Synthetic methods for preparation of 4-(2-chloro-4-methoxy-5-methylphenyl)-n-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-n-prop-2-ynyl-1,3-thiazol-2-amine

Abstract

The present disclosure relates to the fields of chemistry and medicine, more particularly to processes for making 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2 -cyclopropyl-1-(3 -fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-1,3-thiazol-2-amine (Compound 1), pharmaceutically acceptable salts, and crystalline forms thereof, for the treatment of congenital adrenal hyperplasia (CAH).

Description

[0001] SYNTHETIC METHODS FOR PREPARATION OF 4-(2-CHLORO-4-METHOXY-5- METHYLPHENYL)-N-[(1S)-2-CYCLOPROPYL-1-(3-FLUORO-4- METHYLPHENYL)ETHYL]-5-METHYL-N-PROP-2-YNYL-l,3-THIAZOL-2-AMINE

[0002] FIELD OF THE INVENTION

[0003] The present disclosure relates to the fields of chemistry and medicine, more particularly to processes for making 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4- methylphenyl )ethyl] -5-methyl-N-prop-2-ynyl- 1 ,3-thiazol-2-amine (Compound 1), pharmaceutically acceptable salts, and crystalline forms thereof, for the treatment of congenital adrenal hyperplasia (CAH).

[0004] BACKGROUND OF THE INVENTION

[0005] Classic congenital adrenal hyperplasia (CAH) is a disease that includes a group of autosomal recessive disorders that result in an enzyme deficiency that alters the production of adrenal steroids due to 21 -hydroxylase deficiency, a condition that results in little or no cortisol biosynthesis. One clinical manifestation of the absence of cortisol is the lack of feedback inhibition of pituitary adrenocorticotropic hormone (ACTH) secretion. Increased ACTH levels cause adrenal hyperplasia and the enzyme mutation causes a shunting of cortisol precursor steroids to alternate pathways. Most notably, the shunting of androgens leads to virilization and other developmental complications in females and the over-accumulation of ACTH is associated with the formation of testicular adrenal rest tumors in males. In addition, since the same enzyme (21 -hydroxylase) is used in the pathway for the biosynthesis of the mineralocorticoids, a number of these patients suffer from aldosterone deficiency which can result in dehydration and death due to salt-wasting. The prevalence of classic 21- hydroxylase deficiency CAH in the US general population, based on newborn screening, has been documented as 1:10,000 to 1:20,800 (Trakakis et al., “An update to 21 -hydroxylase deficient congenital adrenal hyperplasia,” Gynecol. Endocrinol. (2010) 26(1):63-71; Hertzberg et al., “Birth prevalence rates of newborn screening disorders in relation to screening practices in the United States,” / . Pediatr. (2011) 159(4):555-560).

[0006] Pediatric patients from birth through adolescence, and females in particular, appear to be the most vulnerable population of CAH sufferers and represent the subgroup of patients with the greatest unmet medical need (Cheng and Speiser, “Treatment outcomes in congenital adrenal hyperplasia,”

[0007] Adv. Pediatr. (2012) 59(1):269-281; Merke and Poppas, “Management of adolescents with congenital adrenal hyperplasia,” Lancet Diabetes Endocrinol. (2013) 1(4):341 -352). Excessive androgen production in these younger patients results in early onset puberty and adrenarche, changes in skeletal maturation patterns, short stature caused by premature growth plate fusion, as well as significant hirsutism and acne problems. While survival is properly ensured through steroid replacement strategies based on physiologic dosing of glucocorticoids (e.g., hydrocortisone) and mineralocorticoids (e.g., fludrocortisone), these doses are often inadequate to suppress the accumulating ACTH and overproduction of progestogens and androgens (e.g., 17-hydroxyprogesterone [17-OHP], androstenedione, and testosterone). The uncontrolled symptoms of androgen excess, indeed, have a substantial impact on the day-to-day functioning and development of these patients.

[0008] Currently, exogenous corticosteroids are the standard of care for treating patients with classic CAH. This treatment is used to correct the cortisol deficiency and reduce the excessive ACTH levels and androgen excess. However, the dose and duration of steroid use required to suppress ACTH are typically well above the normal physiological level used for cortisol replacement alone (as in patients with Addison’s disease). This increased exposure to glucocorticoids can lead to iatrogenic Cushing’s syndrome, increased cardiovascular risk factors, glucose intolerance, reduced growth velocity, and decreased bone mineral density in CAH patients (Elnecave et al, “Bone mineral density in girls with classical congenital adrenal hyperplasia due to CYP21 deficiency,” J. Pediatr. Endocrinol. Metab. (2008) 21(12): 1155-1162; King et al., “Long-term corticosteroid replacement and bone mineral density in adult women with classical congenital adrenal hyperplasia,” J. Clin. Endocrinol. Metab. (2006) 91(3):865-869; and Migeon and Wisniewski, “Congenital adrenal hyperplasia owing to 21- hydroxylase deficiency. Growth, development, and therapeutic considerations,” Endocrinol Metab. Clin. North Am. (2001) 30(1): 193-206).

[0009] It has been demonstrated in clinical trials that orally active compounds that block CRFi, such as 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[( 1S)-2-cyclopropyl- l-(3-fluoro-4-methylphenyl)ethyl]- 5-methyl-JV-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1), provide a reduction from baseline in 17- hydroxyprogesterone ( 17-OHP) and androstenedione levels in amounts believed to allow use of lower, more physiologic doses of glucocorticoid (e.g. hydrocortisone) in patients with CAH. The structure of Compound 1 is shown below:

[0010] Compound 1 Accordingly, a significant need exists for efficient methods for the preparation of 4-(2-chloro- 4-methoxy-5 -methylphenyl)-N-[( 1S)-2-cyclopropyl- 1 -(3 -fluoro-4-methylphenyl)ethyl] -5 -methyl-N- prop-2-ynyl- 1,3-thiazol -2-amine (Compound 1) to support further clinical trials and commercial efforts.

[0011] SUMMARY OF THE INVENTION

[0012] The present invention provides, inter alia, processes for the preparation of 4-(2-chloro-4- methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1) and intermediates related thereto.

[0013] The processes and intermediates of the present invention are useful in preparing 4-(2-chloro-4- methoxy-5-methylphenyl)-N-[(15)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1), pharmaceutical salts, crystalline forms, and pharmaceutical compositions that are useful in the treatment of corticotropin releasing factor 1 (CRFi) receptor-mediated disorders.

[0014] One aspect of the present invention pertains to processes for preparing 4-(2-chloro-4-methoxy- 5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl- 1,3-thiazol -2-amine (Compound 1) or a pharmaceutically acceptable salt thereof: comprising: alkylating (S)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A) or a salt thereof: with a Compound of Formula (Ii): wherein: LG is a leaving group; in the presence of an alkylating-step solvent, a phase-transfer catalyst, an alkylating-step base, and water to form 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1) or a pharmaceutically acceptable salt thereof.

[0015] One aspect of the present invention pertains to processes for preparing (S)-4-(2-chloro-4- methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2- amine (Compound 9A) or a salt thereof: comprising: cyclizing (5)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-l -amine (Compound 6A) or a salt thereof: with l-(2-chloro-4-methoxy-5-methylphenyl)-2-thiocyanatopropan-1-one (Compound 8A) or a tautomeric form thereof: in the presence of a cyclizing-step solvent to form (S)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A) or a salt thereof.

[0016] One aspect of the present invention pertains to processes for preparing (5)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethan-l -amine (Compound 6A) or a salt thereof: comprising: deprotecting a Compound of Formula (Ig), or a salt thereof, wherein:

[0017] R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen; in the presence of a deprotec ting-catalyst, hydrogen, and a deprotecting-step solvent to form (S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-amine (Compound 6A) or a salt thereof.

[0018] One aspect of the present invention pertains to processes for preparing a Compound of Formula (Ig), or a salt thereof, wherein:

[0019] R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen; comprising: comprising: reacting 2-cyclopropyl-N-methoxy-N-methylacetamide (Compound 2A): with an organomagnesium reagent of 4-bromo-2-fluoro- 1 -methylbenzene in the presence of a reacting- step solvent to form 2-cycloprOpyl-1-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A).

[0020] One aspect of the present invention pertains an anhydrous crystalline form of 4-(2-chloro-4- methoxy-5 -methylpheny l)-N-[( 1 S)-2-cyclopropyl- 1 -(3-fluoro-4-methylpheny l)ethy 1] -5 -methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1, free base).

[0021] One aspect of the present invention pertains to an anhydrous crystalline form of 4-(2-chloro-4- methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1, tosylate salt).

[0022] One aspect of the present invention pertains to pharmaceutical compositions comprising a crystalline form (Compound 1, free base) as described herein, and a pharmaceutically acceptable earner.

[0023] One aspect of the present invention pertains to pharmaceutical products selected from: a pharmaceutical composition, a formulation, a unit dosage form, and a kit; each comprising a crystalline form (Compound 1, free base) as described herein.

[0024] One aspect of the present invention pertains to pharmaceutical compositions comprising a crystalline form (Compound 1, tosylate salt) as described herein, and a pharmaceutically acceptable carrier.

[0025] One aspect of the present invention pertains to pharmaceutical products selected from: a pharmaceutical composition, a formulation, a unit dosage form, and a kit; each comprising a crystalline form (Compound 1, tosylate salt) as described herein.

[0026] One aspect of the present invention pertains to compositions comprising: a. 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1), or a pharmaceutically acceptable salt thereof; and b. at least one compound selected from:

[0027] (S)-4-(2-chloro-4-methoxy-5 -methylphenyl)-N-(2-cyclopropyl- 1 -(3 -fluoro-4- methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A);

[0028] (S)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(p-tolyl)ethyl)-5-methyl-N- (prop-2-yn- 1 -y l)thiazol-2-amine (Compound Ha);

[0029] (S)-4-(2-chloro-5 -methyl-4-(prop-2-yn- 1 -y loxy)phenyl)-N-(2-cyclopropyl- 1 -(3-fluoro-4- methy lphenyl)ethyl)-5 -methyl-N-(prop-2-yn- 1 -yl)thiazol-2-amine (Compound lib);

[0030] 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1R )-2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-(2-propyn-1-yl)-2-thiazolamine (Compound IIc ); ethanol; and propargyl bromide.

[0031] One aspect of the present invention pertains to methods of treating a disorder in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a crystalline form (Compound 1, free base) as described herein; a crystalline form (Compound 1, tosylate salt) as described herein; Compound 1 (with high e.e.%), or a pharmaceutically acceptable salt thereof as described herein; a pharmaceutical composition as described herein; a pharmaceutical product as described herein; or a composition as described herein; wherein the subject has abnormal levels of CRFi.

[0032] One aspect of the present invention pertains to methods of treating a Corticotropin Releasing Factor 1 (CRFi) disorder in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a crystalline form (Compound 1, free base) as described herein; a crystalline form (Compound 1, tosylate salt) as described herein; Compound 1 (with high e.e.%), or a pharmaceutically acceptable salt thereof as described herein; a pharmaceutical composition as described herein; a pharmaceutical product as described herein; or a composition as described herein.

[0033] One aspect of the present invention pertains to methods of treating congenital adrenal hyperplasia (CAH), in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a crystalline form (Compound 1, free base) as described herein; a crystalline form (Compound 1, tosylate salt) as described herein; Compound 1 (with high e.e.%), or a pharmaceutically acceptable salt thereof as described herein; a pharmaceutical composition as described herein; a pharmaceutical product as described herein; or a composition as described herein. In some embodiments, the congenital adrenal hypoplasia is classic congenital adrenal hypoplasia. In some embodiments, the method fiirtho comprises administering to the subject a glucocorticoid. In some embodiments, the glucocorticoid is hydrocortisone. One aspect of the present invention pertains to uses of an anhydrous crystalline form (Compound 1, free base) as described herein; the crystalline form (Compound 1, tosylate salt) as described herein; or Compound 1 (with high e.e.%), or a pharmaceutically acceptable salt thereof as described herein; for the manufacture of a medicament for the treatment of a subject wherein the subject has abnormal levels of CRFi.

[0034] One aspect of the present invention pertains to uses of an anhydrous crystalline form (Compound 1, free base) as described herein; the crystalline form (Compound 1, tosylate salt) as described herein; or Compound 1 (with high e.e.%), or a pharmaceutically acceptable salt thereof as described herein; for the manufacture of a medicament for the treatment of a Corticotropin Releasing Factor 1 (CRFi) disorder.

[0035] One aspect of the present invention pertains to uses of an anhydrous crystalline form (Compound 1, free base) as described herein; the crystalline form (Compound 1, tosylate salt) as described herein; or Compound 1 (with high e.e.%), or a pharmaceutically acceptable salt thereof as described herein; for the manufacture of a medicament for the treatment of congenital adrenal hyperplasia (CAH). In some embodiments, the congenital adrenal hypoplasia is classic congenital adrenal hypoplasia. In some embodiments, the treatment of congenital adrenal hyperplasia comprises administering a glucocorticoid. In some embodiments, the medicament is formulated for administration with a glucocorticoid. In some embodiments, the glucocorticoid is hydrocortisone.

[0036] One aspect of the present invention pertains to an anhydrous crystalline form (Compound 1, free base) as described herein; a crystalline form (Compound 1, tosylate salt) as described herein; Compound 1 (with high e.e.%), or a pharmaceutically acceptable salt thereof as described herein; a pharmaceutical composition as described herein; a pharmaceutical product as described herein; or a composition as described herein; for use in a method of treatment of the human or animal body by therapy.

[0037] One aspect of the present invention pertains to an anhydrous crystalline form (Compound 1, free base) as described herein; a crystalline form (Compound 1, tosylate salt) as described herein; Compound 1 (with high e.e.%), or a pharmaceutically acceptable salt thereof as described herein; a pharmaceutical composition as described herein; a pharmaceutical product as described herein; or a composition as described herein; for use in a method of treatment of a disorder in a subject wherein the subject has abnormal levels of CRFi.

[0038] One aspect of the present invention pertains to an anhydrous crystalline form (Compound 1, free base) as described herein; a crystalline form (Compound 1, tosylate salt) as described herein; Compound 1 (with high e.e.%), or a pharmaceutically acceptable salt thereof as described herein; a pharmaceutical composition as described herein; a pharmaceutical product as described herein; or a composition as described herein; for use in a method of treatment of a Corticotropin Releasing Factor 1 (CRFi) disorder.

[0039] One aspect of the present invention pertains to an anhydrous crystalline form (Compound 1, free base) as described herein; a crystalline form (Compound 1, tosylate salt) as described herein; Compound 1 (with high e.e.%), or a pharmaceutically acceptable salt thereof as described herein; a pharmaceutical composition as described herein; a pharmaceutical product as described herein; or a composition as described herein; for use in a method of treating congenital adrenal hyperplasia (CAH). In some embodiments, the congenital adrenal hyperplasia is classic congenital adrenal hyperplasia. In some embodiments, the method of treating congenital adrenal hyperplasia comprises administering a glucocorticoid. In some embodiments, the glucocorticoid is hydrocortisone.

[0040] One aspect of the present invention pertains to Compounds of Formula (Ie): wherein:

[0041] R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen.

[0042] One aspect of the present invention pertains to Compounds of Formula (Ig) or a salt thereof: wherein:

[0043] R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen.

[0044] One aspect of the present invention pertains to processes for preparing a pharmaceutical composition comprising admixing a crystalline form (Compound 1, free base) as described herein; a crystalline form (Compound 1, tosylate salt) as described herein; or a composition according as described herein; and a pharmaceutically acceptable carrier.

[0045] These and other aspects of the invention disclosed herein will be set forth in greater detail as the patent disclosure proceeds.

[0046] BRIEF DESCRIPTION OF THE FIGURES FIG. 1 shows an exemplary X-ray powder diffraction (XRPD) pattern for a sample of crystalline Form I of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl- l-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1) prepared according to Example 3.

[0047] FIG.2 shows an exemplary Differential Scanning Calorimetry (DSC) and Thermogravimetric Analysis (TGA) thermograms for a sample of crystalline Form I of 4-(2-chloro-4-methoxy-5- methylphenyl)-N-[( 1 S)-2-cyclopropyl- 1 -(3 -fluoro-4-methylpheny l)ethy 1] -5-methyl-N-prop-2-y ny 1- 1,3- thiazol-2-amine (Compound 1) prepared according to Example 3.

[0048] FIG.3 shows an exemplary Gravimetric Vapor Sorption (GVS) for a sample of crystalline Form I of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[( 15)-2-cyclopropyl- l-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1) as described in Example 4.

[0049] FIG.4 shows general synthetic schemes for the preparation of l-(2-chloro-4-methoxy-5- methylphenyl)-2-thiocyanatopropan-1-one (Compound 8A), 4-chloro-2-(methoxy-13C-d3)-1- methylbenzene (Compound 7A’), and l-(2-chloro-4-(methoxy-13C-d3)-5-methylphenyl)-2- thiocyanatopropan-1-one (Compound 8A’). The synthesis of l-(2-chloro-4-methoxy-5- methylphenyl)-2-thiocyanatopropan- 1 -one (Compound 8A) has previously been described in International Publication Number W02010 / 125414 by Sanofi-Aventis.

[0050] FIG.5 shows a general scheme for the preparation of 4-(2-chloro-4-methoxy-5- methylphenyl)-N- [(1S)-2-cyclopropyl- 1 -(3 -fluoro-4-methylpheny l)ethy 1] -5-methyl-N-prop-2-y ny 1- 1,3- thiazol-2-amine (Compound 1).

[0051] FIG.6 shows a general scheme for the preparation of (S)-4-(2-chloro-4-(methoxy-13C-d3)-5- methylphenyl)-N-(2-cyclopropyl- 1 -(3 -fluoro-4-methy lphenyl)ethyl)-5 -methyl-N-(prop-2-y n- 1 - yl)thiazol-2-amine (Compound 3).

[0052] FIG.7 shows an exemplary X-ray powder diffraction (XRPD) pattern for a sample of crystalline Form I of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[( 1S)-2-cyclopropyl- l-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1). FIG.8 shows an overlay of the exemplary X-ray powder diffraction (XRPD) patterns from Figure 1 and Figure 7 for crystalline Form I of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1), and although the intensities for certain peaks are rather dramatic, the overlay clearly shows substantially the same peak positioning.

[0053] FIG. 9 shows an exemplary X-ray powder diffraction (XRPD) pattern for a sample of crystalline (S)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A).

[0054] FIG. 10 shows an exemplary Differential Scanning Calorimetry (DSC) and Thermogravimetric Analysis (TGA) thermograms for a sample of crystalline (S)-4-(2-chloro-4- methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2- amine (Compound 9A).

[0055] FIG. 11 shows an exemplary X-ray powder diffraction (XRPD) pattern for a sample of crystalline l-(2-chloro-4-methoxy-5-methylphenyl)-2-thiocyanatopropan-1-one (Compound 8A).

[0056] FIG. 12 shows an exemplary Differential Scanning Calorimetry (DSC) and Thermogravimetric Analysis (TGA) thermograms for a sample of crystalline l-(2-chloro-4-methoxy- 5-methylphenyl)-2-thiocyanatopropan-1-one (Compound 8A).

[0057] FIG. 13 shows an exemplary X-ray powder diffraction (XRPD) pattern for a sample of crystalline (S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)etlian-1-amine (Compound 6A, HC1 salt).

[0058] FIG. 14 shows an exemplary Differential Scanning Calorimetry (DSC) and Thermogravimetric Analysis (TGA) thermograms for a sample of crystalline (S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethan-l -amine (Compound 6A, HC1 salt).

[0059] FIG. 15 shows an exemplary X-ray powder diffraction (XRPD) pattern for a sample of crystalline 2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A).

[0060] FIG. 16 shows an exemplary Differential Scanning Calorimetry (DSC) and Thermogravimetric Analysis (TGA) thermograms for a sample of crystalline 2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethan-1-one (Compound 3A).

[0061] FIG. 17 shows an exemplary X-ray powder diffraction (XRPD) pattern for a sample of (S)-2- cyclopropyl- 1 -(3 -fluoro-4-methylphenyl)-N-((S)- 1 -pheny lethyl)ethan- 1 -amine (Compound 5A, HC1 salt).

[0062] FIG. 18 shows an exemplary Differential Scanning Calorimetry (DSC) and Thermogravimetric Analysis (TGA) thermograms for a sample of (S)-2-cyclopropyl-1-(3-fluoro-4- methylphenyl)-N-((S)- 1 -phenylethyl)ethan- 1 -amine (Compound 5A, HC1 salt). FIG. 19 shows the dissolution performance of several spray-dried dispersion formulations in 0.5 wt% simulated intestinal fluid (SIF) in phosphate buffered saline (PBS), pH 6.5.

[0063] FIG.20 shows the vertical membrane flux cell integrated in the pDiss Profiler™ used for the membrane flux assay.

[0064] FIG.21 shows non-sink dissolution data for several spray-dried dispersion formulations and Compound 1 in 0.5 wt% SIF in PBS, pH 6.5.

[0065] FIG.22 is a graph showing membrane flux of 1 mg / mL GB / IB 0.5 wt% SIF doses of Compound 1 and various spray-dried dispersion formulations over time. The solid lines indicate flux (pg min-1 cm-2) and the broken lines indicate concentration (pg / mL) in 0.5% SIF.

[0066] FIG.23 is a flow diagram of the spray drying manufacturing process used to prepare a 1000 g batch of an SDD containing 25% of Compound 1 and 75% PVP / VA 64.

[0067] FIG.24 shows an exemplary X-ray powder diffraction (XRPD) pattern for a sample of crystalline Form I of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[( 1S)-2-cyclopropyl- l-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1, tosylate salt).

[0068] FIG.25 shows an exemplary Differential Scanning Calorimetry (DSC) and Thermogravimetric Analysis (TGA) thermograms for a sample of crystalline Form I of 4-(2-chloro-4- methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1, tosylate salt).

[0069] DETAILED DESCRIPTION OF THE INVENTION

[0070] DEFINITIONS

[0071] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure belongs. Methods and materials are described herein for use in the present disclosure; other, suitable methods and materials known in the art can also be used. The materials, methods, and examples are illustrative only and not intended to be limiting. All publications, patent applications, patents, sequences, database entries, and other references mentioned herein are incorporated by reference in their entirety. In case of conflict, the present specification, including definitions, will control.

[0072] The term “about” preceding a temperature have an allowable variability of ±5°C. In all other instances, unless otherwise specified, the term “about” preceding a stated value includes the stated value and also includes ±20% of the stated value, and includes more specifically values of ±10%,

[0073] ±5%, ±2%, and ±1% of the stated value. To provide a more concise description, some of the quantitative expressions herein are recited as a range from about amount X to about amount Y. It is understood that when a range is recited, the range is not limited to the recited upper and lower bounds, but rather includes the full range from about amount X through about amount Y, or any range therein.

[0074] As used herein, “room temperature”, or “RT”, refers to the ambient temperature of a typical laboratory, which is generally around 25°C.

[0075] As used herein, “administration”, or “administering”, refers to a method of giving a dosage of a compound or pharmaceutical formulation to a vertebrate or invertebrate, including a mammal, a bird, a fish, or an amphibian. The preferred method of administration can vary depending on various factors, e.g., the components of the pharmaceutical formulation, the site of the disease, and the severity of the disease.

[0076] The term “C6-C10 aryl” refers to a saturated ring system containing 6 to 10 carbon atoms that can contain a single ring or two fused rings and is aromatic, such as phenyl and naphthalenyl. When one or more substituents are present on the “aryl” ring, the substituent(s) can be bonded at any available ring carbon.

[0077] The term “C1-C6 alkyl” and “C1-C4 alkyl” refers to a saturated straight or branched carbon radical containing 1 to 6 carbons (i.e., “C1-C6 alkyl”) or 1 to 4 carbons (i.e., “C1-C4 alkyl”). Some embodiments are 1 to 5 carbons (i.e., C1-C5 alkyl), some embodiments are 1 to 3 carbons (i.e., C1-C3 alkyl), and some embodiments are 1 or 2 carbons. Examples of an alkyl group include: methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, pentyl, isopentyl, tert-pentyl, neo- pentyl,

[0078] 1-methylbutyl [z.e., the like.

[0079] The term “C1-C4alkylsulphonyloxy” refers to a radical consisting of a C1-C4alkyl group attached directly to the sulfur of an SO3group. The “C1-C4alkylsulphonyloxy” group can be represented by the formula: C1-C4 alky1S(=0)20- or the following:

[0080] The term C1-C4alkyl has the same definition as found herein. Examples include: methanesulfonate [CH3S(=0)2C)-, or (methylsulfonyl)oxy] , ethanesulfonate, propanesulfonate, isopropylsulfonate, butanesulfonate, and the like.

[0081] The term “C1-C6 alkoxy” refers to a radical consisting of a C1-C6 alkyl group attached directly to an oxygen atom, wherein C1-C6 alkyl has the same definition as found herein. Some embodiments contain 1 to 5 carbons (i.e., C1-C5alkoxy). Some embodiments contain 1 to 4 carbons (i.e., C1-C4 alkoxy). Some embodiments contain 1 to 3 carbons (i.e., C1-C3 alkoxy). Some embodiments contain 1 or 2 carbons. Examples include: methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, r-butoxy, isobutoxy, sec-butoxy, and the like.

[0082] The term “amorphous” means a solid that is in a non-crystalline state. Amorphous solids are disordered arrangements of molecules and therefore possess no distinguishable crystal lattice or unit cell and consequently have no definable long-range ordering. The solid-state form of a solid can be determined by polarized light microscopy, X-ray powder diffraction (XRPD), differential scanning calorimetry (DSC), or other standard techniques known to those of skill in the art.

[0083] The term “C6-C10 arylsulfonyloxy” refers to a radical consisting of an aryl group attached directly to the sulfur atom of an SO3group and can be represented by the formula aryl-S(=0)20- or the following:

[0084] The term aryl has the same definition as found herein. Examples include: benzenesulfonate [PhS(=0)2O-, or (phenylsulfonyl)oxy, besylate], (naphthalen- l-ylsulfonyl)oxy, and (naphthalen-2- ylsulfonyl)oxy.

[0085] The term “composition” refers to a compound or crystalline form thereof, including but not limited to, salts, solvates, and hydrates of a compound of the present invention, in combination with at least one additional component, such as, a composition obtained / prepared during synthesis, preformulation, in-process testingZcontrol (e.g., TLC, HPLC, NMR samples), and the like.

[0086] The term “% crystallinity” or “crystalline purity” refers to the percentage of a crystalline form in a preparation or sample. It is understood that the preparation or sample may contain other forms, such as, an amorphous form of the same compound, or different crystalline form(s) of the same compound, or mixtures thereof. In some embodiments, the crystalline form can be isolated as the desired form (i.e., the crystalline form as described herein) with a crystalline purity of at least about 75% by weight, about 80% by weight, about 85% by weight, about 90% by weight, about 95% by weight, about 96% by weight, about 97% by weight, about 98% by weight, or about 99% by weight.

[0087] In some embodiments, the crystalline form can be isolated with a purity of about 90% or greater by weight. In some embodiments, the crystalline form can be isolated with a purity of about 95% or greater by weight. In some embodiments, the crystalline form can be isolated with a purity of about 99% or greater by weight.

[0088] When describing particle size for a sample, “DIO” , “D50” , “D90” are used and have the following definitions: the term “DIO” as used herein means that 10% of the particles (based on volume) are smaller than or equal to the indicated size; the term “D50” as used herein means that 50% of the particles (based on volume) are smaller than or equal to the indicated size; and the term “D90” as used herein means that 90% of the particles (based on volume) are smaller than or equal to the indicated size. As an example, when a sample as a D10 of 21 μΜ, then 10% of the particles in that sample are smaller than or equal to 21 μΜ based on volume.

[0089] The term “enantiomeric excess” or “e.e.%” refers to the excess of one enantiomer over the other enantiomer as a percentage of the whole, and is a measure of the enantiomeric (chiral) purity of a sample which contains the enantiomer. For example, if a sample contains an excess of the R- enantiomer, then the e.e.% can be determined from the expression:

[0090] Similarly, if a sample contains an excess of the 5-enantiomer, then the e.e.% can be determined from the expression: where ARand As in the above two expressions above are the amounts of the R- and 5-enantiomers in the sample, respectively. The amount of the enantiomers can be determined by any method known in the art, for example, chiral HPLC, such as the method described in Example 9.

[0091] The term “high e.e.%” refers to an e.e.% of a compound that is at least 99.3%, 99.4%, 99.5%, 99.6%, 99.7%, 99.8%, 99.9%, 100%, or a range defined by any of the preceding values, such as 99.3% to 99.9%. In some embodiments, “high e.e.%” is at least 99.3%. In some embodiments, “high e.e.%” is at least 99.4%. In some embodiments, “high e.e.%” is at least 99.5%. In some embodiments, “high e.e.%” is at least 99.6%. In some embodiments, “high e.e.%” is at least 99.7%. In some embodiments, “high e.e.%” is at least 99.8%. In some embodiments, “high e.e.%” is at least 99.9%. In some embodiments, “high e.e.%” is 99.3%. In some embodiments, “high e.e.%” is 99.4%. In some embodiments, “high e.e.%” is 99.5%. In some embodiments, “high e.e.%” is 99.6%. In some embodiments, “high e.e.%” is 99.7%. In some embodiments, “high e.e.%” is 99.8%. In some embodiments, “high e.e.%” is 99.9%. In some embodiments, “high e.e.%” is 100%.

[0092] The term “in need of treatment” and the term “in need thereof” when referring to treatment are used interchangeably to mean a judgment made by a caregiver (e.g. physician, nurse, nurse practitioner, etc. in the case of humans; veterinarian in the case of animals, including non-human mammals) that an individual or animal requires or will benefit from treatment. This judgment is made based on a variety of factors that are in the realm of a caregiver's expertise, but that includes the knowledge that the individual or animal is ill, or will become ill, as the result of a disease, condition or disorder that is treatable by the compounds of the invention. Accordingly, the compounds of the invention can be used in a protective or preventive manner; or compounds of the invention can be used to alleviate, inhibit, or ameliorate the disease, condition, or disorder.

[0093] The term “halo” or “halogen” refers to fluoro, chloro, bromo, or iodo. In some embodiments, halogen is chloro, bromo, or iodo. In some embodiments, halogen is fluoro, chloro, or bromo. In some embodiments, halogen is fluoro. In some embodiments, halogen is chloro. In some embodiments, halogen is bromo. In some embodiments, halogen is iodo.

[0094] The term “C1-C6 haloalkyl” refers to a radical consisting of a C1-C6 alkyl group substituted with one or more halogens, wherein C1-C6 alkyl has the same definition as found herein. The C1-C6 haloalkyl may be fully substituted in which case it can be represented by the formula CnL2n+1, wherein L is a halogen and “n” is 1, 2, 3, 4, 5, or 6. When more than one halogen is present then they may be the same or different and selected from: fluorine, chlorine, bromine, and iodine. In some embodiments, haloalkyl contains 1 to 5 carbons (i.e., C1-C5 haloalkyl). In some embodiments, haloalkyl contains 1 to 4 carbons (i.e., C1-C4 haloalkyl). In some embodiments, haloalkyl contains 1 to 3 carbons (i.e., C1-C3 haloalkyl). In some embodiments, haloalkyl contains 1 or 2 carbons. Examples of haloalkyl groups include fluoromethyl, difluoromethyl, trifluoromethyl, chlorodifluoromethyl, 1- fluoroethyl, 2,2,2-trifluoroethyl, pentafluoroethyl, 4,4,4-trifluorobutyl, and the like.

[0095] The term “hydroxyl” refers to the group -OH.

[0096] The term “individual” or “subject” refers to any animal, including mammals, such as, mice, rats, other rodents, rabbits, dogs, cats, swine, cattle, sheep, horses, primates, and humans. In some embodiment “individual” refers to humans. In the context of a clinical trial or screening or activity experiment the subject may be a healthy volunteer or healthy participant without an underlying CFR- mediated disorder or condition or a volunteer or participant that has received a diagnosis for a disorder or condition in need of medical treatment as determined by a health care professional. In the context outside of a clinical trial a subject under the care of a health care professional who has received a diagnosis for a disorder or condition is typically described as a patient.

[0097] The term “inorganic base” refers to a base that does not include at least one C-H bond and includes at least one alkali metal or alkaline earth metal. Examples of an inorganic base include, but are not limited to, barium carbonate, calcium carbonate, cesium carbonate, lithium carbonate, magnesium carbonate, potassium carbonate, sodium carbonate, cesium hydrogen carbonate, potassium hydrogen carbonate, sodium hydrogen carbonate, barium hydroxide, calcium hydroxide, cesium hydroxide, lithium hydroxide, magnesium hydroxide, potassium hydroxide, sodium hydroxide, and the like.

[0098] As used herein, “leaving group” refers to an atom or a group of atoms that is displaced in a chemical reaction as a stable species. Suitable leaving groups are well known in the art, e.g., see, March’s Advanced Organic Chemistry, 5th Ed., Ed.: Smith, M. B. and March, J., John Wiley & Sons, New York: 2001 and T. W. Greene, Protective Groups in Organic Synthesis, 3rd Ed., John Wiley & Sons, New York, 1999. Such leaving groups include, but are not limited to, halogen, optionally substituted alkylsulphonyloxy, and optionally substituted arylsulfonyloxy. Examples of some leaving groups include chloro, bromo, iodo, mesylate, tosylate, triflate, nosylate, and brosylate.

[0099] The term “nitro” refers to the group -NO2.

[0100] The term “pediatric subject” refers to a subject under the age of 21 years at the time of diagnosis or treatment. The term “pediatric” can be further divided into various subpopulations including: neonates (from birth through the first month of life); infants (1 month up to two years of age); children (two years of age up to 12 years of age); and adolescents (12 years of age through 21 years of age (up to, but not including, the twenty-second birthday)) see e.g., Berhman et al., Textbook of Pediatrics, 15th Ed. Philadelphia: W.B. Saunders Company, 1996; Rudolph et al., Rudolph’s Pediatrics, 21st Ed. New York: McGraw-Hill, 2002; and Avery et al., Pediatric Medicine, 2nd Ed. Baltimore: Williams & Wilkins; 1994.

[0101] In some embodiments, a “pediatric subject” is from birth through the first 28 days of life, from 29 days of age to less than two years of age, from two years of age to less than 12 years of age, or 12 years of age through 21 years of age (up to, but not including, the twenty-second birthday). In some embodiments, a pediatric subject is from birth through the first 28 days of life, from 29 days of age to less than 1 year of age, from one month of age to less than four months of age, from three months of age to less than seven months of age, from six months of age to less than 1 year of age, from 1 year of age to less than 2 years of age, from 2 years of age to less than 3 years of age, from 2 years of age to less than seven years of age, from 3 years of age to less than 5 years of age, from 5 years of age to less than 10 years of age, from 6 years of age to less than 13 years of age, from 10 years of age to less than 15 years of age, or from 15 years of age to less than 22 years of age.

[0102] The phrase “pharmaceutically acceptable” refers to compounds (and salts thereof), compositions, and / or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit / risk ratio. The term “pharmaceutically acceptable carrier” or “pharmaceutically acceptable exdpient” includes any and all solvents, co-solvents, complexing agents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like, which are not biologically or otherwise undesirable. The use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active ingredient, its use in the therapeutic formulations is contemplated. Supplementary active ingredients can also be incorporated into the formulations. In addition, various excipients, such as are commonly used in the art, can be included. These and other such compounds are described in the literature, e.g., in the Merck Index, Merck & Company, Rahway, NJ. Considerations for the inclusion of various components in pharmaceutical compositions are described, e.g., in Gilman et al. (Eds.) (2010); Goodman and Gilman’s: The Pharmacological Basis of Therapeutics, 12th Ed., The McGraw-Hill Companies.

[0103] The term “pharmaceutical composition” refers to a specific composition comprising at least one active ingredient; including but not limited to, salts, solvates, and hydrates of compounds of the present invention, whereby the composition is amenable to investigation for a specified, efficacious outcome in a mammal (for example, without limitation, a human). Those of ordinary skill in the art will understand and appreciate the techniques appropriate for determining whether an active ingredient has a desired efficacious outcome based upon the needs of the artisan.

[0104] The term “phase-transfer catalyst” is any ionic catalyst, such as quaternary ammonium salts, that can enable the migration of a reactant from one phase into another phase where the reaction occurs. Suitable leaving groups are well known in the art. Examples include, acetylcholine chloride, (2-aminoethyl)trimethylammonium chloride hydrochloride, benzalkonium chloride, benzyldimethyldecylammonium chloride, benzyldimethyldodecylammonium chloride, benzyldimethylhexadecylammonium chloride, benzyldimethylhexylammonium chloride, benzyldimethyloctylammonium chloride, benzyldimethyltetradecylammonium chloride, benzyldodecyldimethylammonium bromide, benzyltributylammonium bromide, benzyltributylammonium chloride, benzyltributylammonium iodide, benzyltriethylammonium bromide, benzyltriethylammonium chloride, benzyltrimethylammonium bromide, benzyltrimethylammonium chloride, (3-carboxypropyl)trimethylammonium chloride, cetyltrimethylammonium chloride, cetyltrimethylammonium hydrogensulfate, choline chloride, decyltrimethylammonium bromide, diallyldimethylammonium chloride, didecyldimethylammonium bromide, didodecyldimethylammonium bromide, dihexadecyldimethylammonium bromide, dimethyldioctadecylammonium bromide, dimethylditetradecylammonium bromide, dimethyloctadecyl[3-(trimethoxysilyl)propyl]ammonium chloride, dodecylethyldimethylammonium bromide, dodecyltrimethylammonium chloride, domiphen bromide, heptadecafluorooctanesulfonic acid tetraethylammonium salt, hexadecyltrimethylammonium bromide, hexadecyltrimethylammonium chloride, hexyltrimethylammonium bromide, malondialdehyde tetrabutylammonium salt, methyltrioctylammonium bromide, methyltrioctylammonium chloride, methyltrioctylammonium hydrogen sulfate, methyltrioctylammonium thiosalicylate, myristyltrimethylammonium bromide, tetrabutylammonium acetate, tetrabutylammonium benzoate, tetrabutylammonium bisulfate, tetrabutylammonium bromide, tetrabutylammonium chloride, tetrabutylammonium cyanide, tetrabutylammonium hexafluorophosphate, tetrabutylammonium hydrogensulfate, tetrabutylammonium iodide, tetrabutylammonium methanesulfonate, tetrabutylammonium methoxide, tetrabutylammonium nonafluorobutanesulfonate, tetrabutylammonium perchlorate, tetrabutylammonium phosphate monobasic, tetrabutylammonium succinimide, tetrabutylammonium sulfate, tetrabutylammonium tetrabutylborate, tetrabutylammonium tetrafluoroborate, tetrabutylammonium tetraphenylborate, tetrabutylammonium thiocyanate, tetrabutylammonium p- toluenesulfonate, tetrabutylammonium trifluoromethanesulfonate, tetradodecylammonium bromide, tetradodecylammonium chloride, tetraethylammonium acetate tetrahydrate, tetraethylammonium benzoate, tetraethylammonium bicarbonate, tetraethylammonium bromide, tetraethylammonium chloride, tetraethylammonium cyanide, tetraethylammonium hexafluorophosphate, tetraethylammonium iodide, tetraethylammonium tetrafluoroborate, tetraethylammonium p- toluenesulfonate, tetraethylammonium trifluoromethanesulfonate, tetraheptylammonium bromide, tetrahexadecylammonium bromide, tetrahexylammonium bromide, tetrahexylammonium chloride, tetrahexylammonium hexafluorophosphate, tetrahexylammonium hydrogensulfate, tetrahexylammonium iodide, tetrahexylammonium tetrafluoroborate, tetrakis(decyl)ammonium bromide, tetramethylammonium acetate, tetramethylammonium bis(trifluoromethanesulfonyl)imide, tetramethylammoniumbisulfate, tetramethylammonium bromide, tetramethylammonium chloride, tetramethylammonium hexafluorophosphate, tetramethylammonium hydrogen sulfate, tetramethylammonium hydrogensulfate, tetramethylammonium iodide, tetramethylammonium silicate, tetramethylammonium sulfate, tetramethylammonium tetrafluoroborate, tetraoctadecylammonium bromide, tetraoctylammonium bromide, tetraoctylammonium chloride, tetrapentylammonium bromide, tetrapentylammonium chloride, tetrapropylammonium bromide, tetrapropylammonium chloride, tetrapropylammonium iodide, tetrapropylammonium tetrafluoroborate, tributylammonium pyrophosphate, tributylmethylammonium bromide, tributylmethylammonium chloride, tridodecylmethylammonium chloride, tridodecylmethylammonium iodide, triethylhexylammonium bromide, triethylmethylammonium chloride, trihexyltetradecylammonium bromide, trimethyloctadecylammonium bromide, trimethyloctylammonium bromide, trimethyloctylammonium chloride, trimethylphenylammonium bromide, trimethylphenylammonium chloride, trimethyl- tetradecylammonium chloride, and the like.

[0105] The term “prescribing” refers to order, authorize, or recommend the use of a drug or other therapy, remedy, or treatment. In some embodiments, a health care provider orally advises, recommends, or authorizes the use of a compound, dosage regimen, or other treatment to an individual. The health care provider may or may not provide a written prescription for the compound, dosage regimen, or treatment. Further, the health care provider may or may not provide the compound or treatment to the individual. For example, the health care provider can advise the individual where to obtain the compound without providing the compound. In some embodiments, a health care provider can provide a written prescription for the compound, dosage regimen, or treatment to the individual. A prescription can be written on paper or recorded on electronic media. In addition, a prescription can be called in (oral) or faxed in (written) to a pharmacy or a dispensary. In some embodiments, a sample of the compound or treatment is given to the individual. As used herein, giving a sample of a compound constitutes an implicit prescription for the compound. Different health care systems around the world use different methods for prescribing and administering compounds or treatments, and these methods are encompassed by the disclosure herein. A health care provider can include, for example, a physician, nurse, nurse practitioner, or other health care professional who can prescribe or administer compounds (drugs) for the disorders disclosed herein. In addition, a health care provider can include anyone who can recommend, prescribe, administer, or prevent an individual from receiving a compound or drug, including, for example, an insurance provider.

[0106] The terms “prevent”, “preventing”, and “prevention” refer to the elimination or reduction of the occurrence or onset of one or more symptoms associated with a specific disorder. For example, the terms “prevent”, “preventing”, and “prevention” can refer to the administration of therapy on a prophylactic or preventative basis to an individual who may ultimately manifest at least one symptom of a disorder but who has not yet done so. Such individuals can be identified on the basis of risk factors that are known to correlate with the subsequent occurrence of the disease, such as the presence of a biomarker. Alternatively, prevention therapy can be administered as a prophylactic measure without prior identification of a risk factor. Delaying the onset of the at least one episode and / or symptom of a disorder can also be considered prevention or prophylaxis.

[0107] As used herein, the term “reacting”, “contacting”, or “treating” when describing a certain chemical reaction or process is used as known in the art and generally refers to the bringing together chemical reagents and / or intermediates in such a manner so as to allow their interaction at the molecular level to achieve a chemical or physical transformation. In some embodiments, the reacting involves two reagents, wherein one or more equivalents of second reagent are used with respect to the first reagent. The reacting steps of the processes described herein can be conducted for a time and under conditions suitable for preparing the identified product. Additional terms are also used herein solely to provide descriptive clarity between the different process steps and each of these terms have the same definition as described above. These additional terms include, “alkylating”, “cyclizing”, “deprotecting”, “reducing”, and “condensing”.

[0108] The term “solvate” as used herein refers to a solid-state form of a compound of the present invention or a pharmaceutically acceptable salt thereof which includes a stoichiometric or non- stoichiometric amount of a solvent bound by non-covalent intermolecular forces. When the solvent is water, the solvate is a hydrate.

[0109] The term “subject”, as used herein, means a human or a non-human mammal, e.g., a dog, a cat, a mouse, a rat, a cow, a sheep, a pig, a goat, a non-human primate or a bird, e.g., a chicken, as well as any other vertebrate or invertebrate. In some embodiments, the subject is a human.

[0110] In some embodiments, the subject has experienced and / or exhibited at least one symptom of the disease or disorder to be treated and / or prevented. In some embodiments, the subject has been identified or diagnosed as having congenital adrenal hyperplasia (CAH). In some embodiments, the subject is suspected of having CAH. In some embodiments, the subject has a clinical record indicating that the subject has CAH (and optionally the clinical record indicates that the subject should be treated with any of the compositions provided herein). In some embodiments, the subject is a pediatric subject.

[0111] As used herein, the term “substituted” refers to the replacement of at least one of hydrogen atom of a chemical group with a non-hydrogen substituent or group, the non-hydrogen substituent can be monovalent or divalent. When the chemical group or substituent is divalent, then it is understood that this group is further substituted with another substituent or group. When a chemical group herein is “substituted” it may have up to the full valance of substitution; for example, a methyl group can be substituted by 1, 2, or 3 substituents, a methylene group can be substituted by 1 or 2 substituents, a phenyl group can be substituted by 1, 2, 3, 4, or 5 substituents, a naphthyl group can be substituted by 1, 2, 3, 4, 5, 6, or 7 substituents, and the like. Likewise, “substituted with one or more substituents” refers to the substitution of a group substituted with one substituent up to the total number of substituents physically allowed by the group. It is understood that “optionally substituted” as used herein refers to the group being either “unsubstituted” or “substituted” with a group. Accordingly, when a group is “optionally substituted with one or more substituents”, it is understood that the group is either “unsubstituted” or “substituted” and when substituted, the group is substituted with one substituent up to the total number of substituents physically allowed by the group as described above. In some embodiments, a group can be “optionally substituted with one, two, three, or four substituents”. In some embodiments, a group can be “optionally substituted with one, two, or three substituents”. In some embodiments, a group can be “optionally substituted with one or two substituents”. In some embodiments, a group can be “optionally substituted with one substituent”. Further, when a group is substituted with more than one substituent, then the substituents can be identical, or they can be different. Examples of substituents include, without limitation, halogen, alkoxy, alkyl, haloalkyl, hydroxy, nitro.

[0112] As used herein, “treat?*, or “treatment”, refer to therapeutic or palliative measures. Beneficial or desired clinical results include, but are not limited to, alleviation, in whole or in part, of symptoms associated with a disease or disorder or condition, diminishment of the extent of disease, stabilized (i.e., not worsening) state of disease, delay or slowing of disease progression, amelioration or palliation of the disease state (e.g., one or more symptoms of the disease), and remission (whether partial or total), whether detectable or undetectable. “Treatment” can also mean prolonging survival as compared to expected survival if not receiving treatment.

[0113] The term “therapeutically effective amount” refers to the amount of the compound of the present invention or a pharmaceutically acceptable salt thereof, or an amount of a pharmaceutical composition comprising the compound of the invention or a pharmaceutically acceptable salt thereof, that elicits the biological or medicinal response in a tissue, system, animal, or human that is being sought by an individual, researcher, veterinarian, medical doctor, or other clinician or caregiver, which can include one or more of the following:

[0114] (1) preventing the disorder, for example, preventing a disease, condition, or disorder in an individual who may be predisposed to the disease, condition, or disorder but does not yet experience or display the relevant pathology or symptomatology;

[0115] (2) inhibiting the disorder, for example, inhibiting a disease, condition, or disorder in an individual who is experiencing or displaying the relevant pathology or symptomatology (i.e., arresting further development of the pathology and / or symptomatology); and

[0116] (3) ameliorating the disorder, for example, ameliorating a disease, condition, or disorder in an individual who is experiencing or displaying the relevant pathology or symptomatology (i.e., reversing the pathology and / or symptomatology). CRYSTALLINE FORMS

[0117] The crystalline forms of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethyl] -5 -methyl-N-prop-2-yny 1- 1 ,3 -thiazol-2-amine (Compound 1) and intermediates related thereto can be identified by their unique solid state signatures with respect to, for example, Differential Scanning Calorimetry (DSC), X-ray Powder Diffraction (XRPD), and other solid state methods. Further characterization with respect to water or solvent content of the crystalline forms can be gauged by any of the following methods for example, Thermogravimetric Analysis (TGA), DSC and the like.

[0118] For DSC, it is known that the temperatures observed for thermal events will depend upon sample purity and may also depend on the rate of temperature change, as well as sample preparation technique, and the instrument employed. Thus, the values reported herein relating to DSC thermograms can vary by plus or minus about 5°C (i.e., ± about 5°C). The values reported herein relating to DSC thermograms can also vary by plus or minus about 20 joules per gram (i.e., ± about 20 joules per gram).

[0119] For XRPD, the relative intensities of the peaks can vary, depending upon the sample preparation technique, the sample mounting procedure and the instrument employed. Moreover, instrument variation and other factors can often affect the 2Θ values. Therefore, the peak assignments of diffraction patterns can vary by plus or minus about 0.2° (i.e., ± about 0.2°). For TGA, the temperature features reported herein can vary by plus or minus about 5°C (i.e., ± about 5°C). The TGA % weight changes reported herein over a specified temperature range can vary by plus or minus about 2% weight change (i.e., ± about 2% weight change) due to, for example, variations in sample quality and sample size. All X-ray powder diffraction patterns (diffractograms) were obtained using Cu-Ka radiation.

[0120] Further characterization with respect to hygroscopicity of the crystalline form can be gauged by, for example, Gravimetric Vapor Sorption (GVS). The GVS features reported herein can vary by plus or minus about 5% relative humidity (i.e., ± about 5% relative humidity). The GVS features reported herein can also vary by plus or minus about 2% weight change (i.e., ± about 2% weight change).

[0121] A. 4-(2-Chloro-4-methoxy-5-methylphenyl)-1-[(lS)-2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-1,3-thiazol-2-amine (Compound 1, Anhydrous Crystalline Form I). One aspect of the present invention relates to a novel anhydrous crystalline form of 4-(2- chloro-4-methoxy-5 -methylpheny l)-N-[( 1 S)-2-cyclopropy 1- 1 -(3 -fluoro-4-methylphenyl)ethyl] -5 - methyl-N-prop-2-y ny 1- 1 ,3 -thiazol-2-amine (Compound 1, free base) and processes related thereto. A summary of representative physical properties for the anhydrous crystalline form are provided in Table 1 and Table 2.

[0122] Table 1

[0123] Certain other XRPD peaks for the anhydrous form of 4-(2-chloro-4-methoxy-5- methylphenyl)-N-[( 1 S)-2-cyclopropyl- 1 -(3 -fluoro-4-methylpheny l)ethy 1] -5-methyl-N-prop-2-y ny 1- 1,3- thiazol-2-amine (Compound 1, free base) are shown in Table 2 below.

[0124] Table 2

[0125] Selected X-Ray Powder Diffraction (XRPD) Peaks for Form I of Compound 1 (Free Base)

[0126] The GVS profile (adsorption / desorption isotherm) for the anhydrous crystalline Form I of Compound 1 (free base) is shown in Figure 3. The corresponding data in tabular form is provided in Table 3, where there was substantially no weight change after a cycle from 10% RH to 90% RH and back to 10% RH.

[0127] Table 3

[0128] One aspect of the present invention relates to an anhydrous crystalline form of 4-(2-chloro-4- methoxy-5 -methylpheny l)-N-[( 1 S)-2-cyclopropyl- 1 -(3-fluoro-4-methylpheny l)ethy 1] -5 -methyl-N- prop-2-ynyl-l,3-thiazol-2-amine (Compound 1, free base). Anhydrous crystalline Form I of 4-(2- chloro-4-methoxy-5 -methylpheny l)-N-[( 1 S)-2-cyclopropy 1- 1 -(3 -fluoro-4-methylphenyl)ethyl] -5 - methyl -N-prop-2-ynyl- 1 ,3 -thiazol-2-amine (Compound 1, free base) refers to anhydrous crystalline form that contains 2% or less of water. In some embodiments, the anhydrous crystalline form contains 1% or less water. In some embodiments, the water content is determined by Karl Fischer (KF) analysis.

[0129] One aspect of the present invention relates to an anhydrous crystalline form of 4-(2-chloro-4- methoxy-5 -methylpheny l)-N-[( 1 S)-2-cyclopropyl- 1 -(3-fluoro-4-methylpheny l)ethy 1] -5 -methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1, free base), wherein the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least three peaks, in terms of 2Θ, selected from the group consisting of: 6.0° ± 0.2°, 11.9° ± 0.2°, 13.9° ± 0.2°, 14.3° ± 0.2°, 16.8° ± 0.2°, 17.9° ± 0.2°, 19.7° ± 0.2°, 20.2° ± 0.2°, 20.9° ± 0.2°, 21.8° ± 0.2°, 22.3° ± 0.2°, 23.2° ± 0.2°, 23.9° ± 0.2°, 24.2° ± 0.2°, 25.7° ± 0.2°, 26.8° ± 0.2°, 28.7° ± 0.2°, 29.6° ± 0.2°, 36.1° ± 0.2°, and 43.5° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction pattern comprising at least four peaks, in terms of 20, selected from the group consisting of: 6.0° ± 0.2°, 11.9° ± 0.2°, 13.9° ± 0.2°, 14.3° ± 0.2°, 16.8° ± 0.2°, 17.9° ± 0.2°, 19.7° ± 0.2°, 20.2° ± 0.2°, 20.9° ± 0.2°, 21.8° ± 0.2°, 22.3° ± 0.2°, 23.2° ± 0.2°, 23.9° ± 0.2°, 24.2° ± 0.2°, 25.7° ± 0.2°, 26.8° ± 0.2°, 28.7° ± 0.2°, 29.6° ± 0.2°, 36.1° ± 0.2°, and 43.5° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction pattern comprising at least five peaks, in terms of 20, selected from the group consisting of: 6.0° ± 0.2°, 11.9° ± 0.2°, 13.9° ± 0.2°, 14.3° ± 0.2°, 16.8° ± 0.2°, 17.9° ± 0.2°, 19.7° ± 0.2°, 20.2° ± 0.2°, 20.9° ± 0.2°, 21.8° ± 0.2°, 22.3° ± 0.2°, 23.2° ± 0.2°, 23.9° ± 0.2°, 24.2° ± 0.2°, 25.7° ± 0.2°, 26.8° ± 0.2°, 28.7° ± 0.2°, 29.6° ± 0.2°, 36.1° ± 0.2°, and 43.5° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction pattern comprising at least six peaks, in terms of 20, selected from the group consisting of: 6.0° ± 0.2°, 11.9° ± 0.2°, 13.9° ± 0.2°, 14.3° ± 0.2°, 16.8° ± 0.2°, 17.9° ± 0.2°, 19.7° ± 0.2°, 20.2° ± 0.2°, 20.9° ± 0.2°, 21.8° ± 0.2°, 22.3° ± 0.2°, 23.2° ± 0.2°, 23.9° ± 0.2°, 24.2° ± 0.2°, 25.7° ± 0.2°, 26.8° ± 0.2°, 28.7° ± 0.2°, 29.6° ± 0.2°, 36.1° ± 0.2°, and 43.5° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction pattern comprising at least seven peaks, in terms of 20, selected from the group consisting of: 6.0° ± 0.2°, 11.9° ± 0.2°, 13.9° ± 0.2°, 14.3° ± 0.2°, 16.8° ± 0.2°, 17.9° ± 0.2°, 19.7° ± 0.2°, 20.2° ± 0.2°, 20.9° ± 0.2°, 21.8° ± 0.2°, 22.3° ± 0.2°, 23.2° ± 0.2°, 23.9° ± 0.2°, 24.2° ± 0.2°, 25.7° ± 0.2°, 26.8° ± 0.2°, 28.7° ± 0.2°, 29.6° ± 0.2°, 36.1° ± 0.2°, and 43.5° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction pattern comprising at least eight peaks, in terms of 20, selected from the group consisting of: 6.0° ± 0.2°, 11.9° ± 0.2°, 13.9° ± 0.2°, 14.3° ± 0.2°, 16.8° ± 0.2°, 17.9° ± 0.2°, 19.7° ± 0.2°, 20.2°

[0130] ± 0.2°, 20.9° ± 0.2°, 21.8° ± 0.2°, 22.3° ± 0.2°, 23.2° ± 0.2°, 23.9° ± 0.2°, 24.2° ± 0.2°, 25.7° ± 0.2°, 26.8° ± 0.2°, 28.7° ± 0.2°, 29.6° ± 0.2°, 36.1° ± 0.2°, and 43.5° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction pattern comprising at least nine peaks, in tarns of 20, selected from the group consisting of: 6.0° ± 0.2°, 11.9° ± 0.2°, 13.9° ± 0.2°, 14.3° ± 0.2°, 16.8° ± 0.2°, 17.9° ± 0.2°, 19.7° ± 0.2°, 20.2° ± 0.2°, 20.9° ± 0.2°, 21.8° ± 0.2°, 22.3° ± 0.2°, 23.2° ± 0.2°, 23.9° ± 0.2°, 24.2° ± 0.2°, 25.7° ± 0.2°, 26.8° ± 0.2°, 28.7° ± 0.2°, 29.6° ± 0.2°, 36.1° ± 0.2°, and 43.5° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction pattern comprising at least ten peaks, in terms of 20, selected from the group consisting of: 6.0° ± 0.2°, 11.9° ± 0.2°, 13.9° ± 0.2°, 14.3° ± 0.2°, 16.8° ± 0.2°, 17.9° ± 0.2°, 19.7° ± 0.2°, 20.2° ± 0.2°, 20.9° ± 0.2°, 21.8° ± 0.2°, 22.3° ± 0.2°, 23.2° ± 0.2°, 23.9° ± 0.2°, 24.2° ± 0.2°, 25.7° ± 0.2°, 26.8° ± 0.2°, 28.7° ± 0.2°, 29.6° ± 0.2°, 36.1° ± 0.2°, and 43.5° ± 0.2°.

[0131] One aspect of the present invention relates to an anhydrous crystalline form of 4-(2-chloro-4- methoxy-5 -methylpheny l)-N-[( 1 S)-2-cyclopropyl- 1 -(3-fluoro-4-methylpheny l)ethy 1] -5 -methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1, free base), wherein the anhydrous crystalline form has an X-ray powder diffraction pattern comprising a peak, in terms of 2Θ, at 14.3° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction pattern comprising a peak, in terms of 2Θ, at 19.7° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction pattern comprising a peak, in terms of 2Θ, at 25.1° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 14.3° ± 0.2°, and 25.7° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 14.3° ± 0.2°, and 19.7° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 19.7° ± 0.2°, and 25.7° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 14.3° ± 0.2°, 19.7° ± 0.2°, and 25.1° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 14.3° ± 0.2°, 19.7° ± 0.2°, 20.2° ± 0.2°, and 25.1° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction patter comprising peaks, in terms of 2Θ, at 14.3° ± 0.2°, 19.7° ± 0.2°, 20.2° ± 0.2°, 25.1° ± 0.2°, 26.8° ± 0.2°, and 29.6° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 14.3° ± 0.2°, 19.7° ± 0.2°, 20.2° ± 0.2°, 22.3° ± 0.2°, 25.7° ± 0.2°, 26.8° ± 0.2°, and 29.6° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction patter comprising peaks, in terms of 2Θ, at 14.3° ± 0.2°, 19.7° ± 0.2°, 20.2° ± 0.2°, 22.3° ± 0.2°, 25.7° ± 0.2°, 26.8° ± 0.2°, 29.6° ± 0.2°, and 43.5° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 14.3° ± 0.2°, 19.7° ± 0.2°, 20.2° ± 0.2°, 20.9° ± 0.2°, 22.3° ± 0.2°, 25.7° ± 0.2°, 24.2° ± 0.2°, 26.8° ± 0.2°, 29.6° ± 0.2°, and 43.5° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 14.3° ± 0.2°, 19.7° ± 0.2°, 20.2° ± 0.2°, 20.9° ± 0.2°, 22.3° ± 0.2°, 25.7° ± 0.2°, 24.2° ± 0.2°, 26.8° ± 0.2°, 28.7° ± 0.2°, 29.6° ± 0.2°, and 43.5° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 14.3° ± 0.2°, 19.7° ± 0.2°, 20.2° ± 0.2°, 20.9° ± 0.2°, 21.8° ± 0.2°, 22.3° ± 0.2°, 25.7° ± 0.2°, 24.2° ± 0.2°, 26.8° ± 0.2°, 28.7° ± 0.2°, 29.6° ± 0.2°, and 43.5° ± 0.2°. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has an

[0132] X-ray powder diffraction pattern substantially as shown in Figure 1, wherein by “substantially” is meant that the reported peaks can vary by about ± 0.2 °2Θ.

[0133] It is understood that peak intensities can vary from one diflfractogram to another for the same crystalline form based on any number of factors that are known to those skilled in the art, such as, preferred orientation effects, preparation technique, the sample mounting procedure, the instrument employed, etc. In some instances, peak intensities can be rather dramatical. Accordingly, the diffraction peak intensities shown herein are illustrative and identical diffraction peak intensities are not necessarily required. One example is the XRPD for Form I shown in Figure 7 showing substantially the same peak positions but dramatic peak intensity differences. One skilled in the art would understand that Figure 1 and Figure 7 are the XRPD’s for Form I, despite the differences in the peak intensities. Similarly, those skilled in the art would readily be capable of comparing the diffractograms provided herein with a diflfractogram generated for an unknown crystal form and confirm whether the difflractogram is characterizing the same crystal form as provided herein or a different form.

[0134] One aspect of the present invention relates to an anhydrous crystalline form of 4-(2-chloro-4- methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1, free base), wherein the anhydrous crystalline form has a differential scanning calorimetry (DSC) thermogram comprising an endotherm with an extrapolated onset temperature of about 81°C to about 89.5°C. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 82°C to about 88°C. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 82.5°C to about 88.5°C. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 83°C to about 88°C. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 83.5°C to about 87.5°C. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a differential scanning calorimetry thermogram substantially as shown in Figure 2, wherein by “substantially” is meant that the reported DSC features can vary by about ± 5°C and the reported DSC features can vary by about ± 20 joules per gram.

[0135] One aspect of the present invention relates to an anhydrous crystalline form of 4-(2-chloro-4- methoxy-5 -methylpheny l)-N-[( 1 S)-2-cyclopropyl- 1 -(3-fluoro-4-methylpheny l)ethy 1] -5 -methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1, free base), wherein the anhydrous crystalline form has a thermogravimetric analysis (TGA) profile showing about 1.0% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a thermogravimetric analysis profile showing about 0.9% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a thermogravimetric analysis profile showing about 0.7% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a thermogravimetric analysis profile showing about 0.6% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a thermogravimetric analysis profile showing about 0.5% or less weight loss out to about 125°C.

[0136] One aspect of the present invention relates to an anhydrous crystalline form of 4-(2-chloro-4- methoxy-5 -methylpheny l)-N-[( 1 S)-2-cyclopropyl- 1 -(3-fluoro-4-methylpheny l)ethy 1] -5 -methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1, free base), wherein the anhydrous crystalline form has a thermogravimetric analysis (TGA) profile showing about 0.05% to about 1.0% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a thermogravimetric analysis profile showing about 0.1% to about 0.9% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a thermogravimetric analysis profile showing about 0.1% to about 0.7% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a thermogravimetric analysis profile showing about 0.1% to about 0.6% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a thermogravimetric analysis profile showing about 0.1% to about 0.4% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a thermogravimetric analysis profile substantially as shown in Figure 2, wherein by “substantially” is meant that the reported TGA features can vary by about ± 5°C, and the reported TGA features can vary by about ± 2% weight change (i.e., ± about 2% weight change). One aspect of the present invention relates to an anhydrous crystalline form of 4-(2-chloro-4- methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1, free base), wherein the anhydrous crystalline form has a gravimetric vapor sorption profile showing about 0.015% or less weight change after an adsorption / desorption cycle from 10% relative humidity (RH) to 90% RH and back to 10% RH. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a gravimetric vapor sorption profile showing about 0.01% or less weight change after an adsorption / desorption cycle from 10% RH to 90% RH and back to 10% RH. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a gravimetric vapor sorption profile showing about 0.008% or less weight change after an adsorption / desorption cycle from 10% RH to 90% RH and back to 10% RH. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a gravimetric vapor sorption profile showing about 0.005% or less weight change after an adsoiption / desorption cycle from 10% RH to 90% RH and back to 10% RH. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a gravimetric vapor sorption profile showing about 0.003% or less weight change after an adsorption / desorption cycle from 10% RH to 90% RH and back to 10% RH. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a gravimetric vapor sorption profile showing substantially no weight change after an adsorption / desorption cycle from 10% RH to 90% RH and back to 10% RH.

[0137] One aspect of the present invention relates to an anhydrous crystalline form of 4-(2-chloro-4- methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1, free base), wherein the anhydrous crystalline form has a gravimetric vapor sorption profile showing about 0.1% or less weight change from about 10% relative humidity (RH) to about 90% RH; and about 0.015% or less weight change after an adsorption / desorption cycle from 10% RH to 90% RH and back to 10% RH. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a gravimetric vapor sorption profile showing about 0.08% or less weight change from about 10% relative humidity (RH) to about 90%

[0138] RH; and about 0.01% or less weight change after an adsorption / desorption cycle from 10% RH to 90% RH and back to 10% RH. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a gravimetric vapor sorption profile showing about 0.05% or less weight change from about 10% relative humidity (RH) to about 90% RH; and about 0.008% or less weight change after an adsorption / desorption cycle from 10% RH to 90% RH and back to 10% RH. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a gravimetric vapor sorption profile showing about 0.04% or less weight change from about 10% RH to about 90% RH; and about 0.005% or less weight change after an adsorption / desorption cycle from 10% RH to 90% RH and back to 10% RH. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a gravimetric vapor sorption profile showing about 0.03% or less weight change from about 10% RH to about 90% RH; and about 0.003% or less weight change after an adsorption / desorption cycle from 10% RH to 90% RH and back to 10% RH. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a gravimetric vapor sorption profile showing about 0.2% or less weight change from about 10% RH to about 90% RH; and substantially no weight change after an adsorption / desorption cycle from 10% RH to 90% RH and back to 10% RH. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a gravimetric vapor sorption profile substantially as shown in Figure 3, wherein “substantially” is meant that the reported GVS features can vary by plus or minus about 5% relative humidity (i.e., ± about 5% relative humidity) and also vary by plus or minus about 2% weight change (i.e., ± about 2% weight change).

[0139] One aspect of the present invention relates to an anhydrous crystalline form of 4-(2-chloro-4- methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1, free base), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising at least three peaks, in terms of 2Θ, selected from the group consisting of: 6.0° ± 0.2°, 11.9° ± 0.2°, 13.9° ± 0.2°, 14.3° ± 0.2°, 16.8° ± 0.2°, 17.9° ± 0.2°, 19.7° ± 0.2°, 20.2° ± 0.2°, 20.9° ± 0.2°, 21.8° ± 0.2°, 22.3° ± 0.2°, 23.2° ± 0.2°, 23.9° ± 0.2°, 24.2° ± 0.2°, 25.7° ± 0.2°, 26.8° ± 0.2°, 28.7° ± 0.2°, 29.6° ± 0.2°, 36.1° ± 0.2°, and 43.5° ± 0.2°; a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 81°C to about 89.5°C; a thermogravimetric analysis profile showing about 0.05% to about 1.0% weight loss out to about 125°C; and / or a gravimetric vapor sorption profile showing about 0.015% or less weight change after an adsoiption / desorption cycle from 10% RH to 90% RH and back to 10% RH.

[0140] One aspect of the present invention relates to an anhydrous crystalline form of 4-(2-chloro-4- methoxy-5 -methylpheny l)-N-[( 1 S)-2-cyclopropyl- 1 -(3-fluoro-4-methylpheny l)ethy 1] -5 -methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1, free base), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 14.3° ± 0.2°, 19.7° ± 0.2°, and 25.7° ± 0.2°; a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 82.5°C to about 88.5°C; a thermogravimetric analysis profile showing about 0.7% or less weight loss out to about

[0141] 125°C; and / or a gravimetric vapor sorption profile showing about 0.005% or less weight change after an adsorption / desorption cycle from 10% RH to 90% RH and back to 10% RH.

[0142] One aspect of the present invention relates to an anhydrous crystalline form of 4-(2-chloro-4- methoxy-5 -methylpheny l)-N-[( 1 S)-2-cyclopropyl- 1 -(3-fluoro-4-methylpheny l)ethy 1] -5 -methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1, free base), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 14.3° ± 0.2°, 19.7° ± 0.2°, 20.2° ± 0.2°, 22.3° ± 0.2°, 25.7° ± 0.2°, 26.8° ± 0.2°, 29.6° ± 0.2°, and 43.5° ± 0.2°; a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 83°C to about 88°C; a thermogravimetric analysis profile showing about 0.5% or less weight loss out to about

[0143] 125°C; and / or a gravimetric vapor sorption profile showing about 0.003% or less weight change after an adsorption / desorption cycle from 10% RH to 90% RH and back to 10% RH.

[0144] One aspect of the present invention relates to an anhydrous crystalline form of 4-(2-chloro-4- methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1, free base), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern substantially as shown in Figure 1; a differential scanning calorimetry thermogram substantially as shown in Figure 2; a thermogravimetric analysis profile substantially as shown in Figure 2; and / or a gravimetric vapor sorption profile substantially as shown in Figure 3.

[0145] In some embodiments, the anhydrous crystalline form of 4-(2-chloro-4-methoxy-5 - methylphenyl)-N- [( 1S)-2-cyclopropyl- 1 -(3 -fluoro-4-methylpheny l)ethy 1] -5-methyl-N-prop-2-y ny 1- 1,3- thiazol-2-amine (Compound 1, free base) can be isolated as the crystalline form described herein, with a crystalline purity of at least about 75% by weight. In some embodiments, about 80% by weight. In some embodiments, about 85% by weight. In some embodiments, about 90% by weight. In some embodiments, about 95% by weight. In some embodiments, about 96% by weight. In some embodiments, about 97% by weight. In some embodiments, about 98% by weight. In some embodiments, about 99% by weight.

[0146] The manufacturing batches of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(15')-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1, free base) have been prepared with the following particle size distribution characterization, as shown in Table 4.

[0147] Table 4

[0148] In some embodiments, the anhydrous crystalline form of 4-(2-chloro-4-methoxy-5- methylphenyl 1.S')-2-cyclopropyl-l -(3 -fluoro-4-methylphenyl)ethyl] -5-methyl-N-prop-2-ynyl- 1,3- thiazol -2-amine (Compound 1, free base) has a particle size DIO of about 8 mM to about 35 pM. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a particle size DIO of about 10 pM to about 30 pM. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a particle size D10 of about 10 pM to about 27 pM. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a particle size D10 of about 12 pM to about 25 pM. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a particle size D10 of about 12 pM to about 23 pM.

[0149] In some embodiments, the anhydrous crystalline form of 4-(2-chloro-4-methoxy-5- methylphenyl)-N- [( 15)-2-cyclopropyl- 1 -(3 -fluoro-4-methylphenyl)ethyl] -5-methyl-N-prop-2-ynyl- 1 ,3 - thiazol -2-amine (Compound 1, free base) has a particle size D50 of about 80 pM to about 150 pM. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a particle size D50 of about 90 pM to about 145 pM. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a particle size D50 of about 100 pM to about 140 pM. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a particle size D50 of about 100 pM to about 135 pM. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a particle size D50 of about 105 pM to about 130 pM.

[0150] In some embodiments, the anhydrous crystalline form of 4-(2-chloro-4-methoxy-5- methylphenyl)-N- [( 15)-2-cyclopropyl- 1 -(3 -fluoro-4-methylphenyl)ethyl] -5-methyl-N-prop-2-ynyl- 1 ,3 - thiazol -2-amine (Compound 1, free base) has a particle size D90 of about 280 pM to about 490 pM. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a particle size D90 of about 290 μΜ to about 485 μΜ. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a particle size D90 of about 300 μΜ to about 480 μΜ. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a particle size D90 of about 305 μΜ to about 475 μΜ. In some embodiments, the anhydrous crystalline form (Compound 1, free base) has a particle size D90 of about 310 μΜ to about 470 μΜ.

[0151] B. (S)-4-(2-Chloro-4-methoxy-5-methylphenyl)- / V-(2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A, Anhydrous Crystalline Form).

[0152] One aspect of the present invention relates to a novel anhydrous crystalline form of (S)-4-(2- chloro-4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5- methylthiazol-2-amine (Compound 9A) and processes related thereto.

[0153] A summary of representative physical properties for the anhydrous crystalline form are below in Table 5 and Table 6.

[0154] Table 5

[0155] Certain other XRPD peaks for the crystalline form of (S)-4-(2-chloro-4-methoxy-5- methylphenyl)-N-(2-cyclopropyl- 1-(3 -fluoro-4-methy lphenyl)ethyl)-5 -methylthiazol-2-amine (Compound 9A) are shown in Table 6 below.

[0156] Table 6

[0157]

[0158] One aspect of the present invention relates to a crystalline form of (S)-4-(2-chloro-4-methoxy- 5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A). In some embodiments, the crystal form is an anhydrous crystalline form of (S)-4-(2- chloro-4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5- methylthiazol-2-amine (Compound 9A). An anhydrous crystalline form refers to a crystalline form that contains 2% or less of water. In some embodiments, the anhydrous crystalline form contains 1% or less water. In some embodiments, the water content is determined by Karl Fischer (KF) analysis.

[0159] One aspect of the present invention relates to an anhydrous crystalline form of (S)-4-(2-chloro- 4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2- amine (Compound 9A), «herein the anhydrous crystalline form has an X-ray powder diffraction patter comprising at least three peaks, in terms of 2Θ, selected from the group consisting of: 8.3° ± 0.2°, 11.5° ± 0.2°, 15.2° ± 0.2°, 15.5° ± 0.2°, 16.7° ± 0.2°, 18.4° ± 0.2°, 19.0° ± 0.2°, 19.8° ± 0.2°, 20.7° ± 0.2°, 21.5° ± 0.2°, 23.1° ± 0.2°, 25.2° ± 0.2°, 25.7° ± 0.2°, 26.2° ± 0.2°, 26.9° ± 0.2°, 27.1° ± 0.2°, and 28.0° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least four peaks, in terms of 2Θ, selected from the group consisting of: 8.3° ± 0.2°, 11.5° ± 0.2°, 15.2° ± 0.2°, 15.5° ± 0.2°, 16.7° ± 0.2°, 18.4° ± 0.2°, 19.0° ± 0.2°, 19.8° ± 0.2°, 20.7° ± 0.2°, 21.5° ± 0.2°, 23.1° ± 0.2°, 25.2° ± 0.2°, 25.7° ± 0.2°, 26.2° ± 0.2°, 26.9° ± 0.2°, 27.1° ± 0.2°, and 28.0° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least five peaks, in terms of 2Θ, selected from the group consisting of: 8.3° ± 0.2°, 11.5° ± 0.2°, 15.2° ± 0.2°, 15.5° ± 0.2°, 16.7° ± 0.2°, 18.4° ± 0.2°, 19.0° ± 0.2°, 19.8° ± 0.2°, 20.7° ± 0.2°, 21.5° ± 0.2°, 23.1° ± 0.2°, 25.2° ± 0.2°, 25.7° ± 0.2°, 26.2° ± 0.2°, 26.9° ± 0.2°, 27.1° ± 0.2°, and 28.0° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least six peaks, in terms of 20, selected from the group consisting of: 8.3° ± 0.2°, 11.5° ± 0.2°, 15.2° ± 0.2°, 15.5° ± 0.2°, 16.7° ± 0.2°, 18.4° ± 0.2°, 19.0° ± 0.2°, 19.8° ± 0.2°, 20.7° ± 0.2°, 21.5° ± 0.2°, 23.1° ± 0.2°, 25.2° ± 0.2°, 25.7° ± 0.2°, 26.2° ± 0.2°, 26.9° ± 0.2°, 27.1° ± 0.2°, and 28.0° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least seven peaks, in terms of 2Θ, selected from the group consisting of: 8.3° ± 0.2°, 11.5° ± 0.2°, 15.2° ± 0.2°, 15.5° ± 0.2°, 16.7° ± 0.2°, 18.4° ± 0.2°, 19.0° ± 0.2°, 19.8° ± 0.2°, 20.7° ± 0.2°, 21.5° ± 0.2°, 23.1° ± 0.2°, 25.2° ± 0.2°, 25.7° ± 0.2°, 26.2° ± 0.2°, 26.9° ± 0.2°, 27.1° ± 0.2°, and 28.0° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least eight peaks, in terms of 2Θ, selected from the group consisting of: 8.3° ± 0.2°, 11.5° ± 0.2°, 15.2° ± 0.2°, 15.5° ± 0.2°, 16.7° ±

[0160] 0.2°, 18.4° ± 0.2°, 19.0° ± 0.2°, 19.8° ± 0.2°, 20.7° ± 0.2°, 21.5° ± 0.2°, 23.1° ± 0.2°, 25.2° ± 0.2°, 25.7° ± 0.2°, 26.2° ± 0.2°, 26.9° ± 0.2°, 27.1° ± 0.2°, and 28.0° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least nine peaks, in terms of 2Θ, selected from the group consisting of: 8.3° ± 0.2°, 11.5° ± 0.2°, 15.2° ± 0.2°, 15.5° ± 0.2°, 16.7° ± 0.2°, 18.4° ± 0.2°, 19.0° ± 0.2°, 19.8° ± 0.2°, 20.7° ± 0.2°, 21.5° ± 0.2°, 23.1° ± 0.2°, 25.2° ±

[0161] 0.2°, 25.7° ± 0.2°, 26.2° ± 0.2°, 26.9° ± 0.2°, 27.1° ± 0.2°, and 28.0° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least ten peaks, in terms of 20, selected from the group consisting of: 8.3° ± 0.2°, 11.5° ± 0.2°, 15.2° ± 0.2°, 15.5° ± 0.2°, 16.7° ± 0.2°, 18.4° ± 0.2°, 19.0° ± 0.2°, 19.8° ± 0.2°, 20.7° ± 0.2°, 21.5° ± 0.2°, 23.1° ± 0.2°, 25.2° ± 0.2°, 25.7° ± 0.2°, 26.2° ± 0.2°, 26.9° ± 0.2°, 27.1° ± 0.2°, and 28.0° ± 0.2°.

[0162] One aspect of the present invention relates to an anhydrous crystalline form of (S)-4-(2-chloro- 4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2- amine (Compound 9A), wherein the anhydrous crystalline form has an X-ray powder diffraction pattern comprising a peak, in terms of 20, at 25.7° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising a peak, in terms of 20, at 18.4° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising a peak, in terms of 20, at 19.0° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 20, at 18.4° ± 0.2° and 19.0° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 20, at 18.4° ± 0.2° and 25.7° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 20, at 19.0° ± 0.2° and 25.7° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 18.4° ± 0.2°, 19.0° ± 0.2°, and 25.7° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising peaks, in terms of 2Θ, at 18.4° ± 0.2°, 19.0° ± 0.2°, 23.1° ± 0.2°, and 25.7° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising peaks, in terms of 2Θ, at 15.2° ± 0.2°, 18.4° ± 0.2°, 19.0° ± 0.2°, 23.1° ± 0.2°, and 25.7° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 15.2° ± 0.2°, 16.7° ± 0.2°, 18.4° ± 0.2°, 19.0° ± 0.2°, 19.8° ± 0.2°, 23.1° ± 0.2°, and 25.1° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 15.2° ± 0.2°, 16.7° ± 0.2°, 18.4° ± 0.2°, 19.0° ± 0.2°, 19.8° ± 0.2°, 21.5° ± 0.2°, 23.1° ± 0.2°, and 25.7° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 8.3° ± 0.2°, 15.2° ± 0.2°, 16.7° ± 0.2°, 18.4° ± 0.2°, 19.0° ± 0.2°, 19.8° ± 0.2°, 21.5° ± 0.2°, 23.1° ± 0.2°, and 25.1° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 8.3° ± 0.2°, 15.2° ± 0.2°, 16.7° ± 0.2°, 18.4° ± 0.2°, 19.0° ± 0.2°, 19.8° ± 0.2°, 20.7° ± 0.2°, 21.5° ± 0.2°, 23.1° ± 0.2°, and 25.7° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising peaks, in terms of 2Θ, at 8.3° ± 0.2°, 11.5° ± 0.2°, 15.2° ± 0.2°, 15.5° ± 0.2°, 16.7° ± 0.2°, 18.4° ± 0.2°, 19.0° ± 0.2°, 19.8° ± 0.2°, 20.7° ± 0.2°, 21.5° ± 0.2°, 23.1° ± 0.2°, and 25.7° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter substantially as shown in Figure 9, wherein by “substantially” is meant that the reported peaks can vary by about ±

[0163] 0.2 °20.

[0164] It is understood that peak intensities can vary from one diffractogram to another for the same crystalline form based on any number of factors that are known to those skilled in the art, such as, preferred orientation effects, preparation technique, the sample mounting procedure, the instrument employed, etc. In some instances, peak intensities can be rather dramatical. Accordingly, the diffraction peak intensities shown herein are illustrative and identical diffraction peak intensities are not necessarily required. One skilled in the art would readily be capable of comparing the diffractogram provided herein with a diffractogram generated for an unknown crystal form and confirm whether the diffractogram is characterizing the same crystal form as provided herein or a different form.

[0165] One aspect of the present invention relates to an anhydrous crystalline form of (S)-4-(2-chloro- 4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2- amine (Compound 9A), wherein the anhydrous crystalline form has a differential scanning calorimetry (DSC) thermogram comprising an endotherm with an extrapolated onset temperature of about 129°C to about 136°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 130.5°C to about 135.5°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 131°C to about 134°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 131.5°C to about 133.5°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 132°C to about 133°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram substantially as shown in Figure 10, wherein by “substantially” is meant that the reported DSC features can vary by about ± 5°C and the reported DSC features can vary by about ± 20 joules per gram.

[0166] One aspect of the present invention relates to an anhydrous crystalline form of (S)-4-(2-chloro- 4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2- amine (Compound 9A), wherein the anhydrous crystalline form has a thermogravimetric analysis (TGA) profile showing about 1.0% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.7% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.4% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.2% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.15% or less weight loss out to about 125°C.

[0167] One aspect of the present invention relates to an anhydrous crystalline form of (S)-4-(2-chloro- 4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2- amine (Compound 9A), wherein the anhydrous crystalline form has a thermogravimetric analysis (TGA) profile showing about 0.05% to about 1.0% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.05% to about 0.7% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.05% to about 0.4% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.05% to about 0.2% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.05% to about 0.15% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile substantially as shown in Figure 10, wherein by “substantially” is meant that the reported TGA features can vary by about ± 5°C, and the reported TGA features can vary by about ± 2% weight change (i.e., ± about 2% weight change).

[0168] One aspect of the present invention relates to an anhydrous crystalline form of (S)-4-(2-chloro- 4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2- amine (Compound 9A), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising at least three peaks, in terms of 2Θ, selected from the group consisting of: 8.3° ± 0.2°, 11.5° ± 0.2°, 15.2° ± 0.2°, 15.5° ± 0.2°, 16.7° ± 0.2°, 18.4° ± 0.2°, 19.0° ± 0.2°, 19.8° ± 0.2°, 20.7° ± 0.2°, 21.5° ± 0.2°, 23.1° ± 0.2°, 25.2° ± 0.2°, 25.7° ± 0.2°, 26.2° ± 0.2°, 26.9° ± 0.2°, 27.1° ± 0.2°, and 28.0° ± 0.2°; a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 129°C to about 136°C; and / or a thermogravimetric analysis profile showing about 0.05% to about 1.0% weight loss out to about 125°C.

[0169] One aspect of the present invention relates to an anhydrous crystalline form of (5)-4-(2-chloro- 4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2- amine (Compound 9A), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 18.4° ± 0.2°, 19.0° ± 0.2°, and 25.7° ± 0.2°; a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 131°C to about 134°C; and / or a thermogravimetric analysis profile showing about 0.7% or less weight loss out to about

[0170] 125°C.

[0171] One aspect of the present invention relates to an anhydrous crystalline form of (S)-4-(2-chloro- 4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2- amine (Compound 9A), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 8.3° ± 0.2°, 15.2° ± 0.2°, 16.7° ± 0.2°, 18.4° ± 0.2°, 19.0° ± 0.2°, 19.8° ± 0.2°, 21.5° ± 0.2°, 23.1° ± 0.2°, and 25.7° ± 0.2°; a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 132°C to about 133°C; and / or a thermogravimetric analysis profile showing about 0.4% or less weight loss out to about

[0172] 125°C.

[0173] One aspect of the present invention relates to an anhydrous crystalline form of (S)-4-(2-chloro- 4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2- amine (Compound 9A), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern substantially as shown in Figure 9; a differential scanning calorimetry thermogram substantially as shown in Figure 10; and / or a thermogravimetric analysis profile substantially as shown in Figure 10.

[0174] In some embodiments, the anhydrous crystalline form of (5)-4-(2-chloro-4-methoxy-5- methylphenyl)-N-(2-cyclopropyl- 1 -(3 -fluoro-4-methy lphenyl)ethyl)-5 -methylthiazol-2-amine

[0175] (Compound 9A) can be isolated as the crystalline form described herein, with a crystalline purity of at least about 75% by weight. In some embodiments, about 80% by weight. In some embodiments, about 85% by weight. In some embodiments, about 90% by weight. In some embodiments, about 95% by weight. In some embodiments, about 96% by weight. In some embodiments, about 97% by weight. In some embodiments, about 98% by weight. In some embodiments, about 99% by weight.

[0176] C. l-(2-Chloro-4-methoxy-5-methylphenyl)-2-thiocyanatopropan-1-one (Compound

[0177] 8A, Crystalline Form).

[0178] One aspect of the present invention relates to a novel anhydrous crystalline form of l-(2- chloro-4-methoxy-5-methylphenyl)-2-thiocyanatopropan-1-one (Compound 8A) and processes related thereto.

[0179] A summary of representative physical properties for the crystalline form are provided in Table

[0180] 7 and Table 8.

[0181] Table 7

[0182] Certain other XRPD peaks for the crystalline anhydrous form of l-(2-chloro-4-methoxy-5- methylphenyl)-2-thiocyanatopropan- 1 -one (Compound 8A) are shown in Table 8 below.

[0183] Table 8

[0184]

[0185] One aspect of the present invention relates to a crystalline form of l-(2-chloro-4-methoxy-5- methylphenyl)-2-thiocyanatopropan- 1 -one (Compound 8A). In some embodiments, the crystal form is an anhydrous crystalline form of l-(2-chloro-4-methoxy-5-methylphenyl)-2-thiocyanatopropan-1- one (Compound 8A). An anhydrous crystalline form refers to a crystalline form that contains 2% or less of water. In some embodiments, the anhydrous crystalline form contains 1% or less water. In some embodiments, the water content is determined by Karl Fischer (KF) analysis.

[0186] One aspect of the present invention relates to an anhydrous crystalline form of l-(2-chloro-4- methoxy-5-methylphenyl)-2-thiocyanatopropan-1-one (Compound 8A), wherein the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least three peaks, in terms of 2Θ, selected from the group consisting of: 12.6° ± 0.2°, 13.8° ± 0.2°, 18.9° ± 0.2°, 19.3° ± 0.2°, 21.3° ± 0.2°, 22.2° ± 0.2°, 24.9° ± 0.2°, 25.5° ± 0.2°, 26.7° ± 0.2°, 27.5° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, 39.2° ± 0.2°, and 42.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least four peaks, in terms of 2Θ, selected from the group consisting of: 12.6° ± 0.2°, 13.8° ± 0.2°, 18.9° ± 0.2°, 19.3° ± 0.2°, 21.3° ± 0.2°, 22.2° ± 0.2°, 24.9° ± 0.2°, 25.5° ± 0.2°, 26.7° ± 0.2°, 27.5° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, 39.2° ± 0.2°, and 42.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least five peaks, in terms of 2Θ, selected from the group consisting of: 12.6° ± 0.2°,

[0187] 13.8° ± 0.2°, 18.9° ± 0.2°, 19.3° ± 0.2°, 21.3° ± 0.2°, 22.2° ± 0.2°, 24.9° ± 0.2°, 25.5° ± 0.2°, 26.7° ± 0.2°, 27.5° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, 39.2° ± 0.2°, and 42.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least six peaks, in terms of 2Θ, selected from the group consisting of: 12.6° ± 0.2°, 13.8° ± 0.2°, 18.9° ± 0.2°, 19.3° ± 0.2°, 21.3° ± 0.2°, 22.2° ± 0.2°, 24.9° ± 0.2°, 25.5° ± 0.2°, 26.7° ± 0.2°, 27.5° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, 39.2° ± 0.2°, and 42.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least seven peaks, in terms of 2Θ, selected from the group consisting of: 12.6° ± 0.2°, 13.8° ± 0.2°, 18.9° ± 0.2°, 19.3° ± 0.2°, 21.3° ± 0.2°, 22.2° ± 0.2°, 24.9° ± 0.2°, 25.5° ± 0.2°, 26.7° ± 0.2°, 27.5° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, 39.2° ± 0.2°, and 42.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least eight peaks, in terms of 2Θ, selected from the group consisting of: 12.6° ± 0.2°, 13.8° ± 0.2°, 18.9° ± 0.2°, 19.3° ± 0.2°, 21.3° ± 0.2°, 22.2° ± 0.2°, 24.9° ± 0.2°, 25.5° ± 0.2°, 26.7° ± 0.2°, 27.5° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, 39.2° ± 0.2°, and 42.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising at least nine peaks, in terms of 2Θ, selected from the group consisting of: 12.6° ± 0.2°, 13.8° ± 0.2°, 18.9° ± 0.2°, 19.3° ± 0.2°, 21.3° ± 0.2°, 22.2° ± 0.2°, 24.9° ± 0.2°, 25.5° ± 0.2°, 26.7° ± 0.2°, 27.5° ± 0.2°,

[0188] 27.8° ± 0.2°, 34.8° ± 0.2°, 39.2° ± 0.2°, and 42.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least ten peaks, in terms of 2Θ, selected from the group consisting of: 12.6° ± 0.2°, 13.8° ± 0.2°, 18.9° ± 0.2°, 19.3° ± 0.2°, 21.3° ± 0.2°, 22.2° ± 0.2°, 24.9° ± 0.2°, 25.5° ± 0.2°, 26.7° ± 0.2°, 27.5° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, 39.2° ± 0.2°, and 42.3° ± 0.2°.

[0189] One aspect of the present invention relates to an anhydrous crystalline form of l-(2-chloro-4- methoxy-5-methylphenyl)-2-thiocyanatopropan-1-one (Compound 8A), wherein the anhydrous crystalline form has an X-ray powder diffraction pattern comprising a peak, in terms of 2Θ, at 24.9° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 24.9° ± 0.2° and 26.7° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 24.9° ± 0.2° and 27.8° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 24.9° ± 0.2° and 34.8° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 24.9° ± 0.2° and 42.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 18.9° ± 0.2°, 24.9° ± 0.2°, and 26.7° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X- ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 18.9° ± 0.2°, 24.9° ± 0.2°, and 27.8° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 18.9° ± 0.2°, 24.9° ± 0.2°, and 34.8° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 18.9° ± 0.2°, 24.9° ± 0.2°, and 42.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 24.9° ± 0.2°, 26.7° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, and 42.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 18.9° ± 0.2°, 24.9° ± 0.2°, 26.7° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, and 42.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 18.9° ± 0.2°, 24.9° ± 0.2°, 26.7° ± 0.2°, 27.5° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, and 42.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 18.9° ± 0.2°, 21.3° ± 0.2°, 24.9° ± 0.2°, 26.7° ± 0.2°, 27.5° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, and 42.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 12.6° ±

[0190] 0.2°, 18.9° ± 0.2°, 21.3° ± 0.2°, 24.9° ± 0.2°, 26.7° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, and 42.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 12.6° ± 0.2°, 18.9° ± 0.2°, 21.3° ± 0.2°, 24.9° ± 0.2°, 26.7° ± 0.2°, 27.5° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, and 42.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 12.6° ±

[0191] 0.2°, 18.9° ± 0.2°, 21.3° ± 0.2°, 22.2° ± 0.2°, 24.9° ± 0.2°, 26.7° ± 0.2°, 27.5° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, and 42.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 12.6° ± 0.2°, 18.9° ± 0.2°, 21.3° ± 0.2°, 22.2° ± 0.2°, 24.9° ± 0.2°, 25.5° ± 0.2°, 26.7° ± 0.2°, 27.5° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, and 42.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 12.6° ± 0.2°, 13.8° ± 0.2°, 18.9° ± 0.2°, 21.3° ± 0.2°, 22.2° ± 0.2°, 24.9° ± 0.2°, 25.5° ± 0.2°, 26.7° ± 0.2°, 27.5° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, and 42.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern substantially as shown in Figure 11, wherein by “substantially” is meant that the reported peaks can vary by about ± 0.2 °2Θ.

[0192] It is understood that peak intensities can vary from one diffractogram to another for the same crystalline form based on any number of factors that are known to those skilled in the art, such as, preferred orientation effects, preparation technique, the sample mounting procedure, the instrument employed, etc. In some instances, peak intensities can be rather dramatical. Accordingly, the diffraction peak intensities shown herein are illustrative and identical diffraction peak intensities are not necessarily required. One skilled in the art would readily be capable of comparing the diffractogram provided herein with a diffractogram generated for an unknown crystal form and confirm whether the diffractogram is characterizing the same crystal form as provided herein or a different form.

[0193] One aspect of the present invention relates to an anhydrous crystalline form of l-(2-chloro-4- methoxy-5-methylphenyl)-2-thiocyanatopropan-1-one (Compound 8A), wherein the anhydrous crystalline form has a differential scanning calorimetry (DSC) thermogram comprising an endotherm with an extrapolated onset temperature of about 70.5°C to about 75.5°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 71°C to about 75°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 71.5°C to about 74.5°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 72°C to about 74°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 72.5°C to about 73.5°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram substantially as shown in Figure 12, wherein by “substantially” is meant that the reported DSC features can vary by about ± 5°C and the reported DSC features can vary by about ± 20 joules per gram.

[0194] One aspect of the present invention relates to an anhydrous crystalline form of l-(2-chloro-4- methoxy-5-methylphenyl)-2-thiocyanatopropan-1-one (Compound 8A), wherein the anhydrous crystalline form has a thermogravimetric analysis (TGA) profile showing about 1.0% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.8% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.5% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.4% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.35% or less weight loss out to about 125°C. One aspect of the present invention relates to an anhydrous crystalline form of l-(2-chloro-4- methoxy-5-methylphenyl)-2-thiocyanatopropan-1-one (Compound 8A), wherein the anhydrous crystalline form has a thermogravimetric analysis (TGA) profile showing about 0.1% to about 1.0% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.15% to about 0.8% weight loss out to about

[0195] 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.2% to about 0.5% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.25% to about 0.4% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.3% to about 0.35% weight loss out to about

[0196] 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile substantially as shown in Figure 12, wherein by “substantially” is meant that the reported TGA features can vary by about ± 5°C, and the reported TGA features can vary by about ± 2% weight change (i.e., ± about 2% weight change).

[0197] One aspect of the present invention relates to an anhydrous crystalline form of l-(2-chloro-4- methoxy-5-methylphenyl)-2-thiocyanatopropan-1-one (Compound 8A), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising at least three peaks, in terms of 2Θ, selected from the group consisting of: 12.6° ± 0.2°, 13.8° ± 0.2°, 18.9° ± 0.2°, 19.3° ± 0.2°, 21.3° ± 0.2°, 22.2° ± 0.2°, 24.9° ± 0.2°, 25.5° ± 0.2°, 26.7° ± 0.2°, 27.5° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, 39.2° ± 0.2°, and 42.3° ± 0.2°; a differential scanning calorimetry (DSC) thermogram comprising an endotherm with an extrapolated onset temperature of about 70.5°C to about 75.5°C; and / or a thermogravimetric analysis (TGA) profile showing about 0.1% to about 1.0% weight loss out to about 125°C.

[0198] One aspect of the present invention relates to an anhydrous crystalline form of l-(2-chloro-4- methoxy-5-methylphenyl)-2-thiocyanatopropan-1-one (Compound 8A), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 18.9° ± 0.2°, 24.9° ± 0.2°, 26.7° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, and 42.3° ± 0.2°; a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 71.5°C to about 74.5°C; and / or a thermogravimetric analysis profile showing about 1.0% or less weight loss out to about

[0199] 125°C.

[0200] One aspect of the present invention relates to an anhydrous crystalline form of l-(2-chloro-4- methoxy-5-methylphenyl)-2-thiocyanatopropan-1-one (Compound 8A), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 12.6° ± 0.2°, 18.9° ± 0.2°, 21.3° ± 0.2°, 24.9° ± 0.2°, 26.7° ± 0.2°, 27.8° ± 0.2°, 34.8° ± 0.2°, and 42.3° ± 0.2°; a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 72.5°C to about 73.5°C; and / or a thermogravimetric analysis profile showing about 0.5% or less weight loss out to about

[0201] 125°C.

[0202] One aspect of the present invention relates to an anhydrous crystalline form of l-(2-chloro-4- methoxy-5-methylphenyl)-2-thiocyanatopropan-1-one (Compound 8A), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern substantially as shown in Figure 11; a differential scanning calorimetry thermogram substantially as shown in Figure 12; and / or a thermogravimetric analysis profile substantially as shown in Figure 12.

[0203] In some embodiments, the anhydrous crystalline form of l-(2-chloro-4-methoxy-5- methy lphenyl)-2-thiocyanatopropan- 1 -one (Compound 8A) can be isolated as the crystalline form described herein, with a crystalline purity of at least about 75% by weight. In some embodiments, about 80% by weight. In some embodiments, about 85% by weight. In some embodiments, about 90% by weight. In some embodiments, about 95% by weight. In some embodiments, about 96% by weight. In some embodiments, about 97% by weight. In some embodiments, about 98% by weight. In some embodiments, about 99% by weight.

[0204] D. (S)-2-Cydopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-amine (Compound 6A, Hydrochloride Salt, Crystalline Form).

[0205] One aspect of the present invention relates to a novel anhydrous crystalline form of (S)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-amine (Compound 6A, HQ salt) and processes related thereto.

[0206] A summary of representative physical properties for the crystalline form are provided in Table

[0207] 9 and Table 10. Table 9

[0208] Certain other XRPD peaks for the crystalline form of (S)-2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethan-l -amine (Compound 6A, HQ salt) are shown in Table 10 below.

[0209] Table 10

[0210] One aspect of the present invention relates to a crystalline form of (S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethan-l -amine (Compound 6A, HC1 salt). In some embodiments, the crystal form is an anhydrous crystalline form of (S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-amine (Compound 6A, HQ salt). An anhydrous crystalline form refers to a crystalline form that contains 2% or less of water. In some embodiments, the anhydrous crystalline form contains 1% or less water. In some embodiments, the water content is determined by Karl Fischer (KF) analysis.

[0211] One aspect of the present invention relates to an anhydrous crystalline form of (S)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-amine (Compound 6A, HC1 salt), wherein the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least three peaks, in terms of 26, selected from the group consisting of: 13.7° ± 0.2°, 14.8° ± 0.2°, 15.3° ± 0.2°, 20.5° ± 0.2°, 21.1° ± 0.2°, 21.5° ± 0.2°, 22.3° ± 0.2°, 23.2° ± 0.2°, 23.6° ± 0.2°, 24.3° ± 0.2°, 29.5° ± 0.2°, and 29.8° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least four peaks, in terms of 2Θ, selected from the group consisting of: 13.7° ± 0.2°, 14.8° ± 0.2°, 15.3° ± 0.2°, 20.5° ± 0.2°, 21.1° ± 0.2°, 21.5° ± 0.2°, 22.3° ± 0.2°, 23.2° ± 0.2°, 23.6° ± 0.2°, 24.3° ± 0.2°, 29.5° ± 0.2°, and 29.8° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least five peaks, in terms of 2Θ, selected from the group consisting of: 13.7° ± 0.2°, 14.8° ± 0.2°, 15.3° ± 0.2°, 20.5° ± 0.2°, 21.1° ± 0.2°, 21.5° ± 0.2°, 22.3° ± 0.2°, 23.2° ± 0.2°, 23.6° ± 0.2°, 24.3° ± 0.2°, 29.5° ± 0.2°, and 29.8° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least six peaks, in terms of 2Θ, selected from the group consisting of: 13.7° ± 0.2°, 14.8° ± 0.2°, 15.3° ± 0.2°, 20.5° ± 0.2°, 21.1° ± 0.2°, 21.5° ± 0.2°, 22.3° ± 0.2°, 23.2° ± 0.2°, 23.6° ± 0.2°, 24.3° ± 0.2°, 29.5° ± 0.2°, and 29.8° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least seven peaks, in terms of 2Θ, selected from the group consisting of: 13.7° ± 0.2°, 14.8° ± 0.2°, 15.3° ± 0.2°, 20.5° ± 0.2°, 21.1° ± 0.2°, 21.5° ± 0.2°, 22.3° ± 0.2°, 23.2° ± 0.2°, 23.6° ± 0.2°, 24.3° ± 0.2°, 29.5° ± 0.2°, and 29.8° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least eight peaks, in terms of 2Θ, selected from the group consisting of: 13.7° ± 0.2°, 14.8° ± 0.2°,

[0212] 15.3° ± 0.2°, 20.5° ± 0.2°, 21.1° ± 0.2°, 21.5° ± 0.2°, 22.3° ± 0.2°, 23.2° ± 0.2°, 23.6° ± 0.2°, 24.3° ± 0.2°, 29.5° ± 0.2°, and 29.8° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X- ray powder diffraction pattern comprising at least nine peaks, in terms of 2Θ, selected from the group consisting of: 13.7° ± 0.2°, 14.8° ± 0.2°, 15.3° ± 0.2°, 20.5° ± 0.2°, 21.1° ± 0.2°, 21.5° ± 0.2°, 22.3° ± 0.2°, 23.2° ± 0.2°, 23.6° ± 0.2°, 24.3° ± 0.2°, 29.5° ± 0.2°, and 29.8° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least ten peaks, in terms of 2Θ, selected from the group consisting of: 13.7° ± 0.2°, 14.8° ± 0.2°, 15.3° ± 0.2°, 20.5° ± 0.2°, 21.1° ± 0.2°, 21.5° ± 0.2°, 22.3° ± 0.2°, 23.2° ± 0.2°, 23.6° ± 0.2°, 24.3° ± 0.2°, 29.5° ± 0.2°, and

[0213] 29.8° ± 0.2°.

[0214] One aspect of the present invention relates to an anhydrous crystalline form of (S)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-amine (Compound 6A, HC1 salt), wherein the anhydrous crystalline form has an X-ray powder diffraction pattern comprising a peak, in terms of 2Θ, at 20.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising a peak, in terms of 2Θ, at 21.1° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising a peak, in terms of 2Θ, at 24.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising peaks, in terms of 2Θ, at 20.5° ± 0.2° and 21.1° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 20.5° ± 0.2° and 24.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 21.1° ± 0.2° and 24.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising peaks, in terms of 2Θ, at 20.5° ± 0.2°, 21.1° ± 0.2°, and 24.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 20.5° ± 0.2°, 21.1° ± 0.2°, 24.3° ± 0.2°, and 29.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 20.5° ± 0.2°, 21.1° ± 0.2°, 23.2° ± 0.2°, and 24.3° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 20.5° ± 0.2°, 21.1° ± 0.2°, 23.2° ± 0.2°, 24.3° ± 0.2°, and 29.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 20.5° ± 0.2°, 21.1° ± 0.2°, 23.2° ± 0.2°, 23.6° ± 0.2°, 24.3° ± 0.2°, and 29.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 20.5° ± 0.2°, 21.1° ± 0.2°, 21.5° ± 0.2°, 23.2° ± 0.2°, 24.3° ± 0.2°, and 29.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 20.5° ± 0.2°, 21.1° ± 0.2°, 21.5° ± 0.2°, 23.2° ± 0.2°, 23.6° ± 0.2°, 24.3° ± 0.2°, and 29.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 20.5° ± 0.2°, 21.1° ± 0.2°, 24.3° ± 0.2°, 29.5° ± 0.2°, 23.2° ± 0.2°, 15.3° ± 0.2°, and 14.8° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 15.3° ± 0.2°, 20.5° ± 0.2°, 21.1° ± 0.2°, 21.5° ± 0.2°, 23.2° ± 0.2°, 23.6° ± 0.2°, 24.3° ± 0.2°, and 29.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 14.8° ± 0.2°, 20.5° ± 0.2°, 21.1° ± 0.2°, 21.5° ± 0.2°, 23.2° ± 0.2°, 23.6° ± 0.2°, 24.3° ± 0.2°, and 29.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising peaks, in terms of 2Θ, at 20.5° ± 0.2°, 21.1° ± 0.2°, 21.5° ± 0.2°, 23.2° ± 0.2°, 23.6° ± 0.2°, 24.3° ± 0.2°, 29.5° ± 0.2°, and 29.8° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 14.8° ± 0.2°, 15.3° ±

[0215] 0.2°, 20.5° ± 0.2°, 21.1° ± 0.2°, 21.5° ± 0.2°, 23.2° ± 0.2°, 23.6° ± 0.2°, 24.3° ± 0.2°, 29.5° ± 0.2°, and 29.8° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern substantially as shown in Figure 13, wherein by “substantially” is meant that the reported peaks can vary by about ± 0.2 °20.

[0216] It is understood that peak intensities can vary from one diffractogram to another for the same crystalline form based on any number of factors that are known to those skilled in the art, such as, preferred orientation effects, preparation technique, the sample mounting procedure, the instrument employed, etc. In some instances, peak intensities can be rather dramatical. Accordingly, the diffraction peak intensities shown herein are illustrative and identical diffraction peak intensities are not necessarily required. One skilled in the art would readily be capable of comparing the diffractogram provided herein with a diffractogram generated for an unknown crystal form and confirm whether the diffractogram is characterizing the same crystal form as provided herein or a different form.

[0217] One aspect of the present invention relates to an anhydrous crystalline form of (5)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-amine (Compound 6A, HC1 salt), wherein the anhydrous crystalline form has a differential scanning calorimetry (DSC) thermogram comprising an endotherm with an extrapolated onset temperature of about 154°C to about 164°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 155°C to about 163°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 157°C to about 162°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 158.5°C to about 160.5°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 159°C to about 160°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram substantially as shown in Figure 14, wherein by “substantially” is meant that the reported DSC features can vary by about ± 5°C and the reported DSC features can vary by about ± 20 joules per gram.

[0218] One aspect of the present invention relates to an anhydrous crystalline form of (S)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-amine (Compound 6A, HC1 salt), wherein the anhydrous crystalline form has a thermogravimetric analysis (TGA) profile showing about 1.0% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.8% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.6% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.4% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.35% or less weight loss out to about 125°C.

[0219] One aspect of the present invention relates to an anhydrous crystalline form of (S)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-amine (Compound 6A, HC1 salt), wherein the anhydrous crystalline form has a thermogravimetric analysis (TGA) profile showing about 0.05% to about 1.0% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.1% to about 0.8% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.15% to about 0.6% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.2% to about 0.4% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.25% to about 0.35% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile substantially as shown in Figure 14, wherein by “substantially” is meant that the reported TGA features can vary by about ± 5°C, and the reported TGA features can vary by about ± 2% weight change (i.e., ± about 2% weight change).

[0220] One aspect of the present invention relates to an anhydrous crystalline form of (S)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-amine (Compound 6A, HC1 salt), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising at least three peaks, in terms of 2Θ, selected from the group consisting of: 13.7° ± 0.2°, 14.8° ± 0.2°, 15.3° ± 0.2°, 20.5° ± 0.2°, 21.1° ± 0.2°, 21.5° ± 0.2°, 22.3° ± 0.2°, 23.2° ± 0.2°, 23.6° ± 0.2°, 24.3° ± 0.2°, 29.5° ± 0.2°, and 29.8° ± 0.2°; a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 154°C to about 164°C; and / or a thermogravimetric analysis profile showing about 0.05% to about 1.0% weight loss out to about 125°C.

[0221] One aspect of the present invention relates to an anhydrous crystalline form of (S)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-amine (Compound 6A, HC1 salt), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 20.5° ± 0.2°, 21.1° ± 0.2°, 24.3° ± 0.2°, and 29.5° ± 0.2°; a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 157°C to about 162°C; and / or a thermogravimetric analysis profile showing about 1.0% or less weight loss out to about

[0222] 125°C.

[0223] One aspect of the present invention relates to an anhydrous crystalline form of (5)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-amine (Compound 6A, HC1 salt), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 20.5° ± 0.2°, 21.1° ± 0.2°, 24.3° ± 0.2°, 29.5° ± 0.2°, 23.2° ± 0.2°, 15.3° ± 0.2°, and 14.8° ± 0.2°; a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 159°C to about 160°C; and / or a thermogravimetric analysis profile showing about 0.4% or less weight loss out to about

[0224] 125°C.

[0225] One aspect of the present invention relates to an anhydrous crystalline form of (S)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-amine (Compound 6A, HC1 salt), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern substantially as shown in Figure 13; a differential scanning calorimetry thermogram substantially as shown in Figure 14; and / or a thermogravimetric analysis profile substantially as shown in Figure 14.

[0226] In some embodiments, the anhydrous crystalline form of (S)-2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethan- 1 -amine (Compound 6A, HC1 salt) can be isolated as the crystalline form described herein, with a crystalline purity of at least about 75% by weight. In some embodiments, about 80% by weight. In some embodiments, about 85% by weight. In some embodiments, about 90% by weight. In some embodiments, about 95% by weight. In some embodiments, about 96% by weight. In some embodiments, about 97% by weight. In some embodiments, about 98% by weight. In some embodiments, about 99% by weight.

[0227] E. 2-CycloprOpyl-1-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A, Crystalline Form).

[0228] One aspect of the present invention relates to a novel anhydrous crystalline form of 2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A) and processes related thereto.

[0229] A summary of representative physical properties for the crystalline form are provided in Table 11 and Table 12. Table 11

[0230] Certain other XRPD peaks for the crystalline form of 2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethan-1-one (Compound 3A) are shown in Table 12 below.

[0231] Table 12

[0232] One aspect of the present invention relates to a crystalline form of 2-cyclopropyl-1-(3-fluoro- 4-methylphenyl)ethan-1-one (Compound 3A). In some embodiments, the crystal form is an anhydrous crystalline form of 2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A). An anhydrous crystalline form refers to a crystalline form that contains 2% or less of water. In some embodiments, the anhydrous crystalline form contains 1% or less water. In some embodiments, the water content is determined by Karl Fischer (KF) analysis.

[0233] One aspect of the present invention relates to an anhydrous crystalline form of 2-cyclopropyl- l-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A), wherein the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least three peaks, in terms of 2Θ, selected from the group consisting of: 7.4° ± 0.2°, 7.5° ± 0.2°, 14.7° ± 0.2°, 14.8° ± 0.2°, 22.0° ± 0.2°, 29.5° ± 0.2°, and 37.1° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising at least four peaks, in terms of 2Θ, selected from the group consisting of: 7.4° ± 0.2°, 7.5° ± 0.2°, 14.7° ± 0.2°, 14.8° ± 0.2°, 22.0° ± 0.2°, 29.5° ± 0.2°, and 37.1° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising at least five peaks, in terms of 2Θ, selected from the group consisting of: 7.4° ± 0.2°, 7.5° ± 0.2°, 14.7° ± 0.2°, 14.8° ± 0.2°, 22.0° ± 0.2°, 29.5° ± 0.2°, and 37.1° ± 0.2°.

[0234] One aspect of the present invention relates to an anhydrous crystalline form of 2-cyclopropyl- l-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A), wherein the anhydrous crystalline form has an X-ray powder diffraction pattern comprising a peak, in terms of 2Θ, at 7.4° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising a peak, in terms of 2Θ, at 7.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X- ray powder diffraction pattern comprising a peak, in terms of 2Θ, at 14.7° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising a peak, in terms of 2Θ, at 14.8° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X- ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 7.4° ± 0.2°, and 14.7° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 7.4° ± 0.2°, and 14.8° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 7.5° ± 0.2°, and 14.7° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 7.5° ± 0.2°, and 14.8° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising peaks, in terms of 2Θ, at 7.4° ± 0.2°, 14.7° ± 0.2°, and 22.0° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 7.4° ± 0.2°, 14.8° ± 0.2°, and 22.0° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 7.5° ± 0.2°, 14.7° ± 0.2°, and 22.0° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 7.5° ± 0.2°, 14.8° ± 0.2°, and 22.0° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 7.4° ± 0.2°, 14.7° ± 0.2°, and 29.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising peaks, in terms of 2Θ, at 7.4° ± 0.2°, 14.8° ± 0.2°, and 29.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 7.5° ± 0.2°, 14.7° ± 0.2°, and 29.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 7.5° ± 0.2°, 14.8° ± 0.2°, and 29.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 7.4° ± 0.2°, 14.7° ± 0.2°, 22.0° ± 0.2°, and 29.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising peaks, in terms of 2Θ, at 7.4° ± 0.2°, 14.8° ± 0.2°, 22.0° ± 0.2°, and 29.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising peaks, in terms of 2Θ, at 7.5° ± 0.2°, 14.7° ± 0.2°, 22.0° ± 0.2°, and 29.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising peaks, in terms of 2Θ, at 7.5° ± 0.2°, 14.8° ± 0.2°, 22.0° ± 0.2°, and 29.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising peaks, in terms of 2Θ, at 7.4° ± 0.2°, 14.7° ± 0.2°, 22.0° ± 0.2°, 29.5° ± 0.2°, and 37.1° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising peaks, in terms of 2Θ, at 7.4° ± 0.2°, 14.8° ± 0.2°, 22.0° ± 0.2°, 29.5° ± 0.2°, and 37.1° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising peaks, in terms of 2Θ, at 7.5° ± 0.2°, 14.7° ± 0.2°, 22.0° ± 0.2°, 29.5° ± 0.2°, and 37.1° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising peaks, in terms of 2Θ, at 7.5° ± 0.2°, 14.8° ± 0.2°, 22.0° ± 0.2°, 29.5° ± 0.2°, and 37.1° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction patter comprising peaks, in terms of 2Θ, at 7.4° ± 0.2°, 7.5° ± 0.2°, 14.7° ± 0.2°, 14.8° ± 0.2°, 22.0° ± 0.2°, 29.5° ± 0.2°, and 37.1° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern substantially as shown in Figure 15, wherein by “substantially” is meant that the reported peaks can vary by about ± 0.2 °2Θ.

[0235] It is understood that peak intensities can vary from one diffractogram to another for the same crystalline form based on any number of factors that are known to those skilled in the art, such as, preferred orientation effects, preparation technique, the sample mounting procedure, the instrument employed, etc. In some instances, peak intensities can be rather dramatical. Accordingly, the diffraction peak intensities shown herein are illustrative and identical diffraction peak intensities are not necessarily required. One skilled in the art would readily be capable of comparing the diffractogram provided herein with a diffractogram generated for an unknown crystal form and confirm whether the diffractogram is characterizing the same crystal form as provided herein or a different form.

[0236] One aspect of the present invention relates to an anhydrous crystalline form of 2-cyclopropyl- l-(3-fluoro-4-methylphenyl)etlian-1-one (Compound 3A), wherein the anhydrous crystalline form has a differential scanning calorimetry (DSC) thermogram comprising an endotherm with an extrapolated onset temperature of about 25°C to about 31°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 26.5°C to about 30°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 26.5°C to about 29.5°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 27°C to about 29°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 27.5°C to about 28.5°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram substantially as shown in Figure 16, wherein by “substantially” is meant that the reported DSC features can vary by about ± 5°C and the reported DSC features can vary by about ± 20 joules per gram.

[0237] One aspect of the present invention relates to an anhydrous crystalline form of 2-cyclopropyl- l-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A), wherein the anhydrous crystalline form has a thermogravimetric analysis (TGA) profile showing about 1.0% or less weight loss out to about 70°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.7% or less weight loss out to about 70°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.6% or less weight loss out to about 70°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.4% or less weight loss out to about 70°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.2% or less weight loss out to about 70°C.

[0238] One aspect of the present invention relates to an anhydrous crystalline form of 2-cyclopropyl- l-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A), wherein the anhydrous crystalline form has a thermogravimetric analysis (TGA) profile showing about 0.02% to about 1.0% weight loss out to about 70°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.03% to about 0.7% weight loss out to about 70°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.04% to about 0.6% weight loss out to about 70°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.05% to about 0.4% weight loss out to about 70°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.1% to about 0.2% weight loss out to about 70°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile substantially as shown in Figure 16, wherein by “substantially” is meant that the reported TGA features can vary by about ± 5°C, and the reported TGA features can vary by about ± 2% weight change (i.e., ± about 2% weight change).

[0239] One aspect of the present invention relates to an anhydrous crystalline form of 2-cyclopropyl- l-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising at least three peaks, in terms of 2Θ, selected from the group consisting of: 7.4° ± 0.2°, 7.5° ± 0.2°, 14.7° ± 0.2°, 14.8° ± 0.2°, 22.0° ± 0.2°, 29.5° ± 0.2°, and 37.1° ± 0.2°; a differential scanning calorimetry (DSC) thermogram comprising an endotherm with an extrapolated onset temperature of about 25°C to about 31°C; and / or a thermogravimetric analysis profile showing about 1.0% or less weight loss out to about

[0240] 70°C.

[0241] One aspect of the present invention relates to an anhydrous crystalline form of 2-cyclopropyl- l-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising at least four peaks, in terms of 2Θ, selected from the group consisting of: 7.4° ± 0.2°, 7.5° ± 0.2°, 14.7° ± 0.2°, 14.8° ± 0.2°, 22.0° ± 0.2°, 29.5° ± 0.2°, and 37.1° ± 0.2°; a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 26.5°C to about 29.5°C; and / or a thermogravimetric analysis profile showing about 0.02% to about 1.0% weight loss out to about 70°C.

[0242] One aspect of the present invention relates to an anhydrous crystalline form of 2-cyclopropyl- l-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 7.4° ± 0.2°, 7.5° ± 0.2°, 14.7° ± 0.2°, 14.8° ± 0.2°, 22.0° ± 0.2°, 29.5° ± 0.2°, and 37.1° ± 0.2°; a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 27.5°C to about 28.5°C; and / or a thermogravimetric analysis profile showing about 0.05% to about 0.4% weight loss out to about 70°C. One aspect of the present invention relates to an anhydrous crystalline form of 2-cyclopropyl- l-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern substantially as shown in Figure 15; a differential scanning calorimetry thermogram substantially as shown in Figure 16; and / or a thermogravimetric analysis profile substantially as shown in Figure 16.

[0243] In some embodiments, the anhydrous crystalline form of 2-cyclopropyl-1-(3-fluoro-4- methy lphenyl)ethan- 1 -one (Compound 3A) can be isolated as the crystalline form described herein, with a crystalline purity of at least about 75% by weight. In some embodiments, about 80% by weight. In some embodiments, about 85% by weight. In some embodiments, about 90% by weight. In some embodiments, about 95% by weight. In some embodiments, about 96% by weight. In some embodiments, about 97% by weight. In some embodiments, about 98% by weight. In some embodiments, about 99% by weight.

[0244] F. Crystalline (S)-2-cydopropyl-1-(3-fluoro-4-methylphenyl)-N-((S)-1- phenylethyl)ethan-1-amine (Compound 5A, HC1 salt).

[0245] One aspect of the present invention relates to a novel anhydrous crystalline form of (S)-2- cyclopropyl- 1 -(3 -fluoro-4-methylphenyl)-N-((S)- 1 -pheny lethyl)ethan- 1 -amine (Compound 5A, HC1 salt) and processes related thereto.

[0246] A summary of representative physical properties for crystalline Compound 5A (HC1 salt) are provided in Table 13 and Table 14.

[0247] Table 13

[0248] Certain other XRPD peaks for the anhydrous crystalline form of (S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)-N-((5)- 1 -phenylethyl)ethan- 1 -amine (Compound 5A, HC1 salt) are shown in

[0249] Table 14 below.

[0250] Table 14

[0251] One aspect of the present invention relates to a crystalline form of (S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)-N-((S)-1-phenylethyl)ethan-1-amine (Compound 5A, HC1 salt). In some embodiments, the crystal form is an anhydrous crystalline form of (S)-2-cyclopropyl-1-(3-fluoro-4- methylphenyl)-N-((5)-1-phenylethyl)ethan-1-amine (Compound 5A, HC1 salt). An anhydrous crystalline form refers to a crystalline form that contains 2% or less of water. In some embodiments, the anhydrous crystalline form contains 1% or less water. In some embodiments, the water content is determined by Karl Fischer (KF) analysis.

[0252] One aspect of the present invention relates to an anhydrous crystalline form of (S)-2- cyclopropyl- 1 -(3 -fluoro-4-methylphenyl)-N-((S)- 1-pheny lethyl)ethan- 1 -amine (Compound 5A, HC1 salt), wherein the anhydrous crystalline form has an X-ray powder diffraction patter comprising at least three peaks, in terms of 2Θ, selected from the group consisting of: 6.5° ± 0.2°, 12.1° ± 0.2°, 13.0° ± 0.2°, 14.2° ± 0.2°, 19.5° ± 0.2°, 20.1° ± 0.2°, 20.4° ± 0.2°, 21.9° ± 0.2°, 23.5° ± 0.2°, 24.5° ± 0.2°, 24.8° ± 0.2°, 25.9° ± 0.2°, and 32.1° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least four peaks, in terms of 2Θ, selected from the group consisting of: 6.5° ± 0.2°, 12.1° ± 0.2°, 13.0° ± 0.2°, 14.2° ± 0.2°, 19.5° ± 0.2°, 20.1° ± 0.2°, 20.4° ± 0.2°, 21.9° ± 0.2°, 23.5° ± 0.2°, 24.5° ± 0.2°, 24.8° ± 0.2°, 25.9° ± 0.2°, and 32.1° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least five peaks, in terms of 2Θ, selected from the group consisting of: 6.5° ± 0.2°, 12.1° ± 0.2°, 13.0° ± 0.2°, 14.2° ± 0.2°, 19.5° ± 0.2°, 20.1° ± 0.2°, 20.4° ± 0.2°, 21.9° ± 0.2°, 23.5° ± 0.2°, 24.5° ± 0.2°, 24.8° ± 0.2°, 25.9° ± 0.2°, and 32.1° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least six peaks, in terms of 2Θ, selected from the group consisting of: 6.5° ± 0.2°, 12.1° ± 0.2°, 13.0° ± 0.2°, 14.2° ± 0.2°, 19.5° ± 0.2°, 20.1° ± 0.2°, 20.4° ± 0.2°, 21.9° ± 0.2°, 23.5° ± 0.2°, 24.5° ± 0.2°, 24.8° ± 0.2°, 25.9° ± 0.2°, and

[0253] 32.1° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least seven peaks, in terms of 2Θ, selected from the group consisting of: 6.5° ± 0.2°, 12.1° ± 0.2°, 13.0° ± 0.2°, 14.2° ± 0.2°, 19.5° ± 0.2°, 20.1° ± 0.2°, 20.4° ± 0.2°, 21.9° ± 0.2°, 23.5° ± 0.2°, 24.5° ± 0.2°, 24.8° ± 0.2°, 25.9° ± 0.2°, and 32.1° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least eight peaks, in terms of 2Θ, selected from the group consisting of: 6.5° ± 0.2°, 12.1° ± 0.2°, 13.0° ± 0.2°, 14.2° ± 0.2°, 19.5° ± 0.2°, 20.1° ± 0.2°, 20.4° ± 0.2°, 21.9° ± 0.2°, 23.5° ± 0.2°, 24.5° ± 0.2°, 24.8° ± 0.2°, 25.9° ± 0.2°, and 32.1° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least nine peaks, in terms of 2Θ, selected from the group consisting of: 6.5° ± 0.2°, 12.1° ± 0.2°, 13.0° ± 0.2°, 14.2° ± 0.2°, 19.5° ± 0.2°, 20.1° ± 0.2°, 20.4° ± 0.2°, 21.9°

[0254] ± 0.2°, 23.5° ± 0.2°, 24.5° ± 0.2°, 24.8° ± 0.2°, 25.9° ± 0.2°, and 32.1° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising at least ten peaks, in terms of 2Θ, selected from the group consisting of: 6.5° ± 0.2°, 12.1° ± 0.2°, 13.0° ± 0.2°, 14.2° ± 0.2°, 19.5° ± 0.2°, 20.1° ± 0.2°, 20.4° ± 0.2°, 21.9° ± 0.2°, 23.5° ± 0.2°, 24.5° ± 0.2°, 24.8° ± 0.2°, 25.9° ± 0.2°, and 32.1° ± 0.2°.

[0255] One aspect of the present invention relates to an anhydrous crystalline form of (S)-2- cyclopropyl- 1-(3 -fluoro-4-methylphenyl)-N-((S)- 1 -pheny lethyl)ethan- 1 -amine (Compound 5A, HC1 salt), wherein the anhydrous crystalline form has an X-ray powder diffraction pattern comprising a peak, in terms of 2Θ, at 13.0° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X- ray powder diffraction pattern comprising a peak, in terms of 2Θ, at 19.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising a peak, in terms of 2Θ, at 25.9° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X- ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 13.0° ± 0.2° and 19.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 13.0° ± 0.2° and 25.9° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 19.5° ± 0.2° and 25.9° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 13.0° ± 0.2°, 19.5° ± 0.2°, and 25.9° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 13.0° ± 0.2°, 19.5° ± 0.2°, 20.4° ± 0.2°, and 25.9° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 12.1° ± 0.2°, 13.0° ± 0.2°, 19.5° ± 0.2°, 20.4° ± 0.2°, and 25.9° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 12.1° ± 0.2°, 13.0° ± 0.2°, 14.2° ± 0.2°, 19.5° ± 0.2°, 20.4° ± 0.2°, and 25.9° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 12.1° ± 0.2°, 13.0° ± 0.2°, 14.2° ± 0.2°, 19.5° ± 0.2°, 20.1° ± 0.2°, 20.4° ± 0.2°, 21.9° ± 0.2°, and 25.9° ± 0.2°. In some embodiments, the anhydrous crystalline form has an X-ray powder diffraction pattern substantially as shown in Figure 17, wherein by “substantially” is meant that the reported peaks can vary by about ± 0.2 °2Θ.

[0256] It is understood that peak intensities can vary from one diffractogram to another for the same crystalline form based on any number of factors that are known to those skilled in the art, such as, preferred orientation effects, preparation technique, the sample mounting procedure, the instrument employed, etc. In some instances, peak intensities can be rather dramatical. Accordingly, the diffraction peak intensities shown herein are illustrative and identical diffraction peak intensities are not necessarily required. One skilled in the art would readily be capable of comparing the diffractogram provided herein with a diffractogram generated for an unknown crystal form and confirm whether the diffractogram is characterizing the same crystal form as provided herein or a different form.

[0257] One aspect of the present invention relates to an anhydrous crystalline form of (5)-2- cyclopropyl- 1 -(3 -fluoro-4-methylphenyl)-N-((S)- 1 -pheny lethyl)ethan- 1 -amine (Compound 5A, HC1 salt), wherein the anhydrous crystalline form has a differential scanning calorimetry (DSC) thermogram comprising an endotherm with an extrapolated onset temperature of about 212°C to about 218.5°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 213°C to about 218°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 214°C to about 217.5°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 214.5°C to about 217°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 215°C to about 216.5°C. In some embodiments, the anhydrous crystalline form has a differential scanning calorimetry thermogram substantially as shown in Figure 18, wherein by “substantially” is meant that the reported DSC features can vary by about ± 5°C and the reported DSC features can vary by about ± 20 joules per gram.

[0258] One aspect of the present invention relates to an anhydrous crystalline form of (5)-2- cycloprOpyl-1-(3-fluorO-4-methylphenyl)-N-((S)-1-phenylethyl)ethan-1-amine (Compound 5A, HC1 salt), wherein the anhydrous crystalline form has a thermogravimetric analysis (TGA) profile showing about 1.0% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.8% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.6% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.4% or less weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.2% or less weight loss out to about 125°C.

[0259] One aspect of the present invention relates to an anhydrous crystalline form of (5)-2- cyclopropyl- 1 -(3 -fluoro-4-methylphenyl)-N-((S)- 1 -pheny lethyl)ethan- 1 -amine (Compound 5A, HC1 salt), wherein the anhydrous crystalline form has a thermogravimetric analysis (TGA) profile showing about 0.01% to about 1.0% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.02% to about 0.8% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.03% to about 0.6% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.04% to about 0.4% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.05% to about 0.2% weight loss out to about 125°C. In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile substantially as shown in Figure 18, wherein by “substantially” is meant that the reported TGA features can vary by about ± 5°C, and the reported TGA features can vary by about ± 2% weight change (i.e., ± about 2% weight change).

[0260] One aspect of the present invention relates to an anhydrous crystalline form of (S)-2- cyclopropyl- 1 -(3 -fluoro-4-methylphenyl)-N-((S)- 1-pheny lethyl)ethan- 1 -amine (Compound 5A, HC1 salt), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising at least three peaks, in terms of 2Θ, selected from the group consisting of: 6.5° ± 0.2°, 12.1° ± 0.2°, 13.0° ± 0.2°, 14.2° ± 0.2°, 19.5° ± 0.2°, 20.1° ± 0.2°, 20.4° ± 0.2°, 21.9° ± 0.2°, 23.5° ± 0.2°, 24.5° ± 0.2°, 24.8° ± 0.2°, 25.9° ± 0.2°, and 32.1° ± 0.2°; a differential scanning calorimetry (DSC) thermogram comprising an endotherm with an extrapolated onset temperature of about 212°C to about 218.5°C; and / or a thermogravimetric analysis profile showing about 1.0% or less weight loss out to about

[0261] 125°C.

[0262] One aspect of the present invention relates to an anhydrous crystalline form of (S)-2- cyclopropyl- 1 -(3 -fluoro-4-methylphenyl)-N-((S)- 1-pheny lethyl)ethan- 1 -amine (Compound 5A, HC1 salt), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 13.0° ± 0.2°, 19.5° ± 0.2°, and 25.9° ± 0.2°; a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 214°C to about 217.5°C; and / or a thermogravimetric analysis profile showing about 0.02% to about 0.8% weight loss out to about 125°C.

[0263] One aspect of the present invention relates to an anhydrous crystalline form of (S)-2- cyclopropyl- 1 -(3 -fluoro-4-methylphenyl)-N-((S)- 1 -pheny lethyl)ethan- 1 -amine (Compound 5A, HC1 salt), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 12.1° ± 0.2°, 13.0° ± 0.2°, 14.2° ± 0.2°, 19.5° ± 0.2°, 20.4° ± 0.2°, and 25.9° ± 0.2°; a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 214.5°C to about 217°C; and / or a thermogravimetric analysis profile showing about 0.04% to about 0.4% weight loss out to about 125°C.

[0264] One aspect of the present invention relates to an anhydrous crystalline form of (S)-2- cyclopropyl- 1 -(3 -fluoro-4-methylphenyl)-N-((S)- 1 -pheny lethyl)ethan- 1 -amine (Compound 5A, HC1 salt), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern substantially as shown in Figure 17; a differential scanning calorimetry thermogram substantially as shown in Figure 18; and / or a thermogravimetric analysis profile substantially as shown in Figure 18.

[0265] In some embodiments, the anhydrous crystalline form of (S)-2-cyclopropyl-1-(3-fluoro-4- methylphenyl)-N-((5)-1-phenylethyl)ethan-1-amine (Compound 5A, HC1 salt) can be isolated as the crystalline form described herein, with a crystalline purity of at least about 75% by weight. In some embodiments, about 80% by weight. In some embodiments, about 85% by weight. In some embodiments, about 90% by weight. In some embodiments, about 95% by weight. In some embodiments, about 96% by weight. In some embodiments, about 97% by weight. In some embodiments, about 98% by weight. In some embodiments, about 99% by weight.

[0266] G. Crystalline 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1, Tosylate Salt, Form I).

[0267] One aspect of the present invention relates to a novel crystalline form of 4-(2-chloro-4- methoxy-5 -methylpheny l)-N-[( 1 S)-2-cyclopropyl- 1 -(3-fluoro-4-methylpheny l)ethy 1] -5 -methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1, tosylate salt) and processes related thereto.

[0268] A summary of representative physical properties for crystalline Compound 1 (tosylate salt) are provided in Table 15 and Table 16.

[0269] Table 15

[0270] Certain other XRPD peaks for crystalline 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1, tosylate salt) are shown in Table 16 below.

[0271] Table 16

[0272] Selected X-Ray Powder Diffraction (XRPD) Peaks for Compound 1 (tosylate salt, Form I)

[0273]

[0274] One aspect of the present invention relates to an crystalline form of 4-(2-chloro-4-methoxy-5- methy lphenyl)-N-[( 1 S)-2-cyclopropyl- 1 -(3 -fluoro-4-methylpheny l)ethy 1] -5-methyl-N-prop-2-y ny 1- 1,3- thiazol-2-amine (Compound 1, tosylate salt, Form I).

[0275] One aspect of the present invention relates to an crystalline form of 4-(2-chloro-4-methoxy-5- methy lphenyl)-N-[( 1 S)-2-cyclopropyl- 1 -(3 -fluoro-4-methylpheny l)ethy 1] -5-methyl-N-prop-2-y ny 1- 1,3- thiazol-2-amine (Compound 1, tosylate salt, Form I), wherein the crystalline form has an X-ray powder diffraction pattern comprising at least three peaks, in terms of 2Θ, selected from the group consisting of: 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 13.2° ± 0.2°, 16.3° ± 0.2°, 19.0° ± 0.2°, 19.3° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 22.8° ± 0.2°, 23.3° ± 0.2°, 23.8° ± 0.2°, and 28.5° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising at least four peaks, in terms of 2Θ, selected from the group consisting of: 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 13.2° ± 0.2°, 16.3° ± 0.2°, 19.0° ± 0.2°, 19.3° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 22.8° ± 0.2°, 23.3° ± 0.2°, 23.8° ± 0.2°, and 28.5° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising at least five peaks, in terms of 2Θ, selected from the group consisting of: 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3°

[0276] ± 0.2°, 13.2° ± 0.2°, 16.3° ± 0.2°, 19.0° ± 0.2°, 19.3° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 22.8° ± 0.2°, 23.3° ± 0.2°, 23.8° ± 0.2°, and 28.5° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising at least six peaks, in terms of 2Θ, selected from the group consisting of: 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 13.2° ± 0.2°, 16.3° ±

[0277] 0.2°, 19.0° ± 0.2°, 19.3° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 22.8° ± 0.2°, 23.3° ± 0.2°, 23.8° ± 0.2°, and 28.5° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising at least seven peaks, in terms of 2Θ, selected from the group consisting of: 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 13.2° ± 0.2°, 16.3° ± 0.2°, 19.0° ± 0.2°, 19.3° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 22.8° ± 0.2°, 23.3° ± 0.2°, 23.8° ± 0.2°, and 28.5° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising at least eight peaks, in terms of 20, selected from the group consisting of: 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 13.2° ± 0.2°, 16.3° ± 0.2°, 19.0° ± 0.2°, 19.3° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 22.8° ± 0.2°, 23.3° ± 0.2°, 23.8° ± 0.2°, and 28.5° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising at least nine peaks, in terms of 20, selected from the group consisting of: 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 13.2° ± 0.2°, 16.3° ± 0.2°, 19.0° ± 0.2°, 19.3° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 22.8° ± 0.2°, 23.3° ± 0.2°, 23.8° ± 0.2°, and 28.5° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising at least ten peaks, in terms of 20, selected from the group consisting of: 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 13.2° ± 0.2°, 16.3° ± 0.2°, 19.0° ± 0.2°, 19.3° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 22.8° ± 0.2°, 23.3° ± 0.2°, 23.8° ± 0.2°, and 28.5° ± 0.2°.

[0278] One aspect of the present invention relates to a crystalline form of 4-(2-chloro-4-methoxy-5- methylphenyl)-N-[( 1 S)-2-cyclopropyl- 1 -(3 -fluoro-4-methylpheny l)ethy 1] -5-methyl-N-prop-2-y ny 1- 1,3- thiazol-2-amine (Compound 1, tosylate salt), wherein the crystalline form has an X-ray powder diffraction pattern comprising a peak, in terms of 20, at 9.1° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising a peak, in terms of 2Θ, at 21.1° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction patter comprising a peak, in terms of 2Θ, at 23.3° ±

[0279] 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 9.1° ± 0.2° and 21.1° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction patter comprising peaks, in terms of 20, at 9.1° ± 0.2° and 23.3° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising peaks, in terms of 20, at 21.1° ± 0.2° and 23.3° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising peaks, in terms of 20, at 9.1° ± 0.2°, 21.1° ± 0.2°, and 23.3° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction patter comprising peaks, in terms of 20, at 9.1° ±

[0280] 0.2°, 11.3° ± 0.2°, 21.1° ± 0.2°, and 23.3° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising peaks, in terms of 20, at 9.1° ± 0.2°, 11.3° ± 0.2°, 21.1° ± 0.2°, 22.8° ± 0.2°, and 23.3° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising peaks, in terms of 20, at 9.1° ± 0.2°, 11.3° ± 0.2°, 13.2° ± 0.2°, 16.3° ± 0.2°, and 21.1° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction patter comprising peaks, in terms of 20, at 9.1° ± 0.2°, 11.3° ± 0.2°, 21.1° ± 0.2°, 23.3° ± 0.2°, and

[0281] 23.8° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 9.1° ± 0.2°, 11.3° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 23.3° ± 0.2°, and 23.8° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 23.3° ± 0.2°, and 23.8° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction patter comprising peaks, in terms of 20, at 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 19.0° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 23.3° ± 0.2°, and 23.8° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising peaks, in terms of 20, at 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 19.3° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 23.3° ± 0.2°, and 23.8° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising peaks, in terms of 20, at 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 23.3° ± 0.2°, 23.8° ± 0.2°, and 28.5° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising peaks, in terms of 20, at 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 13.2° ± 0.2°, 19.0° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 23.3° ± 0.2°, and 23.8° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising peaks, in terms of 20, at 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 13.2° ± 0.2°, 19.3° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 23.3° ± 0.2°, and 23.8° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising peaks, in terms of 20, at 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°,

[0282] 13.2° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 23.3° ± 0.2°, 23.8° ± 0.2°, and 28.5° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction patter comprising peaks, in terms of 20, at 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 16.3° ± 0.2°, 19.0° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 23.3° ± 0.2°, and 23.8° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising peaks, in terms of 20, at 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 16.3° ± 0.2°, 19.3° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 23.3° ± 0.2°, and 23.8° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction patter comprising peaks, in terms of 20, at 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 16.3° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 23.3° ± 0.2°, 23.8° ± 0.2°, and 28.5° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 19.0° ± 0.2°, 19.3° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 23.3° ± 0.2°, 23.8° ± 0.2°, and 28.5° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction patter comprising peaks, in terms of 20, at 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 13.2° ± 0.2°, 16.3° ± 0.2°, 19.0° ± 0.2°, 19.3° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 23.3° ± 0.2°, 23.8° ± 0.2°, and 28.5° ± 0.2°. In some embodiments, the crystalline form (Compound 1, tosylate salt) has an X-ray powder diffraction pattern substantially as shown in Figure 24, wherein by “substantially” is meant that the reported peaks can vary by about ± 0.2 °20.

[0283] It is understood that peak intensities can vary from one diffractogram to another for the same crystalline form based on any number of factors that are known to those skilled in the art, such as, preferred orientation effects, preparation technique, the sample mounting procedure, the instrument employed, etc. In some instances, peak intensities can be rather dramatical. Accordingly, the diffraction peak intensities shown herein are illustrative and identical diffraction peak intensities are not necessarily required. One skilled in the art would readily be capable of comparing the diffractogram provided herein with a diffractogram generated for an unknown crystal form and confirm whether the diffractogram is characterizing the same crystal form as provided herein or a different form.

[0284] One aspect of the present invention relates to a crystalline form of 4-(2-chloro-4-methoxy-5- methylphenyl)-N- [( 1S)-2-cyclopropyl- 1 -(3 -fluoro-4-methylpheny l)ethy 1] -5-methyl-N-prop-2-y ny 1- 1,3- thiazol-2-amine (Compound 1, tosylate salt), wherein the crystalline form has a differential scanning calorimetry (DSC) thermogram comprising an endotherm with an extrapolated onset temperature of about 154°C to about 159°C. In some embodiments, the crystalline form (Compound 1, tosylate salt) has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 154.5°C to about 158.5°C. In some embodiments, the crystalline form (Compound 1, tosylate salt) has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 155°C to about 158°C. In some embodiments, the crystalline form (Compound 1, tosylate salt) has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 155.5°C to about 157.5°C. In some embodiments, the crystalline form (Compound 1, tosylate salt) has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 156°C to about 157°C. In some embodiments, the crystalline form (Compound 1, tosylate salt) has a differential scanning calorimetry thermogram substantially as shown in Figure 25, wherein by “substantially” is meant that the reported DSC features can vary by about ± 5°C and the reported DSC features can vary by about ± 20 joules per gram.

[0285] One aspect of the present invention relates to a crystalline form of 4-(2-chloro-4-methoxy-5- methylphenyl)-N-[( 1 S)-2-cyclopropyl- 1 -(3 -fluoro-4-methylpheny l)ethy 1] -5-methyl-N-prop-2-y ny 1- 1,3- thiazol-2-amine (Compound 1, tosylate salt), wherein the crystalline form has a thermogravimetric analysis (TGA) profile showing about 1.0% or less weight loss out to about 125°C. In some embodiments, the crystalline form (Compound 1, tosylate salt) has a thermogravimetric analysis (TGA) profile showing about 0.9% or less weight loss out to about 125°C. In some embodiments, the crystalline form (Compound 1, tosylate salt) has a thermogravimetric analysis (TGA) profile showing about 0.7% or less weight loss out to about 125°C. In some embodiments, the crystalline form (Compound 1, tosylate salt) has a thermogravimetric analysis (TGA) profile showing about 0.6% or less weight loss out to about 125°C. In some embodiments, the crystalline form (Compound 1, tosylate salt) has a thermogravimetric analysis (TGA) profile showing about 0.5% or less weight loss out to about 125°C.

[0286] One aspect of the present invention relates to a crystalline form of 4-(2-chloro-4-methoxy-5- methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3- thiazol-2-amine (Compound 1, tosylate salt), wherein the crystalline form has a thermogravimetric analysis (TGA) profile showing about 0.05% to about 1.0% weight loss out to about 125°C. In some embodiments, the crystalline form (Compound 1, tosylate salt) has a thermogravimetric analysis (TGA) profile showing about 0.1% to about 0.9% weight loss out to about 125°C. In some embodiments, the crystalline form (Compound 1, tosylate salt) has a thermogravimetric analysis (TGA) profile showing about 0.2% to about 0.7% weight loss out to about 125°C. In some embodiments, the crystalline form (Compound 1, tosylate salt) has a thermogravimetric analysis (TGA) profile showing about 0.3% to about 0.6% weight loss out to about 125°C. In some embodiments, the crystalline form (Compound 1, tosylate salt) has a thermogravimetric analysis (TGA) profile showing about 0.4% to about 0.5% weight loss out to about 125°C. In some embodiments, the crystalline form (Compound 1, tosylate salt) has a thermogravimetric analysis profile substantially as shown in Figure 25, wherein by “substantially” is meant that the reported TGA features can vary by about ± 5°C, and the reported TGA features can vary by about ± 2% weight change (i.e., ± about 2% weight change). One aspect of the present invention relates to an crystalline form of 4-(2-chloro-4-methoxy-5- methylphenyl)-N-[( 1 S)-2-cyclopropyl- 1 -(3 -fluoro-4-methylpheny l)ethy 1] -5-methyl-N-prop-2-y ny 1- 1,3- thiazol-2-amine (Compound 1, tosylate salt), wherein the crystalline form has: an X-ray powder diffraction pattern comprising at least three peaks, in terms of 2Θ, selected from the group consisting of: 9.1° ± 0.2°, 10.5° ± 0.2°, 11.3° ± 0.2°, 13.2° ± 0.2°, 16.3° ± 0.2°, 19.0° ± 0.2°, 19.3° ± 0.2°, 20.4° ± 0.2°, 21.1° ± 0.2°, 22.8° ± 0.2°, 23.3° ± 0.2°, 23.8° ± 0.2°, and 28.5° ± 0.2°; a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 154°C to about 159°C; and / or a thermogravimetric analysis profile showing about 0.05% to about 1.0% weight loss out to about 125°C.

[0287] One aspect of the present invention relates to an crystalline form of 4-(2-chloro-4-methoxy-5- methylphenyl)-N-[( 1 S)-2-cyclopropyl- 1 -(3 -fluoro-4-methylpheny l)ethy 1] -5-methyl-N-prop-2-y ny 1- 1,3- thiazol-2-amine (Compound 1, tosylate salt), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 9.1° ± 0.2°, 11.3° ± 0.2°, 21.1° ± 0.2°, 22.8° ± 0.2°, and 23.3° ± 0.2°; a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 155°C to about 158°C; and / or a thermogravimetric analysis profile showing about 0.9% or less weight loss out to about

[0288] 125°C.

[0289] One aspect of the present invention relates to an anhydrous crystalline form of 4-(2-chloro-4- methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1, tosylate salt), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern comprising peaks, in terms of 2Θ, at 9.1° ± 0.2°, 11.3° ± 0.2°, 13.2° ± 0.2°, 16.3° ± 0.2°, and 21.1° ± 0.2°; a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature of about 155.5°C to about 157.5°C; and / or a thermogravimetric analysis profile showing about 0.6% or less weight loss out to about

[0290] 125°C.

[0291] One aspect of the present invention relates to a crystalline form of 4-(2-chloro-4-methoxy-5- methylphenyl)-N-[( 1 S)-2-cyclopropyl- 1 -(3 -fluoro-4-methylpheny l)ethy 1] -5-methyl-N-prop-2-y ny 1- 1,3- thiazol-2-amine (Compound 1, tosylate salt), wherein the anhydrous crystalline form has: an X-ray powder diffraction pattern substantially as shown in Figure 24; a differential scanning calorimetry thermogram substantially as shown in Figure 25; and / or a thermogravimetric analysis profile substantially as shown in Figure 25.

[0292] In some embodiments, the anhydrous crystalline form of 4-(2-chloro-4-methoxy-5 - methylphenyl)-N-[( 1 S)-2-cyclopropyl- 1 -(3 -fluoro-4-methylpheny l)ethy 1] -5-methyl-N-prop-2-y ny 1- 1,3- thiazol-2-amine (Compound 1, tosylate salt) can be isolated as the crystalline form described herein, with a crystalline purity of at least about 75% by weight. In some embodiments, about 80% by weight. In some embodiments, about 85% by weight. In some embodiments, about 90% by weight. In some embodiments, about 95% by weight. In some embodiments, about 96% by weight. In some embodiments, about 97% by weight. In some embodiments, about 98% by weight. In some embodiments, about 99% by weight.

[0293] 4-(2-Chloro-4-methoxy-5-methylphenyl)-N-[(15)-2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine, Compound 1, with High Enantiomeric Excess (e.e.%).

[0294] One aspect of the present invention relates to 4-(2-chloro-4-methoxy-5-methylphenyl)-N- [( 1 S)-2-cyclopropyl- 1 -(3-fluoro-4-methy lphenyl)ethyl] -5 -methy 1-N-prop-2-ynyl- 1 ,3-thiazol-2-amine (Compound 1) with high enantiomeric excess (e.e.%), compositions, and novel processes related thereto.

[0295] In some embodiments, the “high e.e.%” (high enantiomeric excess) of Compound 1, or a pharmaceutically acceptable salt thereof, is an e.e.% of at least 99.3%, 99.4%, 99.5%, 99.6%, 99.7%, 99.8%, 99.9%, 100%, or a range defined by any of the preceding values, such as 99.3% to 99.9%. In some embodiments, the “high e.e.%” of Compound 1, or a pharmaceutically acceptable salt thereof, is an e.e.% of at least 99.3%. In some embodiments, the “high e.e.%” of Compound 1, or a pharmaceutically acceptable salt thereof, is an e.e.% of at least 99.4%. In some embodiments, the “high e.e.%” of Compound 1, or a pharmaceutically acceptable salt thereof, is an e.e.% of at least 99.5%. In some embodiments, the “high e.e.%” of Compound 1, or a pharmaceutically acceptable salt thereof, is an e.e.% of at least 99.6%. In some embodiments, the “high e.e.%” of Compound 1, or a pharmaceutically acceptable salt thereof, is an e.e.% of at least 99.7%. In some embodiments, the “high e.e.%” of Compound 1, or a pharmaceutically acceptable salt thereof, is an e.e.% of at least 99.8%. In some embodiments, the “high e.e.%” of Compound 1, or a pharmaceutically acceptable salt thereof, is an e.e.% of at least 99.9%. In some embodiments, the “high e.e.%” of Compound 1, or a pharmaceutically acceptable salt thereof, is an e.e.% of 99.3%. In some embodiments, the “high e.e.%” of Compound 1, or a pharmaceutically acceptable salt thereof, is an e.e.% of 99.4%. In some embodiments, the “high e.e.%” of Compound 1, or a pharmaceutically acceptable salt thereof, is an e.e.% of 99.5%. In some embodiments, the “high e.e.%” of Compound 1, or a pharmaceutically acceptable salt thereof, is an e.e.% of 99.6%. In some embodiments, the “high e.e.%” of Compound 1, or a pharmaceutically acceptable salt thereof, is an e.e.% of 99.7%. In some embodiments, the “high e.e.%” of Compound 1, or a pharmaceutically acceptable salt thereof, is an e.e.% of 99.8%. In some embodiments, the “high e.e.%” of Compound 1, or a pharmaceutically acceptable salt thereof, is an e.e.% of 99.9%. In some embodiments, the “high e.e.%” of Compound 1, or a pharmaceutically acceptable salt thereof, is an e.e.% of 100%.

[0296] Accordingly, one aspect of the present invention relates to a compound that is 4-(2-chloro-4- methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1): or a pharmaceutically acceptable salt thereof, wherein the enantiomeric excess (e.e.%) of the compound is at least 99.3% as determined by chiral HPLC.

[0297] In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, is the free base. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, is crystalline. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, is the anhydrous crystalline Form I as described herein supra and infra, for example, see: Section A. 4-(2- chloro-4-methoxy-5 -methylpheny 1)-N- [( 1S)-2-cyclopropy 1- 1 -(3 -fluoro-4-methylphenyl)ethyl] -5 - methyl-N-prop-2-y ny 1- 1 ,3 -thiazol-2-amine (Compound 1, Anhydrous Crystalline Form I).

[0298] In some embodiments, the enantiomeric excess (e.e.%) of Compound 1, or a pharmaceutically acceptable salt thereof, is at least 99.4%. In some embodiments, the enantiomeric excess (e.e.%) of Compound 1, or a pharmaceutically acceptable salt thereof, is at least 99.5%. In some embodiments, the enantiomeric excess (e.e.%) of Compound 1, or a pharmaceutically acceptable salt thereof, is at least 99.6%. In some embodiments, the enantiomeric excess (e.e.%) of Compound 1, or a pharmaceutically acceptable salt thereof, is at least 99.7%. In some embodiments, the enantiomeric excess (e.e.%) of Compound 1, or a pharmaceutically acceptable salt thereof, is at least 99.8%. In some embodiments, the enantiomeric excess (e.e.%) of Compound 1, or a pharmaceutically acceptable salt thereof, is at least 99.9%. In some embodiments, the enantiomeric excess (e.e.%) of Compound 1, or a pharmaceutically acceptable salt thereof, is 100% or less. In some embodiments, the enantiomeric excess (e.e.%) of Compound 1, or a pharmaceutically acceptable salt thereof, is 100%.

[0299] In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, has an enantiomeric excess (e.e.%) ranging from 99.3% to 100%. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, has an enantiomeric excess (e.e.%) ranging from 99.3% to 100%. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, has an enantiomeric excess (e.e.%) ranging from 99.4% to 100%. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, has an enantiomeric excess (e.e.%) ranging from 99.5% to 100%. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, has an enantiomeric excess (e.e.%) ranging from 99.6% to 100%. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, has an enantiomeric excess (e.e.%) ranging from 99.7% to 100%. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, has an enantiomeric excess (e.e.%) ranging from 99.8% to 100%. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, has an enantiomeric excess (e.e.%) ranging from 99.9% to 100%.

[0300] One aspect of the present invention relates to compositions comprising a compound that is 4- (2-chloro-4-methoxy-5 -methylpheny 1)-N- [( 1S)-2-cyclopropyl- 1 -(3 -fluoro-4-methylphenyl)ethy 1] -5 - methyl-N-prop-2-y ny 1- 1 ,3 -thiazol-2-amine (Compound 1): or a pharmaceutically acceptable salt thereof, wherein the Compound 1, or a pharmaceutically acceptable salt thereof, has a high enantiomeric excess (e.e.%) as described herein, such as, at least 99.3% as determined by chiral HPLC. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, is the free base. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, is crystalline. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, is the anhydrous crystalline Form I as described herein supra and infra, for example, see: Section A. 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[( 1S)-2-cyclopropyl- l-(3-fluoro- 4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1, Anhydrous Crystalline Form I).

[0301] In some embodiments, the composition further comprises a compound that is (S)-4-(2-chloro- 4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(p-tolyl)ethyl)-5-methyl-N-(prop-2-yn-1-yl)thiazol-2- amine (Compound IIa): or a pharmaceutically acceptable salt thereof.

[0302] In some embodiments, Compound IIa, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount ranging from 1.0% to 0.4%. In some embodiments, Compound IIa, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount ranging from 0.9% to 0.4%. In some embodiments, Compound IIa, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount ranging from 0.8% to 0.4%. In some embodiments, Compound IIa, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount ranging from 0.7% to 0.4%. In some embodiments, Compound IIa, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount ranging from 0.6% to 0.4%.

[0303] In some embodiments, the composition further comprises a compound that is (5)-4-(2-chloro- 4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2- amine (Compound 9A): or a pharmaceutically acceptab le salt thereof. In some embodiments, Compound 9A, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount less than 0.5%. In some embodiments, Compound 9A, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount less than 0.3%. In some embodiments, Compound 9A, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount less than 0.1%. In some embodiments, Compound 9A, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount less than 0.05%.

[0304] In some embodiments, Compound 9A, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount greater than 0.01% and less than 0.5%. In some embodiments, Compound 9A, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount greater than 0.01% and less than 0.3%. In some embodiments, Compound 9A, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount greater than 0.01% and less than 0.1%. In some embodiments, Compound 9A, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount greater than 0.01% and less than 0.05%.

[0305] In some embodiments, the composition further comprises a compound that is (S)-4-(2-chloro- 5-methyl-4-(prop-2-yn-1-yloxy)phenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5- methyl-N-(prop-2-yn- 1 -y l)thiazol-2-amine (Compound nb): or a pharmaceutically acceptable salt thereof.

[0306] In some embodiments, Compound nb, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount less than 0.1%. In some embodiments, the Compound nb, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount greater than 0.01% and less than about 0.1%. In some embodiments, Compound nb, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount less than 0.05%. In some embodiments, the Compound lib, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount greater than 0.01% and less than about 0.05%.

[0307] In some embodiments, the composition further comprises a compound that is 4-(2-chloro-4- methoxy-5-methylphenyl)-N-[(1R )-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-(2- propyn-1-yl)-2-thiazolamine (Compound He):

[0308] or a pharmaceutically acceptable salt thereof.

[0309] In some embodiments, Compound lie, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount less than 0.1% as determined by chiral HPLC. In some embodiments, Compound IIe, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount greater than 0.01% and less than about 0.1%. In some embodiments, Compound IIc, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount greater than 0.01% and less than about 0.05%. In some embodiments, Compound IIc, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount less than 0.05% as determined by chiral HPLC.

[0310] In some embodiments, the composition further comprises ethanol. In some embodiments, ethanol is present in the composition in an amount ranging from 300 ppm to 5000 ppm. In some embodiments, ethanol is present in the composition in an amount ranging from 300 ppm to 3000 ppm. In some embodiments, ethanol is present in the composition in an amount ranging from 300 ppm to 2000 ppm. In some embodiments, ethanol is present in the composition in an amount ranging from

[0311] 300 ppm to 1000 ppm. In some embodiments, ethanol is present in the composition in an amount ranging from 350 ppm to 600 ppm. In some embodiments, ethanol is present in the composition in an amount ranging from 375 ppm to 550 ppm.

[0312] In some embodiments, the composition further comprises propargyl bromide, wherein propargyl bromide is present in the composition in an amount less than 10 ppm. In some embodiments, propargyl bromide is present in the composition in an amount greater than 0.1 ppm and less than 10 ppm.

[0313] One aspect of the present invention relates to compositions comprising: a. 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1), or a pharmaceutically acceptable salt thereof, wherein Compound 1, or a pharmaceutically acceptable salt thereof, has a high enantiomeric excess (e.e.%) as described herein, such as, at least 99.3% as determined by chiral HPLC; and b. at least one compound selected from:

[0314] (5)-4-(2-chloro-4-methoxy-5 -methylphenyl)-N-(2-cyclopropyl- 1 -(3 -fluoro-4- methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A), or a pharmaceutically acceptable salt thereof;

[0315] (S)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(p-tolyl)ethyl)-5-methyl-N- (prop-2-yn- 1 -y l)thiazol-2-amine (Compound IIa), or a pharmaceutically acceptable salt thereof;

[0316] (S)-4-(2-chloro-5 -methyl-4-(prop-2-yn- 1 -y loxy)phenyl)-N-(2-cyclopropyl- 1 -(3-fluoro-4- methylphenyl)ethyl)-5-methyl-N-(prop-2-yn-1-yl)thiazol-2-amine (Compound nb), or a pharmaceutically acceptable salt thereof;

[0317] 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(l / ?)-2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-(2-propyn-1-yl)-2-thiazolamine (Compound lie), or a pharmaceutically acceptable salt thereof; ethanol; and propargyl bromide.

[0318] One aspect of the present invention relates to compositions comprising: a. 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1), or a pharmaceutically acceptable salt thereof, wherein Compound 1, or a pharmaceutically acceptable salt thereof, has a high enantiomeric excess (e.e.%) as described herein, such as, at least 99.3% as determined by chiral HPLC; and b. at least one compound selected from:

[0319] (S)-4-(2-chloro-4-methoxy-5 -methylphenyl)-N-(2-cyclopropyl- 1 -(3 -fluoro-4- methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A), or a pharmaceutically acceptable salt thereof;

[0320] (S)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(p-tolyl)ethyl)-5-methyl-N- (prop-2-yn- 1 -y l)thiazol-2-amine (Compound IIa), or a pharmaceutically acceptable salt thereof;

[0321] (S)-4-(2-chloro-5 -methyl-4-(prop-2-yn- 1 -yloxy)phenyl)-N-(2-cyclopropyl- 1 -(3-fluoro-4- methy lphenyl)ethyl)-5 -methyl-N-(prop-2-yn- 1 -yl)thiazol-2-amine (Compound nb), or a pharmaceutically acceptable salt thereof; ethanol; and propargyl bromide.

[0322] In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, is the free base. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, is crystalline. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, is the anhydrous crystalline Form I as described herein supra and infra, for example, see: Section A. 4-(2- chloro-4-methoxy-5 -methylpheny 1)-N- [( 1S)-2-cyclopropy 1- 1 -(3 -fluoro-4-methylphenyl)ethyl] -5 - methyl-N-prop-2-y ny 1- 1 ,3 -thiazol-2-amine (Compound 1, Anhydrous Crystalline Form I).

[0323] One aspect of the present invention relates Compound 1, or a pharmaceutically acceptable salt thereof, prepared according to any of the synthetic processes or methods as described herein, supra, and infra. According, in some embodiments, the compound that is 4-(2-chloro-4-methoxy-5- methylphenyl)-N- [( 1S)-2-cyclopropyl- 1 -(3 -fluoro-4-methylpheny l)ethy 1] -5-methyl-N-prop-2-y ny 1- 1,3- thiazol-2-amine (Compound 1): or a pharmaceutically acceptable salt thereof, wherein the Compound 1, or a pharmaceutically acceptable salt thereof, has a high enantiomeric excess (e.e.%) as described herein, such as, at least 99.3% as determined by chiral HPLC, is prepared by a process comprising: alkylating (S)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A) or a salt thereof: with a Compound of Formula (Ii): herein: LG is a leaving group; in the presence of an alkylating-step solvent, a phase-transfer catalyst, an alkylating-step base, and water to form 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1) or a pharmaceutically acceptable salt thereof.

[0324] One aspect of the present invention relates compositions comprising Compound 1, or a pharmaceutically acceptable salt thereof, prepared according to any of the synthetic processes or methods as described herein, supra, and infra. According, in some embodiments, the composition comprising the compound that is 4-(2-chloro-4-methoxy-5 -methylpheny l)-N-[( 1 S)-2-cyclopropyl- 1 -(3 - fluoro-4-methylphenyl)ethyl] -5 -methyl-N-prop-2-yny 1- 1 ,3 -thiazol-2-amine (Compound 1): or a pharmaceutically acceptable salt thereof, wherein Compound 1, or a pharmaceutically acceptable salt thereof, has a high enantiomeric excess (e.e.%) as described herein, such as, at least 99.3% as determined by chiral HPLC, is prepared by a process comprising: alkylating (5)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A) or a salt thereof: with a Compound of Formula (Ii): wherein: LG is a leaving group; in the presence of an alkylating-step solvent, a phase-transfer catalyst, an alkylating-step base, and water to form 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[( 1S)-2-cyclopropyl- l-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1) or a pharmaceutically acceptable salt thereof. In some embodiments, the compound and / or the composition can be prepared by any of the processes as described herein, such as, preparing (S)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A) or a salt thereof, comprising: cyclizing (S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-l -amine (Compound 6A) or a salt thereof: with l-(2-chloro-4-methoxy-5-methylphenyl)-2-thiocyanatopropan -1-one (Compound 8A) or a tautomeric form thereof: in the presence of a cyclizing-step solvent to form (S)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A) or a salt thereof.

[0325] In some embodiments, the compound and / or the composition can be prepared by any of the processes as described herein, such as, preparing (5)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)etlian- 1 -amine (Compound 6A) or a salt thereof, comprising: deprotecting a Compound of Formula (Ig), or a salt thereof: wherein: R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen, in the presence of a deprotec ting-catalyst, hydrogen, and a deprotecting-step solvent to form (S)-2-cyclopropyl- l-(3-fluoro-4-methylphenyl)ethan- 1-amine (Compound 6A) or a salt thereof.

[0326] In some embodiments, the compound and / or the composition can be prepared by any of the processes as described herein, such as, preparing a Compound of Formula (Ig), or a salt thereof, comprising: reducing a Compound of Formula (Ie): wherein:

[0327] R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen, in the presence of a reducing-catalyst, hydrogen, and a reducing-step solvent to form the Compound of Formula (Ig), or a salt thereof.

[0328] In some embodiments, the compound and / or the composition can be prepared by any of the processes as described herein, such as, preparing a Compound of Formula (Ie), comprising: condensing 2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A): with a Compound of Formula (Ic), or salt thereof: wherein: R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen, in the presence of a condensing-step acid and a condensing-step solvent to form the Compound of Formula (Ie).

[0329] In some embodiments, the compound and / or the composition can be prepared by any of the processes as described herein, such as, preparing 2-cyclopropyl-1-(3-fluoro-4-methylphenyl)etlian-1- one (Compound 3A), comprising: reacting 2-cyclopropyl-N-methoxy-N-methylacetamide (Compound 2A): with an organomagnesium reagent of 4-bromo-2-fluoro- 1 -methylbenzene in the presence of a reacting-step solvent to form 2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A).

[0330] Pharmaceutical Products and Pharmaceutical Compositions, comprising Compound 1 with High Enantiomeric Excess.

[0331] One aspect of the present invention relates to pharmaceutical products selected from: a pharmaceutical composition, a formulation, a unit dosage form, and a kit; each comprising Compound 1, or a pharmaceutically acceptable salt thereof, wherein Compound 1, or a pharmaceutically acceptable salt thereof, has a high enantiomeric excess (e.e.%) as described herein.

[0332] One aspect of the present invention relates to pharmaceutical compositions comprising the Compound 1, or a pharmaceutically acceptable salt thereof, wherein Compound 1, or a pharmaceutically acceptable salt thereof, has a high enantiomeric excess (e.e.%) as described herein, and a pharmaceutically acceptable carrier.

[0333] In some embodiments, the pharmaceutical product or the pharmaceutical composition comprises Compound 1, or a pharmaceutically acceptable salt thereof, as the free base. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, is crystalline. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, is the anhydrous crystalline Form I as described herein supra and infra, for example, see: Section A. 4-(2-chloro-4- methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N- prop-2-ynyl-l ,3-thiazol-2-amine (Compound 1, Anhydrous Crystalline Form I). In some embodiments, the pharmaceutical product or the pharmaceutical composition is adapted for oral administration.

[0334] One aspect of the present invention relates to pharmaceutical compositions comprising:

[0335] (a) a compound that is 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethyl] -5 -methyl-N-prop-2-yny 1- 1 ,3 -thiazol-2-amine (Compound 1): or a pharmaceutically acceptable salt thereof, wherein the Compound 1, or a pharmaceutically acceptable salt thereof, has a high enantiomeric excess (e.e.%) as described herein; and

[0336] (b) one or more of an oily phase vehicle, an emulsifying agent, a nonionic surfactant, and a solubilizing agent.

[0337] In some embodiments, the pharmaceutical composition comprises about 1 wt% to about 20 wt% of Compound 1, or a pharmaceutically acceptable salt thereof, based on the weight of the free base. In some embodiments, the pharmaceutical composition comprises about 5 wt% to about 15 wt% of Compound 1, or a pharmaceutically acceptable salt thereof, based on the weight of the free base. In some embodiments, the pharmaceutical composition comprises about 10 wt% of Compound 1, or a pharmaceutically acceptable salt thereof, based on the weight of the free base.

[0338] In some embodiments, the pharmaceutical composition comprises an oily phase vehicle. In some embodiments, the pharmaceutical composition comprises about 1 wt% to about 50 wt% of the oily phase vehicle. In some embodiments, the pharmaceutical composition comprises about 20 wt% to about 50 wt% of the oily phase vehicle. In some embodiments, the pharmaceutical composition comprises about 35 wt% to about 45 wt% of the oily phase vehicle. In some embodiments, the pharmaceutical composition comprises about 39 wt% of the oily phase vehicle.

[0339] In some embodiments, the oily phase vehicle is selected from medium-chain triglycerides, glycerin, propylene glycol, polyethylene glycol, olive oil, soybean oil, com oil, and transcutol. In some embodiments, the oily phase vehicle is medium-chain triglycerides. In some embodiments, the medium-chain triglycerides are Labrafac TM Lipophile WL1349. In some embodiments, the medium- chain triglycerides are Miglyol 812N. In some embodiments, the pharmaceutical composition comprises an emulsifying agent. In some embodiments, the pharmaceutical composition comprises about 5 wt% to about 50 wt% of the emulsifying agent. In some embodiments, the pharmaceutical composition comprises about 10 wt% to about 30 wt% of the emulsifying agent. In some embodiments, the pharmaceutical composition comprises about 15 wt% to about 25 wt% of the emulsifying agent. In some embodiments, the pharmaceutical composition comprises about 20 wt% of the emulsifying agent.

[0340] In some embodiments, the emulsifying agent is selected from medium-chain triglycerides, propylene glycol dicaprylate / dicaprate, glycerin, propylene glycol, polyethylene glycol, olive oil, soybean oil, com oil, and transcutol. In some embodiments, the emulsifying agent is propylene glycol dicaprylate / dicaprate. In some embodiments, the propylene glycol dicaprylate / dicaprate is Labrafac TM PC.

[0341] In some embodiments, the pharmaceutical composition comprises a nonionic surfactant.

[0342] In some embodiments, the pharmaceutical composition comprises about 5 wt% to about 50 wt% of the nonionic surfactant. In some embodiments, the pharmaceutical composition comprises about 10 wt% to about 30 wt% of the nonionic surfactant. In some embodiments, the pharmaceutical composition comprises about 15 wt% to about 25 wt% of the nonionic surfactant. In some embodiments, the pharmaceutical composition comprises about 19 wt% of the nonionic surfactant.

[0343] In some embodiments, the nonionic surfactant is selected from oleoyl polyoxyl-6 glycerides, linoleoyl polyoxyl-6 glycerides, Polysorbate 80, Polysorbate 20, Gelucire, lauroyl polyoxyl-32 glycerides, Poloxamer, PEG-32 stearate, and PEG-32 hydrogenated palm glycerides. In some embodiments, the nonionic surfactant is lauroyl polyoxyl-32 glycerides. In some embodiments, the lauroyl polyoxyl-32 glycerides are Gelucire® 44 / 14.

[0344] In some embodiments, the pharmaceutical composition comprises a solubilizing agent. In some embodiments, the pharmaceutical composition comprises about 1 wt% to about 50 wt% of the solubilizing agent. In some embodiments, the pharmaceutical composition comprises about 1 wt% to about 20 wt% of the solubilizing agent. In some embodiments, the pharmaceutical composition comprises about 5 wt% to about 15 wt% of the solubilizing agent. In some embodiments, the pharmaceutical composition comprises about 11 wt% of the solubilizing agent.

[0345] In some embodiments, the solubilizing agent is selected from oleoyl polyoxyl-6 glycerides, linoleoyl polyoxyl-6 glycerides, Polysorbate 80, Polysorbate 20, vitamin E polyethylene glycol succinate, Gelucire, lauroyl polyoxyl-32 glycerides, and Poloxamer. In some embodiments, the solubilizing agent is vitamin E polyethylene glycol succinate. In some embodiments, the vitamin E polyethylene glycol succinate is Kolliphor® TPGS. In some embodiments, the vitamin E polyethylene glycol succinate is Vitamin E / TPGS 260.

[0346] In some embodiments, the pharmaceutical composition comprises:

[0347] (a) 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[( 1S)-2-cyclopropyl- l-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine, or a pharmaceutically acceptable salt thereof;

[0348] (b) an oily phase vehicle;

[0349] (c) an emulsifying agent;

[0350] (d) a nonionic surfactant; and

[0351] (e) a solubilizing agent.

[0352] In some embodiments, the pharmaceutical composition comprises:

[0353] (a) about 5 wt% to about 15 wt% of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-.V-prop-2-ynyl-l,3-thiazol-2-amine, or a pharmaceutically acceptable salt thereof, based on the weight of the free base;

[0354] (b) about 35 wt% to about 45 wt% of an oily phase vehicle;

[0355] (c) about 15 wt% to about 25 wt% of an emulsifying agent;

[0356] (d) about 15 wt% to about 25 wt% of a nonionic surfactant; and

[0357] (e) about 5 wt% to about 15 wt% of a solubilizing agent.

[0358] In some embodiments, the pharmaceutical composition comprises:

[0359] (a) about 10 wt% of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethyl] -5 -methyl-N-prop-2-yny 1- 1 ,3 -thiazol-2-amine, or a pharmaceutically acceptable salt thereof, based on the weight of the free base;

[0360] (b) about 39 wt% of an oily phase vehicle;

[0361] (c) about 20 wt% of an emulsifying agent;

[0362] (d) about 19 wt% of a nonionic surfactant; and

[0363] (e) about 11 wt% of a solubilizing agent.

[0364] In some embodiments, the pharmaceutical composition comprises:

[0365] (a) 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[( 1S)-2-cyclopropyl- l-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine;

[0366] (b) a medium-chain triglycerides component;

[0367] (c) a propylene glycol dicaprylate / dicaprate component;

[0368] (d) a lauroyl polyoxyl-32 glycerides component; and

[0369] (e) a vitamin E polyethylene glycol succinate component. In some embodiments, the pharmaceutical composition comprises:

[0370] (a) about 5 wt% to about 15 wt% of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine;

[0371] (b) about 35 wt% to about 45 wt% of medium-chain triglycerides;

[0372] (c) about 15 wt% to about 25 wt% of propylene glycol dicaprylate / dicaprate;

[0373] (d) about 15 wt% to about 25 wt% of lauroyl polyoxyl-32 glycerides; and

[0374] (e) about 5 wt% to about 15 wt% of vitamin E polyethylene glycol succinate.

[0375] In some embodiments, the pharmaceutical composition comprises:

[0376] (a) about 10 wt% of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine;

[0377] (b) about 39 wt% of medium-chain triglycerides;

[0378] (c) about 20 wt% of propylene glycol dicaprylate / dicaprate;

[0379] (d) about 19 wt% of lauroyl polyoxyl-32 glycerides; and

[0380] (e) about 11 wt% of vitamin E polyethylene glycol succinate.

[0381] In some embodiments, the pharmaceutical composition comprises Compound 1 as a free base.

[0382] In some embodiments, Compound 1, or pharmaceutically acceptable salt thereof, is in crystalline form. In some embodiments, the crystalline form comprises Form I of Compound 1.

[0383] In some embodiments, the pharmaceutical composition is formulated in a unit dosage form, wherein Compound 1, or a pharmaceutically acceptable salt thereof, is present in an amount of about 5 mg to about 200 mg, based on the weight of the free base. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, is present in an amount of about 75 mg to about 150 mg, based on the weight of the free base. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, is present in an amount of about 50 mg, based on the weight of the free base. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, is present in an amount of about 100 mg, based on the weight of the free base. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, is present in an amount of about 25 mg, based on the weight of the free base.

[0384] In some embodiments, the pharmaceutical composition is in the form of a tablet, capsule, sachet, powder, granules, coated particle, coated tablet, enterocoated tablet, enterocoated capsule, melting strip, or melting film. In some embodiments, the pharmaceutical composition is in tablet form In some embodiments, the pharmaceutical composition is in capsule form. In some embodiments, the dosage form is coated. One aspect of the present invention relates to pharmaceutical compositions in oral solution dosage form comprising:

[0385] (a) a compound that is 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethyl] -5 -methyl-N-prop-2-yny 1- 1 ,3 -thiazol-2-amine (Compound 1): or a pharmaceutically acceptable salt thereof, wherein the Compound 1, or a pharmaceutically acceptable salt thereof, has a high enantiomeric excess (e.e.%) as described herein;

[0386] (b) one or more of a sweetener, an anti-oxidant, and a flavor; and

[0387] (c) a liquid vehicle, wherein the liquid vehicle is selected from medium-chain triglycerides, propylene glycol dicaprylate / dicaprate, glycerin, propylene glycol, polyethylene glycol, olive oil, soybean oil, com oil, and transcutol.

[0388] In some embodiments, the pharmaceutical composition comprises about 1 w / v% to about 50 w / v% of Compound 1, or a pharmaceutically acceptable salt thereof, based on the weight of the free base. In some embodiments, the pharmaceutical composition comprises about 1 w / v% to about 10 w / v% of Compound 1, or a pharmaceutically acceptable salt thereof, based on the weight of the free base. In some embodiments, the pharmaceutical composition comprises about 5 w / v% of Compound 1, or a pharmaceutically acceptable salt thereof, based on the weight of the free base.

[0389] In some embodiments, the pharmaceutical composition comprises a sweetener. In some embodiments, the pharmaceutical composition comprises about 0.01 w / v% to about 1.5 w / v% of the sweetener. In some embodiments, the pharmaceutical composition comprises about 0.1 w / v% to about 0.5 w / v% of the sweetener. In some embodiments, the pharmaceutical composition comprises about 0.15 w / v% of the sweetener.

[0390] In some embodiments, the sweetener is selected from saccharin, sucrose, sucralose, aspartame, dextrose, fructose, maltitol, mannitol, sorbitol, and avantame. In some embodiments, the sweetener is saccharin.

[0391] In some embodiments, the pharmaceutical composition comprises an anti-oxidant. In some embodiments, the pharmaceutical composition comprises about 0.01 w / v% to about 1.5 w / v% of the anti-oxidant. In some embodiments, the pharmaceutical composition comprises about 0.1 w / v% to about 0.5 w / v% of the anti-oxidant. In some embodiments, the pharmaceutical composition comprises about 0.17 w / v% of the anti-oxidant.

[0392] In some embodiments, the anti-oxidant is selected from butylated hydroxytoluene, vitamin E TPGS, butylated hydroxyanisole, ascorbic acid, lecithin, tert-butylhydroquinone, and citric acid. In some embodiments, the anti-oxidant is butylated hydroxytoluene.

[0393] In some embodiments, the pharmaceutical composition comprises a flavor.

[0394] In some embodiments, the pharmaceutical composition comprises about 0.01 w / v% to about 0.5 w / v% of the flavor. In some embodiments, the pharmaceutical composition comprises about 0.05 w / v% to about 0.2 w / v% of the flavor. In some embodiments, the pharmaceutical composition comprises about 0.10 w / v% of the flavor.

[0395] In some embodiments, the flavor is selected from FONA orange flavor, FONA Juicy Flavor, FONA Grape Flavor, Firmenich SA Lemon Flavor, Firmenich Tetrarome Orange Flavor, IFF Cherry Flavor, and IFF Grape Flavor. In some embodiments, the flavor is FONA orange flavor.

[0396] In some embodiments, the pharmaceutical composition comprises about 50 w / v% to about 99.9 w / v% of the liquid vehicle. In some embodiments, the pharmaceutical composition comprises about 90 w / v% to about 99 w / v% of the liquid vehicle. In some embodiments, the pharmaceutical composition comprises about 92 w / v% to about 97 w / v% of the liquid vehicle. In some embodiments, the pharmaceutical composition comprises about 94.6 w / v% of the liquid vehicle.

[0397] In some embodiments, the liquid vehicle is medium-chain triglycerides. In some embodiments, the medium-chain triglycerides is Labrafac Lipophile WL1349.

[0398] In some embodiments, the pharmaceutical composition further comprises a surfactant. In some embodiments, the pharmaceutical composition comprises about 1 w / v% to about 50 w / v% of the surfactant. In some embodiments, the pharmaceutical composition comprises about 10 w / v% to about 30 w / v% of the surfactant.

[0399] In some embodiments, the pharmaceutical composition comprises about 20 w / v% of the surfactant. In some embodiments, the surfactant is selected from oleoyl polyoxyl-6 glycerides, linoleoyl polyoxyl-6 glycerides, Polysorbate 80, Polysorbate 20, vitamin E polyethylene glycol succinate, Gelucire, lauroyl polyoxyl-32 glycerides, sodium lauryl sulfate, Poloxamer, com oil PEG-6 esters, and hydrogenated palm / palm kernel oil PEG-6 esters. In some embodiments, the surfactant is oleoyl polyoxyl-6 glycerides. In some embodiments, the oleoyl polyoxyl-6 glycerides is LABRAFIL M 1944 CS. In some embodiments, the pharmaceutical composition comprises about 70 w / v% to about 80 w / v% of the liquid vehicle. In some embodiments, the pharmaceutical composition comprises about 75 w / v% of the liquid vehicle. In some embodiments, the liquid vehicle is selected from medium- chain triglycerides, propylene glycol dicaprylate / dicaprate, glycerin, propylene glycol, polyethylene glycol, olive oil, soybean oil, com oil, and transcutol. In some embodiments, the liquid vehicle is medium-chain triglycerides. In some embodiments, the medium-chain triglycerides is Labrafac Lipophile WL1349.

[0400] In some embodiments, the pharmaceutical composition comprises:

[0401] (a) 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[( 1S)-2-cyclopropyl- l-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l ,3-thiazol-2-amine, or a pharmaceutically acceptable salt thereof;

[0402] (b) a sweetener;

[0403] (c) an anti-oxidant;

[0404] (d) a flavor; and

[0405] (e) a liquid vehicle.

[0406] In some embodiments, the pharmaceutical composition further comprises a surfactant.

[0407] In some embodiments, the pharmaceutical composition comprises:

[0408] (a) about 4 w / v% to about 6 w / v% of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine, or a pharmaceutically acceptable salt thereof, based on the weight of the free base;

[0409] (b) about 0.1 w / v% to about 0.2 w / v% of a sweetener;

[0410] (c) about 0.1 w / v% to about 0.2 w / v% of an anti-oxidant;

[0411] (d) about 0.05 w / v% to about 0.2 w / v% of a flavor; and

[0412] (e) about 92 w / v% to about 97 w / v% of a liquid vehicle.

[0413] In some embodiments, the pharmaceutical composition comprises:

[0414] (a) about 5 w / v% of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine, or a pharmaceutically acceptable salt thereof, based on the weight of the free base;

[0415] (b) about 0.15 w / v% of a sweetener;

[0416] (c) about 0.17 w / v% of an anti-oxidant;

[0417] (d) about 0.1 w / v% of a flavor; and

[0418] (e) about 94.6 w / v% of a liquid vehicle.

[0419] In some embodiments, the pharmaceutical composition comprises: (a) about 4 w / v% to about 6 w / v% of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-tliiazol-2-atnine, or a pharmaceutically acceptable salt thereof, based on the weight of the free base;

[0420] (b) about 0.1 w / v% to about 0.2 w / v% of a sweetener;

[0421] (c) about 0.1 w / v% to about 0.2 w / v% of an anti-oxidant;

[0422] (d) about 0.05 w / v% to about 0.2 w / v% of a flavor;

[0423] (e) about 15 w / v% to about 25 w / v% of a surfactant; and

[0424] (f) about 70 w / v% to about 80 w / v% of a liquid vehicle.

[0425] In some embodiments, the pharmaceutical composition comprises:

[0426] (a) about 5 w / v% of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-atnine, or a pharmaceutically acceptable salt thereof, based on the weight of the free base;

[0427] (b) about 0.15 w / v% of a sweetener;

[0428] (c) about 0.17 w / v% of an anti-oxidant;

[0429] (d) about 0.1 w / v% of a flavor;

[0430] (e) about 20 w / v% of a surfactant; and (0 about 75 w / v% of a liquid vehicle.

[0431] In some embodiments, the pharmaceutical composition comprises:

[0432] (a) 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l ,3-thiazol-2-amine, or a pharmaceutically acceptable salt thereof;

[0433] (b) saccharin;

[0434] (c) butylated hydroxytoluene;

[0435] (d) FONA orange flavor, and

[0436] (e) medium-chain triglycerides.

[0437] In some embodiments, the pharmaceutical composition further comprises oleoyl polyoxyl-6 glycerides.

[0438] In some embodiments, the pharmaceutical composition comprises:

[0439] (a) about 4 w / v% to about 6 w / v% of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine, or a pharmaceutically acceptable salt thereof, based on the weight of the free base;

[0440] (b) about 0.1 w / v% to about 0.2 w / v% of saccharin;

[0441] (c) about 0.1 w / v% to about 0.2 w / v% of butylated hydroxytoluene; (d) about 0.05 w / v% to about 0.2 w / v% of FONA orange flavor; and

[0442] (e) about 92 w / v% to about 97 w / v% of medium-chain triglycerides.

[0443] In some embodiments, the pharmaceutical composition comprises:

[0444] (a) about 5 w / v% of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine, or a pharmaceutically acceptable salt thereof, based on the weight of the free base;

[0445] (b) about 0.15 w / v% of saccharin;

[0446] (c) about 0.17 w / v% of butylated hydroxytoluene;

[0447] (d) about 0.1 w / v% of FONA orange flavor; and

[0448] (e) about 94.6 w / v% of medium-chain triglycerides.

[0449] In some embodiments, the pharmaceutical composition comprises:

[0450] (a) about 4 w / v% to about 6 w / v% of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine, or a pharmaceutically acceptable salt thereof, based on the weight of the free base;

[0451] (b) about 0.1 w / v% to about 0.2 w / v% of saccharin;

[0452] (c) about 0.1 w / v% to about 0.2 w / v% of butylated hydroxytoluene;

[0453] (d) about 0.05 w / v% to about 0.2 w / v% of FONA orange flavor;

[0454] (e) about 15 w / v% to about 25 w / v% of oleoyl polyoxyl-6 glycerides; and

[0455] (f) about 70 w / v% to about 80 w / v% of medium-chain triglycerides.

[0456] In some embodiments, the pharmaceutical composition comprises:

[0457] (a) about 5 w / v% of 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine, or a pharmaceutically acceptable salt thereof, based on the weight of the free base;

[0458] (b) about 0.15 w / v% of saccharin;

[0459] (c) about 0.17 w / v% of butylated hydroxytoluene;

[0460] (d) about 0.1 w / v% of FONA orange flavor;

[0461] (e) about 20 w / v% of oleoyl polyoxyl-6 glycerides; and (0 about 75 w / v% of medium-chain triglycerides.

[0462] In some embodiments, the pharmaceutical composition comprises Compound 1 as a free base.

[0463] In some embodiments, the pharmaceutical composition is formulated in a unit dosage form, wherein Compound 1, or a pharmaceutically acceptable salt thereof, is present in an amount of about 5 mg / mL to about 200 mg / mL, based on the weight of the free base. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, is present in an amount of about 75 mg / mL to about 150 mg / mL, based on the weight of the free base. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, is present in an amount of about 50 mg / mL, based on the weight of the free base. In some embodiments, Compound 1, or a pharmaceutically acceptable salt thereof, is present in an amount of about 100 mg / mL, based on the weight of the free base.

[0464] In some embodiments, the pharmaceutical composition has a viscosity between about 15 to about 40 centipoise at about 45 °C.

[0465] Another aspect of the present invention relates to methods for preparing a pharmaceutical composition comprising the step of admixing Compound 1, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, wherein Compound 1, or a pharmaceutically acceptable salt thereof, has a high enantiomeric excess (e.e.%) as described herein.

[0466] ISOTOPICALLY LABELED COMPOUNDS OF THE INVENTION

[0467] The compounds disclosed and described herein allow atoms at each position of the compound independently to have an isotopic distribution for a chemical element in proportional amounts to those usually found in nature or an isotopic distribution in proportional amounts different to those usually found in nature unless the context clearly dictates otherwise. Accordingly, one aspect of the present invention relates to Compounds of Formula (la): wherein:

[0468] R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, and R11are each independently selected from the group consisting of hydrogen and deuterium; and

[0469] X is selected from the group consisting of carbon-12 (12C) and carbon-13 (13C); provided that at least one R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, and R11is deuterium.

[0470] In some embodiments, each R1is independently deuterium. In some embodiments, each R2is independently deuterium. In some embodiments, each R3is independently deuterium. In some embodiments, R4is deuterium. In some embodiments, each R5is independently deuterium. In some embodiments, each R6is independently deuterium. In some embodiments, each R7is independently deuterium. In some embodiments, each R8is independently deuterium. In some embodiments, each R9is independently deuterium. In some embodiments, R10is deuterium. In some embodiments, R11is deuterium.

[0471] In some embodiments, X is carbon-12 (12C). In some embodiments, X is carbon-13 (13C).

[0472] In some embodiments, each R1is independently deuterium and X is carbon-13 (13C).

[0473] Compounds of Formula (la) can be prepared using processes described herein by introducing one or more isotopes into any of the intermediates using methods known in the art, such as, the representative process shown in Example 6.

[0474] A chemical element has an atomic number defined by the number of protons within the atom’s nucleus. Each atomic number identifies a specific element, but not the isotope; an atom of a given element can have a wide range in its number of neutrons. The number of both protons and neutrons in the nucleus is the atom's mass number, and each isotope of a given element has a different mass number. A compound wherein one or more atoms have an isotopic distribution for a chemical element in proportional amounts different to those usually found in nature is commonly referred to as being an isotopically labeled compound. Each chemical element as represented in a compound structure can include any isotopic distribution of said element. For example, in a compound structure a hydrogen atom can be explicitly disclosed or understood to be present in the compound. At any position of the compound that a hydrogen atom can be present, the hydrogen atom can be an isotopic distribution of hydrogen, including but not limited to protium (1H ) and deuterium (2H) in proportional amounts to those usually found in nature and in proportional amounts different to those usually found in nature. Thus, reference herein to a compound encompasses all potential isotopic distributions for each atom unless the context clearly dictates otherwise. Examples of isotopes include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, sulfur, fluorine, chlorine, bromine and iodine. As one of skill in the art would appreciate, any of the compounds as disclosed and described herein can include radioactive isotopes. Accordingly, also contemplated is use of compounds as disclosed and described herein, wherein one or more atoms have an isotopic distribution different to those usually found in nature, such as having2H or3H in greater proportion, or11C,13C, or14C in greater proportion than found in nature. By way of general example, and without limitation, isotopes of hydrogen include protium (1H ), deuterium (2H) and tritium (3H). Isotopes of carbon include carbon- 11 (11C), carbon-12 (12C), carbon-13 (13C), and carbon-14 (14C). Isotopes of nitrogen include nitrogen-13 (13N),nitrogen- 14 (14N) and nitrogen-15 (15N)· Isotopes of oxygen include oxygen-14 (14O), oxygen-15 (15O), oxygen- 16 (160), oxygen- 17 (170), and oxygen-18 (180). Isotope of fluorine include fluorine-17 (17F), fluorine- 18 (18F) and fluorine-19 (19F). Isotopes of phosphorous include phosphorus-31 (31P), phosphorus-32 (32P), phosphorus-33 (33P), phosphorus-34 (34P), phosphorus-35 (35P) and phosphorus-36 (36P).

[0475] Isotopes of sulfur include sulfur-32 (32S), sulfiir-33 (^S), sulfur-34 (34S), sulfiir-35 (35S), sulfiir-36 (36S) and sulfiir-38 (38S). Isotopes of chlorine include chlorine-35 (35C1), chlorine-36 (36C1) and chlorine-37 (37Cl). Isotopes of bromine include bromine-75 (75Br), bromine-76 (76Br), bromine-77 (77Br), bromine-79 (79Br), bromine-81 (81Br) and bromine-82 (82Br). Isotopes of iodine include iodine- 123 (123I), iodine-124 (124I), iodine-125 (125I), iodine-131 (131I) and iodine-135 (135I). In some embodiments, atoms at every position of the compound have an isotopic distribution for each chemical element in proportional amounts to those usually found in nature. In some embodiments, atoms in at least one position of the compound has an isotopic distribution for a chemical element in proportional amounts different to those usually found in nature (remainder atoms having an isotopic distribution for a chemical element in proportional amounts to those usually found in nature). In some embodiments, atoms in at least two positions of the compound independently have an isotopic distribution for a chemical element in proportional amounts different to those usually found in nature (remainder atoms having an isotopic distribution for a chemical element in proportional amounts to those usually found in nature). In some embodiments, atoms in at least three positions of the compound independently have an isotopic distribution for a chemical element in proportional amounts different to those usually found in nature (remainder atoms having an isotopic distribution for a chemical element in proportional amounts to those usually found in nature). In some embodiments, atoms in at least four positions of the compound independently have an isotopic distribution for a chemical element in proportional amounts different to those usually found in nature (remainder atoms having an isotopic distribution for a chemical element in proportional amounts to those usually found in nature). In some embodiments, atoms in at least five positions of the compound independently have an isotopic distribution for a chemical element in proportional amounts different to those usually found in nature (remainder atoms having an isotopic distribution for a chemical element in proportional amounts to those usually found in nature). In some embodiments, atoms in at least six positions of the compound independently have an isotopic distribution for a chemical element in proportional amounts different to those usually found in nature (remainder atoms having an isotopic distribution for a chemical element in proportional amounts to those usually found in nature).

[0476] With regard to the compounds provided herein, when a particular atomic position is designated as having deuterium or "D" or “d”, it is understood that the abundance of deuterium at that position is substantially greater than the natural abundance of deuterium, which is about 0.015%. A position designated as having deuterium typically has a minimum isotopic enrichment factor of, in certain embodiments, at least 3500 (52.5% deuterium incorporation), at least 4000 (60% deuterium incorporation), at least 4500 (67.5% deuterium incorporation), at least 5000 (75% deuterium incorporation), at least 5500 (82.5% deuterium incorporation), at least 6000 (90% deuterium incorporation), at least 6333.3 (95% deuterium incorporation), at least 6466.7 (97% deuterium incorporation), at least 6600 (99% deuterium incorporation), or at least 6633.3 (99.5% deuterium incorporation) at each designated deuterium position.

[0477] CERTAIN PROCESSES OF THE INVENTION

[0478] The present invention is directed, inter alia, to processes useful in the preparation of 4-(2- chloro-4-methoxy-5 -methylpheny 1)-N- [( 1 S)-2-cyclopropy 1- 1 -(3 -fluoro-4-methylphenyl)ethyl] -5 - methyl-N-prop-2-ynyl- 1 ,3 -thiazol-2-amine (Compound 1) and crystalline forms thereof.

[0479] Any of the processes either, collectively as one or more steps together, or individual steps as described herein, infra and supra, can be conducted under an inert atmosphere. Accordingly, in some embodiments, the process step as described herein is conducted under a substantially inert atmosphere.

[0480] In some embodiments, the process step as described herein is conducted under a substantially inert atmosphere comprising argon or nitrogen. In some embodiments, the process step as described herein is conducted under a substantially inert atmosphere comprising nitrogen.

[0481] The reactions of the processes described herein can be carried out in suitable solvents which can be readily selected by one of skill in the art of organic synthesis. Suitable solvents can be substantially nonreactive with the starting materials (reactants), the intermediates, or products at the temperatures at which the reactions are carried out, e.g., temperatures which can range from the solvent's freezing temperature to the solvent's boiling temperature. A given reaction can be carried out in one solvent or a mixture of more than one solvent. Depending on the reaction step, suitable solvents for a particular reaction step can be selected. In some embodiments, reactions can be carried out in the absence of solvent, such as when at least one of the intermediates or reagents is a liquid.

[0482] Suitable solvents can include halogenated solvents such as: carbon tetrachloride, bromodichloromethane, dibromochloromethane, bromoform, chloroform, bromochloromethane, dibromomethane, butyl chloride, dichloromethane, tetrachloroethylene, trichloroethylene, 1,1,1- trichloroethane, 1 , 1 ,2-trichloroethane, 1,1-dichloroethane, 1 ,2-dichloroethane, 2-chloropropane, hexafluorobenzene, 1 ,2,4-trichlorobenzene, 1 ,2-dichlorobenzene, 1 ,3-dichlorobenzene, 1,4- dichlorobenzene, chlorobenzene, fluorobenzene, fluorotrichloromethane, chlorotrifluoromethane, bromotrifluoromethane, carbon tetrafluoride, dichlorofluoromethane, chlorodifluoromethane, trifluoromethane, 1 ,2-dichlorotetrafluorethane, hexafluoroethane, and mixtures thereof.

[0483] Suitable solvents can include ether solvents, such as: 1 ,2-dimethoxyethane (DME), tetrahydrofiiran (THF), cyclopentyl methyl ether (CPME), 2-methyltetrahydrofuran (2-MeTHF), 1,3- dioxane, 1,4-dioxane, diethyl ether, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, triethylene glycol dimethyl ether, 5- methyl-2-hexanone (MIAK), 4-methyl-2-pentanone (ΜIBΚ), tert-amyl methyl ether (TAME, also referred to as 2-methoxy-2-methylbutane), methyl tert-butyl ether (MTBE), and mixtures thereof.

[0484] Suitable solvents can include alcohol or protic solvents, such as: methanol, ethanol, 2- nitroethanol, 2-fluoroethanol, 2,2,2-trifluoroethanol, ethylene glycol, 1-propanol, 2-propanol, 2- methoxyethanol, 1 -butanol, 2-butanol, isobutyl alcohol, t-butyl alcohol, 2-ethoxyethanol, diethylene glycol, 1-pentanol, 2-pentanol, 3-pentanol, neo-pentyl alcohol, t-pentyl alcohol, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, cyclohexanol, benzyl alcohol, glycerol, and mixtures thereof.

[0485] Suitable solvents can include aprotic solvents, such as: benzene, chlorobenzene, cyclohexane, pentane, hexane, toluene, cycloheptane, methylcyclohexane, heptanes, n-heptane, ethylbenzene, o- xylene, m-xylene, p-xylene, mixtures of xylenes, octane, indane, nonane, naphthalene, tetrahydrofiiran, acetonitrile, dimethyl sulfoxide, propionitrile, ethyl formate, methyl acetate, hexachloroacetone, acetone, ethyl methyl ketone, ethyl acetate, isopropyl acetate, sulfolane, 1,3- dimethyl-3, 4, 5, 6-tetrahydro-2(lH)-pyrimidinone, l,3-dimethyl-2-imidazolidinone, N- methylpyrrolidinone, tetramethylurea, nitromethane, and nitrobenzene, and amides, including but not limited to, N,N-dimethylforrnarnide, N,N-dimethylacetamide, formamide, / V-methylacetamide, N- methylformamide, N,N-dimethylpropionamide, hexamethylphosphoramide, and mixtures thereof.

[0486] Suitable hydrocarbon solvents include benzene, cyclohexane, pentane, hexane, toluene, cycloheptane, methylcyclohexane, heptane, ethylbenzene, m-, o-, or p-xylene, octane, indane, nonane, naphthalene, and mixtures thereof.

[0487] The processes described herein can be monitored according to any suitable method known in the art. For example, product formation can be monitored by spectroscopic means, such as nuclear magnetic resonance spectroscopy (e.g.,1H or13), infrared spectroscopy, spectrophotometry (e.g., UV-visible), mass spectrometry, gas chromatography (GC), or by chromatography, such as, high performance liquid chromatography (HPLC) or thin layer chromatography.

[0488] Upon carrying out preparation of compounds according to the processes described herein, the usual isolation and purification operations such as concentration, filtration, extraction, solid-phase extraction, recrystallization, enantiomeric-enrichment via recrystallization, chromatography, and the like, may be used to isolate the desired product.

[0489] Example processes and certain intermediates of the present invention are shown in Scheme I to Scheme VII below.

[0490] A representative Coupling-Step of 2-cyclopropylacetic acid (Compound 1A) with N,0- dimethylhydroxylamine or a salt thereof in the presence of a coupling-step reagent (e.g., 1,1’- carbonyldiimidazole), a coupling-step base (e.g., triethylamine), and a coupling-step solvent (e.g., dichloromethane) to prepare 2-cyclopropyl-N-methoxy-N-methylacetamide (Compound 2A) is provided below in Scheme I.

[0491] A representative Reacting-Step between 2-cyclopropyl-N-methoxy-N-methylacetamide (Compound 2A) with an organomagnesium reagent of 4-bromo-2-fluoro- 1 -methylbenzene in the presence of a reacting-step solvent (e.g., tetrahydrofuran (THF)) to prepare 2-cyclopropyl-1-(3-fluoro- 4-methylphenyl)ethan- 1 -one (Compound 3A) is provided below in Scheme Π.

[0492] A representative Condensing-Step of 2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A) with a Compound of Formula (Ic) or a salt thereof, in the presence of a condensing- step acid (e.g., p-toluenesulfonic acid) and a condensing-step solvent (e.g., toluene) to prepare a Compound of Formula (Ie) is provided below in Scheme ΙΠ. wherein:

[0493] R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen.

[0494] A representative Reducing-Step of a Compound of Formula (Ie) in the presence of a reducing- catalyst (e.g., sponge nickel and Pd / Cu-C), hydrogen, and a reducing-step solvent (e.g., ethanol) to prepare a Compound of Formula (Ig) is provided below in Scheme IV. wherein:

[0495] R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen.

[0496] A representative Deprotecting-Step of a Compound of Formula (Ig), or a salt thereof, in the presence of a deprotecting-catalyst (e.g., Pd), hydrogen, and a deprotecting-step solvent (e.g., ethanol) to prepare (S)-2-cyclopropyl- l-(3-fluoro-4-methylphenyl)ethan- 1-amine (Compound 6A) or a salt thereof is provided below in Scheme V. wherein:

[0497] R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen.

[0498] A representative Cyclizing-Step of (S)-2-cyclopropyl-1-(3-fluoro-4wmethylphenyl)ethan-1- amine (Compound 6A) or a salt thereof, with l-(2-chloro-4-methoxy-5-methylphenyl)-2- thiocy anatopropan- 1 -one (Compound 8A) or a tautomeric form thereof, in the presence of a cyclizing-step solvent (e.g., n-heptane) to prepare (S)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A) or a salt thereof is provided below in Scheme VI.

[0499]

[0500] A representative Alkylating-Step of (S)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A) or a salt thereof, with a Compound of Formula (Ii), wherein LG is suitable leaving group (e.g., Br), in the presence of an alkylating-step solvent (e.g., methyl tert-butyl ether (MTBE), toluene, and mixtures thereof), a phase-transfer catalyst (e.g., tetra-n-butylammonium bromide (TBAB)), an alkylating-step base (e.g., potassium hydroxide), and water to prepare 4-(2-chloro-4-methoxy-5-methylphenyl)-N- [( 1 S)-2-cyclopropyl- 1 -(3-fluoro-4-methy lphenyl)ethyl] -5 -methy 1-N-prop-2-ynyl- 1 ,3-thiazol-2-amine (Compound 1) or a pharmaceutically acceptable salt thereof is provided below in Scheme VII.

[0501] One aspect of the present invention includes every combination of one or more process steps and intermediates related thereto used in the preparation of 4-(2-chloro-4-methoxy-5-methylphenyl)- N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2- amine (Compound 1), and / or pharmaceutically acceptable salts, and crystalline forms thereof, such as those processes exemplified by Schemes I, Π, ΙΠ, IV, V, VI, VII, and VII (supra) and Compounds contained therein.

[0502] One aspect of the present invention pertains to one or more of the intermediates, such as, Compounds (2A), (3A), (4A), (5A), (6A), (7A), (8A), and (9A); and compounds of Formulae (la),

[0503] (Ic), (Ie), (Ig), and (Ii), and those compounds prepared by the processes exemplified in Schemes I, Π, ΠΙ, IV, V, VI, Vn, and VII (supra), that are useful in the preparation of 4-(2-chloro-4-methoxy-5- methylphenyl)-N-[( 1 S)-2-cyclopropyl- 1 -(3 -fluoro-4-methylpheny l)ethy 1] -5-methyl-N-prop-2-ynyl- 1,3- thiazol-2-amine (Compound 1), and / or pharmaceutically acceptable salts, and crystalline forms thereof.

[0504] Certain synthetic processes for the preparation of 4-(2-chloro-4-methoxy-5-methylphenyl)-N- [( 1 S)-2-cyclopropyl- 1 -(3-fluoro-4-methy lphenyl)ethyl] -5 -methy 1-W-prop-2-ynyl- 1 ,3-thiazol-2-amine (Compound 1) have been described in PCT application PCT / FROO / 01995 , filed 11 July 2000

[0505] (International Publication Number W02001 / 05776). Several improvements have been discovered and are described herein.

[0506] One such improvement is the use of PTC conditions as shown in Scheme VII which eliminated the need for moisture sensitive bases, such as sodium hydride, and dimethylformamide as described in WO2001 / 05776 (see Example 25).

[0507] Other improvements include the steps as shown in Scheme into IV which converted ketone (Compound 3A) to the chiral amine (Compound 6A) in high yield and high enantiomeric excess.

[0508] Compounds of the invention also include all isotopes of atoms occurring in the intermediates and / or final compounds. Isotopes include those atoms having the same atomic number but different mass numbers, for example, isotopes of hydrogen include deuterium and tritium.

[0509] I. Processes useful for the preparation of 4-(2-chloro-4-methoxy-5-methylphenyl> V-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l^-thiazol-2- amine (Compound 1) or a pharmaceutical salt thereof (Alkylating-Step).

[0510] One aspect of the present invention relates to processes for preparing 4-(2-chloro-4-methoxy- 5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl- 1,3-thiazol -2-amine (Compound 1) or a pharmaceutically acceptable salt thereof: comprising: alkylating (5)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A) or a salt thereof: with a Compound of Formula (Ii): herein: LG is a leaving group; in the presence of an alkylating-step solvent, a phase-transfer catalyst, an alkylating-step base, and water to form 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[( 1S)-2-cyclopropyl- l-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1) or a pharmaceutically acceptable salt thereof.

[0511] In some embodiments, LG is selected from the group: C1-C4alkylsulphonyloxy, C6-C10 arylsulfonyloxy, halogen, and hydroxy; wherein C1-C4alkylsulphonyloxy and C6-C10 arylsulfonyloxy are each optionally substituted with one or more groups selected from the group: C1-C4alkyl, C1-C4alkoxy, halogen, C1-C4haloalkyl, C1-C4haloalkoxy, and nitro.

[0512] In some embodiments, the Compound of Formula (H) is a compound of the following

[0513] Formula: wherein the alkyl group is optionally substituted with one or more groups selected from the group: C1-C4alkoxy, halogen, C1-C4haloalkyl, C1-C4haloalkoxy, and nitro. In some embodiments, the phrase “one or more groups” is one, two, or three groups. In some embodiments, the alkyl group is optionally substituted with one or more halogen groups. In some embodiments, the alkyl group is optionally substituted with one or more fluoro groups.

[0514] In some embodiments, the Compound of Formula (H) is a compound of the following

[0515] Formula: wherein: Rla, R2*, and R3* are each selected independently from the group consisting of: H, Ci- Ct alkyl, C1-C4 alkoxy, halogen, C1-C4 haloalkyl, C1-C4 haloalkoxy, and nitro. In some embodiments, Rla, R2*, and R3· are each selected independently from the group consisting of: H, methyl, methoxy, fluoro, chloro, bromo, iodo, trifluoromethyl, trifluoromethoxy, and nitro. In some embodiments, Rla, R2*, and R3· are each selected independently from the group consisting of: H, methyl, methoxy, fluoro, chloro, bromo, trifluoromethyl, trifluoromethoxy, and nitro. In some embodiments, R1c, R2c, and R3care each selected independently from the group consisting of: H, methyl, fluoro, trifluoromethyl, trifluoromethoxy, and nitro. In some embodiments, R1c, R2c, and R3aare each selected independently from the group consisting of: H and methyl.

[0516] In some embodiments, LG is halogen.

[0517] In some embodiments, LG is Cl, Br, or I.

[0518] In some embodiments, LG is Br.

[0519] In some embodiments, the Compound of Formula (H) is selected from the group consisting of: propargyl bromide, propargyl chloride, propargyl alcohol, propargyl methanesulfonate, propargyl trifluoromethanesulfonate, propargyl benzenesulfonate, and propargyl p-toluenesulfonate. In some embodiments, the Compound of Formula (H) is selected from the group consisting of: propargyl bromide, propargyl methanesulfonate, propargyl trifluoromethanesulfonate, propargyl benzenesulfonate, and propargyl p-toluenesulfonate.

[0520] In some embodiments, the Compound of Formula (H) is propargyl bromide.

[0521] In some embodiments, the Compound of Formula (II) and Compound 9A are present in substantially equal molar quantities. In some embodiments, the Compound of Formula (H) is present in a molar excess compared to Compound 9A. In some embodiments, the Compound of Formula (II) is present in about 30% molar excess compared to Compound 9A. In some embodiments, the Compound of Formula (Ii) is present in about 25% molar excess compared to Compound 9A. In some embodiments, the Compound of Formula (H) is present in about 20% molar excess compared to Compound 9A.

[0522] In some embodiments, Compound 9A and the phase-transfer catalyst are present in substantially equal molar quantities. In some embodiments, the molar ratio between Compound 9A and the phase-transfer catalyst is about 1:0.05 to about 1:0.9. In some embodiments, the molar ratio between Compound 9A and the phase-transfer catalyst is about 1:0.05 to about 1:0.8. In some embodiments, the molar ratio between Compound 9A and the phase-transfer catalyst is about 1:0.05 to about 1:0.7. In some embodiments, the molar ratio between Compound 9A and the phase-transfer catalyst is about 1:0.05 to about 1:0.6. In some embodiments, the molar ratio between Compound 9A and the phase-transfer catalyst is about 1:0.05 to about 1:0.5.

[0523] In some embodiments, the molar ratio between Compound 9A and the phase-transfer catalyst is about 1:0.05 to about 1:0.4. In some embodiments, the molar ratio between Compound 9A and the phase-transfer catalyst is about 1:0.1 to about 1.3:0.2. In some embodiments, the molar ratio between Compound 9A and the phase-transfer catalyst is about 1:0.15.

[0524] In some embodiments, the molar ratio between Compound 9A, the phase-transfer catalyst, and the alkylating-step base is about 1:0.05:5 to about 1:0.4:25. In some embodiments, the molar ratio between Compound 9A, the phase-transfer catalyst, and the alkylating-step base is about 1:0.1:10 to about 1:0.2:20. In some embodiments, the molar ratio between Compound 9A, the phase-transfer catalyst, and the alkylating-step base is about 1:0.15:16.

[0525] In some embodiments, the alkylating-step solvent is any suitable solvent, such as, a solvent as described herein, or mixtures thereof.

[0526] In some embodiments, the alkylating-step solvent is selected from a halogenated solvent, an ether solvent, an aptotic solvent, and mixtures thereof. In some embodiments, the alkylating-step solvent is selected from: dichloromethane, tetrachloroethylene, 1,1-dichloroethane, 1 ,2-dichloroethane, 1 ,2-dichlorobenzene, chlorobenzene, 1 ,2-dimethoxyethane (DME), cyclopentyl methyl ether (CPME),

[0527] 2-methyltetrahydrofuran (2-MeTHF), 1,4-dioxane, ethylene glycol diethyl ether, fert-amyl methyl ether (TAME, also referred to as 2-methoxy-2-methylbutane), methyl tert-butyl ether (MTBE), benzene, cyclohexane, hexane, toluene, cycloheptane, methylcyclohexane, heptanes, n-heptane, ethylbenzene, o-xylene, m-xylene, p-xylene, mixtures of xylenes, octane, and mixtures thereof. In some embodiments, the alkylating-step solvent is selected from: 1 ,2-dimethoxyethane (DME), cyclopentyl methyl ether (CPME), 2-methyltetrahydrofiiran (2-MeTHF), 1,4-dioxane, ethylene glycol diethyl ether, tert-amyl methyl ether (TAME, also referred to as 2-methoxy-2-methylbutane), methyl tert-butyl ether (MTBE), benzene, toluene, and mixtures thereof. In some embodiments, the alkylating-step solvent is selected from: methyl tert-butyl ether (MTBE), toluene, and mixtures thereof.

[0528] In some embodiments, the phase-transfer catalyst is a quaternary ammonium salt. In some embodiments, the phase-transfer catalyst is a quaternary ammonium salt selected from: tricaprylyl methyl ammonium chloride (Aliquat 336), tetra-n-butylammonium bromide (TBAB), benzyltriethylammonium chloride (BTEAC), cetyltrimethylammonium bromide (CTAB), tetra-n- butylammonium chloride (TBAQ, tetra-n-butylammonium hydroxide, tetra-n-butylammonium iodide, tetraethylammonium chloride (TEAC), benzyltributylammonium chloride (BTBAQ, cetyltrimethylammonium chloride (CTAC), tetramethylammonium chloride, cetyltrimethylammonium chloride (CTAC), octyltrimethylammonium chloride, and combinations thereof. In some embodiments, the phase-transfer catalyst is tetra-n-butylammonium bromide (TBAB).

[0529] In some embodiments, the alkylating-step base is any suitable base, such as, a base as described herein, or mixtures thereof.

[0530] In some embodiments, the alkylating-step base is an “inorganic base” as described herein.

[0531] In some embodiments, the alkylating-step base is an alkali metal hydroxide. In some embodiments, the alkylating-step base is an alkali metal hydroxide selected from: lithium hydroxide, sodium hydroxide, potassium hydroxide, and cesium hydroxide. In some embodiments, the alkylating- step base is an alkali metal hydroxide selected from: sodium hydroxide and potassium hydroxide. In some embodiments, the alkylating-step base is potassium hydroxide.

[0532] In some embodiments, the alkylating step further comprises the steps of: forming a first-alkylating mixture comprising the alkylating-step solvent, the alkylating- catalyst, and Compound 9A at a first-alkylating temperature; and adding the alkylating-step base and the Compound of Formula (H) to the first-alkylating mixture at the first-alkylating temperature to form an alkylating-biphasic mixture at a second- alkylating temperature.

[0533] In some embodiments, the alkylating step further comprises heating the first-alkylating mixture comprising the alkylating-step solvent, the alkylating-catalyst, and Compound 9A to a temperature of about 40 °C to about 75 °C and subsequently cooling to the first-alkylating temperature. In some embodiments, the alkylating step further comprises heating first-alkylating mixture comprising the alkylating-step solvent, the alkylating-catalyst, and Compound 9A to a temperature of about 55 °C to about 65 °C and subsequently cooling to the first-alkylating temperature. In some embodiments, the alkylating step further comprises heating first-alkylating mixture comprising the alkylating-step solvent, the alkylating-catalyst, and Compound 9A to a temperature of about 60 °C and subsequently cooling to the first-alkylating temperature.

[0534] In some embodiments, adding the alkylating-step base to the first-alkylating mixture is conducted as a solution of the alkylating-step base in water.

[0535] In some embodiments, adding the alkylating-step base to the first-alkylating mixture is conducted as a solution of the alkylating-step base in water and the concentration in terms of percent weight / weight (% w / w) of the alkylating-step base and water is about 40 to about 60. In some embodiments, adding the alkylating-step base to the first-alkylating mixture is conducted as a solution of the alkylating-step base in water and the concentration in terms of percent weight / weight (% w / w) of the alkylating-step base and water is about 45 to about 55. In some embodiments, adding the alkylating-step base to the first-alkylating mixture is conducted as a solution of the alkylating-step base in water and the concentration in terms of percent weight / weight (% w / w) of the alkylating-step base and water is about 52 to about 53. In some embodiments, adding the alkylating-step base to the first-alkylating mixture is conducted as a solution of the alkylating-step base in water and the concentration in terms of percent weight / weight (% w / w) of the alkylating-step base and water is about 52.4.

[0536] In some embodiments, adding the Compound of Formula (Ii) to the first-alkylating mixture is conducted as a solution of the Compound of Formula (H) in the alkylating-step solvent. In some embodiments, adding the Compound of Formula (Ii) to the first-alkylating mixture is conducted as a solution of the Compound of Formula (Ii) in the alkylating-step solvent and the concentration in terms of percent weight / weight (% w / w) of the Compound of Formula (H) in the alkylating-step solvent is about 65 to about 90. In some embodiments, adding the Compound of Formula (H) to the first- alkylating mixture is conducted as a solution of the Compound of Formula (Ii) in the alkylating-step solvent and the concentration in terms of percent weight / weight (% w / w) of the Compound of Formula (Ii) in the alkylating-step solvent is about 75 to about 85. In some embodiments, adding the Compound of Formula (Ii) to the first-alkylating mixture is conducted as a solution of the Compound of Formula (Ii) in the alkylating-step solvent and the concentration in terms of percent weight / weight (% w / w) of the Compound of Formula (H) in the alkylating-step solvent is about 80.

[0537] In some embodiments, adding the alkylating-step base and the Compound of Formula (Ii) to the first-alkylating mixture is conducted concurrently at a rate to maintain the first-alkylating temperature.

[0538] In some embodiments, adding the alkylating-step base and the Compound of Formula (Ii) to the first-alkylating mixture is conducted serially at a rate to maintain the first-alkylating temperature. In some embodiments, serially is conducted by adding the alkylating-step base followed by adding the Compound of Formula (Ii) to the first-alkylating mixture at a rate to maintain the first-alkylating temperature during each addition.

[0539] In some embodiments, the first-alkylating temperature is about -15 °C to about 15 °C. In some embodiments, the first-alkylating temperature is about -10 °C to about 10 °C. In some embodiments, the first-alkylating temperature is about -5 °C to about 7 °C. In some embodiments, the first-alkylating temperature is about 0 °C to about 5 °C.

[0540] In some embodiments, the second-alkylating temperature is about -10 °C to about 20 °C. In some embodiments, the second-alkylating temperature is about -5 °C to about 15 °C. In some embodiments, the second-alkylating temperature is about 0 °C to about 10 °C. In some embodiments, the second-alkylating temperature is about 4 °C to about 6 °C.

[0541] In some embodiments, alkylating is conducted with stirring. In some embodiments, alkylating is conducted with vigorous stirring. In some embodiments, alkylating is conducted with vigorous stirring at a rate to increase the water and organic interface.

[0542] In some embodiments, the alkylating step further comprises preparing (S)-4-(2-chloro-4- methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2- amine (Compound 9A) or a salt thereof, by the step of: cyclizing (S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-l -amine (Compound 6A) or a salt thereof: with l-(2-chloro-4-methoxy-5-methylphenyl)-2-thiocyanatopropan-1-one (Compound 8A) or a tautomeric form thereof: in the presence of a cyclizing-step solvent to form (S)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A) or a salt thereof.

[0543] In some embodiments, the alkylating step further comprises preparing (S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethan-l -amine (Compound 6A) or a salt thereof, by the step of: deprotecting a Compound of Formula (Ig), or a salt thereof, herein:

[0544] R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen; in the presence of a deprotec ting-catalyst, hydrogen, and a deprotecting-step solvent to form (5)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-amine (Compound 6A) or a salt thereof.

[0545] In some embodiments, the alkylating step further comprises preparing a Compound of Formula (Ig), or a salt thereof, wherein:

[0546] R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen; comprising: reducing a Compound of Formula (Ie): wherein:

[0547] R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen; in the presence of a reducing-catalyst, hydrogen, and a reducing-step solvent to form the Compound of Formula (Ig), or a salt thereof. In some embodiments, the alkylating step further comprises preparing a Compound of

[0548] Formula (Ie): wherein:

[0549] R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen; comprising: condensing 2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A): with a Compound of Formula (Ic), or a salt thereof in the presence of a condensing-step acid and a condensing-step solvent to form the Compound of Formula (Ie).

[0550] In some embodiments, the alkylating step further comprising preparing 2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethan-1-one (Compound 3A), by the step of: reacting 2-cyclopropyl-N-methoxy-N-methylacetamide (Compound 2A): with an organomagnesium reagent of 4-bromo-2-fluoro- 1 -methylbenzene in the presence of a reacting- step solvent to form 2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A).

[0551] In some embodiments, the alkylating step further comprising the step of isolating 4-(2-chloro- 4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N- prop-2-ynyl-l ,3-thiazol-2-amine (Compound 1) or a pharmaceutically acceptable salt thereof. In some embodiments, 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[( 1S)-2-cyclopropyl- l-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine is the free base. In some embodiments, 4-(2-chloro-4-methoxy-5 -methylphenyl)-N- [( 1 S)-2-cyclopropyl- 1 -(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine is crystalline. In some embodiments, wherein 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[( 1S)-2-cyclopropyl- l-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine is crystalline Form I.

[0552] In some embodiments, the alkylating step further comprising the step of formulating 4-(2- chloro-4-methoxy-5 -methylpheny l)-N-[( 1 S)-2-cyclopropy 1- 1 -(3 -fluoro-4-methylphenyl)ethyl] -5 - methyl-N-prop-2-ynyl- 1 ,3 -thiazol-2-amine to form a pharmaceutical composition. In some embodiments, the step of formulating comprises admixing 4-(2-chloro-4-methoxy-5-methylphenyl)-N- [(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine with a pharmaceutical excipient.

[0553] In some embodiments, the alkylating step further comprises the step of isolating 4-(2-chloro- 4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N- prop-2-ynyl-l,3-thiazol -2-amine (Compound 1), or a pharmaceutically acceptable salt thereof.

[0554] In some embodiments, the alkylating step comprises the step of formulating 4-(2-chloro-4- methoxy-5 -methylpheny l)-N-[( 15)-2-cyclopropyl- 1 -(3-fluoro-4-methylpheny l)ethy 1] -5 -methyl-N- prop-2-ynyl-l,3-thiazol -2-amine, or a pharmaceutically acceptable salt thereof, to form a pharmaceutical composition. In some embodiments, the step of formulating comprises admixing 4-(2- chloro-4-methoxy-5 -methylpheny l)-N-[( 1 S)-2-cyclopropy 1- 1 -(3 -fluoro-4-methylphenyl)ethyl] -5 - methyl-N-prop-2-ynyl- 1 ,3 -thiazol-2-amine, or a pharmaceutically acceptable salt thereof, with a pharmaceutical excipient. In some embodiments, the step of formulating comprises preparing a spray- dried dispersion as described in the examples.

[0555] In some embodiments, 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(15)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethyl] -5 -methyl-N-prop-2-yny 1- 1 ,3 -thiazol-2-amine is the free base. In some embodiments, 4-(2-chloro-4-methoxy-5 -methylphenyl)-N- [( 15)-2-cyclopropyl- 1 -(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine is crystalline. In some embodiments, 4-(2-chloro-4-methoxy-5 -methylphenyl)-N- [( 15)-2-cyclopropyl- 1 -(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine is crystalline Form I. Π. Processes useful for the preparation of (S)-4-(2-chloro-4-methoxy-5- methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A) or a salt thereof (Cyclizing-Step).

[0556] One aspect of the present invention relates to processes for preparing (S)-4-(2-chloro-4- methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2- amine (Compound 9A) or a salt thereof: comprising: cyclizing (S)2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-l -amine (Compound 6A) or a salt thereof: with l-(2-chloro-4-methoxy-5-methylphenyl)-2-thiocyanatopropa - 1-one (Compound 8A) or a tautomeric form thereof: in the presence of a cyclizing-step solvent to form (S)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A) or a salt thereof.

[0557] In some embodiments, the tautomeric form of Compound 8A has the following chemical structure:

[0558] In some embodiments, the cyclizing-step solvent is any suitable solvent, such as, a solvent as described herein, or mixtures thereof.

[0559] In some embodiments, the cyclizing-step solvent is an aptotic solvent. In some embodiments, the cyclizing-step solvent is an aptotic solvent selected from: benzene, cyclohexane, pentane, hexane, acetonitrile, toluene, o-xylene, m-xylene, p-xylene, a mixture of xylenes, heptanes, n-heptane, octanes, n-octanes, ethylbenzene, and mixtures thereof. In some embodiments, the cyclizing-step solvent is an aptotic solvent selected from: benzene, cyclohexane, hexane, toluene, cycloheptane, o-xylene, m- xylene, p-xylene, a mixture of xylenes, heptanes, n-heptane, octanes, n-octane, ethylbenzene, and mixtures thereof. In some embodiments, the cyclizing-step solvent comprises a mixture of heptanes. In some embodiments, the cyclizing-step solvent is n-heptane.

[0560] In some embodiments, Compound 6A and Compound 8A are present in substantially equal molar quantities. In some embodiments, Compound 6A is present in a molar excess compared to Compound 8A. In some embodiments, Compound 6A is present in about 5% molar excess compared to Compound 8A. In some embodiments, Compound 6A is present in about 2% molar excess compared to Compound 8A. In some embodiments, Compound 6A is present in about 1% molar excess compared to Compound 8A.

[0561] In some embodiments, the cyclizing step further comprises the step of adding Compound 6A to a first-cyclizing mixture comprising Compound 8A and the cyclizing-step solvent at a first- cyclizing temperature.

[0562] In some embodiments, the first-cyclizing temperature is about 50°C to about 110°C. In some embodiments, the first-cyclizing temperature is about 60°C to about 95°C. In some embodiments, the first-cyclizing temperature is about 70°C to about 90°C. In some embodiments, the first-cyclizing temperature is about 80°C to about 87°C. In some embodiments, the first-cyclizing temperature is about 85°C.

[0563] In some embodiments, cyclizing is conducted with stirring.

[0564] ΙΠ. Processes useful for the preparation (S>2-cydopropyl-1-(3-fluoro-4- methylphenyl)ethan-1-amine (Compound 6A) or a salt thereof (Deprotecting-Step). One aspect of the present invention relates to processes for preparing (S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethan-l -amine (Compound 6A) or a salt thereof: comprising: deprotecting a Compound of Formula (Ig), or a salt thereof, wherein:

[0565] R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen; in the presence of a deprotec ting-catalyst, hydrogen, and a deprotecting-step solvent to form (5)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-amine (Compound 6A) or a salt thereof.

[0566] In some embodiments, the deprotec ting-catalyst comprises palladium. In some embodiments, the deprotec ting-catalyst comprises palladium on carbon. In some embodiments, the deprotecting- catalyst comprises about 2% palladium on carbon to about 20% palladium on carbon. In some embodiments, the deprotecting-catalyst comprises about 5% palladium on carbon to about 15% palladium on carbon. In some embodiments, the deprotecting-catalyst comprises about 10% palladium on carbon.

[0567] In some embodiments, the weight ratio between the Compound of Formula (Ig) and the deprotecting-catalyst is about 1:0.01 to about 1:0.15. In some embodiments, the weight ratio between the Compound of Formula (Ig) and the deprotecting-catalyst is about 1 :0.02 to about 1 :0.1. In some embodiments, the weight ratio between the Compound of Formula (Ig) and the deprotecting-catalyst is about 1:0.03 to about 1:0.07. In some embodiments, the weight ratio between the Compound of Formula (Ig) and the deprotecting-catalyst is about 1:0.05.

[0568] In some embodiments, the deprotecting-step solvent is any suitable solvent, such as, a solvent as described herein, or mixtures thereof. In some embodiments, the deprotecting-step solvent comprises an alcohol solvent. In some embodiments, the deprotecting-step solvent comprises an alcohol solvent selected from: methanol, ethanol, ethylene glycol, 1-propanol, 2-propanol, 2-methoxyethanol, 1-butanol, 2-butanol, isobutyl alcohol, 2-ethoxyethanol, 1-pentanol, 2-pentanol, 3-pentanol, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, and mixtures thereof. In some embodiments, the deprotecting-step solvent comprises an alcohol solvent selected from: methanol, ethanol, 1 -propanol, 2-propanol, and mixtures thereof. In some embodiments, the deprotecting-step solvent comprises an alcohol solvent selected from: methanol, ethanol, and mixtures thereof. In some embodiments, the deprotecting-step solvent is methanol.

[0569] In some embodiments, the deprotecting step further comprises the steps of: forming a first-deprotecting mixture comprising the Compound of Formula (Ig), the deprotecting-catalyst, and the deprotecting-step solvent; pressurizing the first-deprotecting mixture with hydrogen to form a second-deprotecting mixture; and heating the second-deprotecting mixture to a first-deprotecting temperature.

[0570] In some embodiments, pressurizing the first-deprotecting mixture with hydrogen is conducted at about 5 to about 12 bar. In some embodiments, pressurizing the first-deprotecting mixture with hydrogen is conducted at about 9 to about 11 bar. In some embodiments, pressurizing the first- deprotecting mixture with hydrogen is conducted at about 9.8 to about 10.2 bar.

[0571] In some embodiments, the first-deprotecting temperature is about 40°C to about 80°C. In some embodiments, the first-deprotecting temperature is about 50°C to about 70°C. In some embodiments, the first-deprotecting temperature is about 58°C to about 62°C.

[0572] Some embodiments relate to compounds of Formula (Ig), wherein R1c, R2c, and R3care each independently selected from: H, methoxy, methyl, trifluoromethyl, fluoro, chloro, and bromo. Some embodiments relate to compounds of Formula (Ig), wherein R1c, R2c, and R3care each H (i.e., (S)-2- cyclopropyl- 1 -(3 -fluoro-4-methylphenyl)-N-((S)- 1 -pheny lethyl)ethan- 1 -amine (Compound 5A)).

[0573] In some embodiments, deprotecting is conducted with stirring.

[0574] IV. Processes useful for the preparation of Compounds of Formula (Ig) or salts thereof (Reducing-Step).

[0575] One aspect of the present invention relates to processes for preparing a Compound of Formula (Ig), or a salt thereof: wherein:

[0576] R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen; comprising: reducing a Compound of Formula (Ie): in the presence of a reducing-catalyst, hydrogen, and a reducing-step solvent to form the Compound of Formula (Ig), or a salt thereof.

[0577] In some embodiments, the reducing-catalyst is sponge nickel or Pd / Cu-C.

[0578] In some embodiments, the reducing-catalyst is sponge nickel. In some embodiments, the weight ratio between the Compound of Formula (Ie) and the reducing-catalyst is about 1 :0.5 to about 1:0.9. In some embodiments, the weight ratio between the Compound of Formula (Ie) and the reducing-catalyst is about 1:0.6 to about 1:0.8. In some embodiments, the weight ratio between the Compound of Formula (Ie) and the reducing-catalyst is about 1:0.65 to about 1:0.75. In some embodiments, the weight ratio between the Compound of Formula (Ie) and the reducing-catalyst is about 1:0.7.

[0579] In some embodiments, the reducing-catalyst is Pd / Cu-C. In some embodiments, the Pd / Cu-C catalyst comprises about 1% to about 10% Pd and about 0.2% to about 4% Cu. In some embodiments, the Pd / Cu-C catalyst comprises about 2% to about 6% Pd and about 0.5% to about 2% Cu. In some embodiments, the Pd / Cu-C catalyst comprises about 4% Pd and 1% Cu. In some embodiments, the weight ratio between the Compound of Formula (Ie) and the reducing-catalyst is about 1:0.01 to about 1:0.3. In some embodiments, the weight ratio between the Compound of Formula (Ie) and the reducing-catalyst is about 1:0.015 to about 1:0.1. In some embodiments, the weight ratio between the Compound of Formula (Ie) and the reducing-catalyst is about 1:0.02 to about 1:0.05. In some embodiments, the weight ratio between the Compound of Formula (Ie) and the reducing-catalyst is about 1:0.03.

[0580] In some embodiments, the reducing-step solvent is any suitable solvent, such as, a solvent as described herein, or mixtures thereof.

[0581] In some embodiments, the reducing-step solvent comprises an alcohol solvent. In some embodiments, the reducing-step solvent comprises an alcohol solvent selected from: methanol, ethanol, ethylene glycol, 1-propanol, 2-propanol, 2-methoxyethanol, 1-butanol, 2-butanol, isobutyl alcohol, 2-ethoxyethanol, 1-pentanol, 2-pentanol, 3-pentanol, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, and mixtures thereof. In some embodiments, the reducing-step solvent comprises an alcohol solvent selected from: methanol, ethanol, 1 -propanol, 2-propanol, and mixtures thereof. In some embodiments, the reducing-step solvent comprises an alcohol solvent selected from: methanol, ethanol, and mixtures thereof. In some embodiments, the reducing-step solvent comprises ethanol.

[0582] In some embodiments, the reducing step further comprises the steps of: forming a first-reducing mixture comprising the reducing-catalyst and the reducing-step solvent; adding the Compound of Formula (Ie) to the first-reducing mixture to form a second-reducing mixture; pressurizing the second-reducing mixture with hydrogen to form a third-reducing mixture; and heating the third-reducing mixture to a first-reducing temperature.

[0583] In some embodiments, adding the Compound of Formula (Ie) to the first-reducing mixture is conducted as a solution of the Compound of Formula (Ie) in toluene. In some embodiments, adding the Compound of Formula (Ie) to the first-reducing mixture is conducted as a solution of about 40% to about 80% of the Compound of Formula (Ie) in toluene. In some embodiments, adding the Compound of Formula (Ie) to the first-reducing mixture is conducted as a solution of about 50% to about 70% of the Compound of Formula (Ie) in toluene. In some embodiments, adding the Compound of Formula (Ie) to the first-reducing mixture is conducted as a solution of about 60% to about 65% of the Compound of Formula (Ie) in toluene.

[0584] In some embodiments, pressurizing the second-reducing mixture with hydrogen is conducted at about 5 to about 12 bar. In some embodiments, pressurizing the second-reducing mixture with hydrogen is conducted at about 9 to about 11 bar. In some embodiments, pressurizing the second- reducing mixture with hydrogen is conducted at about 9.8 to about 10.2 bar. In some embodiments, the first-reducing temperature is about 25°C to about 55°C. In some embodiments, the first-reducing temperature is about 30°C to about 45°C. In some embodiments, the first-reducing temperature is about 33°C to about 37°C.

[0585] Some embodiments relate to compounds of Formula (Ie), wherein R1c, R2c, and R3care each independently selected from: H, methoxy, methyl, trifluoromethyl, fluoro, chloro, and bromo. Some embodiments relate to compounds of Formula (Ie), wherein R1c, R2c, and R3care each H (i.e., (S)-2- cyclopropyl- 1 -(3 -fluoro-4-methylphenyl)-N-( 1 -phenylethyl)ethan- 1 -imine (Compound 4A)).

[0586] In some embodiments, reducing is conducted with stirring.

[0587] V. Processes useful for the preparation of Compounds of Formula (Ie) (Condensing-

[0588] Step).

[0589] One aspect of the present invention relates to processes for preparing a Compound of Formula

[0590] (Ie): wherein:

[0591] R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen; comprising: condensing 2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A): with a Compound of Formula (Ic), or a salt thereof: in the presence of a condensing-step acid and a condensing-step solvent to form the Compound of Formula (Ie).

[0592] In some embodiments, the Compound of Formula (Ic) and Compound 3A are present in substantially equal molar quantities. In some embodiments, the Compound of Formula (Ic) is present in a molar excess compared to Compound 3A. In some embodiments, the molar ratio between Compound 3A and the Compound of Formula (Ic) is about 1:1 to about 1:1.5. In some embodiments, the molar ratio between Compound 3A and the Compound of Formula (Ic) is about 1:1.1 to about 1:1.3. In some embodiments, the molar ratio between Compound 3A and the Compound of Formula (Ic) is about 1:1.2.

[0593] In some embodiments, the molar ratio between Compound 3A, the Compound of Formula (Ic), and the condensing-step acid is about 1:1:0.01 to about 1:1.5:0.2. In some embodiments, the molar ratio between Compound 3A, the Compound of Formula (Ic), and the condensing-step acid is about 1:1.1:0.03 to about 1:1.3:0.1. In some embodiments, the molar ratio between Compound 3A, the Compound of Formula (Ic), and the condensing-step acid is about 1:1.2:0.05.

[0594] In some embodiments, the condensing-step acid comprises a Br0nsted acid. In some embodiments, the condensing-step acid comprises a Br0nsted acid selected from: acetic acid, trifluoroacetic acid (TFA), p-toluenesulfonic acid (pTSA), H3PO4, H2SO4, methanesulfonic acid (MSA), formic acid, and HC1. In some embodiments, the condensing-step acid is p-toluenesulfonic acid (pTSA).

[0595] In some embodiments, the condensing-step solvent is any suitable solvent, such as, a solvent as described herein, or mixtures thereof.

[0596] In some embodiments, the condensing-step solvent is an aptotic solvent. In some embodiments, the condensing-step solvent is an aptotic solvent selected from: benzene, cyclohexane, pentane, hexane, acetonitrile, toluene, cycloheptane, o-xylene, m-xylene, p-xylene, a mixture of xylenes, heptanes, n-heptane, octanes, n -octanes, ethylbenzene, and mixtures thereof. In some embodiments, the condensing-step solvent is acetonitrile or toluene. In some embodiments, the condensing-step solvent is acetonitrile. In some embodiments, the condensing-step solvent is toluene.

[0597] In some embodiments, condensing is conducted at the boiling point of the condensing-step solvent.

[0598] In some embodiments, condensing further comprises the removal of water. In some embodiments, condensing further comprises the removal of water using a Dean-Stark process, a desiccant, or a combination thereof. In some embodiments, condensing further comprises the removal of water using a desiccant. In some embodiments, condensing further comprises the removal of water using a Dean-Stark process.

[0599] In some embodiments, condensing further comprises the step of isolating the Compound of Formula (Ie) from a condensing-step mixture comprising the Compound of Formula (Ie) and the Compound of Formula (Ic). In some embodiments, isolating comprises substantially removing the Compound of Formula (Ic) from the condensing-step mixture using an isolating-step acid. In some embodiments, the isolating-step acid is a water-soluble acid. In some embodiments, the isolating-step acid is an ammonium halide. In some embodiments, the isolating-step acid is ammonium chloride (i.e.,

[0600] NH4C1).

[0601] Some embodiments relate to compounds of Formula (Ic), wherein R1c, R2c, and R3care each independently selected from: H, methoxy, methyl, trifluoromethyl, fluoro, chloro, and bromo. Some embodiments relate to compounds of Formula (Ic), wherein R1c, R2c, and R3care each H (i.e., (S)-(-)-1- phenylethylamine). In some embodiments, the compound of Formula (Ic) is (S)-(-)- 1- phenylethylamine.

[0602] In some embodiments, condensing is conducted with stirring.

[0603] VI. Processes useful for the preparation of 2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethan-1-one (Compound 3A) (Reacting-Step).

[0604] One aspect of the present invention relates to processes for preparing 2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethan-1-one (Compound 3A), comprising: reacting 2-cyclopropyl-N-methoxy-N-methylacetamide (Compound 2A): with an organomagnesium reagent of 4-bromo-2-fluoro- 1 -methylbenzene in the presence of a reacting- step solvent to form 2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethan-1-one (Compound 3A).

[0605] In some embodiments, the organomagnesium reagent of 4-bromo-2-fluoro-1-methylbenzene is prepared by the process comprising the steps of: forming a first-reacting mixture comprising magnesium and the reacting-step solvent; adding a magnesium activator to the first-reacting mixture at a first-reacting temperature to form a second-reacting mixture; and adding 4-bromo-2-fluoro- 1 -methylbenzene to the second-reacting mixture at a second-reacting temperature to form the organomagnesium reagent of 4-bromo-2-fluoro-1-methylbenzene.

[0606] In some embodiments, the first-reacting temperature is about 15°C to about 45°C. In some embodiments, the first-reacting temperature is about 25°C to about 40°C. In some embodiments, the first-reacting temperature is about 25°C to about 35°C.

[0607] In some embodiments, the second-reacting temperature is about 20°C to about 65°C. In some embodiments, the second-reacting temperature is about 25°C to about 60°C. In some embodiments, the second-reacting temperature is about 30°C to about 50°C.

[0608] In some embodiments, the reacting-step solvent is any suitable solvent, such as, a solvent as described herein or mixtures thereof.

[0609] In some embodiments, the reacting-step solvent is an ether solvent. In some embodiments, the reacting-step solvent is selected from: diethyl ether, 1 ,2-dimethoxyethane (DME), tetrahydroftiran (THF), cyclopentyl methyl ether (CPME), and 2-methyltetrahydrofuran (2-MeTHF). In some embodiments, the reacting-step solvent is selected from: tetrahydroftiran (THF), cyclopentyl methyl ether (CPME), and 2-methyltetrahydroftiran (2-MeTHF). In some embodiments, the reacting-step solvent is tetrahydroftiran (THF).

[0610] In some embodiments, the magnesium activator is I2, 1 ,2-dibromoethane, diisobutylaluminium hydride , sodium bis(2-methoxyethoxy)aluminum hydride (Red-Al), and borane dimethyl sulfide complex (BH3-SMe2). In some embodiments, the magnesium activator is diisobutylaluminium hydride (DIBAL-H).

[0611] In some embodiments, the organomagnesium reagent of 4-bromo-2-fluoro-1-methylbenzene is:

[0612] In some embodiments, reacting is conducted with stirring.

[0613] VII. Processes useful for the preparation 2-cyclopropyl-N-methoxy-N-methylacetamide (Compound 2A) (Coupling-Step). One aspect of the present invention relates to processes for preparing 2-cyclopropyl-N- methoxy-N-methylacetamide (Compound 2A), comprising: coupling 2-cyclopropylacetic acid (Compound 1A) with N,O-dimethylhydroxylamine or a salt thereof in the presence of a coupling-step reagent, a coupling-step base, and a coupling-step solvent to form 2- cyclopropyl-N-methoxy-N-methylacetamide (Compound 2A).

[0614] In some embodiments, the coupling step further comprises mixing 2-cyclopropylacetic acid (Compound 1A), the coupling-step reagent, and the coupling-step solvent together to form a first- coupling mixture.

[0615] In some embodiments, the first-coupling mixture is at a suitable first temperature to form 2- cyclopropyl-N-methoxy-N-methylacetamide (Compound 2A).

[0616] In some embodiments, the first-coupling mixture is at a first-coupling temperature of about - 15°C to about 35°C. In some embodiments, the first-coupling mixture is at a first-coupling temperature of about -10°C to about 30°C. In some embodiments, the first-coupling mixture is at a first-coupling temperature of about -10°C to about 25°C. In some embodiments, the first-coupling mixture is at a first-coupling temperature of < 25 °C.

[0617] In some embodiments, coupling further comprising adding N.O-dimethylhydroxylamine or a salt thereof to the first-coupling mixture to form a second-coupling mixture at a second-coupling temperature.

[0618] In some embodiments, the second-coupling temperature is < 30 °C. In some embodiments, the second-coupling temperature is about -15°C to about 30°C. In some embodiments, the second- coupling temperature is about -10°C to about 25°C. In some embodiments, the second-coupling temperature is about 20°C to about 25°C.

[0619] In some embodiments, N, 0-dimethylhydroxylamine or a salt thereof is added to the first- coupling mixture at a rate to maintain the temperature at the second-coupling temperature.

[0620] In some embodiments, the coupling step further comprises adding the coupling-step base to the second-coupling mixture.

[0621] In some embodiments, the coupling step further comprises adding the coupling-step base to the second-coupling mixture and maintaining a third-coupling temperature at about -10°C to about 25°C. In some embodiments, the coupling step further comprising adding the coupling-step base to the second-coupling mixture and maintaining a third-coupling temperature at about 20°C to about 25°C.

[0622] In some embodiments, the coupling-step reagent is a tetramethyluronium-based coupling reagent. In some embodiments, the coupling-step reagent is a tetramethyluronium-based coupling agent selected from: 2-( 1H-benzotriazole- 1 -yl)- 1 , 1 ,3,3-tetramethyluronium hexafluorophosphate

[0623] (HBTU), 2-( 1H-benzotriazole- 1 -yl)- 1,1,3 ,3-tetramethyluronium tetrafluoroborate (TBTU), 2-(7-aza- 1H-benzotriazole- 1 -yl-) 1,1,3 ,3-tetramethyluronium hexafluorophosphate (HATU), 2-(6-chloro-l / / - benzotriazole-1-yl)-l, 1, 3, 3-tetramethylaminium hexafluorophosphate (HCTU), and tetramethyl-0-(3,4-dihydro-4-oxo-l,2,3-benzotriazin-3-yl)uronium tetrafluoroborate (TDBTU). In some embodiments, the coupling-step reagent is 1,1’ -carbonyldiimidazole (GDI).

[0624] In some embodiments, the coupling-step solvent is any suitable solvent, such as, a solvent as described herein or mixtures thereof.

[0625] In some embodiments, the coupling-step solvent is an aprotic solvent. In some embodiments, the coupling-step solvent is selected from a halogenated solvent, an ether solvent, and mixtures thereof. In some embodiments, the coupling-step solvent comprises dichloromethane (DCM).

[0626] In some embodiments, the coupling-step base is a tertiary amine. In some embodiments, the coupling-step base is selected from: / V, / V-diisopropylethylamine (DIEA), triethylamine (TEA), N- methylmorpholine (NMM), 4-dimethylaminopyridine (DMAP), 2,4,6-trimethylpyridine (collidine), 2,3,5 ,6-tetramethylpyridine (TEMP), and 2,6-di-tert-butyl-4-(dimethylamino)pyridine (DBDMAP). In some embodiments, the coupling-step base is triethylamine.

[0627] In some embodiments, coupling is conducted with stirring.

[0628] Intermediate Compounds

[0629] One aspect of the present invention includes every combination of one or more compounds as described herein, and salts, solvates, and hydrates thereof.

[0630] One aspect of the present invention pertains to certain compounds of Formula (Ic): wherein:

[0631] R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen. Some embodiments relate to compounds of Formula (Ic), wherein R1c, R2c, and R3care each independently selected from: H, methoxy, methyl, trifluoromethyl, fluoro, chloro, and bromo.

[0632] Some embodiments relate to compounds of Formula (Ic), wherein R1c, R2c, and R3care each H (z.e., (S)-(-)-1-phenylethylamine):

[0633] One aspect of the present invention pertains to certain compounds of Formula (Ie): wherein:

[0634] R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen.

[0635] Some embodiments relate to compounds of Formula (Ie), wherein R1c, R2c, and R3care each independently selected from: H, methoxy, methyl, trifluoromethyl, fluoro, chloro, and bromo.

[0636] Some embodiments relate to compounds of Formula (Ie), wherein R1c, R2c, and R3care each H (i.e., (S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)-N-( l-phenylethyl)ethan- 1-imine (Compound 4A)):

[0637] One aspect of the present invention pertains to certain compounds of Formula (Ig): or a salt thereof: wherein:

[0638] R1c, R2c, and R3care each independently selected from: H, C1-C6 alkoxy, C1-C6 alkyl, C1-C6 haloalkyl, and halogen.

[0639] Some embodiments relate to compounds of Formula (Ig), wherein R1c, R2c, and R3care each independently selected from: H, methoxy, methyl, trifluoromethyl, fluoro, chloro, and bromo.

[0640] Some embodiments relate to compounds of Formula (Ig), wherein R1c, R2c, and R3care each H (i.e., (S)-2-cyclopropyl- l-(3-fluoro-4-methylphenyl)-N-((S)- 1 -phenylethyl)ethan- 1 -amine (Compound 5A)):

[0641] Some embodiments relate to compounds of Formula (Ig), wherein R1c, R2c, and R3care each H as the HQ salt.

[0642] Some embodiments relate to compounds of Formula (Ig), wherein R1c, R2c, and R3care each H and is an HQ salt. In some embodiments, the HC1 salt is crystalline. In some embodiments, the crystalline form of the HQ salt is the crystalline (S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)-N- ((S)-1-phenylethyl)ethan-1-amine (Compound 5A, HQ salt) as described herein.

[0643] DISORDERS, USES, AND METHODS OF TREATMENT

[0644] 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1) is a Corticotropin Releasing Factor 1 (CRFi) antagonist. Accordingly, Compound 1, as the free base, a pharmaceutically acceptable salt, such as the tosylate salt, and crystal forms thereof are useful in methods of antagonizing a Corticotropin Releasing Factor 1 by contacting the receptor. In some embodiments, the contacting is conducted in vivo. In some embodiments, the contacting is conducted ex vivo. In some embodiments, Compound 1, as the free base, a pharmaceutically acceptable salt, and a crystal form thereof, can be used in methods of antagonizing Corticotropin Releasing Factor 1 in a patient in need thereof by administering an effective amount of Compound 1, as the free base, a pharmaceutically acceptable salt, or a crystal form thereof.

[0645] Methods are provided herein for treating or preventing (i.e., reducing the likelihood of occurrence) a Corticotropin Releasing Factor 1 disorder. In some embodiments, Compound 1, pharmaceutical salts, and crystal forms thereof, are useful for the treatment or prevention of a disorder. In some embodiments, Compound 1, pharmaceutical salts, and crystal forms thereof, are useful for the treatment or prevention of a subtype of a disorder. In some embodiments, Compound 1, pharmaceutical salts, and crystal forms thereof, are useful for the treatment or prevention of a symptom of a disorder. In some embodiments,

[0646] Compound 1 is a free base. In some embodiments, Compound 1 (free base) is anhydrous crystalline Form I as described herein. In some embodiments, Compound 1 is as a pharmaceutical salt, wherein the salt is a tosylate salt. In some embodiments, the Compound 1 tosylate salt is crystal Form I as described herein.

[0647] One aspect of the present invention relates to methods of treating a disorder in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of an anhydrous crystalline form (Compound 1, free base) as described herein, a crystalline form (Compound 1, tosylate salt) as described herein, a pharmaceutical composition as described herein, a pharmaceutical product as described herein, or a composition as described herein, wherein the subject has abnormal levels of CRFi.

[0648] One aspect of the present invention relates to methods of treating a Corticotropin Releasing Factor 1 (CRFi) disorder in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of an anhydrous crystalline form (Compound 1, free base) as described herein, a crystalline form (Compound 1, tosylate salt) as described herein, a pharmaceutical composition as described herein, a pharmaceutical product as described herein, or a composition as described herein.

[0649] One aspect of the present invention relates to methods of treating congenital adrenal hyperplasia (CAH), in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of an anhydrous crystalline form (Compound 1, free base) as described herein, a crystalline form (Compound 1, tosylate salt) as described herein, a pharmaceutical composition as described herein, a pharmaceutical product as described herein, or a composition as described herein.

[0650] One aspect of the present invention relates to uses of an anhydrous crystalline form (Compound 1, free base) as described herein, or the crystalline form (Compound 1, tosylate salt) as described herein, for the manufacture of a medicament for the treatment of a subject wherein the subject has abnormal levels of CRFi.

[0651] One aspect of the present invention relates to uses of an anhydrous crystalline form (Compound 1, free base) as described herein, or the crystalline form (Compound 1, tosylate salt) as described herein, for the manufacture of a medicament for the treatment of a Corticotropin Releasing Factor 1 (CRFi) disorder.

[0652] One aspect of the present invention relates to uses of an anhydrous crystalline form (Compound 1, free base) as described herein, or the crystalline form (Compound 1, tosylate salt) as described herein, for the manufacture of a medicament for the treatment of congenital adrenal hyperplasia (CAH).

[0653] One aspect of the present invention relates to an anhydrous crystalline form (Compound 1, free base) as described herein; a crystalline form (Compound 1, tosylate salt) as described herein; a pharmaceutical composition as described herein, a pharmaceutical product as described herein, or a composition as described herein; for use in a method of treatment of the human or animal body by therapy.

[0654] One aspect of the present invention relates to an anhydrous crystalline form (Compound 1, free base) as described herein; a crystalline form (Compound 1, tosylate salt) as described herein; a pharmaceutical composition as described herein; a pharmaceutical product as described herein; or a composition as described herein; for use in a method of treatment of a disorder in a subject wherein the subject has abnormal levels of CRFi.

[0655] One aspect of the present invention relates to an anhydrous crystalline form (Compound 1, free base) as described herein; a crystalline form (Compound 1, tosylate salt) as described herein; a pharmaceutical composition as described herein; a pharmaceutical product as described herein; or a composition as described herein; for use in a method of treatment of a Corticotropin Releasing Factor 1 (CRFi) disorder.

[0656] One aspect of the present invention relates to an anhydrous crystalline form (Compound 1, free base) as described herein; a crystalline form (Compound 1, tosylate salt) as described herein; a pharmaceutical composition as described herein; a pharmaceutical product as described herein; or a composition as described herein; for use in a method of treating congenital adrenal hyperplasia

[0657] (CAH).

[0658] PHARMACEUTICAL COMPOSITIONS, COMPOSITIONS, FORMULATION, AND DOSAGE FORMS

[0659] The present disclosure further provides for compositions comprising the crystalline forms of Compound 1, e.g., the free base and tosylate salt of Compound 1 as described herein, and an excipient such as a pharmaceutically acceptable excipient for use in the methods for treating Corticotropin Releasing Factor 1 (CRFi) diseases or disorders, such as congenital adrenal hypoplasia. A pharmaceutically acceptable excipient is a physiologically and pharmaceutically suitable non-toxic and inactive material or ingredient that does not interfere with the activity of the drug substance; an excipient also may be called a carrier. The formulation methods and excipients described herein are exemplary and are in no way limiting. Pharmaceutically acceptable excipients are well known in the pharmaceutical art and described, for example, in Rowe et al., Handbook of Pharmaceutical

[0660] Excipients: A Comprehensive Guide to Uses, Properties, and Safety, 5th Ed., 2006, and in Remington : The Science and Practice of Pharmacy (Gennaro, 21st Ed. Mack Pub. Co., Easton, PA (2005)). Exemplary pharmaceutically acceptable excipients include sterile saline and phosphate buffered saline at physiological pH. Preservatives, stabilizers, dyes, buffers, and the like may be provided in the pharmaceutical composition. In addition, antioxidants and suspending agents may also be used.

[0661] For compositions formulated as liquid solutions, acceptable carriers and / or diluents include saline and sterile water, and may optionally include antioxidants, buffers, bacteriostats and other common additives. The compositions can also be formulated as pills, capsules, granules, or tablets which contain, diluents, dispersing and surface active agents, binders, and lubricants. One skilled in this art may further formulate the active pharmaceutical ingredient (e.g., the free base and tosylate salt of Compound 1 as described herein) in an appropriate manner, and in accordance with accepted practices, such as those disclosed in Remington, supra.

[0662] Methods of administration include systemic administration of the active pharmaceutical ingredient (e.g., the free base and tosylate salt of Compound 1 as described herein), preferably in the form of a pharmaceutical composition as discussed above. As used herein, systemic administration includes oral and parenteral methods of administration. For oral administration, suitable pharmaceutical compositions include powders, granules, pills, tablets, and capsules as well as liquids, syrups, suspensions, and emulsions. These compositions may also include flavorants, preservatives, suspending, thickening and emulsifying agents, and other pharmaceutically acceptable additives. For parental administration, the active pharmaceutical ingredient (e.g., the free base and tosylate salt of Compound 1 as described herein) can be prepared in aqueous injection solutions which may contain buffers, antioxidants, bacteriostats, and other additives commonly employed in such solutions.

[0663] Pharmaceutical preparations for oral administration can be obtained by any suitable method, typically by uniformly mixing the active pharmaceutical ingredient (e.g., the free base and tosylate salt of Compound 1 as described herein) with liquids or finely divided solid carriers, or both, in the required proportions and then, if necessary, processing the mixture, after adding suitable auxiliaries, if desired, forming the resulting mixture into a desired shape to obtain tablets or dragee cores. Conventional excipients, such as binding agents, fillers, adjuvant, carrier, acceptable wetting agents, tabletting lubricants and disintegrants may be used in tablets and capsules for oral administration. Liquid preparations for oral administration may be in the form of solutions, emulsions, aqueous or oily suspensions and syrups. Alternatively, the oral preparations may be in the form of dry powder that can be reconstituted with water or another suitable liquid vehicle before use. Additional additives such as suspending or emulsifying agents, non-aqueous vehicles (including edible oils), preservatives and flavorings and colorants may be added to the liquid preparations. Parenteral dosage forms may be prepared by dissolving the compound of the invention in a suitable liquid vehicle and filter sterilizing the solution before lyophilization, or simply filling and sealing an appropriate vial or ampule.

[0664] As used herein, an “excipient” refers to a substance that is added to a composition to provide, without limitation, bulk, consistency, stability, binding ability, lubrication, disintegrating ability, etc., to the composition. A “diluent” is a type of excipient and refers to an ingredient in a pharmaceutical composition that lacks pharmacological activity but may be pharmaceutically necessary or desirable. For example, a diluent may be used to increase the bulk of a potent drug whose mass is too small for manufacture and / or administration. It may also be a liquid for the dissolution of a drug to be administered by injection, ingestion, or inhalation. A pharmaceutically acceptable excipient is a physiologically and pharmaceutically suitable non-toxic and inactive material or ingredient that does not interfere with the activity of the drug substance. Pharmaceutically acceptable excipients are well known in the pharmaceutical art and described, for example, in Rowe et al., Handbook of Pharmaceutical Excipients : A Comprehensive Guide to Uses, Properties, and Safety, 5th Ed., 2006, and in Remington: The Science and Practice of Pharmacy (Gennaro, 21st Ed. Mack Pub. Co., Easton, PA (2005)). Preservatives, stabilizers, dyes, buffers, and the like may be provided in the pharmaceutical composition. In addition, antioxidants and suspending agents may also be used. For compositions formulated as liquid solutions, acceptable carriers and / or diluents include saline and sterile water, and may optionally include antioxidants, buffers, bacteriostats and other common additives. In some embodiments, the diluents may be a buffered aqueous solution such as, without limitation, phosphate buffered saline. The compositions can also be formulated as capsules, granules, or tablets which contain, in addition to a compound as disclosed and described herein, diluents, dispersing and surface-active agents, binders, and lubricants. One skilled in this art may further formulate a compound as disclosed and described herein in an appropriate manner, and in accordance with accepted practices, such as those disclosed in Remington, supra. One aspect of the present inventio...

Claims

CLAIMS1. A compound that is 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethyl] -5 -methyl-N-prop-2-yny 1- 1 ,3 -thiazol-2-amine (Compound 1):or a pharmaceutically acceptable salt thereof, wherein the enantiomeric excess (e.e.%) of the compound is at least 99.3% as determined by chiral HPLC.

2. The compound according to claim 1, wherein Compound 1, or a pharmaceutically acceptable salt thereof, is the free base.

3. The compound according to claim 1 or 2, wherein the enantiomeric excess (e.e.%) of Compound 1, or a pharmaceutically acceptable salt thereof, is at least 99.4%.

4. The compound according to claim 1 or 2, wherein the enantiomeric excess (e.e.%) of Compound 1, or a pharmaceutically acceptable salt thereof, is at least 99.5%.

5. The compound according to claim 1 or 2, wherein the enantiomeric excess (e.e.%) of Compound 1, or a pharmaceutically acceptable salt thereof, is at least 99.6%.

6. The compound according to claim 1 or 2, wherein the enantiomeric excess (e.e.%) of Compound 1, or a pharmaceutically acceptable salt thereof, is at least 99.7%.

7. The compound according to claim 1 or 2, wherein the enantiomeric excess (e.e.%) of Compound 1, or a pharmaceutically acceptable salt thereof, is at least 99.8%.

8. The compound according to claim 1 or 2, wherein the enantiomeric excess (e.e.%) of Compound 1, or a pharmaceutically acceptable salt thereof, is at least 99.9%.

9. The compound according to any one of claims 1 to 8, wherein the enantiomeric excess (e.e.%) of Compound 1, or a pharmaceutically acceptable salt thereof, is 100% or less.

10. The compound according to any one of claims 1 to 9, wherein Compound 1, or a pharmaceutically acceptable salt thereof, is crystalline.

11. The compound according to any one of claims 1 to 10, wherein Compound 1, or a pharmaceutically acceptable salt thereof, is crystalline Form I.

12. A composition comprising a compound that is 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[( 1 S)-2-cyclopropyl- 1 -(3-fluoro-4-methy lphenyl)ethyl] -5 -methy l-N-prop-2-ynyl- 1 ,3-thiazol-2- amine (Compound 1) according to any one of claims 1 to 11:or a pharmaceutically acceptable salt thereof.

13. The composition according to claim 12, wherein Compound 1, or a pharmaceutically acceptable salt thereof, is the free base.

14. The composition according to claim 12 or 13, further comprising a compound that is (5)-4-(2- chloro-4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(p-tolyl)ethyl)-5-methyl-N-(prop-2- yn-1-yl)thiazol-2-amine (Compound Da), or a pharmaceutically acceptable salt thereof:

15. The composition according to claim 14, wherein Compound Da, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount ranging from 1.0% to 0.4%.

16. The composition according to claim 14, wherein Compound IIa, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount ranging from 0.9% to 0.4%.

17. The composition according to claim 14, wherein Compound IIa, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount ranging from 0.8% to 0.4%.

18. The composition according to claim 14, wherein Compound IIa, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount ranging from 0.7% to 0.4%.

19. The composition according to claim 14, wherein Compound IIa, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount ranging from 0.6% to 0.4%.

20. The composition according to any one of claims 12 to 19, further comprising a compound that is (S)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A), or a pharmaceutically acceptable salt thereof:

21. The composition according to claim 20, wherein Compound 9A, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount less than 0.5%.

22. The composition according to claim 20, wherein Compound 9A, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount less than 0.3%.

23. The composition according to claim 20, wherein Compound 9A, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount less than 0.1%.

24. The composition according to claim 20, wherein Compound 9A, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount less than 0.05%.

25. The composition according to any one of claims 12 to 24, further comprising a compound that is (S)-4-(2-chloro-5 -methyl-4-(prop-2-y n- 1 -yloxy)phenyl)-N-(2-cyclopropy 1- 1 -(3-fluoro-4- methylphenyl)ethyl)-5 -methyl-N-(prop-2-yn- 1 -yl)thiazol-2-amine (Compound nb), or a pharmaceutically acceptable salt thereof:wherein the compound is present in the composition in an amount less than 0.1%.

26. The composition according to claim 25, wherein Compound lib, or a pharmaceutically acceptable salt thereof, is present in the composition in an amount less than 0.05%.

27. The composition according to any one of claims 12 to 26, further comprising ethanol.

28. The composition according to claim 27, wherein ethanol is present in the composition in an amount ranging from 300 ppm to 5000 ppm.

29. The composition according to claim 27, wherein ethanol is present in the composition in an amount ranging from 300 ppm to 3000 ppm.

30. The composition according to claim 27, wherein ethanol is present in the composition in an amount ranging from 300 ppm to 2000 ppm.

31. The composition according to claim 27, wherein ethanol is present in the composition in an amount ranging from 300 ppm to 1000 ppm.

32. The composition according to claim 27, wherein ethanol is present in the composition in an amount ranging from 350 ppm to 600 ppm.

33. The composition according to claim 27, wherein ethanol is present in the composition in an amount ranging from 375 ppm to 550 ppm.

34. The composition according to any one of claims 12 to 33, further comprising propargyl bromide, wherein propargyl bromide is present in the composition in an amount less than 10 ppm.

35. A composition comprising: a. 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1), or a pharmaceutically acceptable salt thereof, wherein the enantiomeric excess (e.e.%) of the compound is at least 99.3% as determined by chiral HPLC; and b. at least one compound selected from:(S)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro-4- methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A), or a pharmaceutically acceptable salt thereof;(S)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(p-tolyl)ethyl)-5- methyl-N-(prop-2-yn-1-yl)thiazol-2-amine (Compound Ila), or a pharmaceutically acceptable salt thereof;(S)-4-(2-chloro-5 -methyl-4-(prop-2-yn- 1 -y loxy)phenyl)-N-(2-cyclopropyl- 1 -(3- fluoro-4-methylphenyl)ethyl)-5-methyl-N-(prop-2-yn-1-yl)thiazol-2-atnine (Compound lib), or a pharmaceutically acceptable salt thereof; ethanol; and propargyl bromide.

36. The composition according to claim 35, wherein Compound 1, or a pharmaceutically acceptable salt thereof, is the free base.

37. A compound that is 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethyl] -5 -methyl-N-prop-2-yny 1- 1 ,3 -thiazol-2-amine (Compound 1) according to any one of claims 1 to 11:or a pharmaceutically acceptable salt thereof, prepared by a process comprising: alkylating (S)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro- 4-methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A) or a salt thereof:with a Compound of Formula (Ii):wherein: LG is a leaving group;in the presence of an alkylating-step solvent, a phase-transfer catalyst, an alkylating-step base, and water to form 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3- fluoro-4-methylphenyl)ethyl] -5 -methyl-N-prop-2-yny 1- 1 ,3 -thiazol-2-amine (Compound 1) or a pharmaceutically acceptable salt thereof.

38. The compound according to claim 37, wherein Compound 1, or a pharmaceutically acceptable salt thereof, is the free base.

39. A composition comprising the compound that is 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[( 1 S)-2-cyclopropyl- 1 -(3-fluoro-4-methy lphenyl)ethyl] -5 -methy l-N-prop-2-ynyl- 1 ,3-thiazol-2- amine (Compound 1) according to any one of claims 1 to 11:or a pharmaceutically acceptable salt thereof, prepared by a process comprising: alkylating (S)-4-(2-chloro-4-methoxy-5-methylphenyl)-N-(2-cyclopropyl-1-(3-fluoro- 4-methylphenyl)ethyl)-5-methylthiazol-2-amine (Compound 9A) or a salt thereof:with a Compound of Formula (Ii):wherein: LG is a leaving group; in the presence of an alkylating-step solvent, a phase-transfer catalyst, an alkylating-step base, and water to form 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl] -5 -methyl-N-prop-2-yny 1- 1 ,3 -thiazol-2-amine (Compound 1) or a pharmaceutically acceptable salt thereof.

40. The composition according to claim 39, wherein Compound 1, or a pharmaceutically acceptable salt thereof, is the free base.

41. A pharmaceutical product selected from: a pharmaceutical composition, a formulation, a unit dosage form, and a kit; each comprising Compound 1, according to any one of claims 1 to 11, 37, and 38, or a pharmaceutically acceptable salt thereof.

42. The pharmaceutical product according to claim 41, wherein Compound 1, or a pharmaceutically acceptable salt thereof, is the free base.

43. The pharmaceutical product according to claim 41 or 42, wherein the pharmaceutical product is adapted for oral administration.

44. A pharmaceutical composition comprising Compound 1, according to any one of claims 1 to 11, 37, and 38 or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

45. A pharmaceutical composition comprising:(a) a compound that is 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1) according to any one of claims 1 to 11:or a pharmaceutically acceptable salt thereof; and(b) one or more of an oily phase vehicle, an emulsifying agent, a nonionic surfactant, and a solubilizing agent.

46. A pharmaceutical composition in oral solution dosage form comprising:(a) a compound that is 4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2- cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-prop-2-ynyl-l,3-thiazol-2-amine (Compound 1) according to any one of claims 1 to 11:or a pharmaceutically acceptable salt thereof;(b) one or more of a sweetener, an anti-oxidant, and a flavor; and(c) a liquid vehicle, wherein the liquid vehicle is selected from medium-chain triglycerides, propylene glycol dicaprylate / dicaprate, glycerin, propylene glycol, polyethylene glycol, olive oil, soybean oil, com oil, and transcutol.

47. The pharmaceutical composition according to any one of claims 44 to 46, wherein Compound 1, or a pharmaceutically acceptable salt thereof, is the free base.

48. A compound according to any one of claims 1 to 11, 37, and 38, or a pharmaceutically acceptable salt thereof; a composition according to any one of claims 12 to 36, 39, and 40; a pharmaceutical product according to any one of claims 41 to 43; or a pharmaceutical composition according to any one of claims 44 to 47; for use in a method of treatment or prophylaxis of the human or animal body by therapy.

49. A compound according to any one of claims 1 to 11, 37, and 38, or a pharmaceutically acceptable salt thereof; a composition according to any one of claims 12 to 36, 39, and 40; a pharmaceutical product according to any one of claims 41 to 43; or a pharmaceutical composition according to any one of claims 44 to 47; for use in a method of treatment of a disorder in a subject wherein the subject has abnormal levels of CRFi.

50. A compound according to any one of claims 1 to 11, 37, and 38, or a pharmaceutically acceptable salt thereof; a composition according to any one of claims 12 to 36, 39, and 40; a pharmaceutical product according to any one of claims 41 to 43; or a pharmaceutical composition according to any one of claims 44 to 47; for use in a method of treatment of a Corticotropin Releasing Factor 1 (CRFi) disorder.

51. A compound according to any one of claims 1 to 11, 37, and 38, or a pharmaceutically acceptable salt thereof; a composition according to any one of claims 12 to 36, 39, and 40; a pharmaceutical product according to any one of claims 41 to 43; or a pharmaceutical composition according to any one of claims 44 to 47; for use in a method of treating congenital adrenal hypoplasia (CAH).

52. The compound, or a pharmaceutically acceptable salt thereof; the composition; the pharmaceutical product; or the pharmaceutical composition for use according to claim 51; wherein the congenital adrenal hyperplasia is classic congenital adrenal hyperplasia.

53. The compound, or a pharmaceutically acceptable salt thereof; the composition; the pharmaceutical product; or the pharmaceutical composition for use according to claim 51 or 52; wherein the method of treating congenital adrenal hyperplasia comprises administering a glucocorticoid.

54. The use of a compound according to any one of claims 1 to 11, 37, and 38, or a pharmaceutically acceptable salt thereof; for the manufacture of a medicament for the treatment of a subject wherein the subject has abnormal levels of CRFi.

55. The use of a compound according to any one of claims 1 to 11, 37, and 38 or a pharmaceutically acceptable salt thereof; for the manufacture of a medicament for the treatment of a Corticotropin Releasing Factor 1 (CRFi) disorder.

56. The use of a compound according to any one of claims 1 to 11, 37, and 38 or a pharmaceutically acceptable salt thereof; for the manufacture of a medicament for the treatment of congenital adrenal hypoplasia (CAH).

57. The use according to claim 56; wherein the congenital adrenal hyperplasia is classic congenital adrenal hypoplasia.

58. The use according to claim 56 or 57; wherein the treatment of congenital adrenal hyperplasia comprises administering a glucocorticoid.

59. A method of treating a disorder in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound according to any one of claims 1 to 11, 37, and 38, or a pharmaceutically acceptable salt thereof; a composition according to any one of claims 12 to 36, 39, and 40; a pharmaceutical product according to any one of claims 41 to 43; or a pharmaceutical composition according to any one of claims 44 to 47; wherein the subject has abnormal levels of CRFi.

60. A method of treating a Corticotropin Releasing Factor 1 (CRFi) disorder in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound according to any one of claims 1 to 11, 37, and 38, or a pharmaceutically acceptable salt thereof; a composition according to any one of claims 12 to 36, 39, and 40; a pharmaceutical product according to any one of claims 41 to 43; or a pharmaceutical composition according to any one of claims 44 to 47.

61. A method of treating congenital adrenal hypoplasia (CAH), in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound according to any one of claims 1 to 11, 37, and 38, or a pharmaceutically acceptable salt thereof; a composition according to any one of claims 12 to 36, 39, and 40; a pharmaceutical product according to any one of claims 41 to 43; or a pharmaceutical composition according to any one of claims 44 to 47.

62. The method according to claim 61 ; wherein the congenital adrenal hyperplasia is classic congenital adrenal hypoplasia.

63. The method according to claim 61 or 62; wherein the method further comprises administering to the subject a glucocorticoid.

64. A method for preparing a pharmaceutical composition comprising the step of admixing a compound according to any one of claims 1 to 11, 37, and 38, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.