to warm to ambient temperature and stirred for 18 hours. The e was diluted with EtOAc. The organic layer was washed with 1M aqueous HCl (x 2), saturated s NaHC03 (x 2) and brine (x 1). The organic layer was dried (MgSO4), filtered and concentrated in vacuo to give the sub-title compound as a white solid that was used without further purification (1.93 g, 98% Yield); 1H NMR (400 MHz, DMSO) 5 1.40 (s, 9H), 3.85 (s, 3H), 4.20 (d, J = 6.1 Hz, 2H), 7.38 (d, J = 8.2 Hz, 2H), 7.49 (t, l = 6.1 Hz, 1H) and 7.92 (d, J = 8.2 Hz, 2H) ppm; MS (ES+) 251.1 (M-Mc).

Step 2: Methyl 4-[[tert-butoxycarbonyl(trideuteriomethyl)amino]methyl]benzoate LiHMDS (1M in THF) (8.112 mL of 1 M, 8.112 mmol) was added dropwise to a stirred solution of methyl 4-[(tert—butoxycarbonylamino)methyl]benzoate (1.93 g, 7.275 mmol) in THF (10 mL) at —78 °C. The solution was stirred at this temperature for 30 minutes then trideuterio(iodo)methane (1.360 g, 9.385 mmol) was added dropwise and the mixture allowed to warm to t temperature over 3 hours. The reaction was cooled to —78 °C and a further portion of LiHMDS (1M in THF) (2.182 mL of 1 M, 2.182 mmol) was added. After minutes a further n of trideuterio(iodo)methane (527.4 mg, 3.638 mmol) was added and the reaction allowed to warm to ambient temperature over 17 hours. The mixture was diluted with EtOAc and the organic layer washed with ted aqueous NaHCO; (x 2), brine (x 1), dried (MgSO4) filtered and concentrated in vacuo. The residue was purified by PCT/USZ012/058127 column chromatography (ISCO Companion, 120 g column, eluting with 0 to 30% EtOAc/Petroleum Ether, loaded in DCM) to give the sub-title product as a pale yellow oil (1.37 g, 67% Yield); 1H NMR (400 MHz, DMSO) 5 1.38 (d, J = 44.2 Hz, 9H), 3.83 (s, 3H), 4.43 (s, 2H), 7.33 (d, J = 8.2 Hz, 2H) and 7.94 (d, J = 8.1 Hz, 2H) ppm; MS (ES+) 268.1 (M— Step 3: tert-Butyl N—[[4-(hydroxymethyl)phenyl]methyl]-N- (trideuteriomethy1)carbamate LiBH4 (158.5 mg, 7.278 mmol) was added to a stirred solution of methyl 4— [[tert-butoxycarbonyl(trideuteriomethy1)amino]methyl]benzoate (1.37 g, 4.852 mmol) in THF (10 mL) and the reaction warmed to 85 °C for 15 hours. A further portion of LiBH4 (158.5 mg, 7.278 mmol) was added and the reaction stirred at 65 °C for a r 7 hours. The reaction mixture was cooled to ambient temperature then poured onto crushed ice and whilst stirring, ]M HCl was added dropwise until no effervescence was observed. The mixture was stirred for 10 minutes then saturated s NaHCO3 was added until the mixture was at pH 8. The aqueous layer was ted with EtOAc (x 3) and the combined c extracts dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by column chromatography (lSCO Companion, 120 g column, elueting with 0 to 100% EtOAc/Petroleum Ether, loaded in DCM) to give the sub—title product as a colourless oil (1.03 g, 84% Yield); 1H NMR (400 MHz, DMSO) 5 1.42 (d, J = 14.6 Hz, 9H), 4.35 (s, 2H), 4.48 (d, J = 5.7 Hz, 2H), 5.15 (t, J = 5.7 Hz, 1H), 7.18 (d, J = 7.9 Hz, 2H) and 7.30 (d, J = 7.7 Hz, 2H) ppm; MS (ES+) 181.1 (M—O’Bu).

Step 4: tert-Butyl formylphenyl)methyl]-N-(trideuteriomethyl)carbamate KE:|\/| D D\|/D N\n/OK MnOz (5.281 g, 1.051 mL, 60.75 mmol) was added to a d solution of tert- butyl N-[[4—(hydroxymethyl)phenyl]methyl]~N-(trideuteriomethyl)carbamate (1.03 g, 4.050 mmol) in DCM (10 mL) and the reaction stirred at ambient temperature for 20 hours. The reaction was filtered through a pad of Celite and washed with DCM. The filtrate was concentrated in vacuo to give the sub-title nd as a colourless oil (891 mg, 88% Yield); 1H NMR (400 MHz, DMSO) 8 1.40 (d, J = 43.4 Hz, 9H), 4.48 (s, 2H), 7.43 (d, J = 8.0 Hz, 2H), 7.91 (d, J = 7.9 Hz, 2H) and 10.00 (s, 1H), ppm.

Step 5: tert—butyl N—[[4—[hydroxyiminomethyl]phenyl]methyl]-N- (trideuteriomethyl)carbamate xxii Hydroxylamine (466.0 uL of 50 %w/V, 7.054 mmol) was added to a stirred solution of tert-butyl N-[(4-formy1pheny1)methy1]-N—(trideuteriomethyl)carbamate (890 mg, 3.527 mmol) in ethanol (5 mL) and the on e stirred at t temperature for 45 minutes. The reaction mixture was concentrated in vacuo and the residue taken up in water and extracted with EtOAc (x 3). The combined organic extracts were washed with brine (x 1), dried (MgSO4), filtered and concentrated in vacuo. The residue was triturated from petroleum ether and the precipitate ed by filtration to give the sub-title product as a white solid (837 mg, 89% Yield); 1H NMR (400 MHz, DMSO) 5 1.41 (d, J = 25.8 Hz, 9H), 4.38 (s, 2H), 7.24 (d, J = 8.0 Hz, 2H), 7.58 (d, J = 8.0 Hz, 2H), 8.13 (s, 1H) and 11.20 (s, 1H) ppm; MS (138+) 212.0 (M-tBu).

Step 6: tert-Butyl N-[[4-[chloro-N—hydroxy—carbonimid0y1]phenyl]methyl]-N- (trideuteriomethyl)carbamatep xxiii tert—butyl N—[[4—[hydroxyiminomethy1]pheny1]methyl]~N— (trideuteriomethyl)carbamate (250 mg, 0.9351 mmol) in DMF (2.5 mL) was treated with NCS (124.9 mg, 0.9351 mmol) and the reaction warmed to 65 °C for 1 hour. The reaction was cooled to ambient temperature and diluted with water. The e was extracted with WO 49726 EtOAc (x 2) and the combined organic ts washed with brine (x 4), dried (MgSO4), filtered and concentrated in vacuo to give the sub—title nd as a white solid (259 mg, 92% Yield); 1H NMR (400 MHz, DMSO) 5 1.41 (d, J = 29.6 Hz, 9H), 4.42 (s, 2H), 7.31 (d, J = 8.3 Hz, 2H), 7.78 (d, J = 8.0 Hz, 2H), and12.38 (s, 1H), ppm.

Step 7: tert-Butyl N—[[4-[5—[3-[bis(tert—but0xycarbonyl)amino](4- isopropylsulfonylphenyl)pyrazin-Z-yllisoxazolyl]phenyl] methyl]-N- (trideuteriomethyl)carbamate , O=< (800w O N\ N+D N \ D xxiv [001831 Eth (48.41 mg, 66.68 uL, 0.4784 mmol) was added dropwise to a stirred solution of tert-butyl N—tert-butoxycarbonyl-N-[3-ethynyl-5~(4- isopropy1sulfonylphenyl)pyrazin—2—yl]carbamate (200 mg, 0.3987 mmol) and tert—butyl N— [[4—[chloro-N-hydroxy—carbonimidoyl]phenyl]methyl]~N-(trideuteriomethyl)carbamate (120.3 mg, 0.3987 mmol) in anhydrous THF (5 mL) and the reaction mixture heated at 65 °C for 2.5 hours. The reaction mixture was cooled to ambient temperature and diluted with EtOAc/brine. Water was added until the s layer became clear and the layers were separated. The aqueous layer was extracted with EtOAc (x 1) and the combined organic extracts were washed with brine (x 1), dried (MgSO4), filtered and trated in vacuo.

The residue was purified by column chromatography (ISCO Companion, 40 g column, elueting with 0 to 20% EtOAc/Petroleum Ether, loaded in DCM) to give the sub—title product as a white solid (213.5 mg, 70% Yield); 1H NMR (400 MHz, DMSO) 8 1.22 (d, J = 6.8 Hz, 6H), 1.31 (s, 18H), 1.43 (d, J = 26.2 Hz, 9H), 3.51 = - 3.60 (m, 1H), 4.47 (s, 2H), 7.42 (d, J 8.1 Hz, 2H), 8.03 (d, J = 5.2 Hz, 3H), 8.08 (d, J = 8.6 Hz, 2H), 8.65 (d, J = 8.6 Hz, 2H) and 9.52 (s, 1H) ppm; MS (138+) 667.4 (M-Boc).

Step 8: 5-(4-Isopropylsulfonylphenyl)-3—[3—[4-[(trideuteriomethylamino)methyl] phenyl]isoxazol-S-yl]pyrazin-Z-amine (Compound 11-3) PCT/U32012/058127 NH2 0"‘{ HN {D N \ D o=s=o 11-3 3M HCl in MeOH (1.5 mL of 3 M, 4.500 mmol) was added to a stirred solution of tert—butyl N—[[4-[5—[3—[bis(tert-butoxycarbonyl)amino](4— isopropylsulfonylphenyl)pyrazin—2-y1]isoxazol—3—yl]phenyl]methyl]~N- (trideuteriomethyl)carbamate (213 mg, 0.2777 mmol) in DCM (6 mL) and the reaction heated at reflux for 15 hours. A further portion of 3M HCl in M6011 (0.5 mL of 3 M, 1.500 mmol) was added and the reaction heated at reflux for a further 7 hours. The reaction was cooled to ambient temperature and the ant precipitate was isolated by ion and dried under vacuum at 40 °C to give the di-HCl salt of the title compound as a yellow solid (97.6 mg, 65% Yield); 1H NMR (400 MHz, DMSO) 5 1.20 (d, J = 6.8 Hz, 6H), 3.47 (tt, J = 14.0, 6.9 Hz, 1H), 4.19 — 4.25 (m, 2H), 7.23 (s, 2H), 7.72 (d, J = 8.4 Hz, 2H), 7.85 (s, 1H), 7.95 (d, J = 8.7 Hz, 2H), 8.11 (d, J = 8.4 Hz, 2H), 8.39 (d, J = 8.7 Hz, 2H), 8.97 (s, 1H) and 9.11 (s, 2H) ppm; MS (ES+) 467.2.

PCT/U82012/058127 tetradeuterio-l- trideuteriometh leth lsulfon l hen l Z-amine Com ound 11-41 /\O \/n S_g__>fection 4m? Oxime Formation Amination /O —--—---—> xxvil Chlorooxime (BOC)2N . 0‘N\ N~ Formation 0T0 [3+2] cycloaddlton \ —-————> N \ xxviii xxix Br xxx Br a: Br w O~ ,O Bornate Alkylation 8 ion Suzuki SH ——> ion ——> Dbz/*w<”fl 0W: D D o=s=o D D o o D D D n n xxxi xxxii xxxiii xxxiv O NH2 o—N\ HN‘ (80an 0'N\ =<N~ N \ \ /N Deprotection DC):S=O O=S=O xxxv o o n o 0 XXV] 2M methylamine in MeOH (288.1 mL, 576.2 mmol) was diluted with methanol (1.000 L) and stirred at ~20 °C. 4-(Dieth0xymethy1)benzaldehyde (100 g, 480.2 mmol) was added dropwise over 1 minute and the reaction stirred at ambient temperature for 1.25 hours.

Sodium borohydride (29.07 g, 30.76 mL, 768.3 mmol) was added portionwise over 20 minutes while maintaining the temperature between 20 and 30 °C with an ice-water bath. The reaction solution was stirred at ambient temperature overnight then quenched by the dropwise addition ofNaOH (960.4 mL of 1.0 M, 960.4 mmol) over 20 minutes. The reaction was W0 2013/049726 stirred for 30 minutes and concentrated in vacuo to remove MeOH. The reaction was partitioned with MTBE (1.200 L) and the phases separated. The c phase was washed with water (3000 mL), dried (N212804), and concentrated in vacuo to give the title compound as a yellow oil (102.9 g, 96% Yield); 1H NMR (400 MHZ, CDC13) 6 1.25 (t, 6H), 2.46 (s, 3H), 3.45 ~ 3.65 (m, 4H), 3.75 (s, 2H), 5.51 (s, 1H), 7.32 (d, 2H) and 7.44 (d, 2H) ppm.

Step 2: tert-Buty] N-[[4—(diethoxymethyl)pheny1]methyl]-N-methyl-carbamate LO d/ “co"N\ xxvu A l-L glass-jacketed reactor was fitted with an overhead stirrer, thermocouple, and chiller. A solution of l-[4-(diethoxymethyl)phenyl]-N—methyl-methanamine (80.0 g, 358.2 mmol) in DCM (480.0 mL) was stirred at 18 °C. A solution of B00 anhydride (79.75 g, 83.95 mL, 365.4 mmol) in DCM (160.0 mL) was added over 10 minutes and the on was stirred at 20 ~ 25 °C overnight. The reaction e was filtered, rinsed with DCM (3 x 50 mL) and the filtrate concentrated in vacuo to afford give the title compound as a pale yellow liquid (116.6 g, quantitative ; 1H NMR (400 MHz, CDCl3) 5 1.25 (t, 6H), 1.49 — 1.54 (2 x s, 9H), 2.78 — 2.83 (2 x s, 3H), 3.50 4 3.66 (m, 4H), 4.42 (s, 2H), 5.49 (s, 1H), 7.22 (d, 2H) and 7.45 (d, 2H) ppm.

Step 3: tert-Butyl N—[[4-[hydroxyiminomethyl]phenyl]methyl]-N-methyl-carbamate xxviii A biphasic on of tert-butyl N—[[4-(diethoxymethyl)phenyl]methyl]-1V— methyl-carbamate (50.0 g, 154.6 mmol) in F (400.0 mL) and Na2S04 (100.0 mL of %w/v, 70.40 mmol) was stirred at 8 — 10 °C in a l—L, glass—jacketed reactor.

Hydroxylamine hydrochloride (46.38 mL of 5.0 M, 231.9 mmol) was added and the biphasic solution was stirred at 30 °C for 16 hours. The reaction was diluted with MTBE (200.0 mL) and the layers separated. The organic phase was washed with water (200.0 mL), dried (Na2S04), filtered and concentrated in vacuo. The residue was diluted with heptane (200.0 PCT/U82012/058127 mL) and the ant suspension was stirred at ambient ature for 30 minutes. The solid was collected by filtration to give the title compound as a white solid (36.5 g, 89% Yield); 1H NMR (400 MHz, CDC13) 5 1.50 (s, 9H), 2.88 (br s, 3H), 4.60 (s, 2H), 7.26 (d, 2H), 7.52 (d, 2H) and 8.15 (s, 1H) ppm.

Step 4: tert—Butyl N-I[4-[chloro-N-hydroxy-carbonimidoyl]phenyl]methyl]-N-methyl— carbamate A suspension of tert~butyl [hydroxyiminomethyl]phenyl]methyl]-N— methyl—carbamate (100 g, 378.3 mmol) in isopropyl acetate (1.000 L) was stirred at ambient temperature. N-Chlorosuccinimide (53.04 g, 397.2 mmol) was added and stirred at ambient temperature for 16 hours. The reaction was partitioned with water (500.0 mL) and the phases separated. The organic phase was washed with water (500.0 mL) (2 x), dried (Na2804), filtered and concentrated in vacuo to remove most of the solvent. Heptane (1.000 L) was added and the mixture concentrated in vacuo to remove most of the solvent. Heptane (1.000 L) was added and the resultant precipitate isolated by filtration. The filter-cake was washed with heptanc (500 mL) and ied to give the title compound as an off—white powder (105.45 g, 93% Yield); 1H NMR (400 MHz, CDC13) 8 1.48 (2 x s, 9H), 2.90 (2 x s, 3H), 4.47 (s, 2H), 7.26 (d, 2H), 7.77 (d, 2H) and 8.82 (s, 1H) ppm.

Step 5: tert-Butyl N—[[4-[5-[3-[bis(tert-butoxycarbonyl)amino]bromo-pyrazin—2- yllisoxazol—3-yl]phenyl] methyl]—N-methyl-carbamate (BOC)2N 0’11 N\ A suspension of tert-butyl [chloro-N-hydroxy- carbonimidoyl]phenyl]methyl]-N-methyl-carbamate (100.0 g, 334.7 mmol) and tert—butyl N- tert—butoxycarbonyl-N—[3—ethynyl—5—(4—isopropylsulfonylphenyl)pyrazin—2—yl]carbamate W0 2013f049726 PCT/USZ012/058127 (121.2 g, 304.3 mmol) in DCM (1.212 L) was stirred at ambient temperature. Triethylamine (33.87 g, 46.65 mL, 334.7 mmol) was added in one portion and the reaction stirred at ambient temperature for 16 hours. The reaction was partitioned with water (606.0 mL) and the phases ted. The organic phase was washed with water (606.0 mL), dried (NaZSO4), filtered and concentrated in vacuo to near dryness. Heptane (3 63.6 mL) was added and the mixture concentrated to about 300 mL, Further heptane (1.212 L) was added and the mixture heated to 90 °C with stirring. The mixture was slowly cooled to ambient ature and stirred at this temperature for 1 hour. The resultant precipitate was isolated by filtration and the filter— cake washed with e (2 x 363.6 mL) and air-dried to give the title nd as a beige solid (181.8 g, 90% Yield); 1H NMR (400 MHz, CDCl3) 6 1.41 (s, 18H), 1.51 (s, 9H), 2.88 (2 x s, 3H), 4.50 (s, 2H), 7.36 — 7.38 (m, 3H), 7.86 (d, 2H) and 8.65 (s, 1H) ppm.

Step 6: l-Bromo[1,2,2,2-tetradeuterio(trideutcri0methyl)ethyl]sulfanyl-benzene xxxii Sodium hydride (246.5 mg, 6.163 mmol) was added pofiionwise to a stirred solution of 4—br0mobenzenethiol (compound xxxi) (970.9 mg, 5.135 mmol) in DMF (10 mL) at 0 °C. After stirring at this temperature for 15 minutes 1,1 l ,2,3,3,3 -heptadeutetio-2—iodo— e (l g, 5.649 mmol) was added and the reaction allowed to warm to ambient temperature over 18 hours. The reaction was quenched by the addition of water and the mixture stirred for 10 minutes. The mixture was extracted with diethyl ether (x 3) and the combined organic extracts washed with water (x 2), brine (x 2), dried (MgSO4), filtered and trated in vacuo to give the sub—title compound that was used directly without further ation assuming 100% Yield and purity; 1H NMR (500 MHz, DMSO) 5 7.25 — 7.37 (m, 2H) and 7.48 — 7.55 (m, 2H) ppm.

WO 49726 Step 7: 1-Bromo[1,2,2,2-tetradeuterio(trideuteriomethyl)ethyl]sulfonyl—benzene xxxiii mCPBA (2.875 g, 12.83 mmol) was added in portions to a stirred solution of 1— bromo—4—[1,2,2,2—tetradeuterio—1-(trideuteriomethyl)ethyl]sulfanyl—benzene (1.223 g, 5.134 mmol) in DCM (20 mL) at 0 °C and the reaction allowed to warm to ambient temperature over 17 hours. The mixture was washed 1M aqueous NaOH (X 2), saturated aqueous Na28203 (x 3), brine (x 1), dried (MgSO4), d and trated in vacuo. The residue was purified by column chromatography (ISCO Companion, 80 g column, eluting with 0 to 40% EtOAc/Petroleum Ether, loaded in DCM) to give the sub—title compound as a colourless oil (1.19 g, 86% Yield); 1H NMR (500 MHz, DMSO) 8 7.77 - 7.81 (m, 2H) and 7.88 - 7.92 (m, 2H) ppm.

Step 8: 4,4,5,5-Tetramethyl—2-[4-[l,2,2,2-tetradeuterio(trideuteriomethyl)ethyl] sulfonylphenyl]-1,3,2-dioxaborolane xxxiv Pd(dppf)Clz.DCM (179.8 mg, 0.2202 mmol) was added to a stiired suspension of 1—bremo—4-[1,2,2,2—tetradeuterio-l~(trideuteriomethyl)ethyl]sulfonyl—benzene (1.19 g, 4.404 mmol), bis(dipinaeolato)diboron (1.342 g, 5.285 mmol) and KOAc (1.296 g, 13.21 mmol) in dioxane (10 mL). The reaction placed under an atmosphere of nitrogen via 5 x nitrogen/vacuum cycles and the e was heated at 80 °C for 4.5 hours. The reaction was cooled to ambient temperature and the solvent removed in vacuo. The e was partitioned between EtZO and water and the layers separated. The organic layer was dried (MgSO4), PCT/U52012/058127 filtered and concentrated in vacuo. The residue was ved in 30% EtOAc/Petroleum ether (35 mL) and 1.2 g of Florosil was added. The mixture was stirred for 30 minutes then filtered, washing the solids with further alliquots of 30% EtOAc/Petrol (x 3). The filtrate was concentrated in vacuo and tritruated from 10% EtOAc/petroleum ether. The resultant solid was isolated by filtration, washed with petroleum ether and dried in vacuo to give the sub— title nd as an off—white solid (1052.1 mg, 75% Yield); 1H NMR (400 MHz, DMSO) 8 1.33 (s, 12H), 7.87 (d, J = 8.4 Hz, 2H) and 7.94 (d, J = 8.4 Hz, 2H) ppm.

Step 9: tert—Butyl N—[[4-[5-[3-[bis(tert—but0xycarbonyl)amino]-6—[4—[1,2,2,2— tetradeuterio-l-(trideuteriomethyl)ethyl]sulfonylphenyl]pyrazin-Z-yl]isoxazol yllphenyl]methyl]-N—methyl—carbamate (BOC>2N O’N N\ xxxv ] [1, 1’-Bis(di-tert-butylphosphino)ferrocene]dichloropalladium(H) (106.8 mg, 0.1639 mmol) was added to a mixture of 4,4,5,5—tetramethy1—2—[4-[1,2,2,2—tetradeuterio—1— (trideuteriomethyl)ethyl]sulfonylphenyl}l,3,2-dioxaborolane (1.3 g, 4.098 mmol), tert—butyl N-[[4—[5—[3-[bis(teit-butoxycarbonyl)amino]bromo—pyrazinyl]isoxazol—3- yl]pheny1]methyl]—N—methyl~carbamate (2.707 g, 4.098 mmol) and K2CO3 (1.133 g, 8.200 mmol) in toluene (9.100 mL), EtOH (2.600 mL) and water (2.600 mL) and the reaction mixture was degassed with a flow of nitrogen (5 cycles).

The e was heated at 75 °C for 1.5 hours. The reaction was ccoled to ambient temperature and water (5.2 mL) was added. After stirring the layers were separated and the organic layer dried (Na2304), filtered, and concentrated in vacuo. The residue was triturated with IPA and the resultant precipitate isolated by filtration, washed with IPA (3 x 4 mL) and dried in vacuo at 50 °C to give the title compound as a white solid (2.4 g, 76% Yield); 1H NMR (400 MHz, CDC13) 6 1.41 (s, 18H), 1.50 (s, 9H), 2.85 — 2.89 (m, 3H), 4.50 (s, 2H), 7.36 ~ 7.38 (m, 3H), 7.87 (d, 2H), 8.09 (d, 2H), 8.35 (d, 2H) and 9.06 (s, 1H) ppm. 2012/058127 Step 10: 3-[3—[4-(Methylaminomethy1)phenyl]isoxazol—S-yl][4—[1,2,2,2-tetradeuterio- 1{trideuteriomethyDethyl]sulfonylphenyl]pyrazin—Z-amine (compound 11-4) NH2 O'N\ HN‘ II-4 Concentrated HCl (3.375 g, 2.812 mL of 37 %w/w, 34.25 mmol) was added to a solution of utyl N—[[4~[5—[3-[bis(tert~butoxycarbonyl)amino]-6—[4~[l,2,2,2-tetradeuterio(trideuteriomethyl)ethy1]sulfonylphenyl]pyrazin—2—yl]isoxazol—3—yl]phenyl]methy1]-N— methyl-carbamate (2.2 g, 2.854 mmol) in acetone (28.60 mL) and the reaction heated at reflux for 7 hours. The reaction was cooled to ambient temperature and the resultant precipitate isolated by filtration, washed with acetone (2 x 4.5 mL) and dried in vacuo at 50 °C to give the di-l-lCl salt of the title compound as a yellow solid ( 1.42 g, 92% Yield); 1H NMR (400 MHz, DMSO) 5 2.58 (t, 3H), 4.21 (t, 2H), 5.67 (br s, 2H), 7.74 (d, 2H), 7.85 (s, 1H), 7.94 (d, 2H), 8.10 (d, 2H), 8.38 (d, 2H), 8.96 (s, 1H) and 9.33 (br s, 2H) ppm; MS (ES+) 471.8.

PCT/U52012/058127 Exam 1e 6: S nthesis of 5- 4— tert-bu lsulfon l hen l 3- 4- meth lamino meth l hen lisoxazol-S- l razin-Z-amine Com ound 1-2 HO‘N Step 1 HO‘N Step 2 l I 300 N08, IPAc TEA. DCM __._____..__, | \ c|)\©\/BocN\ N(BOC)2 4-i 4-ii N,v\ 8%N 4-iii Step 3 800‘ [Boo 800 N O Boo [Boo B(OH)2 \ \N \ W0"! \N\ .'POr 23 N] \ 8%“l ——-—~—————-——-—> 4-iv 1. cat. Pd(dtbpf)ClZ, PhCHB, 5-i Br aq. K2C03 2. IPA crystallization SOQiPI’ NH2 0% HN‘ NH2 4 O’r‘i HN‘ Step \ Step5 \ \ N \ conc.HCl N! I acetone / N 4:1 IPA/water -2HC| / N 'HCI SOZiPr SOQIPF Compound I2HC1 Compound I Step 1: Preparation of Compound 4-ii Hot Step 1 HO\ I I 53°C NCS, IPAc ————-—-——-> N\ cg/K©\/I§ocN\ 4-i 4-ii A suspension of tert—butyl 4~((hydroxyimino)methy1)benzyl (methyl)carbamate (Compound 4-i) (650 g, 2.46 mol) in isopropyl acetate (6.5 L) is stirred at ambient ature. rosuccinimide (361 g, 2.71 mol) is added and the reaction temperature maintained overnight at 20—28 °C to ensure te reaction. The reaction mixture is diluted with water (3.25 L) and EtOAc (1.3 L) and the phases are separated. The organic phase is washed with water (2 x 3.25 L), dried (Na2SO4), and concentrated to a wet-cake. The concentrate is diluted with heptane (9.1 L), ~2 L of solvent removed, and then stirred at ambient temperature for 2—20 h. The solid is collected by filtration. The filter-cake is washed with heptane (2 x 975 mL) and dried to afford Compound 4-ii (692 g; 94% yield, 99.2 area % purity by HPLC) as a colorless powder.

Ste 2: Pre aration of tart—but 1 5—bromo 3— 4- tert—butox carbon 1 meth lamino meth 1 hen lisoxazol—S- 1 razin-Z— l tert—butox carbon lcarbamate Com ound 4—iv HO‘N EtaN,DCM B0C\N,Boc N Boc\ ..______, ..

' O\\ N‘ N(Boc)2 Cl 800 // N \ 111\ N \ l l /N 4'"-- Br 4-m 4-Iv_ A suspension of rerr-butyl N—(S-bromo-3 «ethynylpyrazin-Z~yl)~N-tert— hutoxycarbonylcarbamate (Compound 4-iii)(1.59 kg, 3.99 mol) and tert—butyl 4- (chloro(hydroxyimino)methyl)benzyl(tetrahydro-2H—pyran—4—y1)carbamate (1.31 kg, 4.39 mol; 1.10 equiv.) in CH2C12 (12.7 L) is stirred at ambient ature. Triethylamine (444 g, 611 mL, 4.39 mol) is added to the suspension and the reaction ature is maintained between 20—30 °C for 20—48 h to ensure complete reaction. The reaction mixture is d with water (8 L) and thoroughly mixed, then the phases are separated. The organic phase is washed with water (8 L), dried (NaZSO4), and then trated until about 1 L of CH2C12 s. The trate is diluted with heptane (3.2 L) and re-concentrated at 40 °C/200 torr until no distillate is observed. The concentrate is d and further diluted with heptane (12.7 L) to precipitate a solid. The suspension is d overnight. The solid is collected by filtration, washed with heptane (2 x 3 L) then dried to afford Compound 4-iv (2.42 kg; 92% yield, 100 area % purity by HPLC) as a light tan powder. 1H NMR (400 MHz, CDC13) 5 8.61 (s, 1H), 7.82 (d, J= 8.2 Hz, 2H), 7.31 (m, 3H), 4.46 (br s, 2H), 2.84 (br d, 3H), 1.57 (s, 2H), 1.44 (br s, 9H), 1.36 (s, 18H).

PCT/U52012/058127 Ste 3: Pre aration of Com ound 5-i Boos ,Boc N B 8(0le o—N\ °°‘N\ Boo Boo \ / Bog N OvN \ \ \ N~ iPrOZS NI \ \ /N | "_““““‘——’ 1. cat. Pd(dtbpf)012, PhCHg, 5" 4 , IN Br 3‘1 choa 2. i—PrOH crystallization SOzlPr ] A mixture of tert-butyl (5-bromo—3—(3 (tert— butoxycarbonyl)(methyl)amino)methyl)phenyl)isoxazol—S—yl)pyrazin-2~yl)(tert~ butoxycarbony1)carbamate (Compound 4-iv )( 1.00 kg, 1.51 mol), K2CO3 (419 g, 3.02 mol), and (4—(isopropylsulfonyl)pheny1)boronic acid (345 g, 1.51 mol) in toluene (7.0 L) and water (2.0 L) was stirred and degassed with N2 for 30 min. 1,1’—bis(di—t-butylphosphino)ferrocen- dichloro-palladium(ll) [Pd(dtbpf)C12; 19.7 g, 30.3 mmol] was then added and degassed an additional 20 min. The reaction mixture was warmed at 70 °C for at least 1 h to ensure complete reaction. The reaction mixture was cooled to ambient temperature then filtered through Celite. The reaction vessel and filter pad are rinsed with toluene (2 x 700 mL). The filtrates are combined and the phases are separated. The organic phase is stirred with Biotage MP—TMT resin (170 g) for 4—20 h. The resin is d by filtration through Celite and the filter pad is washed with toluene (2 x 700 mL). The filtrate and washings are combined and trated to near s then diluted with i—PrOH (5.75 L) and re—concentrated. The concentrate is again dissolved in warm (45 °C) i~PrOH (5.75 L) and then cooled to ambient temperature with stirring to induce crystallization then stirred for around 16 — 20 h. The solid is collected by filtration, washed with i—PrOH (2 x 1 L), and dried to afford VRT—1018729 (967 g; 84%) as a beige powder. 1H NMR (400 MHz, CDC13) 6 9.04 (s, 1H), 8.33 (d, J = 8.6 Hz, 2H), 8.06 (d, J = 8.5 Hz, 2H), 7.85 (d, J = 8.1 Hz, 2H), 7.34 (m, 3H), 4.47 (br s, 2H), 3.25 (hept, J= 7.0 Hz, 1H), 2.85 (br d, 3H), 1.47 (s, 9H), 1.38 (s, 18H), 1.33 (d, J= 6.9 Hz, 6H).

Step 4: Preparation of Compound 1-2 ' 2HCl A solution of Compound S-i (950 g, 1.24 mol) in acetone (12.35 L) is warmed to 40 °C then concentrated HCl (1.23 kg, 1.02 L of 37 %w/w, 12.4 mol) is added at a rate to maintain the reaction temperature between 40 - 45 °C for at least 5 h to ensure complete reaction. The sion is cooled to below 30 °C and the solid ted by filtration. The filter—cake is washed with acetone (2 x 950.0 mL) then dried to afford Compound I—2 ' 2HC1 (578 g; 87% yield, 99.5 area % purity by HPLC) as a yellow powder. 1H NMR (400 MHz, DMSO) 6 9.53 (br d, J= 4.8 Hz, 2H), 8.93 (s, 1H), 8.37 (d, J= 8.5 Hz, 2H), 8.07 (d, J= 8.3 Hz, 2H), 7.92 (d, J = 8.6 Hz, 2H), 7.84 (s, 1H), 7.75 (d, J = 8.3 Hz, 2H), 4.23 — 4.15 (m, 2H), 3.43 (hept, J= 6.8 Hz, 1H), 2.55 (t, J= 5.3 Hz, 3H), 1.17 (d, J= 6.8 Hz, 6H).

Ste 5: Pre aration of Com ound I-2 - HCI from Corn ound 1-2 - 2HC1 NH2 O‘N\ HN‘ NH2 O’N\ HN\ \ \ N \ N \ I . | / N 4.1 I-PrOH/water / N -HCl -2HCI SOZiPI' SOQiPr Compound l-2 0 2HC| Compound l-2 - HCI t process A stirred suspension of Compound I-2 ' 2HC1 (874 g, 1.63 mol) in i-PrOH (3.50 L) and water (0.87 L) is warmed at 50 °C for 1—2 h, cooled to ambient ature, and stirred for 1-20 h. XRPD is performed on a small sample to ensure that Compound 1—2 ° 2HC1 has been converted to another form. The sion is cooled to 5 °C and stirred for 1 h. The solid is collected by ion then the filter-cake is washed with 80/20 i-PrOH/water (2 x 874 mL), and briefly dried.

IfXRPD shows the Compound 1—2 - HCI/anhydrate form, the solid is dried to afford Compound 1—2 °HCl/anhydrate (836 g, 99% yield, 99.2 area % purity by HPLC) as a yellow solid. 1H NMR (400 MHZ, DMSO) 5 9.38 (s, 2H), 8.96 (s, 1H), 8.46 ~ 8.34 (m, 2H), 8.10 (d, J= 8.3 Hz, 2H), 7.94 (d, J= 8.6 Hz, 2H), 7.85 (s, 1H), 7.75 (d, J= 8.3 Hz, 2H), 7.23 (br s, 2H), 4.21 (3, 21-1), 3.47 (hept, J = 6.7 Hz. 11-1), 2.58 (s, 3H), 1.19 (d, J= 6.8 Hz, 6H).

IfXRPD shows the Compound 1-2 -HCl/hydrate form the solid is stirred in fresh i-PrOH (3.50 L) and water (0.87 L) at 50 °C for at least 2 h until XRPD shows complete conversion to Compound 1—2 'HCI/anhydrate. The suspension is then cooled to 5 °C and stirred for 1 h. The solid is collected by filtration then the filter-cake is washed with 80/20 i- ater (2 x 874 mL) then dried to afford Compound 1HC1/anhydrate.

Alternative procedure (single pot) used Compound 1-2 0 2HC1 (392 g) is charged to the reactor. 4:] ter (8 L) is charged to a reactor and stirred at ambient temperature overnight. XRPD is used to confirm the conversion to the mono-HCI salt mono—hydrate form. The mixture is heated to 50 °C.

Seeds of Compound 1-2 ' hydrate (16 g) are added and the mixture heated at 50 °C until XRPD confirms complete conversion to the desired anhydrate form. The mixture is to cooled to ambient, filtered and the solid washed with 4:1 IPA/water (2 x 800 mL) then dried to afford Compound 1—2 - HCI/anhydrate (343 g, 94% yield).

Ste 4: Alternate Method 1: Pre aration of Com ound I-2 free base fl;W 1. TFA N/Me DCM HNrMe 25 c'C - 2 NaOH 0~N tPrOZS EtOH/water iPrOZS Compound 1-2 (free base) A solution of Compound 5-i (100 g, 131 mmol) in DCM (200 mL) was stirred at ambient temperature then TFA (299 g, 202 mL, 2.62 mol) was added. After 2 h on solution was cooled to 5 °C. The reaction mixture was diluted with EtOH (1.00 L) over about min ing in a bright yellow suspension. The suspension was cooled to 10 °C then NaOH (1.64 L of 2.0 M, 3.28 mol) was added over 30 min then stirred at t temperature overnight. The solid was collected by filtration then washed with water (2 x 400 mL), EtOH (2 x 200 mL) then dried to afford Compound 1—2 free—base (57.0 g, 94% yield, 99.7 area % purity by HPLC) as a fine, yellow powder. 1H NMR (400 MHz, DMSO) 5 8.95 (s, 1H), 8.39 (d, J= 8.5 Hz, 2H), 7.95 (dd, J: 11.6, 8.4 Hz, 4H), 7.78 (s, 1H), 7.51 (d, J= 8.2 112,211), 7.21 (br s, 2H), 3.72 (s, 2H), 3.47 (hept, J= 6.8 Hz, 1H), 2.29 (s, 3H), 1.19 (d, J= 6.8 Hz, 6H).

Ste 4: Alternate Method 2: Pre aration of Com ound 1-2 - HCI N NHZ / 'HCI ’Me [M N / Acetone OxN iPrOZS 1P1’028 Compound I-2 Compound I-2 HCI W0 2013I049726 2012/058127 A suspension of nd I—2 free base (10.0 g, 21.6 mmol) in acetone (80 mL) was stirred and heated to 35 °C. An aqueous solution of HCl (11.9 mL of 2.0 M, 23.8 mmol) diluted with water (8.0 mL) was added and the mixture heated at 50 °C for 4 h. The suspension was allowed to cool to ambient temperature then stirred overnight. The solid was ted by filtration. The filter—cake was washed with acetone (2 x 20 mL) then dried to afford 10.2 g Compound 1-2 hydrochloride (95% yield) as a yellow . [002051 Exam 1e 7: S nthesis of 5- 4- Iso ro lsulfon l hen l 3- 4- tetrah dro ran~4- lamina meth 1 hen l isoxazol—S- l razin—Z-amine Com ound Scheme: Exam le S nthesis of Com ound 1-3 B(OH)2 oC>——NBoc OC>7N,Boc N(Boc)} /N SOQi-Pr A—5-i A4 " NCS, i-PrOAc Br *—'~’ _.__..__> , 1. cat Pd(dtbpf)C|2, ,N~ 20 — 30 °c ,N— TEA, DCM PhCHg, aq. K2003 HO HO Cl 20 - 30 °C 2. EtOH crystallization 3. MP-TMT resin A-4 Ai A.5 1. TFA NHZ I \N DCM , - 25 °C __.. N, \ 2. NaOH EtOH/water SOzi—Pr 502“Pr A-6 L3 2012/058127 EtN(i—Pr)2, NaBH4 ———-———> ti?) MeOH NH2'HCI 20 - 25 °C A solution of tetrahydro-2H—pyran-4—amine hloride (1.13 kg, 8.21 mol) in MeOH (14.3 L) is stirred at about 20 °C. then Et3N (1.06 kg, 1.43 L, 8.21 mol) is added.

The mixture is d for at least 5 min then terephthalaldehyde diethyl acetal (1.43 kg, 6.84 mol) is added while maintaining the reaction temperature between 20—25 °C. The mixture is stirred for at least 45 min to form the imine. NaBH4 caplets (414 g, 11.0 mol) are added while maintaining the reaction temperature below about 25 °C. The mixture is stirred for 1 h after the addition is completed. The reaction e is quenched by adding 1 M NaOH (13.7 L) then extracted with MTBE. The organic solution was washed with brine (7.13 L) then dried (Na2SO4) and concentrated to afford Compound A—2 (2197 g; 109% yield, 94.4 area % purity by HPLC) as a hazy oil. 1H NMR (400 MHz, CDC13) 8 7.43 (d, J= 8.1 Hz, 2H), 7.31 (d, J= 8.1 Hz, 2H), 5.49 (s, 1H), 4.66 (br s, 1H), 4.03 — 3.91 (m, 2H), 3.82 (s, 2H), 3.69 — 3.47 (m, 4H), 3.38 (td, J= 11.6, 2.1 Hz, 2H), 2.78 — 2.65 (m, 1H), 1.90— 1.81 (m, 2H), 1.53 — 1.37 (m, 2H), 1.23 (t, J = 7.1 Hz, 6H).

Ste 2: Pre aration of tert-but l4- diethox meth lben ltetrah dro-ZH- ran-4— yllcarbamate gA-32 O Boc 0, Et N NH DCM — 25 °C tMQOC A mixture of N—(4-(diethoxymethyl)benzyl)tetrahydro-ZH—pyran-4—amine (A-2) (2195 g, 7.48 mol) in CH2C12 (22.0 L) is stirred at 25 °C then di—t-butyl onate (1.71 kg, 7.86 mol) is added. RN (795 g, 1.10 L) is then added while maintaining the reaction temperature between 20 — 25 °C. The reaction mixture is stirred at about 25 °C for 12 — 20 h.

After the reaction is ted, the mixture is cooled to about 20 °C and quenched with 0.5 M aqueous citric acid (7.48 L, 3.74 mol) while maintaining the reaction temperature between W0 20131049726 PCT/U52012/058127 — 25 °C. The organic phase is collected, washed with sat. NaHC03 (6.51 L, 7.48 mol), washed with brine (6.59 L), and dried (N212804) then concentrated to afford tert-butyl 4- (diethoxymethyl)benzy1(tetrahydro-2H-pyran-4—yl)carbamate (A-3) (2801 g; 95% yield, 98.8 area % purity by HPLC) as a thick, amber oil.1H NMR (400 MHZ, CDC13) 6 7.40 (d, J= 8.1 Hz, 2H), 7.21 (d, J= 7.9 Hz, 2H), 5.49 (s, 1H), 4.39 (br s, 3H), 3.93 (br dd, J: 10.8, 3.8 Hz, 2H), 3.67 — 3.47 (m, 4H), 3.40 (br m, 2H), 1.68 - 1.59 (m, 4H), 1.39 (br s, 9H), 1.23 (t, J= 7.1 Hz, 6H).

Ste 3: Pre aration of tert-bu l4- 4—yl)carbamate gA-4) 0 0 OEt HOT" Etc/‘\[>V NH20H'HCI ——————-—-> N‘Boc K©V THF/HZO N‘Boc - 25 ‘JC A-3 A-4 A solution of tert—butyl 4—(diethoxymethy1)benzyl(tetrahydro—2H—pyran—4— yl)carbamate (A-3) (2.80 kg, 7.12 mol) in THF (28.0 L) and water (2.80 L) is stirred at about °C. Hydroxylamine hydrochloride (593 g, 8.54 mol) is added while maintaining the reaction temperature n 20—25 °C. The reaction mixture is stirred at about 20 °C for 16 — 20 h then d with CHzClz (8.4 L) and 50% brine (11.2 L) and stirred for at least 5 min.

The phases are separated then the organic phase is washed with 50% brine (2 x 2.8 L), dried (Na2SO4) and concentrated. The concentrate is diluted with MeOI—I (1.4 L) and re— concentrated. The concentrate is d with MeOH (14.0 L) and transferred to a reaction vessel. The on is warmed to about 25 °C then water ( 14.0 L) is added over about 1 — 1.5 h; after about 10 L of water is added, the mixture is seeded and a hazy suspension is observed. Additional water (8.4 L) is added over 1.5 h to r precipitate the product. After aging, the solid is collected by filtration. The filter-cake is washed with heptane (5.6 L) and dried to afford tert—butyl 4-((hydroxyimin0)methyl)benzy1(tetrahydro—2H-pyran yl)carbamate (A—4) (1678 g; 71%, 91.5 area % purity by HPLC) as an ite powder. 1H NMR (400 MHz, CDCl3) 6 8.12 (s, 1H), 7.51 (d, J= 8.2 Hz, 2H), 7.24 (d, .I= 7.9 Hz, 2H), 4.40 (br s, 3H), 3.96 (dd, J= 10.4, 3.6 Hz, 2H), 3.41 (br m, 2H), 1.69 — 1.61 (m, 4H), 1.39 (br s, 9H).

PCT/U52012/058127 Ste 4: Pre n of tart—bu 14— chloro h drox imino meth lbenz l tetrah dro- 2H- ran lcarbamate Ai HO\ O B00 20 30 °C A-4 i A suspension of (E)-z‘erIf—buty1 4—((hydroxyimino)methy1)benzyl(tetrahydro—2H— pyran~4—y1)carbamate (A4) (1662 g, 4.97 mol) in i—PrOAc (16.6 L) is stirred at 20 °C in a r. N—chlorosuccinimide (730 g, 5.47 mol) is added maintaining about 20 °C. The suspension is stirred at about 20 °C to complete the reaction. The suspension is diluted with water (8.3 L) and stirred to dissolve the solid. The phases are separated and the organic phase is washed with water (8.3 L). The organic phase is concentrated then diluted with i—PrOAc (831 mL). Heptane (13.3 L; 8 V) is slowly added to induce crystallization. The thick suspension is then stirred for 1 h. The solid is collected by filtration; the filter—cake is washed with heptane (2 x 1.6 L; 2 x 1 V) and dried to afford (Z)—tert—butyl 4- (chloro(hydroxyimino)methy1)benzy1 (tetrahydro-2H-pyranyl)carbamate (A—4-i) (1628 g; 89%, 98.0 area % purity by HPLC) as a white powder.

Ste 5: Pre n of (err-but l 5-bromo 3- 4- tert-butox carbon 1 tetrah dro- ZH- ran-4— lamino meth l hen lisoxazol-S- l razin-Z- l tert- butox carbon lcarbamate A-5 TEA, DCM Boc\ / QKKNZAii \ NBC N \ Br 00 Al A solution of terl-butyl 4-(ch1oro(hydroxyimino)methy1)benzy1(tetrahydro-2H- pyrany1)carbamate (Ai) (1.60 kg, 4.34 mol) and utyl N—(S—bromo lpyrazin-2—yl)—N—tert—butoxycarbonylcarbamate (Compound A—4-ii) (1.73 kg, 4.34 mol) in CH2C12 (12.8 L) is stirred at 20 °C. Et3N (483 g, 665 mL; 4.77 mol) is added and the reaction temperature ined below 30 °C. The suspension stirred at 20 °C to complete PCT/U52012/058127 the reaction then diluted with water (8.0 L) and agitated. The phases are separated and the organic phase is washed with water (8.0 L) and then concentrated. i-PrOAc (1.6 L) is added and the mixture and heated at 50 °C. Heptane (4.0 L) was slowly added then the suspension is allowed to cool to t temperature and stirred overnight. Additional heptane (7.2 L) is added to the suspension and it is stirred for l h. The solid is collected by filtration. The filter- cake is washed with hcptane (2 x 1.6 L) and dried to afford tert—butyl (5-bromo—3 — (((tert-butoxycarbony1)(tetrahydro—2H-pyran-4—yl)amino)methyl)phenyl)isoxazol—5— yl)pyrazin—2—yl)(tert—butoxycarbonyl)carbamate (A~5) (2.478 kg; 78%, 97.8 area % purity by HPLC) as a fine, tan powder. 1H NMR (400 MHz, CDC13) 5 8.60 (s, 1H), 7.78 (d, J= 8.3 Hz, 2H), 7.31 (m, 3H), 4.42 (br m, 3H), 4.03 — 3.82 (m, 2H), 3.38 (br s, 2H), 1.60 (m, 4H), 1.36 (s, 27H).

Ste 6: Pre aration of tert-bu ltert-butox carbon 13- 3— 4— tert- butox carbon 1 tetrah dro-ZH- ran lamino meth l hen lisoxazol-S- 1 4- iso r0 lsulfon l hen 1 razin-Z— lcarbamate i-PrOzS NWl N‘Boc N \ Ai / N l N\BOC ..........___..—> ’ N (j 1. cat. pf)C|2, PhCHg. o aq. K2C03 2. EtOH crystallization A-5 A's 3. MP-TMT resin sozi'Pr A mixture of terl—butyl (5-bromo~3—(3 —(4—(((tert-butoxycarbonyl)(tetrahydro— 2H—pyran-4~yl)amino)methyl)phenyl)isoxazol—5—yl)pyrazin-2—yl)(zert- butoxycarbonyl)carbamatc (A-S) (425 g, 582 mmol), K2C03 (161 g, 1.16 mol; 2.0 equiv.), and (4-(isopropylsulfonyl)phenyl)boronic acid (133 g, 582 mmol) in e (2.98 L) and water (850 mL) is stirred and degassed with N2 at ambient temperature. The st [1,1’- bis(di-Zert—butylphosphino)ferrocenc]dichloropalladium(ll), (Pd(dtbpf)Clz; 1.90 g, 2.91 mmol) is added and the mixture is degassed for an additional 10 min. The mixture is heated at 70 °C until the reaction is complete. The mixture is cooled to 50 °C, diluted with water (850 mL) and filtered through a bed of Celite. The phases are ted. The organic phase is concentrated then the residue is diluted with EtOH (1.70 L) and rc-conccntrated. With mixing at 40 °C, the concentrate is diluted with EtOl—l (1.70 L) to induce crystallization. The W0 49726 suspension is cooled to 20 °C and d for 4 h. The solid is collected by filtration. The filter-cake is washed with EtOH (2 x 425 mL) and air-dried to afford tert-butyl tert- butoxycarbonyl(3-(3 -(4-(((tert—butoxycarbonyl)(tetrahydro-2H—pyran-4— yl)amino)methyl)phenyl)isoxazol—S—yl)—5—(4—(isopropylsulfonyl)pheny1)pyrazin y1)carbamate (A—6) as a beige powder. The solid is dissolved in THF (2.13 L) and ed with Biotage MP—TMT resin (48 g) at ambient temperature. The resin is removed by filtration and the e concentrated to remove most of the THF. The concentrate is diluted with EtOH (970 mL) and re—concentrated to about half the original volume. The concentrate is diluted again with EtOH (970 mL) and mixed for 1 h at 40 °C. The suspension is cooled to ambient temperature and the solid is collected by filtration then dried to afford tert—butyl tert— butoxycarbonyl(3—(3 —(4—(((tert-butoxycarbonyl)(tetrahydro—ZH—pyran—4- y1)amino)methyl)phenyl)isoxazol~5-yl)-5—(4—(isopropy1sulfonyl)pheny1)pyrazin yl)carbamate (A—6) (416 g; 86% yield, 99.3 area % purity by HPLC) as a white powder. 1H NMR (400 MHz, CDC13) 5 9.04 (s, 1H), 8.38 — 8.28 (m, 2H), 8.10 — 8.01 (m, 2H), 7.82 (d, J = 8.2 Hz, 2H), 7.34 (m, 3H), 4.44 (br s, 2H), 3.94 (dd, J= 10.5, 3.5 Hz, 2H), 3.40 (br s, 2H), 3.25 (hept, .]= 6.8 Hz, 1H), 1.65 (m, 4H), 1.38 (br s, 27H), 1.33 (d, .]= 6.9 Hz, 6H).

Ste 7: Pre aration of 5- 4- ’ 4- lamina meth l hen lisoxazol—S- l Z-amine 1-3 freebase form BOC‘N’BO(Z)"‘1\NW NH2 0—11 1. TFA NW I N‘Boc DCM I NH / N (j N — 25 °c / ———-——>‘ o 2. NaOH (:30 EtOH/water A-6 [-3 SOziPr SOziPr A suspension of tert—butyl tert—butoxycarbonyl(3—(3—(4-(((tert— butoxycarbonyl)(tetrahydro-2H-pyranyl)amino)methyl)phenyl)isoxazol-5—yl)-5—(4- (isopropylsulfony1)phenyl)pyrazin—2-y1)carbamate (A~6) (410 g; 492 mmol) in CH2C12 (410 mL) is d at ambient temperature in a flask. TFA (841 g, 568 mL; 7.4 mol) is added while maintaining the reaction temperature between 20—25 °C. The solution is stirred at ambient ature for about 3 h when analysis shows reaction completion. The solution is cooled to about 5—10 °C and diluted with EtOH (3.3 L) while maintaining the temperature below 20 °C. A 5.0 M aqueous solution ofNaOH (1.77 L; 8.85 mol) is added while ng the reaction temperature to rise from about 14°C to about 42 °C. The suspension is heated at 70 — 75 °C for 6 h while removing distillate. The suspension is allowed to cool to ambient temperature. The solid is collected by filtration and the filter-cake is washed with water (4 x 1.64 L). The filter—cake is washed with EtOH (2 x 820 mL) and dried to afford 5—(4— (isopropylsulfonyl)phenyl)—3~(3—(4—(((tetrahydro—ZH—pyrany1)amino)methyl)phenyl) isoxazol-S-yl)pyrazin—2—amine (Compound 1—1) (257 g; 98% yield, 99.5 area % purity by HPLC) as a yellow powder. 1H NMR (400 MHz, DMSO) 6 8.94 (s, 1H), 8.44 - 8.33 (m, 2H), 7.94 (t, J= 8.2 Hz, 4H), 7.76 (s, 1H), 7.53 (d, J= 8.2 Hz, 2H), 7.20 (s, 2H), 3.83 (m, 1H), 3.80 (s, 3H), 3.46 (hept, J= 6.8 Hz, 1H), 3.25 (td, J= 11.4, 2.1 Hz, 2H), 2.66 — 2.54 (m, 1H), 1.79 (br dd, 2H), 1.36 — 1.22 (m, 2H), 1.19 (d, J= 6.8 Hz, 6H).13C NMR (101 MHz, DMSO) 5 167.57, 151.76, , 137.58, 135.75, 129.16, 128.53, 126.57, 126.41, 125.69, , 102.13, 65.83, 54.22, 52.60, 49.19, 33.18, 15.20.

Compound Analytical Data Cmpd LCMS LCMS HNMR N0. ES + Rt min H NMR (400 MHz, DMSO) 6 9.63 (d, J = 4.7 Hz, 2H), 9.05 (s, 1H), 8.69 (d, J= 5.2 Hz, 1H), 8.21 (s, 1H), 8.16 — 8.03 (m, 3H), 7.84 (t, J= 4.1 Hz, 3H), 7.34 (br s, 2H), 4.40 — 4.18 (m, 2H), 3.94 (dd, J=11.2, 3.9 Hz, 2H), 3.32 (t, J= 11.2 Hz, 3H), 2.17 — 2.00 (m, 2H), 1.81 (s, 6H), 1.75 (dd, J 12.1, 4.3 Hz, 2H.

H NMR (400 MHz, DMSO) 5 8.94 (s, 1H), 8.44 - 8.33 (m, 2H), 7.94 (t, J= 8.2 Hz, 4H), 7.76 (s, 1H), 7.53 (d, J= 8.2 Hz, 2H), 7.20 (s, 2H), 3.83 (m, 1H), 3.80 (s, 3H), 3.46 (hept, J= 6.8 Hz, 1H), 3.25 (td, J= 11.4, 2.1 Hz, 2H), 2.66 — 1.22 (m, 2H), 1.19 — 2.54 (m, 1H), 1.79 (br dd, 2H), 1.36 (d, J= 6.8 Hz, 6H). 1H NMR (500 MHz, DMSO) 9.10 (d, J = 5.8 Hz, 2H), 8.97 (s, 1H), 8.42 — 8.37 (m, 2H), 8.15 - 8.08 (m, 2H), 7.99 — 7.92 II—l 466.2 0.83 (m, 2H), 7.85 (s, 1H), 7.75 — 7.69 (m, 2H), 7.22 (br s, 2H), 3.48 (hept, J = 6.8 Hz, 1H), 2.60 (t, J = 5.4 Hz, 3H), 1.20 (d, J = 6.8 Hz, 6H). 1H NMR (500 MHz, DMSO) 9.14 (s, 2H), 8.96 (s, 1H), 8.42 ~ 8.36 (m, 2H), 8.13 - 8.08 (m, 2H), 7.99 — 7.91 (m, II—2 469.1 0.82 2H), 7.85 (s, 1H), 7.78 - 7.68 (m, 2H), 7.21 (s, 2H), 3.48 (d J= 13.6, 6.7 Hz, 1H 1.20 , , d, J= 6.8 Hz, 6H).

WO 2013049726 PCT/U52012/058127 1H NMR (500 MHz, DMSO) 9.11 (s, 2H), 8.97 (s, 1H), 8.39 (d, J = 8.7 Hz, 2H), 8.11 (d, J = 8.4 Hz, 2H), 7.95 (d, J = 8.7 Hz, 2H), 7.85 (s, 1H), 7.72 (d, J = 8.4 Hz, 2H), 7.23 (s, 2H), 4.25 - 4.19 (m, 2H), 3.47 (tt, J = 14.0, 6.9 Hz, 1H), 1.20 (d, J = 6.8 Hz, 6H). 1H NMR (400 MHz, DMSO) 5 2.58 (t, 3H), 4.21 (t, 2H), .67 (br s, 2H), 7.74 (d, 2H), 7.85 (s, 1H), 7.94 (d, 2H), 8.10 (d, 2H), 8.38 (d, 2H), 8.96 (s, 1H) and 9.33 tbr s, 2H} ppm INTERMEDIATES Example 8: Preparation of Oxime 5a SCHEME BB: Step 1b OEt Step 2b ——-————> NaBH4 N\ DCM OEt HO‘ Et0)\©\/§OC Step 3b 1“ NHZOH'HCI 1300 N _...____., I \ N THF/water \ 3b 53 Step 1b Add MeOH (28.00 L) and 4—(diethoxymethyl)benzaldehyde (Compound 1b) (3500 g, 16.81 mol) into a reactor at 20 °C. Add methylamine, 33% in EtOH (1.898 kg, 2.511 L of 33 %w/w, 20.17 mol) maintaining 20-30 °C then stir for 1.5 h to form the iminc. Add NaBH4 (381.7 g, 10.09 mol)cap1ets ining the temperature between 20 - 30 °C. Stir at room temperature for at least 30 min to ensure te reaction. Add aqueous NaOH (16.81 L of 2.0 M, 33.62 mol) maintaining approximately 20 °C. Add MTBE (17.50 L) and brine (7.0 L), stir for at least 5 min then allow the phases to separate. Extract the aqueous layer with MTBE (7.0 L) then combine the organic phases and wash with brine (3.5 L) then dry (N212804) then trate to 6 L. The biphasic mixture was erred to a separatory funnel and the aqueous phase removed. The organic phase was concentrated to afford 1-(4- (diethoxymethyl)phenyl)-N-methylmethanamine (Compound 2b) (3755 g, 16.82 mol, 100% WO 49726 ‘ PCT/U82012/058127 yield) as an oil. ‘H NMR (400 MHz, CDClg) 5 7.43 (d, J= 8.1 Hz, 2H), 7.31 (d, J: 8.1 Hz, 2H), 5.49 (s, 1H), 3.75 (s, 2H), 3.68 — 3.46 (m, 4H), 2.45 (s, 3H), 1.23 (t, J= 7.1 Hz, 6H).

Steps 2b and 3b Add 2-MeTHF (15.00 L) and l—(4-(diethoxymethyl)phenyl)—N— methylmethanamine (Compound 2b) (3750 g, 16.79 mol) to a reactor at 20 °C. Add a solution of B00 anhydride (3.848 kg, 4.051 L, 17.63 mol) in 2-MeTHF (7.500 L) maintaining imately 25 °C. Stir for at least 30 min to ensure te conversion to tert—butyl 4- oxymethyl)benzyl(methyl)carbamate (Compound 3b), then add a solution ofNaZSO4 _ (1.192 kg, 8.395 mol) in water (11.25 L). Heat to 35 °C then add a solution of ylamine hydrochloride (1.750 kg, 25.18 mol) in water (3 .75 L) then stir for at least 6 h to ensure complete reaction. Cool to 20 °C, stop the stirring and remove the aqueous phase. Wash the organic layer with brine (3.75 L), dry (Na2SO4), filter and concentrate to about 9 L. Add heptane (15.00 L) and crystalline tert—butyl 4—((hydroxyimino)methyl)benzy1(methyl) carbamate (Compound 5a) (1.0g portions every 10 min) until nucleation was evident, then concentrate to afford a solid slurry. Add heptane (3.75 L) then cool to room temp and filter.

Wash with heptane (5.625 L) then dry to afford tert—butyl 4—((hydroxyimino)methyl) benzyl(methyl)carbamate (Compound 5a) (4023 g, 15.22 mo], 91 % yield, 972 area % purity by HPLC) as a colorless solid. 1H NMR (400 MHz, CDC13) 5 8.13 (s, 1H), 7.54 (d, J= 8.1 Hz, 2H), 7.25 (br (1, 2H), 4.44 (br s, 2H), 2.83 (br d, 3H), 1.47 (br s, 9H).

Scheme CC: Synthesis of Intermediate Aii NH2 NH2 TMS N)\rBr / ' l , N 'PTSA Sonogashira BOC protection Bf --——-——-———-———> Br > C-1 C-2 N B TMS N Boc N \ N \ RN TMS removal / RN/ Br Br C-3 Aii The compound of formula A-4—ii may be made according to the steps outlined in Scheme C. Sonogashira coupling reactions are known in the art (see e.g., Chem. Rev.

WO 2013049726 PCT/U82012/058127 2007, 874-922). In some embodiments, suitable Sonogashira coupling conditions comprise adding 1 equivalent of the compound of formula C-1, 1 equivalent of TMS-acetylene, 0.010 equivalents of Pd(PPh3)2C12, 0.015 equivalents of CuI and 1.20 equivalents ofNMM in isopropanol. The product can be isolated by adding water to the lic reaction mixture.

Amine salts of a product maybe formed by dissolving the amine in a common, organic solvent and adding an acid. Examples of suitable solvents include chlorinated solvents (e. g., dichloromethane (DCM), dichloroethane (DCE), CHzClz, and chloroform), ethers (e.g., THF, 2—MeTI-IF and dioxane), esters (e.g., EtOAc, IPAC) and other c solvents. Examples of le acids e but are not limited to HCl, H3PO4, H2304, MSA, and PTSA. In some embodiments, the solvent is IPAC and the acid is PTSA. In some embodiments, the acid addition salt is converted back to the free amine base in the presence of a suitable solvent and a suitable base. le solvents include EtOAc, IPAC, dichloromethane (DCM), dichloroethane (DCE), , chloroform, 2—MeTHF, and suitable bases include NaOH, NaHCO3, Na2C03, KOH, KHCOg, K2C03, and C52CO3. In some embodiments, the suitable solvent is EtOAc and the suitable base is KHCO3, The amine of Compound 02 may be protected with various amine protecting , such as Boc (tert-butoxycarbonyl). Introduction of Boc protecting groups is known in the art (see e.g. ting Groups in Organic Synthesis, Greene and Wuts). In some embodiments, le conditions involve adding 1.00 equivalents of the amine, 2.10 equivalents of di—tert—butyl dicarbonate, and 0.03 equivalents ofDMAP in EtOAc. ] ion in Pd is ed by treating with a metal scavenger (silica gel, functionalized resins, charcoal). In some embodiments, suitable ions involve adding charcoal.

The TMS (trimethylsilyl) protecting group on Compound C-3 may be removed via conditions known to one of skill in the art. In some embodiments, TMS removal conditions se reacting the TMS-protected compound with a suitable base in a suitable solvent. Examples of suitable solvents include chlorinated solvents (e.g., dichloromethane (DCM), dichloroethane (DCE), CH2C12, and chloroform), ethers (e.g., THF, 2—MeTHF and dioxane), esters (e.g., EtOAc, IPAC), other aprotic solvents and alcohol solvents (e. g., MeOH, EtOH, iPrOI—I). es of suitable bases include but are not limited to (e.g., NaOH, KOH, K2CO3, Na2C03). In certain embodiments, suitable conditions comprise adding 1.00 equivalents ofthe TMS-protected acetylene, 1.10 equivalents of K2CO3, EtOAc and EtOH. In some emboments, the alcoholic solvent, such as EtOH, is added last in the reaction. In some embodiments the product acetylene is isolated by adding water.

PCT/U82012/058127 Scheme DD: Example Synthesis of Compound Aii NH2 1. TMS4acetylene NH2 TMS cat. Pd(PPh3)ZCI2 Br ¢ 1. EtOAc, aq. KHCOS N \ cat. Cul, NMM, IPA N \ 2. Boch, cat. DMAP, RN 2. water ”\fN °PTSA EtOAc 3. PTSA, EtOAc 3. charcoal Br —-——————> Br ———"‘“> C4 (65-75%) 0.2 (95-10005) }/ TMS 1. K2003, EtOAc, EtOH 2. water NV”(800); krN/ ————-> K/N/ Br %) Br C-3 Aii Exam 1e 9: S nthesis of Com ound Aii N(Boc)2 NIV/ A—4-ii Ste 1: Pre aration of 5-bromo trimeth lsil leth n l razin-Z-amine Com ound 9.2.1 NH2 1. TMS—acetylene NH2 TMS cat. Pd(PPh3)2C|2 Br é NI \ cat. Cul, NMM, [PA N \ RN 2. water “\(N 'PTSA 3. PTSA, EtOAc Br —.__——.———.> Br c-1 (65—75%) c-2 Charge isopropanol (8.0 L) to a reactor the stir and sparge with a stream of N2.

Add 3,5—dibromopyrazinamine (Compound GD (2000 g, 7.91 moles), Pd(PP'h3)2C12 (56 g, 0.079 moles), CuI (23 g, 0.119 , and NMM (1043 mL, 9.49 moles) to the reactor under a N2 atmosphere. Adjust the reaction temperature to 25 °C. Purge the reactor with N2 by doing at least three /N2 purge cycles. Charge ”EMS—acetylene (1.12 L, 7.91 moles) to the reaction mixture and maintain the reaction temperature below 30 °C. When the reaction is te lower the temperature of the reaction mixture to 15 °C then add water (10 L) and PCTfUS2012/058127 stir for at least 2 h. The solid is ted by filtration washing the solid with 1:1 IPA/water (2 x 6 L). The filter cake is dried under vacuum then charged to a reactor and dissolved in EtOAc (12.5 L). PTSA hydrate (1.28 kg, 6.72 mol) is charged as a solid to the r. The mixture is stirred at ambient temperature for at least 5 h then the solid is collected by filtration, washed with 1:1 heptane/EtOAc (3.5 L) ed by heptane (3.5 L). The filter cake is dried to afford 5—bromo-3 —((trimethylsily1)ethynyl)pyrazin-2—aminc(Compound 02) as a PTSA salt (2356 g, 67% yield, 98.9 area % purity by HPLC).1H NMR (400 MHZ, DMSO) 8 8.12 (s, 1H), 7.48 (d, J= 8.1 Hz, 2H), 7.12 (d, J: 8.0 Hz, 2H), 2.29 (s, 3H), 0.26 (s, 9H).

Steps 2 and 3 1. EtOAc, aq. KHC03 2. 80020. cat. DMAP.

NH2 TMS 1. KZCOS EtOAc é EtOAc N(BOC)} TMS EtOH ”(300); N \ 3.charcoa| NV 2.water / l \ /N oPTSA W9 | (es—100%) N (75-80%) / Br Br c.3 Aii Ste 2: Pre n of tert-bu lN-tert-butox carbon l—N— 5-brom0 eth n l razin-Z- lcarbamate Com ound C-3 A solution of5-brom0—3—((trimethylsilyl)ethynyl)pyrazin—2—amine PTSA salt (Compound C-2) (2350 g, 5.31 mol) in EtOAc (11.5 L) is stirred with a 20% w/w aq. solution of KHC03 (4.5 kg, 1.5 eq.) for at least 30 min. The layers are separated and the organic layer is concentrated then dissolved in EtOAc (7 L) and added to a reactor. DMAP (19.5 g, 0.16 mol) is added followed a solution of Boczo (2436 g, 11.16 mol) in EtOAc (3 L) is added lowly. The reaction is stirred for at least 30 min to ensure complete reaction then activated al (Darco G—60, 720 g) and Celite (720 g) are added and stirred for at least 2 h. The mixture is filtered washing the solid pad with EtOAc (2 x 1.8 L). The filtrate is concentrated to afford tert-butyl N—tert-butoxycarbonyl—N—[5—br0m0—3-((trimethylsilyl)ethynyl) pyrazin yl]carbamate (Compound C-3) that is used directly in the next step.

PCT/U32012/058127 Ste 3: Pre aration of tart-bu 'lN— 5—bromoethvnvi vrazin-Z-vl butoxycarbonylcarbamate {Compound Aii) K2CO3 (811 g, 5.87 mol) is charged to a reactor followed by a solution of Compound O3 (2300 g, 4.89 mol) ved in EtOAc (4.6 L) agitation started. EtOH (9.2 L) is added slowly and the mixture stirred for at least 1 h to ensure that the on is complete then water (4.6 L) is added and stirred for at least 2 h. The solid is collected by ion and washed with 1:1 EtOH/water (4.6 L followed by 2.3 L) followed by EtOH (2.3 L). The filter cake is dried to afford zen—butyl romo~3—ethynylpyrazinyl)~N—tert— butoxycarbonylcarbamate (Compound ) (1568 g, 78% yield, 97.5 area % by HPLC).1H NMR (400 MHz, CDC13) 5 8.54 (s, 1H), 3.52 (s, 1H), 1.42 (s, 1811).

Solid Forms of Compound I—2 Compound I-2 has been prepared in s solid forms, including salts, and co- solvates. The solid forms of the present invention are useful in the cture of medicaments for the treatment of cancer. One embodiment provides use of a solid form described herein for treating cancer. In some embodiments, the cancer is pancreatic cancer or non—small cell lung cancer. Another embodiment provides a pharmaceutical composition comprising a solid form described herein and a pharmaceutically acceptable carrier.

Applicants be herein five novel solid forms of Compound 1—2. The names and stoichiometry for each of these solid forms are provided in Table 8—1 below: - Table 3-1 Exam-1e Examle l3 Comound 1—2 free base Examle 14 Comoound I—2 - HCl Example 15 Compound I-2 - 2HC1 12.

Examle 16 Comoound I-2 ° HCl ' H20 1:2:1 Examle l7 Comound I-2 ° HCl - 2H20 1:1:2 Solid state NMR a were acquired on the -Biospin 400 MHz Advance III wide—bore spectrometer equipped with Bruker~Biospin 4mm HFX probe.

Samples were packed into 4mm ZrOz rotors (approximately 70mg or less, depending on sample availability). Magic angle spinning (MAS) speed of typically 12.5 kHz was applied.

The temperature of the probe head was set to 275K to minimize the effect of onal heating during spinning. The proton relaxation time was measured using lH MAS T1 saturation recovery relaxation experiment in order to set up proper recycle delay of the C 13C CPMAS experiment cross—polarization (CP) MAS experiment. The recycle delay of was WO 2013049726 PCT/U$2012/058127 adjusted to be at least 1.2 times longer than the measured lH T1 relaxation time in order to ze the carbon spectrum signal-to-noise ratio. The CP contact time of 13C CPMAS experiment was set to 2 ms. A CP proton pulse with linear ramp (from 50% to 100%) was employed. The Hartmann-Hahn match was optimized on external reference sample (glycine). Carbon spectra were acquired with SPINAL 64 decoupling with the field strength of approximately 100 kHz. The chemical shift was referenced t external rd of adamantane with its upfield resonance set to 29.5 ppm.

XRPD data for Examples 13—14 were measured on Bruker D8 Advance System (Asset V014333) equipped with a seal ed tube Cu source and a Vantec—l or (Bruker AXS, Madison, WI) at room temperature. The X—ray generator was operating at a voltage of 40 kV and a current of 40 mA. The powder sample was placed in a shallow silicon holder.

The data were recorded in a reflection scanning mode (locked coupled) over the range of 3°— 40° 2 theta with a step size of 00144" and a dwell time of 0.253 (105 s per step). le divergence slits were used.

Example 10: Compound I-2 (free base) Compound 1-2 free base can be formed according to the methods described in Example 6, Step 4: ate Method 1.

XRPD of Compound I—2 (free base) Figure la shows the X—ray powder diffractogram of the sample which is characteristic of crystalline drug substance.

Representative XRPD peaks from nd I-2 free base: XRPD Angle Intensity % Peaks (2-Theta :1: 0.2) ~ 23.8 100.0 *2 14.2 43.9 3 22.5 . 39.3 19.3 28.6 6 27.2 27.6 7 17.0 25.4 18.1 25.2 9 17.6 19.6 20.2 17.2 12 20.8 14.5' 13 29.9 14.5 33.2 14.3 .1 13.5 PCT/U82012/058127 XRPD Angle Intensity % Peaks (2-Theta :1: 0.2) .6 .6 Thermo Analysis of Compound 1-2 free base A thermal gravimetric analysis of Compound 1—2 free base was performed to determine the percent weight loss as a function of time. The sample was heated from ambient temperature to 350°C at the rate of 10°C/min on TA ment TGA Q5000 (Asset V01425 8). Figure 2a shows the TGA result with a one-step weight loss before evaporation or thermal decomposition. From t temperature to 215°C, the weight was ~l .9 %.

Differential Scanning Calorimetry of Compound I-2 free base The thermal properties of Compound 1-2 free base were measured using the TA Instrument DSC Q2000 (Asset V014259). A Compound I—2 free base sample (1.6900 mg) was weighed in a nched pinhole aluminum hermetic pan and heated from ambient ature to 350°C at 10°C/min. One endothermic peak is observed at 210°C with its onset temperature at 201°C e 3a). The enthalpy associated with the endothermic peak is 78 J/g.

Solid State NMR of Compound I—2 free base 13C CPMAS on Compound I—2 free base 275K; 1H Tl=l.30s 12.5 kHz spinning; ref. adamantane 29.5 ppm For the full spectrum, see Figure 4a.

W0 49726 PCT/U82012/058127 Representative Peaks um rel l_—— 126.6 100.0 ' 123.5 38.1 Crystal Structure of Compound 1-2 free base The free form of Compound 1-2 was prepared from the Compound 1—2 HCl salt. 200mg Compound 1—2 HCl salt was added to lmL of 6N NaOH solution. 20mL of dichloromethane was used to extract the free form. The dichloromethane layer was dried over K2C03. The solution was filtered off and SmL of n—heptane was added to it. Crystals were obtained by slow evaporation of the solution at room temperature over night.

Most crystals obtained were thin plates. Some tic shape crystals were found among them.

A yellow prismatic l with ions of 0.2>< 0.1><0.l mm3 was selected, mounted on a MicroMount and centered on a Bruker APEX II diffractometer. Three batches of 40 frames separated in reciprocal space were obtained to provide an orientation matrix and initial cell parameters. Final cell parameters were obtained and refined after data collection was completed based on the full data set.

A diffraction data set of reciprocal space was obtained to a resolution of 11696" 20 angle using 0.5" steps with 10 s exposure for each frame. Data were collected at 100 (2) K temperature with a nitrogen flow cryosystem. Integration of intensities and refinement of cell parameters were accomplished using APEXII software.

PCT/U52012/058127 CRYSTAL DATA Example 11: Compound I-2 - HCl Compound 1-2 ° HCl can be formed according to the s described in Example 6, Step 4: Alternate Method 2 and Example 6, Step 5.

XRPD ofCompound I-2 - HCl Figure 1b shows the X—ray powder diffractogram of the sample which is characteristic of crystalline drug nce.

Representative XRPD peaks from Compound I—2 ' HCl XRPD Angle Intensity % Peaks (2—Theta :l: 0.2) 16.4 23.6 .5 .4 Thermo Analysis of Compound I—2 - HCl A thermal gravimetric analysis of Compound 1—2 - HCl was performed to determine the percent weight loss as a function of time. The sample was heated from ambient temperature to 350°C at the rate of 10°C/min on TA Instrument TGA Q5000 (Asset W0 2013f049726 V01425 8). Figure 2b shows the TGA result with a ep weight loss before ation or thermal osition. From ambient temperature to 100°C, the weight was ~l .1 %, and from 110°C to 240°C the weight loss is ~0.8%.

Differential Scanning Calorimetry of Compound 1—2 0 HCl The thermal properties of Compound I~2 ° HCl were measured using the TA Instrument DSC Q2000 (Asset V014259). A nd I—2 - HCI sample (3.8110 mg) was weighed in a pre—punched pinhole aluminum hermetic pan and heated from ambient temperature to 350°C at 10°C/min. One endothermic peak is observed at 293°C with its onset temperature at 291°C (Figure 3b). The enthalpy associated with the endothermic peak is 160.3 J/g. The second endothermic peak is around 321°C. Both peaks were coupled with sample evaporation and decomposition.

Solid State NMR of Com ound 1-2 - HCl CPMAS on Compound 12 - HCl 275K;_12.5 kHz spinning; ref. adamantane 29.5 ppm For the full spectrum, Sfi Figure 4b.

Representative Peaks Peak Chem Shift Intensity # o um rel 142.9 54 14 138.7 44 06 136.7 60 O6 129.8 73.58 127.9 63.71 124.1 34.91 53.52 W0 2013f049726 PCT/U82012/058127 Crystal Structure of Compound l-2 - HCl 180mg Compound l-2 ° HCl was added to a vial with 0.8mL 2-propanol and 0.2 mL water. The sealed vial was kept in an oven at 70°C for two weeks. Diffraction y crystals were observed.

A yellow needle shape c1ystal with dimensions of 0.15X 0.02X0.02 mm3 was selected, mounted on a ount and centered on a Bruker APEX II diffractometer (V011510). Three batches of 40 frames separated in reciprocal space were obtained to provide an orientation matrix and initial cell parameters. Final cell parameters were collected and refined was completed based on the full data set.

A diffraction data set of ocal space was ed to a resolution of 106° 29 angle using 05" steps with re times 20 s each frame for low angle frames and 603 each frame for high angle frames. Data were collected at room temperature.

To obtain the data in table 1, dry nitrogen was blown to the crystal at 6 Litre/min speed to keep the ambient moisture out. Data in table 2 was obtained without nitrogen. Integration of intensities and refinement of cell parameters were conducted using the APEXII software. The water occupancy can vary n 0 and l. masosoaa V= 2510.87 (17) A3 v = 2527.2 (4) A3 CHN Elemental Analysis CHN elemental analysis of Compound 1—2 - HCI suggest a mono HCl salt. mesons %Theory 57.60 5.20 14.00 7.10 %Foooo so-sa sass Example 12: Compound I-2 - 2HC1 Compound I-2 ° ZHCI can be formed according to the s bed in Example 6, Step 4.

XRPD ofCompound I—2 - ZHCl ] The XRPD patterns are acquired at room temperature in reflection mode using a Bruker D8 Discover system (Asset Tag V012842) equipped with a sealed tube source and a Hi—Star area detector (Bruker AXS, Madison, WI). The X-Ray tor is operated at a voltage of40 kV and a current of 35 mA. The powder sample is placed in a nickel holder.

Two frames are registered with an exposure time of 120 3 each. The data is subsequently integrated over the range of 4.5°—39° 2 theta with a step size of 002° and merged into one continuous pattern.

Figure 1c shows the X—ray powder diffractogram of the sample which is characteristic of crystalline drug substance.

Representative XRPD peaks from Compound I—2 ° 2HC1 Peaks 2—Theta :t 0.2) 100.0 92.2 91.3 91.3 91.2 _—89.0 89.0 l=-_88.8 9 88.1 *10 87.5 11 87.4 12 86.6 *13 86.0 14 86.0 86.0 85.9 85.9 85.7 85.7 85.4 85.2 85.2 84.9 84.7 84.1 PCT/U82012/058127 Thermo Analysis of nd 1—2 ' 2HC1 A thermal gravimetric analysis of Compound I-2 ' 2HC1 was performed on the TA Instruments TGA model Q5000. nd I-2 ° 2HCl was placed in a platinum sample pan and heated at 10°C/min to 350°C from room temperature. Figure 20 shows the TGA , which demonstrates a weight loss of 7.0% from room temperature to 188°C, which is consistent with the loss of 1 equivalent of HCl (6.8%). The onset temperature of degradation/melting is 263°C.

Differential Scanning metg}: of Compound l~2 ° 2HC1 A DSC thermogram for Compound 1—2 - 2HC1 drug substance lot 3 was obtained using TA Instruments DSC Q2000. Compound 1-2 - ZHCI was heated at 2°C/min to 275°C from —20°C, and modulated at i 1°C every 60 sec. The DSC thermogram (Figure 3c) reveals an endothermic peak below 200°C, which could corresponds to the loss of 1 equivalent of HCl. Melting/recrystallization occurs n 215—245°C, followed by degradation.

Solid State NMR of Compound I-2 - 2HC1 13c CPMAS on Compound 1-2 - 2HCl 275K; 1H T1=l.7s 12.5 kHz spinning; ref. adamantane 29.5 ppm For the full spectrum, s_e§ Figure 4c.

Chem Shift um Cmstal Structure of Compound I—2 ' 2HCl 180mg Compound I—2 ' HCl was added to a vial with 0.8mL 2-propanol and 0.2 mL water. The sealed Vial was kept in an oven at 70°C for two weeks. Diffraction quality crystals were observed.

A yellow needle shape crystal with dimensions of 0. 15X 0.02 X0.02 mm3 was selected, mounted on a ount and centered on a Bruker APEX II diffractometer (V011510). Three batches of 40 frames ted in reciprocal space were obtained to provide an orientation matrix and initial cell parameters Final cell parameters were collected and refined was completed based on the full data set.

A diffraction data set of reciprocal space was obtained to a tion of 106° 20 angle using 0.5° steps with exposure times 20 s each frame for low angle frames and 605 each frame for high angle frames. Data were collected at room temperature. Dry nitrogen was blown to the crystal at 6 Litre/min speed to keep the t moisture out. Integration of intensities and refinement of cell parameters were conducted using the APEXH software.

CRYSTAL DATA V= 2510.87 (17) A3 e 13: Compound I-2 - HCl 0 H20 Compound I—2 - HCl- H20 can be formed from Compound 1—2 - 2 HCl. 4—17) A suspension of Compound I—2 - 2 HCl (10.0 g, 18.6 mmol) in isopropyl alcohol (40 mL) and water (10 mL) is warmed at 50 °C for about 1 h and then cooled to below 10 °C. The solid is ted by filtration. The filter-cake is washed with 80/20 isopropyl alcohol/water (2X 10 mL) and air—dried to afford Compound I-2 - HCl- 2H20 as a yellow powder.

WO 49726 PCT/U82012/058127 XRPD of Compound I-2 - HCl - HZPQ The XRPD patterns are acquired at room temperature in reflection mode using a Bruker D8 Discover system (Asset Tag V012842) equipped with a sealed tube source and a Hi—Star area detector (Bruker AXS, Madison, WI). The X-Ray generator is operated at a voltage of40 kV and a t of 35 mA. The powder sample is placed in a nickel holder.

Two frames are registered with an exposure time of 120 5 each. The data is subsequently integrated over the range of 4.5°—39° 2 theta with a step size of 0.02° and merged into one continuous pattern.

Figure 1d shows the X—ray powder diffractogram of the sample which is characteristic of crystalline drug nce.

Representative XRPD peaks from Compound l-2 - HCl - H20 XRPD Angle Intensity % Peaks (2—Theta :l: 0.2) *1—n_ 17-7 11 31-1 12 15-8 14 17-1 12.7 16 16-0 18 20.6 16.0 *20 11.2 15.2 21 33.9 11.3 Thermo Analysis of Compound l—2 - HCl ° H20 Thermogravimetric analysis (TGA) for Compound 1-2 - l-lCl - H20 was performed on the TA ments TGA model Q5000. Compound I—2 - HCl 0 H20 was placed in a platinum sample pan and heated at 10°C/min to 400°C from room temperature.

The thermogram (Figure 2d) demonstrates a weight loss of 2.9% from room temperature to PCT/U52012/058127 100°C, and a weight loss of 0.6% from 100°C to 222°C, which is consistent with theoretical monohydrate (3.5%).

Differential ng Calorimetry of Compound 1-2 - HCl - H29 A DSC thermogram for Compound 1-2 ° HCI - H20 was obtained using TA Instruments DSC Q2000. Compound 12 - HCl ° H20 was heated at 2°C/min to 275°C from — °C, and modulated at :r 1°C every 60 sec. The DSC thermogram (Figure 3d) reveals an endothermic peak below 200°C, which could corresponds to the loss of 1 equivalent of HCl.

Melting/recrystallization occurs between 215-245°C, followed by ation.

Example 14: Compound I-2 - HCI - 2H20 Compound 1—2 - HCl- 213120 can be formed from Compound I-2 ° 2 I-ICl.

(E29244—17) A suspension of Compound 1—2 - 2 HCl (10.0 g, 18.6 mmol) in isopropyl alcohol (40 mL) and water (10 mL) is warmed at 50 °C for about 1 h and then cooled to below 10 °C. The solid is collected by filtration. The filter-cake is washed with 80/20 isopropyl alcohol/water (2 x 10 mL) and ied to afford nd 1—2 - HC1° 2H20 as a yellow powder.

XRPD of Compound 1-2 - 1-1C1 0 21-129 The powder x—ray diffraction measurements were performed using PANalytical’s X—pert Pro diffractometer at room temperature with copper radiation (1.54060 °A). The incident beam optic was comprised of a variable divergence slit to ensure a constant illuminated length on the sample and on the diffracted beam side, a fast linear solid state detector was used with an active length of 2. 12 degrees 2 theta measured in a ng mode.

The powder sample was packed on the indented area of a zero background silicon holder and ng was performed to achieve better statistics. A symmetrical scan was measured from 4 ~ 40 degrees 2 theta with a step size of 0.017 degrees and a scan step time of 15.53.

Figure 1d shows the X—ray powder diffractogram of the sample which is characteristic of lline drug substance.

Representative XRPD peaks from Compound 1—2 - HCl - 2H20 XRPD Angle (2- Intensity % Peaks Theta i 0.2) 100.0 82.0 69.2 66.3 63.8 ‘i_ 5:33 .3- 51.8 9 20.7 49.7 15.3 46.2 44.6 41.2 19.9 40.4 14 17.6 39.1 39.0 36.1 33.6 33.5 32.2 29.1 28.7 28.0 23.8 22.6 26 14.3 22.4 .8 28 25.1 19.7 29 I 13.7 19.0 UJWUJUJUJUJUJ \OOOQOM-PUJN—‘O 14.0 17.4 33.0 16.2 9(- 23.3 15.7 16.6 15.1 29.6 14.9 29.9 14.8 27.6 14.8 32.1 13.3 -X- 24.6 13.1 .8 11.1 1 O4 W0 2013l049726 PCT/U82012/058127 Thermo Analysis of Compound 1-2 - HC1° 2HZQ The TGA (Thermogravimetric Analysis) thermographs were obtained using a TA instrument TGA Q500 respectively at a scan rate of lO°C/min over a temperature range of °C. For TGA analysis, samples were placed in an open pan. The thermogram demonstrates a weight loss of~6 from room temperature to 100°C, which is consistent with theoretical ate (6.7%).

Differential Scanning Calorimetm of nd I—2 - HCl ' 2H__20 A DSC (Differential Scanning Calorimetry) thermographs were obtained using a TA instruments DSC Q2000 at a scan rate of 10°C/min over a temperature range of 25~ 300°C. For DSC analysis, samples were weighed into aluminum hermetic T-zero pans that were sealed and punctured with a single hole. The DSC thermogram reveals dehydration between room temperature and 120°C followed by melting/recrystallization between 170— 250°C.

Crystal Structure of Compound 1—2 - HCl with water 180mg Compound I-2 - HCl was added to a vial with 0.8mL 2—propanol and 0.2 mL water.

The sealed vial was kept in an oven at 70°C for two weeks. Diffraction quality crystals were observed.

] A yellow needle shape crystal with dimensions of 0.15>< 0.02><0.02 mm3 was ed, mounted on a MicroMount and centered on a Bruker APEX II diffractometer (V011510). Then a kapton tube with water inside covered the pin. The tube was sealed to make sure the l is equilibrated with water for two days before the ction experiments. Three batches of 40 frames separated in reciprocal space were obtained to provide an orientation matrix and initial cell parameters Final cell ters were collected and refined was ted based on the full data set.

A diffraction data set of reciprocal space was obtained to a resolution of 106° 20 angle using 0.5° steps with exposure times 20 3 each frame for low angle frames and 60s each frame for high angle frames. Data were collected at room temperature. Integration of intensities and refinement of cell parameters were ted using the APEXII software.

PCT/U52012/058127 CRYSTAL DATA Example 15: ar ATR Inhibition Assay: Compounds can be screened for their ability to inhibit intracellular ATR using an immunofluorescence microscopy assay to detect phosphorylation of the ATR substrate histone H2AX in hydroxyurea treated cells. HT29 cells are plated at 14,000 cells per well in 96—well black imaging plates (BD 353219) in McCoy’s 5A media (Sigma M8403) mented with 10% foetal bovine serum (JRl-I Biosciences 12003), Penicillin/Streptomycin solution diluted 1:100 (Sigma , and 2mM L—glumtamine (Sigma G7513), and allowed to adhere overnight at 37°C in 5% C02. Compounds are then‘ added to the cell media from a final concentration of 25uM in 3-fold serial dilutions and the cells are incubated at 37°C in 5% C02. After 15min, hydroxyurea (Sigma H8627) is added to a final concentration of 2mM.

After 45min of treatment with hydroxyurea, the cells are washed in PBS, fixed for 10min in 4% formaldehyde diluted in PBS (Polysciences Inc 18814), washed in 0.2% Tween—20 in PBS (wash buffer), and permeabilised for 10min in 0.5% Triton X-100 in PBS, all at room temperature. The cells are then washed once in wash buffer and blocked for 30min at room temperature in 10% goat serum (Sigma G9023) diluted in wash buffer (block buffer). To detect H2AX phosphorylation levels, the cells are then incubated for 1h at room temperature in primary antibody (mouse monoclonal hosphorylated histone H2AX Serl39 antibody; Upstate 05-636) diluted 1:250 in block buffer. The cells are then washed five times in wash buffer before incubation for 1h at room temperature in the dark in a mixture of secondary antibody (goat ouse Alexa Fluor 488 conjugated dy; Invitrogen A11029) and Hoechst stain rogen H3570); diluted 1:500 and 1:5000, tively, in wash buffer. The cells are then washed five times in wash buffer and finally 100ul PBS is added to each well before imaging.

PCTIU52012/058127 Cells are imaged for Alexa Fluor 488 and Hoechst intensity using the BD Pathway 855 Bioimager and Attovision software (BD Biosciences, Version 1.6/855) to fy phosphorylated H2AX Serl39 and DNA staining, respectively. The percentage of orylated H2AX-positive nuclei in a montage of 9 images at 20x magnification is then calculated for each well using BD Image Data Explorer software (BD Biosciences Version 2.2.15). Phosphorylated H2AX-positive nuclei are defined as Hoechst—positive regions of interest containing Alexa Fluor 488 intensity at 1.75—fold the average Alexa Fluor 488 intensity in cells not treated with hydroxyurea. The percentage ofH2AX positive nuclei is finally plotted against concentration for each compound and ICSOs for ellular ATR inhibition are ined using Prism software (GraphPad Prism version 3.ch for Macintosh, GraphPad Software, San Diego California, USA).

The compounds described herein can also be tested according to other methods known in the art (5% Sarkaria et a1, “Inhibition ofATM and ATR Kinase Activities by the Radiosensitizing Agent, Caffeine: Cancer Research 59: 4375—5382 (1999); Hickson et al, “Identification and Characterization of a Novel and Specific Inhibitor of the Ataxia- iectasia Mutated Kinase ATM” Cancer ch 64: 9152-9159 (2004); Kim et a1, “Substrate cities and Identification of Putative Substrates of ATM Kinase Family Members” The Journal ofBiological Chemistry, 274(53): 37538-37543 (1999); and Chiang et a1, “Determination of the catalytic activities of mTOR and other members of the phosphoinositide-3—kinase—related kinase family” Methods M01. Biol. 281 :125—41 (2004)).

Example 16: ATR Inhibition Assay: ] Compounds can be screened for their ability to inhibit ATR kinase using a radioactive—phosphate incorporation assay. Assays are d out in a mixture of SOmM Tris/HCl (pH 7.5), lOmM MgClz and 1mM DTT. Final substrate concentrations are lOuM [y—33P]ATP (3mCi 33P ATP/mmol ATP, Perkin Elmer) and 800 uM target peptide (ASELPASQPQPFSAKKK).

Assays are carried out at 25°C in the presence of 5 nM full—length ATR. An assay stock buffer solution is prepared containing all of the reagents listed above, with the exception of ATP and the test compound of interest. 13.5 pL of the stock solution is placed in a 96 well plate followed by addition of 2 pL of DMSO stock containing serial dilutions of the test compound ally ng from a final concentration of 15 uM with 3-fold serial dilutions) in duplicate (final DMSO concentration 7%). The plate is cubated for 10 minutes at 25°C and the reaction initiated by addition of 15 uL [y—33P]ATP (final WO 49726 2012/058127 tration 10 uM).

The reaction is stopped after 24 hours by the addition of 30uL 0.1M phosphoric acid containing 2mM ATP. A multiscreen phosphocellulose filter 96-well plate (Millipore, Cat no. MAPHNOBSO) is pretreated with IOOuL 0.2M phosphoric acid prior to the addition of 45uL of the stopped assay mixture. The plate is washed with 5 x 200nL 0.2M phosphoric acid. After drying, 100 uL Optiphase ‘SuperMix’ liquid llation il (Perkin Elmer) is added to the well prior to scintillation counting (1450 Microbeta Liquid Scintillation r, Wallac).

After ng mean background values for all of the data points, Ki(app) data are calculated from non—linear regression analysis of the l rate data using the Prism re package (GraphPad Prism version 3.0cx for Macintosh, GraphPad Software, San Diego California, USA).

In general, the compounds of the present invention are effective for inhibiting ATR.

Compounds I-l, 1—2, 11—1, 11-2, 11-3 and 11—4 inhibit ATR at Ki values below 0.001 pM.

Example 17: Cisplatin Sensitization Assay Compounds can be screened for their ability to sensitize HCT116 colorectal cancer cells to Cisplatin using a 96h cell viability (MTS) assay. HCTI 16 cells, which possess a defect in ATM signaling to Cisplatin (s_e_e, Kim et al.; Oncogene 21 :3864 (2002); m, Takemura et al.; JBC 281230814 (2006)) are plated at 470 cells per well in 96-well polystyrene plates (Costar 3596) in 150g] of McCoy’s 5A media (Sigma M8403) supplemented with 10% foetal bovine serum (JRH Biosciences 12003), Penicillin/Streptomycin solution diluted 1:100 (Sigma P7539), and 2mM L—glumtamine (Sigma 67513), and allowed to adhere overnight at 37°C in 5% C02. Compounds and Cisplatin are then both added simultaneously to the cell media in 2—fold serial dilutions from a top final concentration of IOuM as a full matrix of concentrations in a final cell volume of 200ul, and the cells are then incubated at 37°C in 5% C02. After 96h, 40ul ofMTS reagent (Promega G358a) is added to each well and the cells are incubated for 111 at 37°C in 5% C02.

Finally, absorbance is measured at 490nm using a SpectraMax Plus 384 reader (Molecular Devices) and the concentration of compound required to reduce the ICSO of tin alone by at least 3—fold (to 1 decimal place) can be reported.

PCT/U52012/058127 Example 18: Single Agent HCT116 Activity Compounds can be screened for single agent activity against HCT116 ctal cancer cells using a 96h cell viability (MTS) assay. HCTl 16 are plated at 470 cells per well in 96—well polystyrene plates (Costar 3596) in 150m of McCoy’s 5A media (Sigma M8403) supplemented with 10% foetal bovine serum (JRH Biosciences , Penicillin/ Streptomycin solution diluted 1:100 (Sigma P7539), and 2mM tamine (Sigma G7513), and allowed to adhere overnight at 37°C in 5% C02. Compounds are then added to the cell media in 2—fold serial dilutions from a top final concentration of lOuM as a full matrix of concentrations in a final cell volume of 2001,11, and the cells are then ted at 37°C in 5% 002. After 96h, 40m ofMTS reagent (Promega G35 8a) is added to each well and the cells are incubated for lh at 37°C in 5% C02. Finally, ance is measured at 490nm using a SpectraMax Plus 384 reader (Molecular Devices) and IC50 values can be calculated. _________pl___esData for Exam 18-21 Cisplatin sensitization While we have described a number of ments of this invention, it is apparent that our basic examples may be altered to provide other embodiments that utilize the compounds, methods, and processes 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 herein.

Claims (5)

1. A solid form of a compound of a I-2: wherein the form is crystalline Compound I-2 free base.

2. The solid form of claim 1, having a monoclinic crystal system, having a P21/n space group, and having the following unit cell dimensions in Å when measured at 120K: a = 8.9677 (1) Å b = 10.1871 (1) Å c = 24.5914 (3) Å.

3. The solid form of claim 1 or 2, characterized by a weight loss of from about 1.9 % in a temperature range of from about 25 °C to about 215 °C.

4. The solid form of any one of claims 1-3, characterized by one or more peaks expressed in 2-theta ± 0.2 at about 14.2, 25.6, 18.1, 22.0, and 11.1 degrees in a X-ray powder diffraction n obtained using Cu K alpha radiation.

5. The solid form of any one of claims 1-4, characterized as having an X-ray powder diffraction n substantially the same as that shown in