Aminopyridine derivatives and their use as selective ALK-2 inhibitors

Abstract

To provide a compound as an ALK-2 inhibitor, a pharmaceutically acceptable salt thereof, and a pharmaceutical composition thereof.SOLUTION: The invention relates to a compound of formula (I) in free form or in pharmaceutically acceptable salt form (I), to pharmaceutical compositions comprising the compound, and to the use of the compound in the treatment of heterotopic ossification and fibrodysplasia ossificans progressiva.SELECTED DRAWING: None

Description

[Technical field]

[0001] ALK-2, also known as activin A receptor type I (ACVR1) or as serine-threonine protein kinase receptor R1 (SKR1), is a protein kinase that in humans is encoded by the ACVR1 gene.

[0002] ALK-2 is a ubiquitously expressed type I BMP receptor. It comprises an extracellular ligand-binding domain and a regulated intracellular serine / threonine kinase domain, both of which are required for signal transduction. [Background technology]

[0003] Bone morphogenetic proteins (BMPs) are multifunctional growth factors that are members of the transforming growth factor beta (TGFβ) superfamily. BMP signaling plays a role in cardiac, neural and cartilage development, as well as postnatal bone formation. BMPs induce ectopic endochondral bone formation and play an important role in skeletal and joint morphogenesis (Urist, Science 110:893-899 (1965); Olsen et al, Annu. Rev. Cell Dev. Biol. 16:191-220 (2000); Kronenberg, Nature 423:332-336 (2003); Thomas et al, Nat. Genet. 12:315-317 (1996); Thomas et al, Nat. Genet. 17:58-64 (1997); Polinkowsky et al, Nat. Genet. 17:18-19 (1997); Storm et al., Nature 368:639-643 (1994); and Wozney, Prog. Growth Factor Res. 1:267-280 (1989)).

[0004] BMP signaling is controlled at many levels, including through extracellular antagonists such as Noggin (Massague, Nat. Rev. MoI. Cell. Biol. 1:169-178 (2000)). It has been suggested that untimely or unwanted activation of signaling pathways essential for normal development can promote disease processes such as spondyloarthropathy. The effect of BMP signaling on the initiation and progression of arthritis by gene transfer of Noggin has also been described (Lories et al, J. Clin. Invest., 115, 1571-1579 (2005)). The physiological role of BMP and BMP receptor signaling in normal bone formation, including skeletal and limb development, has been studied and reviewed in Zhao, Genetics 35:43-56 (2003).

[0005] Experiments with BMP antagonists demonstrate that regulation of BMP signaling proteins is central to bone formation in vivo (Devlin et al., Endocrinology 144:1972-1978 (2003) and Wu et al., J. Clin. Invest., 112:924 (2003)).

[0006] Fibrodysplasia ossificans progressiva (FOP) is a rare, disabling genetic disorder characterized by congenital malformations of the great toe and by progressive ectopic endochondral ossification in a predictable anatomical pattern. Ectopic expression of BMP4 has been found in FOP patients (Gannon et al., Hum. Pathol. 28:339-343 (1997) and Xu et al., Clin. Genet. 58:291-298 (2000)). Patients with FOP have been shown to have activating mutations in ALK-2 (Shore et al., Nat. Genet., 38(5):525-7 (2006)).

[0007] It has been established that excessive BMP signaling leads to several of the pathologies mentioned above. WO2008033408 and WO2009114180 describe inhibitors of the BMP signaling pathway. Summary of the Invention [Problem to be solved by the invention]

[0008] However, there remains a need to find alternative ways in which BMP signaling can be regulated.

[0009] Such a need may be met by designing selective ALK-2 inhibitors.

[0010] Specific ALK-2 antibodies are described, for example, in WO 1994011502 and WO 2008030611. Bone morphogenetic proteins that bind to ALK-2 are described in WO 2012023113 and WO 2012077031.

[0011] WO2007123896 describes a method for treating pathologies associated with heterotopic ossification by administering siRNA specific for a nucleic acid encoding ALK-2.

[0012] WO2014160203 and WO2014138088 describe inhibitors of the BMP pathway. WO2015152183 describes ALK-2 inhibitors for the treatment of FOP. ALK-2 inhibitors are also described in WO2014151871. [Means for solving the problem]

[0013] There is a continuing need to develop new ALK-2 inhibitors that are good drug candidates that would find use, among other things, in the treatment of fibrodysplasia ossificans progressiva (FOP) or non-hereditary heterotopic ossification (HO).

[0014] The present invention provides compounds that are ALK-2 inhibitors, their pharma- ceutical acceptable salts, and pharmaceutical compositions thereof.The present invention further provides a method for treating, preventing, or ameliorating fibrodysplasia ossificans progressiva (FOP) or non-hereditary heterotopic ossification (HO), comprising administering an effective amount of an ALK-2 inhibitor to a subject in need thereof.

[0015] Various embodiments of the present invention are described herein.

[0016] In certain embodiments herein, a compound of formula (I), in free form or in pharma- ceutically acceptable salt form, [ka] The compound of formula (1) is provided.

[0017] In another embodiment, the present invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of formula (I) or any of its sub-formulas (Ia), (II), (IIa), (IIb) as defined herein, in free form or in pharma- ceutically acceptable salt form, and one or more pharma- ceutically acceptable carriers.

[0018] In a further aspect, the present invention relates to a method of inhibiting ALK-2 receptor activity in a subject comprising the step of administering to the subject a therapeutically effective amount of a compound of formula (I) or subformulas (Ia), (II), (IIa), (IIb) as defined herein, in free form or in a pharma- ceutically acceptable salt form.

[0019] In yet another aspect, the present invention relates to a method for treating a disorder or disease selected from heterotopic ossification or fibrodysplasia ossificans progressiva, comprising the step of administering to a subject a therapeutically effective amount of a compound of formula (I) or sub-formulas (Ia), (II), (IIa), (IIb) as defined herein, in free form or in a pharma- ceutically acceptable salt form.

[0020] The compounds of the present invention show favorable pharmacokinetic properties, are non-toxic, and have few side effects.In particular, the compounds of the present invention are selective inhibitors of ALK-2 over other receptors.In addition, the ideal drug candidates are stable, non-hygroscopic, and easily formulated. [Brief description of the drawings]

[0021] [Figure 1] μCT quantification of ectopic bone formed in the right hind limb of mice 6 weeks after FOP-induced flare-up with adenovirus / CTX, showing the effect of 6 weeks of Compound A treatment on HO formation. Mean ± SEM. *: p<0.05, **: p<0.01, ***: p<0.01 vs. vehicle treatment; One-way ANOVA with Dunnett's post-hoc test. [Diagram 2] μCT quantification of ectopic bone formed in the right hind limb of mice 8 weeks after FOP-induced flare-up with adenovirus / CTX, showing the effect of 6 weeks of Compound A treatment on HO formation. Mean ± SEM. *: p<0.05, **: p<0.01, ***: p<0.01 vs. vehicle treatment; T-test [Diagram 3] 1 shows the X-ray powder diffraction pattern of crystalline free form modified HA crystals of Compound A. [Figure 4] 1 shows a differential scanning diagram of crystalline free form modified HA crystals of Compound A. [Diagram 5] FIG. 1 shows the thermogravimetric analysis diagram of crystalline free form modified HA of compound A. [Figure 6] FIG. 1 shows a Fourier transform infrared diagram of crystalline free form modified HA of compound A. [Figure 7]1 shows the X-ray powder diffraction pattern of the crystalline free form modification A of Compound A. [Figure 8] 1 shows a differential scanning diagram of the crystalline free form modification A of Compound A. [Figure 9] 1 shows a thermogravimetric analysis diagram of the crystalline free form modification A of Compound A. [Figure 10] FIG. 2 shows the Fourier transform infrared diagram of the crystalline free form modified A of Compound A. [Figure 11] 1 shows the X-ray powder diffraction pattern of crystalline fumarate-modified HA of Compound A. [Figure 12] FIG. 1 shows a differential scanning diagram of crystalline fumarate-modified HA of Compound A. [Figure 13] FIG. 1 shows the thermogravimetric analysis diagram of crystalline fumarate modified HA of compound A. [Figure 14] FIG. 1 shows a Fourier transform infrared diagram of crystalline fumarate-modified HA of compound A. [Figure 15] FIG. 2 shows the dynamic gas sorption diagram of crystalline fumarate modified HA of Compound A at 25° C., method 50%-0%-90% relative humidity (RH). [Figure 16] FIG. 2 shows the dynamic gas sorption diagram of crystalline fumarate modified HA of Compound A at 40° C., method 50%-0%-90% RH. [Figure 17] 1 shows an X-ray powder diffraction pattern of the crystalline phosphate salt of Compound A. [Figure 18] FIG. 1 shows the X-ray powder diffraction pattern of the crystalline free form anhydrate (Example 89C). [Figure 19] FIG. 1 shows the X-ray powder diffraction pattern of the crystalline free form trihydrate (Example 89D). DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0022] In particular, the present invention provides a compound of formula (I), in free form or in an acceptable salt form: [ka] (In the formula, L is a bond, (CH2) n , -CH(CH3)-, -O-(CH2) n -, -C(O)-, -C(O)-NH-(CH2) n - and; n is 1, 2, 3; R1 is a C3-C7 cycloalkyl optionally substituted one or more times with substituents independently selected from hydroxyl, halogen, C1-C3 alkyl; a bridged C5-C alkyl optionally substituted one or more times with substituents independently selected from hydroxyl, hydroxy C1-C3 alkyl; 10 cycloalkyl; R2 and R3 are independently selected from H, halogen, and C1-C3 alkyl; R4 is an N-containing heterocyclic non-aromatic ring optionally comprising one or more additional heteroatoms selected from N, O or S, optionally substituted one or more times with R7; R7 is C1-C3 alkyl, hydroxy C1-C3 alkyl, halo C1-C3 alkyl, C1-C3 alkoxy C1-C3 alkyl, halo C1-C3 alkoxy C1-C3 alkyl, C2-C4 alkynyl, cyano C1-C3 alkyl, (CH2) m - selected independently from R8; m is 0, 1, 2 or 3; R8 is a 4-, 5-, or 6-membered saturated or unsaturated non-aromatic heterocycle comprising one or more heteroatoms selected from N, O, or S, optionally substituted one or more times with substituents independently selected from oxo, SO2C1-C3 alkyl, haloC1-C3 alkyl, or C3-C6 cycloalkyl optionally substituted one or more times with halo (selected from The present invention relates to a compound of the formula:

[0023] Unless otherwise indicated, the term "compounds of the present invention" or "compounds of the invention" refers to compounds of formula (I), (Ia), (II), (IIa), (IIb) and salts thereof, as well as all stereoisomers (such as diastereoisomers and enantiomers), rotamers, tautomers, and isotopically labeled compounds (such as deuterium substitutions), and naturally formed moieties.

[0024] As used herein, the term "C1-C3 alkyl" refers to a straight or branched hydrocarbon chain radical containing no unsaturation, having from 1 to 3 carbon atoms, and consisting solely of carbon and hydrogen atoms, attached to the remainder of the molecule by a single bond. Examples of C1-C3 alkyl include methyl, ethyl, n-propyl, and 1-methylethyl (isopropyl).

[0025] As used herein, the term "hydroxy C1-C3 alkyl" refers to a group of the formula: a refers to the free radical of —OH, where R a is a C1-C3 alkyl as defined above.

[0026] As used herein, the term "C3-C7 cycloalkyl" refers to a saturated monocyclic hydrocarbon group of 3 to 7 carbon atoms. Examples of C3-C7 cycloalkyl include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and cycloheptyl.

[0027] As used herein, the term "C1-C3 alkoxy" refers to a group of the formula: a In the formula, R a is a C1-C3 alkyl radical as generally defined above. Examples of C1-C3 alkoxy include, but are not limited to, methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, pentoxy, and hexoxy.

[0028] As used herein, the term "C1-C3 alkoxy C1-C3 alkyl" refers to a group of the formula: b -OR a In the formula, R a is a C1-C3 alkyl radical as defined above, R b is a C1-C3 alkyl radical as defined above. The oxygen atom may be bonded to any carbon atom of either alkyl radical. Examples of C1-C3 alkoxy C1-C3 alkyl include, for example, methoxymethyl, methoxy-ethyl, and ethoxyethyl.

[0029] "Halogen" or "halo" refers to bromo, chloro, fluoro or iodo.

[0030] As used herein, the term "halogen C1-C3 alkyl" or "halo C1-C3 alkyl" refers to a C1-C3 alkyl radical, as defined above, substituted by one or more halo radicals, as defined above. Examples of halogen C1-C3 alkyl include, for example, trifluoromethyl, difluoromethyl, fluoromethyl, trichloromethyl, 2,2,2-trifluoroethyl, 1-fluoromethyl-2-fluoroethyl, 3-bromo-2-fluoropropyl, and 1-bromomethyl-2-bromoethyl.

[0031] As used herein, the term "halo C1-C3 alkoxy C1-C3 alkyl" refers to a group of the formula: b -OR a In the formula, R a is a C1-C3 alkyl radical as defined above, R b is a haloC1-C3 alkyl radical as defined above.

[0032] As used herein, the term "N-containing heterocyclic non-aromatic ring optionally containing one or more additional heteroatoms selected from N, O or S" for R4 refers to a saturated or unsaturated non-aromatic ring or ring system that is a 4-, 5-, 6-, or 7-membered monocyclic ring containing 1, 2, or 3 heteroatoms selected from O, S, and N, where at least one heteroatom is N, a 6-, 7-, 8-, 9-, 10-, 11-, or 12-membered bicyclic ring system containing 1, 2, 3, 4, or 5 heteroatoms selected from O, S, and N, where at least one heteroatom is N, or a 10-, 11-, 12-, 13-, 14-, or 15-membered tricyclic ring system containing 1, 2, 3, 4, 5, 6, or 7 heteroatoms selected from O, S, and N, where at least one heteroatom is N, and where N and S can also be optionally oxidized to various oxidation states. The N-containing heterocyclic non-aromatic ring can be attached via a heteroatom or carbon atom. N-containing heterocyclic non-aromatic rings may include fused or bridged rings as well as spiro rings. In a preferred embodiment, the "N-containing heterocyclic non-aromatic ring optionally containing one or more additional heteroatoms selected from N, O or S" is an N-containing 5-membered saturated monocyclic ring, an N-containing 6-membered saturated monocyclic or bicyclic ring, an N-containing 7-membered saturated spiro ring. Examples of N-containing heterocyclic non-aromatic rings include morpholine, piperazine, piperidine, imidazolidine, imidazoline, pyrroline, pyrrolidine, thiomorpholine, and 3-azabicyclo[3.1.0]hexane.

[0033] As used herein, the term "N-containing 5-membered heterocyclic non-aromatic ring optionally containing one or more additional heteroatoms selected from N, O or S" for R4 includes, by way of example, pyrrolidine, 2,3-dihydropyrrole, oxazolidine, imidazolidine. In a preferred embodiment, it refers to pyrrolidine. The ring is attached to the remainder of the molecule via a ring carbon atom.

[0034] As used herein, the term "N-containing 6-membered heterocyclic non-aromatic mono- or bicyclic rings optionally containing one or more additional heteroatoms selected from N, O or S" for R4 includes, by way of example, morpholine, thiomorpholine, piperidine, piperazine, 3-azabicyclo[3.1.0]hexane. In a preferred embodiment, it refers to 3-azabicyclo[3.1.0]hexane. The ring is attached to the remainder of the molecule via a ring carbon atom.

[0035] As used herein, with respect to the embodiment in which R5 and R6 together with the N atom to which they are attached form a ring, the term "5-membered ring optionally comprising one additional heteroatom selected from N, O or S" includes, by way of example, pyrrolidine, 2,3-dihydropyrrole, oxazolidine, imidazolidine. In a preferred embodiment, it refers to pyrrolidine.

[0036] As used herein, with respect to embodiments in which R5 and R6 together with the N atom to which they are attached form a ring, the term "6-membered ring optionally comprising one additional heteroatom selected from N, O or S" includes, by way of example, piperidinyl, morpholinyl, piperazinyl.

[0037] As used herein, with respect to embodiments in which R5 and R6 together with the N atom to which they are attached form a ring, the term "7-membered spiro ring optionally comprising one additional heteroatom selected from N, O or S" includes, by way of example, 2-azaspiro[3.3]heptane, 2-oxa-6-azaspiro[3.3]heptane.

[0038] As used herein, "bridged C5-C 10 The term "cycloalkyl" refers to a saturated bicyclic or tricyclic ring system comprising at least one bridge. 10 Examples of cycloalkyl include, for example, bicyclo[1.1.1]pentane, bicyclo[2.2.2]octane, bicyclo[2.2.1]heptane, tricyclo[3.3.1.1] 3,7] Deccan is one example.

[0039] As used herein, the term "C2-C4 alkynyl" refers to a straight chain group consisting only of carbon and hydrogen atoms, containing at least one triple bond, having 2-4 carbon atoms, and attached to the remainder of the molecule by a single bond. Examples of C2-C4 alkynyl include, for example, ethynyl, prop-1-ynyl, and but-1-ynyl.

[0040] As used herein, the term "cyano C1-C3 alkyl" refers to a group of the formula: a -CN, where R a is a C1-C3 alkyl as defined above.

[0041] As used herein, the term "4-, 5-, or 6-membered saturated or unsaturated non-aromatic heterocycle comprising one or more heteroatoms selected from N, O, or S" includes, by way of example, tetrahydropyran, morpholine, piperidine, oxetane. In a preferred embodiment, it is tetrahydropyran.

[0042] As used herein, the term "ALK-2" refers to activin A receptor, type I (ACVRI), also known as ACVRLK2; SKR1; ACVR1A; activin receptor type I; activin receptor-like kinase 2; serine / threonine-protein kinase receptor R1; TGF-B superfamily receptor type I; ACTRI; TSRI; activin A receptor, type II-like kinase 2; activin receptor type-1; hydroxyalkyl-protein kinase; ACTR-I; TSR-I.

[0043] Various embodiments of the invention are described herein. It will be appreciated that the features specified in each embodiment may be combined with other specific features to provide further embodiments of the invention.

[0044] Embodiment 1. Formula (I), in free form or in a pharma- ceutically acceptable salt form: [ka] (In the formula, L is a bond, (CH2) n , -CH(CH3)-, -O-(CH2) n -, -C(O)-, -C(O)-NH-(CH2) n - and; n is 1, 2, 3; R1 is a C3-C7 cycloalkyl optionally substituted one or more times with substituents independently selected from hydroxyl, halogen, C1-C3 alkyl; a bridged C5-C alkyl optionally substituted one or more times with substituents independently selected from hydroxyl, hydroxy C1-C3 alkyl; 10 cycloalkyl; R2 and R3 are independently selected from H, halogen, and C1-C3 alkyl; R4 is an N-containing heterocyclic non-aromatic ring optionally comprising one or more additional heteroatoms selected from N, O or S, optionally substituted one or more times with R7; R7 is C1-C3 alkyl, hydroxy C1-C3 alkyl, halo C1-C3 alkyl, C1-C3 alkoxy C1-C3 alkyl, halo C1-C3 alkoxy C1-C3 alkyl, C2-C4 alkynyl, cyano C1-C3 alkyl, (CH2) m - selected independently from R8; m is 0, 1, 2 or 3; R8 is a 4-, 5-, or 6-membered saturated or unsaturated non-aromatic heterocycle comprising one or more heteroatoms selected from N, O, or S, optionally substituted one or more times with substituents independently selected from oxo, SO2C1-C3 alkyl, haloC1-C3 alkyl, or C3-C6 cycloalkyl optionally substituted one or more times with halo (selected from Compound.

[0045] Embodiment 2. Formula (Ia) as defined in embodiment 1, in free form or in pharma- ceutically acceptable salt form; [ka] Compound.

[0046] Embodiment 3. A compound according to any of embodiments 1 or 2, in free form or in pharma- ceutically acceptable salt form, wherein R4 is NR5R6, and R5 and R6, together with the N atom to which they are attached, form a 5-membered ring, optionally comprising one additional heteroatom selected from N, O or S, and optionally substituted one or more times with R7.

[0047] Embodiment 4. A compound according to any of embodiments 1 or 2, in free form or in pharma- ceutically acceptable salt form, wherein R4 is NR5R6, and R5 and R6, together with the N atom to which they are attached, form a 6-membered ring, optionally comprising one additional heteroatom selected from N, O or S, and optionally substituted one or more times with R7.

[0048] Embodiment 5. A compound according to any of embodiments 1 or 2, in free form or in pharma- ceutically acceptable salt form, wherein R4 is NR5R6, and R5 and R6, together with the N atom to which they are attached, optionally contain one additional heteroatom selected from N, O or S, and form a 7-membered spiro ring, optionally substituted one or more times with R7.

[0049] Embodiment 6. The compound of any of embodiments 1 or 2, in free form or in pharma- ceutically acceptable salt form, wherein R4 is an N-containing 5-membered heterocyclic non-aromatic ring optionally comprising one or more additional heteroatoms selected from N, O, or S, said ring being optionally substituted one or more times with R7; and said ring being attached to the remainder of the molecule via a ring carbon atom.

[0050] Embodiment 7. The compound of any of embodiments 1 or 2, in free form or in pharma- ceutically acceptable salt form, wherein R4 is an N-containing 6-membered heterocyclic non-aromatic mono- or bicyclic ring, optionally comprising one or more additional heteroatoms selected from N, O, or S, said ring being optionally substituted one or more times with R7; and said ring being attached to the remainder of the molecule via a ring carbon atom.

[0051] Embodiment 8. Formula (II) according to any of embodiments 1, 2 or 7, in free form or in pharma- ceutically acceptable salt form; [ka] (In the formula, R7 is C1-C3 alkyl, hydroxy C1-C3 alkyl, halo C1-C3 alkyl, C1-C3 alkoxy C1-C3 alkyl, halo C1-C3 alkoxy C1-C3 alkyl, C2-C4 alkynyl, cyano C1-C3 alkyl, (CH2) m - selected independently from R8; m is 0, 1, 2 or 3. Compound.

[0052] Embodiment 9. Formula (IIa) as defined in embodiment 8, in free form or in pharma- ceutically acceptable salt form; [ka] Compound.

[0053] Embodiment 10. Formula (IIb) as defined in embodiment 8, in free form or in pharma- ceutically acceptable salt form; [ka] Compound.

[0054] Embodiment 11. R7 is (CH2) m - R8; R8 is a 6-membered heterocycle comprising one or more heteroatoms selected from N, O, or S, optionally substituted one or more times with substituents independently selected from oxo, SO2C1-C3 alkyl, haloC1-C3 alkyl; m is 0, 1, 2 or 3; A compound according to any of the preceding embodiments, in free form or in a pharma- ceutically acceptable salt form.

[0055] Embodiment 12. A compound according to embodiment 11, in free form or in a pharma- ceutically acceptable salt form, wherein R8 is unsubstituted tetrahydropyran and m is 0.

[0056] Embodiment 13. A compound according to embodiment 11, in free form or in a pharma- ceutically acceptable salt form, wherein R8 is unsubstituted morpholine and m is 2 or 3.

[0057] Embodiment 14. A compound according to any of the preceding embodiments, in free form or in a pharma- ceutically acceptable salt form, wherein R1 is cyclohexyl optionally substituted one or more times with substituents independently selected from hydroxyl, halogen, C1-C3 alkyl.

[0058] Embodiment 15. R1 is [ka] The compound according to any of the preceding embodiments, in free form or in pharma- ceutically acceptable salt form, wherein:

[0059] Embodiment 16. R1 is [ka] The compound according to any of the preceding embodiments, in free form or in pharma- ceutically acceptable salt form, wherein:

[0060] Embodiment 17. A compound according to any one of embodiments 1 to 13, in free form or in a pharma- ceutically acceptable salt form, wherein R1 is bicyclo[2.2.2]octanyl substituted once with hydroxyl.

[0061] Embodiment 18. R1 is [ka] The compound according to embodiment 17, in free form or in a pharma- ceutically acceptable salt form, wherein:

[0062] Embodiment 19. A compound according to any one of embodiments 1 to 13, in free form or in a pharma- ceutically acceptable salt form, wherein R1 is bicyclo[1.1.1]pentanyl substituted with hydroxymethyl.

[0063] Embodiment 20.R1 is [ka] The compound according to embodiment 19, in free form or in a pharma- ceutically acceptable salt form, wherein:

[0064] Embodiment 21. 2-amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(1-(methylsulfonyl)piperidin-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 5-(4-(-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-(-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(3-morpholinopropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-(-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-(-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-5-(2-fluoro-4-(4-isopropylpiperazin-1-yl)phenyl)-N-(-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-5-(4-(-3-(2-fluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-(-4-hydroxycyclohexyl)-5-(4-(1-isopropylpyrrolidin-3-yl)phenyl)nicotinamide; 2-Amino-N-(-4-hydroxy-4-methylcyclohexyl)-5-(4-(-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-(-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)-5-(4-(-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(3,3,3-trifluoropropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(-4-hydroxycyclohexyl)-5-(4-(pyrrolidin-3-yl)phenyl)nicotinamide; 2-Amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(3-fluoro-4-hydroxycyclohexyl)-5-(4-(-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 5-(4-(2-azaspiro[3.3]heptan-2-ylmethyl)phenyl)-2-amino-N-(-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-(-4-hydroxy-4-methylcyclohexyl)-5-(4-(-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-(-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(oxetan-3-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)-5-(4-(-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-5-(2-fluoro-4-(piperazin-1-yl)phenyl)-N-(-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-(-4-hydroxycyclohexyl)-5-(4-((2-methylpyrrolidin-1-yl)methyl)phenyl)nicotinamide; 2-Amino-N-(4-hydroxycyclohexyl)-5-(4-(3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-(3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-(-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide; 2-amino-5-(4-(-3-(but-2-yn-1-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(oxetan-3-ylmethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(1-(2,2,2-trifluoroethyl)piperidin-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(2-(2,2,2-trifluoroethoxy)ethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-cyclohexyl-5-(4-(3-(piperidin-1-yl)propoxy)phenyl)nicotinamide; 2-Amino-5-(4-(-3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-cyclohexyl-5-(4-(4-methylpiperazine-1-carbonyl)phenyl)nicotinamide 2-amino-5-(3-fluoro-4-(2-methylpyrrolidin-1-yl)methyl)phenyl)-N-(-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-Amino-N-cyclohexyl-5-(4-morpholinophenyl)nicotinamide; 2-Amino-5-(4-(-3-(2,2-difluoropropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(-4-hydroxycyclohexyl)nicotinamide; 2-Amino-5-(4-(-3-(2-cyanoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-cyclohexyl-5-(4-(3-morpholinopropoxy)phenyl)nicotinamide; 2-Amino-N-(4-hydroxycyclohexyl)-5-(4-(3-(prop-2-yn-1-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 5-(4-(-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)-2-chlorophenyl)-2-amino-N-(-4-hydroxycyclohexyl)nicotinamide; 2-Amino-5-(2-fluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-N-(-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-Amino-5-(4-(-3-(2-fluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide; 2-amino-5-(4-(-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(-4-hydroxy-4-methylcyclohexyl)nicotinamide; 5-(4-(-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-(-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-Amino-N-cyclohexyl-5-(4-(piperidin-1-yl)phenyl)nicotinamide; 2-Amino-N-(4-hydroxy-4-methylcyclohexyl)-5-(4-(3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-(-3-(oxetan-3-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-cyclohexyl-5-(4-((2-(4-methylpiperazin-1-yl)ethyl)carbamoyl)phenyl)nicotinamide; 2-Amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(2,2,2-trifluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 5-(4-(-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-(-3-hydroxyadamantan-1-yl)nicotinamide; 2-Amino-N-cyclohexyl-5-(4-(morpholine-4-carbonyl)phenyl)nicotinamide; 2-Amino-N-(-4-hydroxy-4-methylcyclohexyl)-5-(4-((2-methylpyrrolidin-1-yl)methyl)phenyl)nicotinamide; 2-Amino-5-(2,3-difluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-N-(-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-Amino-N-(-4-hydroxycyclohexyl-4-d)-5-(4-(-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(-4-hydroxycyclohexyl)-5-(4-(4-methylpiperazine-1-carbonyl)phenyl)nicotinamide; 2-Amino-5-(2-chloro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-N-(-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-Amino-N-(3-(2-hydroxypropan-2-yl)bicyclo[1.1.1]pentan-1-yl)-5-(4-(-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-cyclohexyl-5-(3-(morpholine-4-carbonyl)phenyl)nicotinamide; 2-Amino-5-(3-chloro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-N-(-4-hydroxy-4-methylcyclohexyl)nicotinamide; 5-(4-(-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-(-4-hydroxy-1-methylcyclohexyl)nicotinamide; 2-amino-N-(-4-hydroxy-4-methylcyclohexyl)-5-(2-methyl-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)nicotinamide; and 2-Amino-N-cyclohexyl-5-(3-(4-(2-hydroxyethyl)piperazine-1-carbonyl)phenyl)nicotinamide The compound according to embodiment 1, in free form or in pharma- ceutically acceptable salt form, selected from:

[0065] Embodiment 22. 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(1-(methylsulfonyl)piperidin-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide; 5-(4-((S)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(3-morpholinopropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1S,5R)-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-5-(2-fluoro-4-(4-isopropylpiperazin-1-yl)phenyl)-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-5-(4-((1S,5R)-3-(2-fluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-((1r,4r)-4-hydroxycyclohexyl)-5-(4-(1-isopropylpyrrolidin-3-yl)phenyl)nicotinamide; 2-Amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(3,3,3-trifluoropropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-((1r,4r)-4-hydroxycyclohexyl)-5-(4-(pyrrolidin-3-yl)phenyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1R,3S,4R)-3-fluoro-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-((1s,4S)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 5-(4-(2-azaspiro[3.3]heptan-2-ylmethyl)phenyl)-2-amino-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-5-(4-((1R,5S)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(oxetan-3-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-5-(4-((1S,5R)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-(3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)-5-(4-((1S,5R)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-5-(2-fluoro-4-(piperazin-1-yl)phenyl)-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide 2-Amino-N-(3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)nicotinamide; 2-Amino-N-((1r,4S)-4-hydroxy-4-methylcyclohexyl)-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-((1S,5R)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide; 2-Amino-N-(3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-((1S,5R)-3-(but-2-yn-1-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(oxetan-3-ylmethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(1-(2,2,2-trifluoroethyl)piperidin-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1S,5R)-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(2-(2,2,2-trifluoroethoxy)ethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1S,5R)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-((1R,5S)-3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide; 2-amino-5-(3-fluoro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(3,3,3-trifluoropropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-5-(4-((1R,5S)-3-(2-fluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide; 2-amino-5-(4-((1R,5S)-3-(2,2-difluoropropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide; 2-Amino-5-(4-((1S,5R)-3-(2-cyanoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(prop-2-yn-1-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(prop-2-yn-1-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)-2-chlorophenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide; 2-amino-5-(2-fluoro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-Amino-5-(4-((1R,5S)-3-(2-fluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide; 2-amino-5-(4-((1S,5R)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxy-4-methylcyclohexyl)nicotinamide; 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-amino-5-(4-((1R,5S)-3-(but-2-yn-1-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-((1r,4S)-4-hydroxy-4-methylcyclohexyl)-5-(4-((1S,5R)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1S,5R)-3-(oxetan-3-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(oxetan-3-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-cyclohexyl-5-(4-((2-(4-methylpiperazin-1-yl)ethyl)carbamoyl)phenyl)nicotinamide; 2-amino-5-(4-((1S,5R)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(2,2,2-trifluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1R,3R)-3-hydroxyadamantan-1-yl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(oxetan-3-ylmethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-((1s,4R)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)-5-(4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)nicotinamide; 2-amino-5-(4-((1S,5R)-3-(2-fluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide; 2-amino-5-(2,3-difluoro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-Amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-5-(4-((1S,5R)-3-(2,2-difluoropropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(2,2,2-trifluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-((1r,4S)-4-hydroxycyclohexyl-4-d)-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-N-((1s,4s)-4-hydroxycyclohexyl)-5-(4-(4-methylpiperazine-1-carbonyl)phenyl)nicotinamide; 2-amino-5-(4-((1R,5S)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide; 2-Amino-5-(2-chloro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-amino-5-(4-((1R,5S)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-amino-N-(3-(2-hydroxypropan-2-yl)bicyclo[1.1.1]pentan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-5-(3-chloro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide; 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1r,4R)-4-hydroxy-1-methylcyclohexyl)nicotinamide; and 2-Amino-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)-5-(2-methyl-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)nicotinamide 22. The compound according to embodiment 21, in free form or in pharma- ceutically acceptable salt form, selected from:

[0066] Embodiment 23. A pharmaceutical composition comprising a therapeutically effective amount of a compound according to any of the preceding embodiments, in free form or in a pharma- ceutically acceptable salt form, and one or more pharma- ceutically acceptable carriers.

[0067] Embodiment 24. A combination comprising a therapeutically effective amount of a compound according to any of embodiments 1 to 22, in free form or in pharma- ceutically acceptable salt form, and one or more therapeutically active agents.

[0068] Embodiment 25. A compound according to any of embodiments 1 to 22, in free form or in a pharma- ceutically acceptable salt form, for use as a medicament.

[0069] Embodiment 26. A compound according to any of embodiments 1-22, in free form or in a pharma- ceutically acceptable salt form, for use in the treatment of a disorder or disease selected from heterotopic ossification or fibrodysplasia ossificans progressiva.

[0070] Embodiment 27. In particular, a modified H in free form, in particular having (i) the first two, the first three, the first four, the first five, the first six, the first eight, in particular the first ten or in particular all of the 2θ values ​​in the reflection XRPD shown in Table A below; or (ii) exhibiting a DSC diagram as shown in FIG. 4; or (iii) having a TGA diagram as shown in FIG. 5; or (iv) having an FT-IR diagram as shown in FIG. 6; or having two or three, or in particular all of (i) to (iv) above; or in particular having an XRPD diagram as shown in FIG. 3. A of 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide in its free form.

[0071] Embodiment 28. In particular, 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide in free form, in particular in modified A form, having (i) the first two, the first three, the first four, the first five, the first six, the first eight, in particular the first ten or in particular all of the 2θ values ​​in the reflection XRPD shown in Table B below; or (ii) a DSC diagram as shown in FIG. 8; or (iii) a TGA diagram as shown in FIG. 9; or (iv) an FT-IR diagram as shown in FIG. 10; or having two or three, or in particular all of (i) to (iv) above; or in particular an XRPD diagram as shown in FIG. 7.

[0072] Embodiment 29. 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide, as free form anhydrate, having in particular the XRPD diagram shown in FIG. 18.

[0073] Embodiment 30. 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide, as the free form trihydrate, having in particular the XRPD diagram shown in FIG. 19.

[0074] Embodiment 31. In particular, a fumarate modified H having (i) the first two, the first three, the first four, the first five, the first six, the first eight, in particular the first ten or especially all of the 2θ values ​​in the reflection XRPD shown in Table C below; or (ii) a DSC diagram as shown in Figure 12; or (iii) a TGA diagram as shown in Figure 13; or (iv) an FT-IR diagram as shown in Figure 14; or (v) a DVS diagram at 25°C as shown in Figure 15; or (vi) a DVS diagram at 40°C as shown in Figure 16; or two or three or four or five, or especially all of (i) to (iv) above; or in particular an XRPD diagram as shown in Figure 11. A in the form of a fumarate salt form, particularly having a compound A to fumaric acid molar ratio of 1:1.

[0075] Embodiment 32. 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide of fumarate salt amorphous form variant 1, particularly having a 1:1 molar ratio of Compound A to fumaric acid, exhibiting a glass transition of about 143° C. when analyzed by modulated DSC at a heating rate of 1 K / min, amplitude temperature of 1 K for 60 seconds.

[0076] Embodiment 33. 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide of fumaric acid amorphous form variant 2, particularly having a compound A to fumaric acid molar ratio of 1:1, exhibiting a glass transition of about 78° C. when analyzed by DSC at a heating rate of 10 K / min.

[0077] Embodiment 34. In particular, (i) 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide in phosphate form, having 2θ values ​​in the first two, the first three, the first four, the first five, the first six, the first eight, in particular the first ten or in particular all of the 2θ values ​​shown in Table D below; or in particular having an XRPD diagram as shown in Figure 17, in particular having a compound A to phosphoric acid molar ratio of 1:1.5.

[0078] Embodiment 35. A compound in the form of any one of embodiments 27 to 34 for use as a medicament.

[0079] Embodiment 36. A compound in the form of any one of embodiments 27-34 for use in the treatment of a disorder or disease selected from heterotopic ossification or fibrodysplasia ossificans progressiva.

[0080] Where 2θ values ​​are given in this disclosure (or in the table "Angles" below), this means the respective value ±0.2, i.e. in particular the value itself.

[0081] When the term "modification" is used, this relates to amorphous forms or in particular crystalline polymorphs (i.e., forms of crystalline structure), and also includes pseudopolymorphs such as solvates or in particular hydrates, of the free form or salts, respectively.

[0082] Depending on the selection of starting materials and procedures, the compounds may exist in the form of pure optical isomers or, depending on the number of asymmetric carbon atoms, as mixtures of isomers, such as racemic and diastereomeric mixtures. The present invention is intended to include all such possible isomers, including racemic mixtures, diastereomeric mixtures and optically pure forms. Optically active (R) and (S) isomers may be prepared using chiral synthons or chiral reagents or separated using conventional techniques. When the compounds contain double bonds, the substituents may be in the E or Z configuration. When the compounds contain disubstituted cycloalkyl, the cycloalkyl substituents may have cis or trans configuration. All tautomers are also intended to be included.

[0083] As used herein, the term "salt" or "salts" refers to an acid or base addition salt of the compound of the present invention. "Salt" specifically includes "pharmaceutically acceptable salt". The term "pharmaceutically acceptable salt" refers to a salt that retains the biological effectiveness and properties of the compound of the present invention and is typically not biologically or otherwise undesirable. In many cases, the compound of the present invention can form acid salts due to the presence of a basic aminopyridine moiety. When "free form" is referred to, this refers to the form without additional acid and / or base, i.e., the compound itself (although if the compound contains basic and acidic groups, it may form internal salts).

[0084] Pharmaceutically acceptable acid addition salts can be formed with inorganic and organic acids.

[0085] Inorganic acids from which salts can be derived include, for example, hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, and the like.

[0086] Organic acids from which salts can be derived include, for example, acetic acid, propionic acid, glycolic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, toluenesulfonic acid, sulfosalicylic acid, and the like.

[0087] In another aspect, the present invention provides an acid salt selected from the group consisting of acetate, ascorbate, adipate, aspartate, benzoate, besylate, bromide / hydrobromide, bicarbonate / carbonate, hydrogensulfate / sulfate, camphorsulfonate, caprate, chloride / hydrochloride, chlorotheophylline, citrate, ethanedisulfonate, fumarate, gluceptate, gluconate, glucuronate, glutamate, glutanate, glycolate, hippurate, hydroiodide / iodide, isethionate, lactate, lactobionate, lauryl salt, and the like. Provided is a compound of formula (I) in the sulfate, malate, maleate, malonate, mandelate, mesylate, methylsulfate, mucate, naphthoate, napsylate, nicotinate, nitrate, octadecanoate, oleate, oxalate, palmitate, pamoate, phosphate / hydrogen phosphate / dihydrogen phosphate, polygalacturonate, propionate, sebacate, stearate, succinate, sulfosalicylate, sulfate, tartrate, tosylate, triphenylacetate, trifluoroacetate or xinafoate salt form.

[0088] Any formula provided herein is intended to represent unlabeled forms of compounds as well as isotopically labeled forms. Isotopically labeled compounds have the structure represented by the formula provided herein, except that one or more atoms are replaced with an atom having a selected atomic mass or mass number. Examples of isotopes that can be incorporated into the compounds of the present invention include, respectively: 2 H, 3 H, 11 C. 13 C. 14 C. 15 N, 18 F 31 P, 32 P, 35 S, 36 Cl, 123 I, 124 I, 125 The present invention includes various isotopically labeled compounds as defined herein, e.g., 3 H and 14 Radioisotopes such as C, or 2 H and 13 Such isotopically labeled compounds may be useful in metabolic studies, including drug or substrate tissue distribution assays. 14 C), reaction kinetic studies (e.g. 2 H or 3 H), positron emission tomography (PET) or single photon emission computed tomography (SPECT), or in radiotherapy of patients. 18 F-labeled compounds may be particularly desirable for PET or SPECT studies. Isotopically labeled compounds of formula (I) may generally be prepared by conventional techniques known to those skilled in the art, or by methods analogous to those described in the accompanying examples, using the appropriate isotopically labeled reagent in place of the previously used unlabeled reagent.

[0089] Additionally, heavier isotopes, especially deuterium (i.e. 2Substitution with H or D) may result in certain therapeutic advantages, for example resulting from greater metabolic stability, such as increased in vivo half-life or reduced dose requirements or improved therapeutic index. It is understood that deuterium in this context is considered a substituent of the compound of formula (I). The concentration of such heavier isotopes, particularly deuterium, may be defined by an isotopic enrichment factor. The term "isotopic enrichment factor" as used herein refers to the ratio between the isotopic abundance and the natural abundance of a particular isotope. When a substituent of a compound of the invention is designated as deuterium, such compounds have an isotopic enrichment factor for each designated deuterium atom of at least 3500 (52.5% deuterium incorporation at each designated deuterium atom), 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).

[0090] Pharmaceutically acceptable solvates in accordance with the invention include, for example, D2O, d6-acetone, d6-DMSO, and the like, in which the solvent of crystallization may be isotopically substituted.

[0091] The compounds of the present invention, i.e., compounds of formula (I), containing groups capable of acting as donors and / or acceptors for hydrogen bonds, may be capable of forming co-crystals with suitable co-crystal formers. These co-crystals may be prepared from compounds of formula (I) by known co-crystal formation procedures. Such procedures include grinding, heating, co-subliming, co-melting, or contacting compounds of formula (I) in solution with a co-crystal former under crystallization conditions, and isolating the co-crystals formed thereby. Suitable co-crystal formers include those described in WO 2004 / 078163. Thus, the present invention further provides co-crystals comprising compounds of formula (I).

[0092] As used herein, the term "pharmaceutical acceptable carrier" includes any and all solvents, dispersion media, coatings, surfactants, antioxidants, preservatives (e.g., antibacterial, antifungal), isotonicity agents, absorption delaying agents, salts, preservatives, drug stabilizers, binders, excipients, disintegrants, lubricants, sweeteners, flavoring agents, dyes, and the like, and combinations thereof, as known to those skilled in the art (see, e.g., Remington's Pharmaceutical Sciences, 18th Ed. Mack Printing Company, 1990, pp. 1289-1329). Except insofar as any conventional carrier is incompatible with the active ingredient, its use in the therapeutic or pharmaceutical compositions is contemplated.

[0093] The term "therapeutically effective amount" of a compound of the present invention refers to an amount of a compound of the present invention that elicits a biological or medical response in a subject, such as, for example, reducing or inhibiting an enzyme or protein activity, or alleviating symptoms, relieving a pathology, slowing or delaying disease progression, or preventing a disease. In one non-limiting embodiment, the term "therapeutically effective amount" refers to an amount of a compound of the present invention that, when administered to a subject, is effective to (1) at least partially reduce, inhibit, prevent, and / or ameliorate a condition or disorder or disease that is (i) mediated by ALK-2, or (ii) associated with ALK-2 activity, or (iii) characterized by the activity (normal or abnormal) of ALK-2; or (2) reduce or inhibit the activity of ALK-2; or (3) reduce or inhibit the expression of ALK-2. In another non-limiting embodiment, the term "therapeutically effective amount" refers to an amount of a compound of the present invention that, when administered to a cell or tissue or non-cellular biological material or medium, is effective to at least partially reduce or inhibit the activity of ALK-2; or to at least partially reduce or inhibit the expression of ALK-2.

[0094] As used herein, the term "subject" refers to a human.

[0095] As used herein, the terms "inhibit," "inhibition," or "inhibiting" refer to the reduction or suppression of a given condition, symptom, or disorder, or disease; or a significant decrease in the baseline activity of a biological activity or process.

[0096] As used herein, the terms "treat", "treating" or "treatment" of any disease or disorder refer, in one embodiment, to ameliorating the disease or disorder (i.e., slowing or arresting or reducing the onset of the disease or at least one clinical symptom thereof). In another embodiment, "treat", "treating" or "treatment" refers to alleviating or improving at least one physical parameter, including one that may not be discernible by the patient. In yet another embodiment, "treat", "treating" or "treatment" refers to modulating the disease or disorder, either physically (e.g., stabilization of a discernible symptom), physiologically (e.g., stabilization of a physical parameter), or both. In yet another embodiment, "treat", "treating" or "treatment" refers to preventing or delaying the onset or development or progression of the disease or disorder.

[0097] As used herein, a subject is "in need of" a treatment if such a subject would benefit biologically, medically, or in quality of life from such treatment.

[0098] As used herein, the terms "a," "an," "the," and similar terms as used in the context of the present invention (particularly in the context of the claims) are intended to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context.

[0099] All methods described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context. Any and all examples provided herein, or the use of exemplary language (e.g., "such as"), are intended merely to facilitate understanding of the invention and do not pose limitations on the scope of the invention unless claimed.

[0100] Any asymmetric atom of the compounds of the present invention (e.g., carbon, etc.) may be present in racemic or enantiomerically enriched, such as (R), (S) or (R,S) configurations. In certain embodiments, each asymmetric atom has at least 50% enantiomeric excess, at least 60% enantiomeric excess, at least 70% enantiomeric excess, at least 80% enantiomeric excess, at least 90% enantiomeric excess, at least 95% enantiomeric excess, or at least 99% enantiomeric excess in the (R) or (S) configuration. Substituents of atoms with unsaturated double bonds may be present in cis-(Z) or trans-(E) form, if possible.

[0101] Thus, as used herein, the compounds of the present invention may be in the form of one of the possible isomers, rotamers, atropisomers, tautomers or mixtures thereof, for example as substantially pure geometric isomers (cis or trans), diastereomers, optical isomers (enantiomers), racemates or mixtures thereof.

[0102] Any resulting mixture of isomers can be separated on the basis of the physical chemical differences of the components into pure or substantially pure geometric or optical isomers, diastereomers, racemates, for example, by chromatography and / or fractional crystallization.

[0103] Any resulting final product or intermediate racemate can be separated into its optical antipodes by known methods, such as, for example, separation of its diastereomeric salts obtained with optically active acids or bases, and liberation of optically active acidic or basic compounds. Thus, the compounds of the present invention can be resolved into their optical antipodes using basic moieties, for example, by fractional crystallization of salts formed with optically active acids, such as tartaric acid, dibenzoyltartaric acid, diacetyltartaric acid, di-O,O'-p-toluoyltartaric acid, mandelic acid, malic acid or camphor-10-sulfonic acid. Racemic products can also be separated by chiral chromatography, such as, for example, high pressure liquid chromatography (HPLC) using a chiral adsorbent.

[0104] Furthermore, the compounds of the present invention, including their salts, may also be obtained in the form of their hydrates, or may include other solvents used in their crystallization. The compounds of the present invention may naturally or intentionally form solvates with pharmaceutically acceptable solvents (including water); in particular, the present invention is therefore intended to encompass both solvated and non-solvated forms. The term "solvate" refers to a molecular complex of the compounds of the present invention (including its pharmaceutically acceptable salts) with one or more solvent molecules. Such solvent molecules are those commonly used in the pharmaceutical arts, for example, water and ethanol, which are known to be harmless to the recipient. The term "hydrate" refers to a complex in which the solvent molecule is water.

[0105] The compounds of the present invention, including their salts, hydrates and solvates, may naturally or by design form polymorphs.

[0106] Typically, compounds of formula (I) may be prepared according to the following scheme:

[0107] Scheme 1 [ka] Step 1: Compounds of formula (III), where R2, R3, R4, and L are as defined herein for compounds of formula (I), can be prepared by coupling a compound of formula (IV), where the B(OR)2 moiety forms a boronic acid derivative (e.g., R is hydrogen or pinacol), with a compound of formula (V), where R2, R3, R4, and L are as defined herein for compounds of formula (I), in the presence of a suitable solvent, such as, for example, dioxane or 2-methyl-2-butanol, a base, such as, for example, potassium carbonate, and a suitable catalyst, preferably a palladium-based catalyst, such as, for example, [1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium(II). Compounds of formulas IV, V, III, and II may be used in free form or in the form of a salt thereof.

[0108] Step 2: Compounds of formula (II), where R2, R3, R4, and L are as defined herein for compounds of formula (I), can be prepared by treating compounds of formula (III), where R2, R3, R4, and L are as defined herein for compounds of formula (I), with a suitable base, such as, for example, lithium hydroxide or sodium hydroxide, in the presence of a suitable solvent, such as, for example, an alkanol, such as tetrahydrofuran or methanol. Addition of an acid, such as HCl, results in the corresponding salt of the compound of formula II, such as, for example, the hydrochloride salt.

[0109] Step 3: Compounds of formula (I), wherein R1, R2, R3, R4, and L are as defined herein for compounds of formula (I), may be prepared by coupling a compound of formula (II), wherein R2, R3, R4, and L are as defined herein for compounds of formula (I), with a suitable amine having the formula R1-NH2, wherein R1 is as defined herein for compounds of formula (I), such as trans-4-aminocyclohexanol, a suitable amide coupling reagent, such as O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium-hexafluorophosphate, a base, such as N-methylmorpholine or triethylamine, in the presence of a suitable solvent, such as N,N-dimethylformamide or acetonitrile.

[0110] Compounds of formula (IV) and (V) may be obtained as described in the Examples below.

[0111] Scheme 2 [ka] Step 1: Compounds of formula (VII), wherein R1 is as defined herein for compounds of formula (I), may be obtained by treating compounds of formula (VIII) with a compound of formula, such as, for example, trans-4-aminocyclohexanol, a suitable amine of R1-NH2, a suitable amide coupling reagent, such as, for example, O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium-hexafluorophosphate, and a base, such as, for example, N-methylmorpholine, in the presence of a suitable solvent, such as, for example, N,N-dimethylformamide.

[0112] Step 2: Compounds of formula (VI), where R is as defined herein for compounds of formula (I) and the B(OR) moiety forms a boronic acid derivative (e.g., R is hydrogen or pinacol), can be obtained by coupling a compound of formula (VII), where R is as defined herein for compounds of formula (I), with a boron compound, such as, for example, bis(pinacolato)diboron, in the presence of a suitable solvent, such as, for example, dioxane, a salt, such as potassium acetate, and a suitable catalyst, preferably a palladium-based catalyst, such as, for example, [1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium(II).

[0113] Step 3: Compounds of formula (I), where R1, R2, R3, R4, and L are as defined herein, may be obtained by coupling a compound of formula (VI), where R1 is as defined herein for compounds of formula (I) and the B(OR)2 moiety forms a boronic acid derivative (e.g., R is hydrogen or pinacol), with a compound of formula (V), where R2, R3, R4, and L are as defined herein for compounds of formula (I), in the presence of a suitable solvent, e.g., dioxane, a base, e.g., sodium hydroxide, and a suitable catalyst, preferably a palladium-based catalyst, e.g., [1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium(II).

[0114] Scheme 3 [ka] Step 1: Compounds of formula (VIII) (wherein R2, R3, L, R4 are as defined herein for compounds of formula (I) and the B(OR)2 moiety forms a boronic acid derivative) (e.g., R is hydrogen or pinacol) can be obtained by coupling a compound of formula (V) (wherein R2, R3, L, R4 are as defined herein for compounds of formula (I)) with a boron compound, such as, for example, bis(pinacolato)diboron, in the presence of a suitable solvent, such as, for example, dioxane, a salt, such as potassium acetate, and a suitable catalyst, preferably, a palladium-based catalyst, such as, for example, [1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium(II), or alternatively, in a suitable solvent, such as tetrahydrofuran, and a strong base, such as a mixture of n-butyllithium or isopropylmagnesium chloride or both with a boron compound, such as trimethylboronic acid.

[0115] Step 2: Compounds of formula (I), where R1, R2, R3, R4, and L are as defined herein, may be obtained by coupling a compound of formula (VIII), where R2, R3, L, R4 are as defined herein for compounds of formula (I), and the B(OR)2 moiety forms a boronic acid derivative, for example, R is hydrogen or pinacol, with a compound of formula (VII), where R1 is as defined herein for compounds of formula (I), in the presence of a suitable solvent, for example dioxane, a base, for example potassium carbonate, and a suitable catalyst, preferably a palladium-based catalyst, for example [1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium(II).

[0116] Scheme 4 [ka] Step 1: Compounds of formula (IX), wherein R2 and R3 are as defined herein for compounds of formula (I), may be obtained by treating compounds of formula (X), wherein R2 and R3 are as defined herein for compounds of formula (I), with N-methyliminodiacetic acid in the presence of a suitable solvent, such as, for example, DMF.

[0117] Step 2: Compounds of formula (VIII-1), where R1, R2, R3, R4, and L are as defined herein, can be obtained by treating compounds of formula (IX), where R2 and R3 are as defined herein for compounds of formula (I), with a suitable amine, with a suitable reducing agent, such as, for example, sodium triacetoxyborohydride, and with an acid, such as acetic acid, in the presence of a suitable solvent, such as, for example, THF.

[0118] Step 3: Compounds of formula (I), where R1, R2, R3, R4, and L are as defined herein, can be obtained by coupling a compound of formula (VIII-1), where R2, R3, L, R4 are as defined herein for compounds of formula (I), with a compound of formula (VII), where R1 is as defined herein for compounds of formula (I), in the presence of a suitable solvent, such as, for example, dioxane, a base, such as, for example, potassium phosphate, and a suitable catalyst, preferably a palladium-based catalyst, such as, for example, (2-dicyclohexylphosphino-2',4',6'-triisopropyl-1,1'-biphenyl)[2-(2-aminoethyl)phenyl)]palladium(II) chloride.

[0119] In a further aspect, the present invention provides a method for producing a method for treating a cancer cell comprising the steps of: a) coupling a compound of formula (II) as defined herein with a compound of formula R1-NH2 as defined herein to obtain a compound of formula (I); b) collecting the compound of formula (I) thus obtained, in free form or in pharma- ceutically acceptable salt form; The present invention relates to a process for preparing a compound of formula (I), in free form or in a pharma- ceutically acceptable salt form, comprising:

[0120] In a further aspect, the present invention provides a method for producing a method for treating a cancer cell comprising the steps of: a) coupling a compound of formula (VI) as defined herein with a compound of formula (V) as defined herein to obtain a compound of formula (I); b) collecting the compound of formula (I) thus obtained, in free form or in pharma- ceutically acceptable salt form; The present invention relates to a process for preparing a compound of formula (I), in free form or in a pharma- ceutically acceptable salt form, comprising:

[0121] In a further aspect, the present invention provides a method for producing a method for treating a cancer cell comprising the steps of: a) coupling a compound of formula (VIII) or a compound of formula (VIII-1) as defined herein with a compound of formula (VII) as defined herein to obtain a compound of formula (I); b) collecting the compound of formula (I) thus obtained, in free form or in pharma- ceutically acceptable salt form; The present invention relates to a process for preparing a compound of formula (I), in free form or in a pharma- ceutically acceptable salt form, comprising:

[0122] The invention further includes any variant of the process of the invention, in which intermediate products available at any stage thereof are used as starting materials to carry out the remaining steps; or the starting materials are formed in situ under the reaction conditions; or the reaction components are used in the form of their salts or optically pure materials.

[0123] The compounds of the present invention and intermediates may also be converted into each other by methods commonly known to those skilled in the art.

[0124] In another aspect, the present invention provides a pharmaceutical composition comprising a compound of the present invention or a pharma- ceutically acceptable salt thereof and a pharma- ceutically acceptable carrier. In a further embodiment, the composition comprises at least two pharma- ceutically acceptable carriers, such as those described herein. For the purposes of the present invention, solvates and hydrates are generally considered to be compositions, unless otherwise specified. Preferably, the pharma- ceutical acceptable carrier is sterile. The pharmaceutical composition may be formulated for a particular route of administration, such as oral, parenteral, rectal, transdermal, etc. Furthermore, the pharmaceutical composition of the present invention may be configured in solid form (such as, but not limited to, capsules, tablets, pills, granules, powders, or suppositories) or in liquid form (such as, but not limited to, solutions, suspensions, or emulsions). The pharmaceutical composition may be subjected to conventional pharmaceutical operations, such as sterilization, and / or may contain conventional inert diluents, lubricants, or buffers, as well as adjuvants, such as preservatives, stabilizers, wetting agents, emulsifiers, buffers, and the like.

[0125] Typically, the pharmaceutical composition is a tablet or gelatin capsule comprising the active ingredient in combination with one or more of the following: an active ingredient such as a sucrose or glycerin (AGA) or an adjuvant (eg, sucrose or glycerin) or an active ingredient such as sucrose or glycerin (eg, sucrose or glycerin) in a pharmaceutical composition comprising an active ingredient such as sucrose or sucrose; a) diluents such as, for example, lactose, dextrose, sucrose, mannitol, sorbitol, cellulose, and / or glycine; b) lubricants such as, for example, silica, talc, stearic acid, its magnesium or calcium salts and / or polyethylene glycol; Tablets also include: c) binders, such as, for example, magnesium aluminum silicate, starch paste, gelatin, tragacanth, methylcellulose, sodium carboxymethylcellulose and / or polyvinylpyrrolidone; if desired d) disintegrants, such as, for example, starch, agar, alginic acid or its sodium salt, or effervescent mixtures; and e) Absorbents, colourants, flavourings and sweeteners.

[0126] Tablets may be either film coated or enteric coated according to methods known in the art.

[0127] Compositions suitable for oral administration contain an effective amount of the compound of the present invention in the form of tablets, lozenges, aqueous or oily suspensions, dispersible powders or granules, emulsions, hard or soft capsules, or syrups or elixirs. Compositions for oral use are prepared according to any method known in the art of manufacturing pharmaceutical compositions, and in order to provide pharma-ceutically elegant and palatable preparations, such compositions may contain one or more agents selected from the group consisting of sweeteners, flavoring agents, coloring agents and preservatives. Tablets may contain the active ingredient in a mixture with non-toxic pharma-ceutically acceptable excipients suitable for the manufacture of tablets. These excipients are, for example, inert diluents such as calcium carbonate, sodium carbonate, lactose, calcium phosphate or sodium phosphate; granulating and disintegrating agents such as corn starch or alginic acid; binding agents such as starch, gelatin or acacia; and lubricating agents such as magnesium stearate, stearic acid or talc. Tablets are uncoated or coated by known techniques to delay disintegration and absorption in the gastrointestinal tract, thereby providing a longer sustained action.For example, time-delay materials such as glyceryl monostearate or glyceryl distearate can be used.The preparation for oral use can be provided as a hard gelatin capsule in which active ingredient is mixed with an inert solid diluent such as calcium carbonate, calcium phosphate or kaolin, or as a soft gelatin capsule in which active ingredient is mixed with water or with an oil medium such as peanut oil, liquid paraffin or olive oil.

[0128] Compounds of formula (I), in free form or in pharma- ceutically acceptable salt form, exhibit beneficial pharmacological properties, e.g., ALK-2 modulating properties, e.g., as demonstrated in the in vitro and in vivo tests provided in the subsequent sections, and are therefore indicated for therapy or for use as research chemicals, e.g., as tool compounds.

[0129] The compounds of the invention may be useful in the treatment of an indication selected from heterotopic ossification or fibrodysplasia ossificans progressiva.

[0130] Without wishing to be bound by theory, it is believed that the compounds of the present invention, being selective ALK-2 inhibitors, reduce / inhibit BMP signaling and the associated aberrant tissue repair.

[0131] Thus, as a further embodiment, the present invention provides the use of a compound of formula (I) or its subformulas (Ia), (II), (IIa), (IIb) in free form or in pharma- ceutically acceptable salt form in therapy. In a further embodiment, the therapy is selected from diseases that may be treated by inhibition of the ALK-2 receptor. In another embodiment, the disease is selected from heterotopic ossification or fibrodysplasia ossificans progressiva.

[0132] Thus, as a further embodiment, the present invention provides a compound of formula (I) or its subformulas (Ia), (II), (IIa), (IIb) in free form or in pharma- ceutically acceptable salt form for use in therapy. In a further embodiment, the therapy is selected from diseases that may be treated by inhibition of the ALK-2 receptor. In another embodiment, the disease is selected from heterotopic ossification or fibrodysplasia ossificans progressiva.

[0133] In another embodiment, the present invention provides a method of treating a disease treated by inhibition of the ALK-2 receptor comprising the step of administering a therapeutically acceptable amount of a compound of formula (I) or its subformulas (Ia), (II), (IIa), (IIb) in free form or in pharma- ceutically acceptable salt form. In a further embodiment, the disease is selected from heterotopic ossification or fibrodysplasia ossificans progressiva.

[0134] Thus, as a further embodiment, the present invention provides the use of a compound of formula (I) or its subformulas (Ia), (II), (IIa), (IIb) in free form or in pharma- ceutically acceptable salt form for the manufacture of a medicament. In a further embodiment, the medicament is for the treatment of a disease that may be treated by inhibition of the ALK-2 receptor. In another embodiment, the disease is selected from heterotopic ossification or fibrodysplasia ossificans progressiva.

[0135] In one embodiment of the present invention, there is provided 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-(3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide in free form or in a pharma- ceutically acceptable salt thereof, in particular in one of the modifications mentioned herein, for use in the treatment of heterotopic ossification or fibrodysplasia ossificans progressiva.

[0136] In one embodiment there is provided 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide in free form or in a pharma- ceutically acceptable salt thereof, in particular in one of the modifications mentioned herein, for use in the treatment of heterotopic ossification or fibrodysplasia ossificans progressiva.

[0137] In one embodiment there is provided 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1S,5R)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide in free form or in a pharma- ceutically acceptable salt thereof, in particular in one of the modifications mentioned herein, for use in the treatment of heterotopic ossification or fibrodysplasia ossificans progressiva.

[0138] The following examples are intended to illustrate the invention and should not be construed as limiting it. Temperatures are given in degrees Celsius. Unless otherwise noted, all evaporations are carried out under reduced pressure, typically about 15 mmHg to 100 mmHg (=20 to 133 mbar). The structures of final products, intermediates, and starting materials are confirmed by standard analytical methods, e.g., microanalysis, and spectroscopic characteristics, e.g., MS, IR, NMR, etc. Abbreviations used are those commonly used in the art.

[0139] All starting materials, building blocks, reagents, acids, bases, dehydrating agents, solvents, and catalysts utilized to synthesize the compounds of the invention are commercially available or can be prepared by organic synthesis methods known to those skilled in the art, or by methods described in the Examples or by methods analogous thereto. Additionally, the compounds of the invention can be prepared by organic synthesis methods known to those skilled in the art, as shown in the Examples below. EXAMPLES

[0140] Abbreviation δ Chemical shift AcOH Acetic acid aq rr aq. Water-based APCI-MS atmospheric pressure chemical ionization mass spectrometry BH3DMS Borane dimethyl sulfide complex Brine Saturated sodium chloride solution n-BuLi n-Butyl lithium DCM Dichloromethane DMAP 4-(Dimethylamino)pyridine DMF N,N-Dimethylformamide DIPEA Diisopropylethylamine DMSO Dimethyl sulfoxide DSC Differential Scanning Calorimetry DVS Dynamic Vapor Sorption eq equivalent Et Ethyl Et3N Triethylamine EtOAc Ethyl acetate EtOH Ethanol ESI-MS Electrospray Ionization Mass Spectrometry FIA-MS Flow Injection Analysis Mass Spectroscopy FT-IR Fourier transform infrared spectroscopy h time HATU O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium-hexafluorophosphate HPLC High Performance Liquid Chromatography HRMS high-resolution mass spectrometry IPA Isopropanol IPAc Isopropyl acetate i-PrOH Isopropanol IT internal temperature K2CO3 Potassium Carbonate K3PO4 Potassium Phosphate KOAc Potassium Acetate L Liter LC-MS Liquid Chromatography Mass Spectrometry LiAlH4 Lithium Aluminum Hydride LiOH Lithium hydroxide M Molar concentration MCC Microcrystalline Cellulose mg milligram mM millimolar concentration MeOH Methanol min mL Milliliters MgSO4 Magnesium Sulfate MHz Megahertz MTBE Methyl tert-butyl ether N Normal Na2SO4 Sodium Sulfate NaHCO3 Sodium bicarbonate NaHMDS Sodium bis(trimethylsilyl)amide NaOH Sodium hydroxide NH4Cl Ammonium chloride NH4OH Ammonium hydroxide NH4OAc Ammonium Acetate NMR nuclear magnetic resonance PdCl2(dppf) or Pd(dppf)Cl2[1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium(II) PdCl2(PPh3)2 Bis(triphenylphosphine)palladium(II) chloride prepHPLC Preparative High Performance Liquid Chromatography ppm parts per million RT or rt Room temperature (23±3℃) sat. saturation SFC Supercritical Fluid Chromatography SPE solid phase extraction TEA Triethylamine TFA Trifluoroacetic acid THF Tetrahydrofuran TGA thermogravimetric analysis t R Residence time UPLC-MS Ultra-High Performance Liquid Chromatography Mass Spectroscopy XPhos Pd (2-Dicyclohexylphosphino-2',4',6'-triisopropyl-1,1'-biphenyl)[2-(2-aminoethyl)phenyl]palladium(II) chloride XRPD X-ray powder diffraction

[0141] Analysis method 1H-NMR Measurements were performed on a Bruker Ultrashield™ 400 (400 MHz), Bruker Ultrashield™ 600 (600 MHz), 400 MHz DRX Bruker Cryo Probe (400 MHz) or 500 MHz DRX Bruker Cryo Probe (500 MHz) spectrometer with or without trimethylsilane as an internal standard. Chemical shifts (δ values) are reported in ppm downfield from tetramethylsilane, and spectral splitting patterns are singlet (s), doublet (d), triplet (t), quartet (q), multiplet, unresolved or more overlapping signals (m), broad signals (bs). Solvents are indicated in parentheses.

[0142] UPLC-MS Column: Waters Acquity HSS T3, C18, 1.8 μm, 2.1 × 50 mm, oven at 60 °C. Flow rate: 1.0 mL / min. Gradient: 5%-98% B for 1.40 min, then 98% B for 0.40 min, 98%-5% B for 0.10 min, 5% B for 0.10 min; A = water + 0.05% formic acid + 3.75 mM NH4OAc, B = acetonitrile + 0.04% formic acid. Detection: UV / VIS (DAD), ESI (±). Mass spectrometer range: 100-1200 Da.

[0143] For Examples 46, 56, 74, 81, 85, and 87: Column: Waters Acquity BEH, C18, 1.7 μm, 2.1 × 50 mm, oven at 50 °C. Flow rate: 1.0 mL / min. Gradient: 2% to 98% B in 4.40 min, then 98% B in 0.75 min, 98% to 2% B in 0.04 min; A = water + 0.1% formic acid, B = acetonitrile + 0.1% formic acid. Detection: UV / VIS (DAD), ESI (±). Mass spectrometer range: 100-1200 Da.

[0144] UPLC-HRMS: Waters Acquity SDS, C18, 1.7 μm, 2.1 × 50 mm, oven at 50 °C. Gradient: 5% to 98% B in 7.50 min, then 98% B in 0.40 min, 98% to 5% B in 0.15 min; A = water + 5 mM NH4OH, B = acetonitrile + 5 mM NH4OH. Detection: UV / VIS (DAD), ESI (±). Mass spectrometer range: 100-1200 Da.

[0145] HPLC-MS Column: Waters Symmetry C8, 3.5 μm, 2.1 × 50 mm, oven at 50 °C; flow rate: 1.0 mL / min. Gradient: 10%-95% B for 2 min, then 95% B for 1 min, 95%-10% B for 0.5 min, 10% B for 0.50 min; A = water + 0.1% TFA, B = acetonitrile + 0.1% TFA. Detection: UV / VIS (DAD), APCI (+). Mass spectrometer range: 100-1200 Da.

[0146] Optical rotation measurement Optical rotations were measured using a polarimeter Perkin Elmer PE241 Series No. 5325 operating at 589 nm using chloroform as the solvent.

[0147] Purification method prepHPLC Gilson GX-281, Pump 331 / 332. Column: Waters Sunfire C18, 30×100 mm, 5 μm. Flow rate: 30 mL / min. Mobile phase: Water (containing 0.1% TFA) and acetonitrile (Method 1a) or: Column: X-Bridge C18, 30×50mm, 5μm. Flow rate: 75mL / min. Mobile phase: Water (containing 5 mM NH4OH) and acetonitrile (Method 1b)

[0148] Normal Phase Flash Chromatography Teledyne ISCO CombiFlash: Column: Redisep Rf Silica Flash Mobile phase: cyclohexane / EtOAc (Method 2a) or DCM / MeOH (Method 2b). Biotage Flash-Master II: Column: prefilled with silica gel 60 (40-63 μm) from Merck Mobile phase: DCM and MeOH (containing 7.3 mM NH4OH) (Method 2c).

[0149] Reversed Phase Flash Chromatography: Teledyne ISCO CombiFlash: Columns Redisep Rf Gold C18 High Performance, 15.5g, 50g or 240g prepacked columns, 20-40μm, 100A Mobile phase: water and acetonitrile (containing 7.3 mM NH4OH) (Method 3a) or water (containing 0.1% TFA) and acetonitrile (Method 3b).

[0150] Example 1: 2-Amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(1-(methylsulfonyl)piperidin-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] To a solution of 5-(4-((1R,5S)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide TFA salt (intermediate 1a, 80 mg, 0.158 mmol) in DCM (4 mL) was added 1-(methylsulfonyl)piperidin-4-one (30.8 mg, 0.174 mmol) and AcOH (0.018 mL, 0.316 mmol) at room temperature under nitrogen atmosphere. The reaction mixture was stirred at 45° C. for 30 min. Sodium triacetoxyborohydride (84 mg, 0.395 mmol) was added at room temperature and the reaction mixture was stirred at 45° C. for 1 h. The reaction mixture was then diluted with a saturated aqueous solution of NaHCO3 and mixed with EtOAc. After phase separation, the aqueous layer was extracted again with EtOAc. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The crude product was purified by normal phase chromatography (Method 2b) to give the title compound as a colorless solid. 1H NMR(400MHz,DMSO-d6)δ 8.39(d,1H),8.31(d,1H),8.11(d,1H),7.59(d,2H),7.24(d,2H),7.12(s,2H),4.58(d,1H),3.80-3.63(m,1H),3.45-3.36(m,4H),3. 15(dd,1H),2.89-2.83(m,5H),2.65(dd,1H),2.35-2.29(m,1H),1.98-1.81(m,7H),1.57-1.18(m,8H),0.83-0.70(m,1H).(UPLC-MS)t R0.49 min; ESI-MS 554[M+H] + .

[0151] Intermediate 1a: 5-(4-((1R,5S)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide To a solution of (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b, 940 mg, 1.55 mmol) in dioxane (10 mL) was added a 4 M solution of HCl in dioxane (1.55 mL, 6.20 mmol) at room temperature. The reaction mixture was stirred at 65° C. for 5 h and then concentrated under reduced pressure to give the title compound as the hydrochloride salt. Sometimes the title compound was further purified by prepHPLC (Method 1a) to give the TFA salt after evaporation of the solvent. (UPLC-MS)t R 0.45 min;ESI-MS 393[M+H] + .

[0152] Intermediate 1b: (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate To a solution of 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c, 630 mg, 1.59 mmol) in DMF (10 mL) was added trans-4-aminocyclohexanol (290 mg, 1.91 mmol), HATU (909 mg, 2.39 mmol) and N-methylmorpholine (0.53 mL, 4.78 mmol) at room temperature. The reaction mixture was stirred for 2 h, diluted with a saturated aqueous solution of NaHCO3 and extracted three times with EtOAc. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The crude product was purified by prepHPLC (Method 1a) to give the title compound as a colorless solid. (UPLC-MS)t R 1.00 min;ESI-MS 493[M+H] + .

[0153] Intermediate 1c: 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid To a solution of (1R,5S)-tert-butyl 1-(4-(6-amino-5-(methoxycarbonyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1d, 1.00 g, 2.44 mmol) in THF (15 mL) was added a 2M aqueous solution of LiOH (3.66 mL, 7.33 mmol) at room temperature. The reaction mixture was stirred at 65° C. for 2 h and then concentrated under reduced pressure. The crude product was purified by prepHPLC (Method 1a) to give the title compound. (UPLC-MS)t R 0.92 min;ESI-MS 396[M+H] + .

[0154] Intermediate 1d: (1R,5S)-tert-butyl-1-(4-(6-amino-5-(methoxycarbonyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate Racemic tert-butyl-1-(4-(6-amino-5-(methoxycarbonyl)pyridin-3-yl)phenyl)-3-aza-bicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1e, 13.5 g, 33.0 mmol) was subjected to chiral preparative SFC (Waters SFC200, CHIRALPAK AD-H500 30 μm). * Separation was performed by SFC (CHIRALPAK AD-3 3μm2, mobile phase CO2 / i-PrOH 70:30, flow rate 120g / min; UV detection at 278nm). After concentration under reduced pressure, the title compound was obtained as an off-white solid. * 100 mm, mobile phase CO2 / MeOH+0.1%DEA 60:40, flow rate 1 mL / min; UV detection at 274 nm):t R 2.30 minutes, ee=98.6%, [α] D 20 =+90°.

[0155] Intermediate 1e: tert-Butyl 1-(4-(6-amino-5-(methoxycarbonyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate To a solution of tert-butyl 1-(4-bromophenyl)-3-aza-bicyclo[3.1.0]hexane-3-carboxylate (prepared as described in WO 2007 / 022935) (3.34 g, 9.38 mmol) in dioxane (75 mL) was added methyl 2-amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (prepared as described in WO 2012 / 087938) (3.91 g, 14.1 mmol). A 2M aqueous solution of K2CO3 (9.38 mL, 18.8 mmol) and Pd(dppf)Cl2-DCM adduct (0.766 g, 0.938 mmol) was added under nitrogen atmosphere and the mixture was heated at 80 °C under nitrogen atmosphere for 18 h. The reaction mixture was diluted with 150 mL of water and extracted three times with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The crude residue was purified by normal phase chromatography (Method 2b) to give the title compound as an off-white solid. (UPLC-MS)t R 1.29 minutes;ESI-MS 410[M+H] + .

[0156] Example 2: 2-Amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] To a solution of 2-amino-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid TFA salt (Intermediate 2a, 117 mg, 0.259 mmol) in DMF (3 mL) was added trans-4-aminocyclohexanol hydrochloride (39.3 mg, 0.259 mmol), HATU (148 mg, 0.389 mmol), and N-methylmorpholine (0.085 mL, 0.778 mmol) at room temperature. The reaction mixture was stirred at room temperature for 2 h, then diluted with a saturated aqueous solution of NaHCO3 and mixed with EtOAc. After phase separation, the aqueous layer was extracted again with EtOAc. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The crude product was purified by prepHPLC (Method 1a) to give the title compound as a yellow solid. 1H NMR(400MHz,DMSO-d6)δ 8.38(d,1H),8.31(d,1H),8.11(d,1H),7.58(d,2H),7.23(d,2H),7.12(s,2H),4.58(d,1H),3.82-3.66(m,1H),3.48-3.3 4(m,3H),3.07(d,1H),2.64-2.55(m,2H),1.96-1.77(m,5H),1.50-1.19(m,5H),1.04(dd,6H),0.75(dd,1H).(UPLC-MS)t R 0.50 min; ESI-MS 435[M+H] + .

[0157] Intermediate 2a: 2-amino-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid TFA salt To a solution of methyl 2-amino-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate (Intermediate 2b, 660 mg, 1.22 mmol) in THF (10 mL) was added a 2M aqueous solution of LiOH (1.22 mL, 2.44 mmol) at room temperature. The reaction mixture was stirred at 65° C. for 2 h and then concentrated under reduced pressure. The crude product was purified by prepHPLC (Method 1a) to give the title compound as a TFA salt. (UPLC-MS)t R0.37 min;ESI-MS 338[M+H] + .

[0158] Intermediate 2b: Methyl 2-amino-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate To a solution of methyl 2-amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (prepared as described in WO 2012 / 087938) (462 mg, 1.663 mmol) in acetonitrile (7 mL) was added (1R,5S)-1-(4-bromophenyl)-3-isopropyl-3-azabicyclo[3.1.0]hexane (intermediate 2c, 466 mg, 1.66 mmol), 2M aqueous K2CO3 (1.66 mL, 3.33 mmol) and PdCl2(dppf)-DCM adduct (67.9 mg, 0.083 mmol) at room temperature. The reaction mixture was sealed and irradiated in a microwave reactor at 120 °C for 10 min, then cooled, filtered over Celite, diluted with a saturated aqueous solution of NaHCO3 and mixed with EtOAc. After phase separation, the aqueous layer was extracted again with EtOAc. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The crude product was used without further purification. (UPLC-MS)t R 0.62 min;ESI-MS 352[M+H] + .

[0159] Intermediate 2c: (1R,5S)-1-(4-bromophenyl)-3-isopropyl-3-azabicyclo[3.1.0]hexane To a solution of (1R,5S)-1-(4-bromophenyl)-3-azabicyclo[3.1.0]hexane (prepared as described in WO 2007 / 022935) (525 mg, 2.21 mmol) in acetonitrile (10 mL) was added 2-iodopropane (0.420 mL, 2.65 mmol) and K2CO3 (609 mg, 4.41 mmol) at room temperature under nitrogen atmosphere. The reaction mixture was stirred at 65°C for 3 h, then diluted with EtOAc and mixed with a saturated aqueous solution of NaHCO3. After phase separation, the aqueous phase was extracted with EtOAc. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound as an off-white solid. (UPLC-MS)t R 0.72 min; ESI-MS 280 / 282[M+H] + .

[0160] Example 3: 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide [ka] To a solution of (6-amino-5-(((1r,4r)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)boronic acid (Intermediate 3a, 300 mg, 0.645 mmol) in dioxane (5 mL), (R)-6-(1-(4-bromophenyl)ethyl)-2-oxa-6-azaspiro[3.3]heptane (Intermediate 3b, 420 mg, 0.774 mmol), PdCl2(dppf) (23.6 mg, 0.032 mmol) and 2N aqueous NaOH (0.645 mL, 1.29 mmol) were added at room temperature under nitrogen atmosphere. The reaction mixture was stirred at 80° C. for 2 h and then diluted with EtOAc and water. After two extractions with EtOAc, the organic layer was washed with a saturated aqueous solution of NaHCO3 and brine, respectively, dried over MgSO4, filtered and concentrated under reduced pressure. The crude product was dissolved in MeOH and passed through a silica-thiol cartridge (500 mg loaded; preconditioned with MeOH) to remove palladium. The filtrate was concentrated under reduced pressure. The residue was purified by normal phase chromatography (Method 2b) to give the title compound as a brownish solid. 1H NMR(400MHz,DMSO-d6)δ 8.37(d,1H),8.27(d,1H),8.09-8.14(m,1H),7.57(bs,2H),7.33(bs,2H),7.12(bs,2H),4.54-4.58(m,1H),4.51-4.66(m,3H),3.55-3.81(m, (UPLC-MS)t R 0.45 min;ESI-MS 437[M+H] + .

[0161] Intermediate 3a: (6-amino-5-(((1r,4r)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)boronic acid. To a solution of 2-amino-5-bromo-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide (Intermediate 3c, 1.00 g, 2.67 mmol) in dioxane (25 mL) was added bis(pinacolato)diboron (0.815 g, 3.21 mmol), PdCl2(dppf) (0.098 g, 0.134 mmol), and KOAc (0.525 g, 5.35 mmol) at room temperature under nitrogen atmosphere. The reaction mixture was stirred at 80 °C for 18 h, cooled, filtered through a celite pad, and concentrated under reduced pressure to give the title compound as a crude brownish solid (the pinacolato ester was hydrolyzed under the reaction conditions), which was used without further purification. (UPLC-MS)t R 0.32 min; ESI-MS 280[M+H] + .

[0162] Intermediate 3b: (R)-6-(1-(4-bromophenyl)ethyl)-2-oxa-6-azaspiro[3.3]heptane. To a solution of (R)-1-(4-bromophenyl)ethanamine (0.216 mL, 1.499 mmol) in DMF (7 mL) was added DIPEA (0.524 mL, 3.00 mmol) and 3,3-bis(bromomethyl)oxetane (439 mg, 1.80 mmol) at room temperature under nitrogen atmosphere. The reaction mixture was stirred at 100° C. for 5 h, cooled and diluted with water and EtOAc. After phase separation, the aqueous layer was extracted twice with EtOAc and the combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound as a yellow oil, which was used without further purification. (UPLC-MS)t R 0.52 min; ESI-MS 282 / 284[M+H] + .

[0163] Intermediate 3c: 2-amino-5-bromo-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide. To a solution of 2-amino-5-bromonicotinic acid (2.00 g, 9.22 mmol) in DMF (30 mL) was added trans-4-aminocyclohexanol (1.68 g, 11.1 mmol), HATU (7.01 g, 18.4 mmol) and N-methylmorpholine (4.05 mL, 36.9 mmol) at room temperature. After stirring for 2 h, the reaction mixture was diluted with EtOAc and a saturated aqueous solution of NaHCO3. The aqueous phase was extracted twice with EtOAc. The combined organic layers were dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by normal phase chromatography (Method 2a) to give the title compound as a yellow solid. (UPLC-MS)t R 0.62 min;ESI-MS 314 / 316[M+H] + .

[0164] Example 4: 5-(4-((S)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 3), except that (S)-6-(1-(4-bromophenyl)ethyl)-2-oxa-6-azaspiro[3.3]heptane (Intermediate 4a) was used instead of (R)-6-(1-(4-bromophenyl)ethyl)-2-oxa-6-azaspiro[3.3]heptane (Intermediate 3b). 1H NMR(400MHz,DMSO-d6)δ 8.37(d,1H),8.27(d,1H),8.09-8.14(m,1H),7.57(bs,2H),7.33(bs,2H),7.12(bs,2H),4.54-4.58(m,1H),4.51-4.66(m,3H),3.55-3.81(m, (UPLC-MS)t R 0.45 min;ESI-MS 437[M+H] + .

[0165] Intermediate 4a: (S)-6-(1-(4-bromophenyl)ethyl)-2-oxa-6-azaspiro[3.3]heptane The title compound was prepared in a similar manner to (R)-6-(1-(4-bromophenyl)ethyl)-2-oxa-6-azaspiro[3.3]heptane (Intermediate 3b), except that (S)-1-(4-bromophenyl)ethanamine was used instead of (R)-1-(4-bromophenyl)ethanamine. (UPLC-MS)t R 0.55 min; ESI-MS 282 / 284[M+H] + .

[0166] Example 5: 2-Amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(3-morpholinopropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] To a solution of 5-(4-((1S,5R)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide TFA salt (Intermediate 5a, 70 mg, 0.138 mmol) in acetonitrile (3 mL), K2CO3 (47.7 mg, 0.345 mmol) and 4-(3-bromopropyl)morpholine (47.9 mg, 0.166 mmol) were added at room temperature. The reaction mixture was stirred at 65 °C for 2 h. The reaction mixture was then diluted with a saturated aqueous solution of NaHCO3 and mixed with EtOAc. After phase separation, the aqueous layer was extracted again with EtOAc. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The crude product was purified by prepHPLC (Method 1a) to give the title compound as a yellow solid. 1H NMR(400MHz,DMSO-d6)δ 8.38(d,1H),8.31(d,1H),8.11(d,1H),7.58(d,2H),7.22(d,2H),7.12(s,2H),4.58(d,1H),3.82-3.67(m,1H),3.61-3.50(m,4) (UPLC-MS)t R 0.40 min;ESI-MS 520[M+H] + .

[0167] Intermediate 5a: 5-(4-((1S,5R)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide To a solution of (1S,5R)-tert-butyl 1-(4-(6-amino-5-(((1r,4S)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 5b, 1.18 g, 1.95 mmol) in dioxane (10 mL) was added a 4 M solution of HCl in dioxane (1.95 mL, 7.78 mmol) at room temperature. The reaction mixture was stirred at 65° C. for 5 h and then concentrated under reduced pressure to give the title compound as the hydrochloride salt. Sometimes the product was further purified by prepHPLC (Method 1a) to give the title compound as the TFA salt after evaporation of the solvent. (UPLC-MS)t R 0.45 min;ESI-MS 393[M+H] + .

[0168] Intermediate 5b: (1S,5R)-tert-butyl 1-(4-(6-amino-5-(((1r,4S)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate The title compound was prepared in a similar manner to (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b), except that 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 5c) was used instead of 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c). (UPLC-MS)t R 1.00 min;ESI-MS 493[M+H] + .

[0169] Intermediate 5c: 2-amino-5-(4-((1S,5R)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c), except that (1S,5R)-tert-butyl 1-(4-(6-amino-5-(methoxycarbonyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 5d) was used instead of (1R,5S)-tert-butyl 1-(4-(6-amino-5-(methoxycarbonyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1d). (UPLC-MS)t R 0.92 min;ESI-MS 396[M+H] + .

[0170] Intermediate 5d: (1S,5R)-tert-butyl 1-(4-(6-amino-5-(methoxycarbonyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate Racemic tert-butyl 1-(4-(6-amino-5-(methoxycarbonyl)pyridin-3-yl)phenyl)-3-aza-bicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1e, 13.5 g, 33.0 mmol) was purified by chiral preparative SFC (CHIRALPAK AD-H 5 μm 30 * Separation was performed by HPLC (CHIRALPAK AD-3 3μm2, 250mm, mobile phase CO2 / i-PrOH 70:30, flow rate 120g / min; UV detection at 278nm). After concentration under reduced pressure, the title compound was obtained as an off-white solid. * 100 mm, mobile phase CO2 / MeOH+0.1%DEA 60:40, flow rate 1 mL / min; UV detection at 274 nm):t R 2.90 minutes, ee=98.7%, [α] D 20 =-87°.

[0171] Example 6: 2-Amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide [ka] To a solution of 5-(4-((1R,5S)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide TFA salt (Intermediate 1a, 70 mg, 0.138 mmol) in acetonitrile (3 mL) was added K2CO3 (38.2 mg, 0.276 mmol) and 1,3-difluoropropan-2-yl trifluoromethanesulfonate (Intermediate 6a) (37.8 mg, 0.166 mmol) at room temperature. The reaction mixture was stirred at room temperature for 1 h, then diluted with a saturated aqueous solution of NaHCO3 and mixed with EtOAc. After phase separation, the aqueous layer was extracted again with EtOAc. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The crude product was purified by prepHPLC (Method 1a) to give the title compound. 1H NMR(400MHz,DMSO-d6)δ 8.41(d,1H),8.37(d,1H),8.18(s,1H),7.62(s,2H),7.35(d,1H),7.25(m,3H),4.64( d,3H),3.74(m,4H),2.89(d,4H),1.87(t,5H),1.34(m,6H),0.82(s,1H).(UPLC-MS)t R 0.68 min;ESI-MS 471[M+H] + .

[0172] Intermediate 6a: 1,3-difluoropropan-2-yl trifluoromethanesulfonate To a solution of 1,3-difluoropropan-2-ol (300 mg, 3.12 mmol) in DCM (8 mL) was added DMAP (26.7 mg, 0.219 mmol) and TEA (0.522 mL, 3.75 mmol) at room temperature under nitrogen atmosphere. The reaction mixture was cooled to 0° C. and trifluoromethanesulfonic anhydride (0.630 mL, 3.75 mmol) was added. After stirring for 60 min at 0° C. and 3 h at room temperature, the reaction mixture was diluted with DCM. The organic layer was washed twice with an aqueous solution of citric acid and twice with a saturated aqueous solution of NaHCO3, dried over MgSO4 and concentrated at 500 mbar. The title compound was obtained as a crude oil, which was used without further purification.

[0173] Example 7: 2-Amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1S,5R)-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was synthesized by using 2-amino-5-(4-((1S,5R)-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 7a) instead of 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c) to obtain the trans-4- Prepared in a similar manner as (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b), except that 4-aminobicyclo[2.2.2]octan-1-ol hydrochloride was used instead of aminocyclohexanol. The crude product was purified first by prepHPLC (Method 1a) and then by reverse-phase flash chromatography (Method 3a) to give the title compound as a colorless solid. 1H NMR(400MHz,DMSO-d6)δ 8.34(d,1H),7.98(d,1H),7.79(s,1H),7.57(d,2H),7.21(d,2H),6.92(s,2H),4.32(s,1H),3.45(t,2H),3.41-3.29(m,2H),3.27(s, (UPLC-MS)t R 0.52 min;ESI-MS 477[M+H] + .

[0174] Intermediate 7a: 2-amino-5-(4-((1S,5R)-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 2c), except that methyl 2-amino-5-(4-((1S,5R)-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate (Intermediate 7b) was used instead of (1R,5S)-tert-butyl 1-(4-(6-amino-5-(methoxycarbonyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1d). (UPLC-MS)t R 0.32 min; ESI-MS 354[M+H] + .

[0175] Intermediate 7b: Methyl 2-amino-5-(4-((1S,5R)-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate To a solution of methyl 5-(4-((1S,5R)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-aminonicotinate hydrochloride (Intermediate 7c, 210 mg, 0.607 mmol) in acetonitrile (6 mL) was added K2CO3 (168 mg, 0.729 mmol) and 1-bromo-2-methoxyethane (0.068 mL, 0.729 mmol) at room temperature. The reaction mixture was stirred at 65 °C for 3 h. The reaction mixture was then diluted with a saturated aqueous solution of NaHCO3 and mixed with EtOAc. After phase separation, the aqueous layer was extracted again with EtOAc. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound, which was used without further purification. (UPLC-MS)t R 0.62 min; ESI-MS 368[M+H] + .

[0176] Intermediate 7c: Methyl 5-(4-((1S,5R)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-aminonicotinate hydrochloride To a solution of (1S,5R)-tert-butyl 1-(4-(6-amino-5-(methoxycarbonyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 5d, 500 mg, 1.22 mmol) in dioxane (7 mL) was added a 4 M solution of HCl in dioxane (1.22 mL, 4.88 mmol) at room temperature. The reaction mixture was stirred at 60° C. for 3 h and then concentrated under reduced pressure to give the title compound as the hydrochloride salt. (UPLC-MS)t R 0.58 min; ESI-MS 310[M+H] + .

[0177] Example 8: 2-Amino-5-(2-fluoro-4-(4-isopropylpiperazin-1-yl)phenyl)-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide [ka] To a solution of 2-amino-5-bromo-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide (Intermediate 3c, 230 mg, 0.731 mmol) in dioxane (4 mL), 1-(3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4-isopropylpiperazine (Intermediate 8a, 463 mg, 0.731 mmol), 2N aqueous K2CO3 (0.73 mL, 1.46 mmol), and PdCl2(dppf)-DCM adduct (29.9 mg, 0.037 mmol) were added at room temperature under nitrogen atmosphere. The reaction mixture was stirred at 80 °C for 60 min and then diluted with EtOAc and aqueous NaHCO3. After phase separation, the aqueous layer was extracted with EtOAc. The organic layer was washed with a saturated aqueous solution of NaHCO3 and brine, respectively, dried over MgSO4, filtered and concentrated under reduced pressure. The crude product was purified by prepHPLC (Method 1a) to give the title compound as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ 8.24-8.16(m,2H), 7.95(d,1H), 7.39(t,1H), 7.06(s,2H), 6.86(d,2H), 4.54(d,1H), 3.69(m,1H), 3.41-3.33(m,2H), 3.15(s,3H), 2.66(q,3H), 1.82(m,4H), 1.42-0.88(m,10H). (UPLC-MS) t R 0.48 min; ESI-MS 456[M+H] + .

[0178] Intermediate 8a: 1-(3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4-isopropylpiperazine To a solution of 1-(4-bromo-3-fluorophenyl)-4-isopropylpiperazine (Intermediate 8b, 212 mg, 0.662 mmol) in dioxane (8 mL), bis(pinacolato)diboron (202 mg, 0.794 mmol), KOAc (130 mg, 1.323 mmol) and PdCl2(dppf)-DCM adduct (27 mg, 0.033 mmol) were added at room temperature under nitrogen atmosphere. The reaction mixture was stirred at 90° C. for 2 h, then filtered through a Celite pad and concentrated under reduced pressure to give the title compound, which was used without further purification. (UPLC-MS)t R 0.79 min;ESI-MS 349[M+H] + .

[0179] Intermediate 8b: 1-(4-bromo-3-fluorophenyl)-4-isopropylpiperazine To a solution of 1-(4-bromo-3-fluorophenyl)piperazine (Intermediate 8c, 215 mg, 0.797 mmol) in acetonitrile (7 mL) was added 2-iodopropane (0.095 mL, 0.956 mmol) and K2CO3 (220 mg, 1.593 mmol) at room temperature. The reaction mixture was stirred at 65 °C for 4 h and then diluted with EtOAc and aqueous NaHCO3. After phase separation, the aqueous layer was extracted with EtOAc. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound as a colorless oil, which was used without further purification. (UPLC-MS)t R 0.66 min;ESI-MS 302[M+H] + .

[0180] Intermediate 8c: 1-(4-bromo-3-fluorophenyl)piperazine To a solution of tert-butyl 4-(4-bromo-3-fluorophenyl)piperazine-1-carboxylate (300 mg, 0.835 mmol) in dioxane (8 mL) was added 4N HCl in dioxane (0.84 mL, 3.34 mmol) at room temperature under nitrogen atmosphere. The reaction mixture was stirred for 2 h and then diluted with EtOAc and aqueous NaHCO3. After phase separation, the aqueous layer was extracted with EtOAc. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound, which was used without further purification. (UPLC-MS)t R 0.60 min; ESI-MS 260[M+H] + .

[0181] Example 9: 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide (Example 2), except that 2-amino-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid TFA salt (Intermediate 9a) was used instead of 2-amino-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid TFA salt (Intermediate 2a). 1H NMR(400MHz,DMSO-d6)δ 8.38(d,1H),8.31(d,1H),8.11(d,1H),7.58(d,2H),7.23(d,2H),7.12(s,2H),4.58(d,1H),3.82-3.66(m,1H),3.48-3.3 4(m,3H),3.07(d,1H),2.64-2.55(m,2H),1.96-1.77(m,5H),1.50-1.19(m,5H),1.04(dd,6H),0.75(dd,1H).(UPLC-MS)t R 0.50 min; ESI-MS 435[M+H] + .

[0182] Intermediate 9a: 2-amino-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid TFA salt The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid TFA salt (Intermediate 2a), except that methyl 2-amino-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate (Intermediate 9b) was used instead of methyl 2-amino-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate (Intermediate 2b). (UPLC-MS)t R 0.37 min;ESI-MS 338[M+H] +.

[0183] Intermediate 9b: Methyl 2-amino-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate The title compound was prepared in a similar manner to methyl 2-amino-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate (Intermediate 2b), except that (1S,5R)-1-(4-bromophenyl)-3-isopropyl-3-azabicyclo[3.1.0]hexane (Intermediate 9c) was used instead of (1R,5S)-1-(4-bromophenyl)-3-isopropyl-3-azabicyclo[3.1.0]hexane (Intermediate 2c). (UPLC-MS)t R 0.62 min;ESI-MS 352[M+H] + .

[0184] Intermediate 9c: (1S,5R)-1-(4-bromophenyl)-3-isopropyl-3-azabicyclo[3.1.0]hexane The title compound was prepared in a similar manner to (1R,5S)-1-(4-bromophenyl)-3-isopropyl-3-azabicyclo[3.1.0]hexane (Intermediate 2c), except that (1S,5R)-1-(4-bromophenyl)-3-azabicyclo[3.1.0]hexane (prepared as described in WO 2007 / 022935) was used instead of (1R,5S)-1-(4-bromophenyl)-3-azabicyclo[3.1.0]hexane. (UPLC-MS)t R 0.70 min;ESI-MS 280 / 282[M+H] + .

[0185] Example 10: 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 6), except that 4-(2-bromoethyl)morpholine was used instead of 1,3-difluoropropan-2-yl trifluoromethanesulfonate (Intermediate 6a), and the reaction mixture was stirred at 65° C. for 1 h. 1H NMR(400MHz,DMSO-d6)δ 8.38(d,1H),8.31(d,1H),8.11(d,1H),7.59(d,2H),7.22(d,2H),7.12(s,2H),4.59(d,1H),3.84-3.67(m,1H),3.63-3.51(m,4H) (UPLC-MS)t R 0.49 min;ESI-MS 506[M+H] + .

[0186] Example 11: 2-Amino-5-(4-((1S,5R)-3-(2-fluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 5), except that 1-bromo-2-fluoroethane was used instead of 4-(3-bromopropyl)morpholine, and the reaction mixture was stirred at 60° C. for 5 h. 1H NMR(400MHz,DMSO-d6)δ 8.38(d,1H),8.31(d,1H),8.11(d,1H),7.59(d,2H),7.22(d,2H),7.13(s,2H),4.59(d,2H),4.50(s,1H) ,3.73(d,1H),3.41(d,3H),2.83-2.78(m,3H),1.85(t,5H),1.47-1.16(m,6H),0.78(s,1H).(UPLC-MS)t R 0.47 min;ESI-MS 439[M+H] + .

[0187] Example 12: 2-Amino-N-((1r,4r)-4-hydroxycyclohexyl)-5-(4-(1-isopropylpyrrolidin-3-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(2-fluoro-4-(4-isopropylpiperazin-1-yl)phenyl)-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide (Example 8), except that 1-isopropyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine (Intermediate 12a) was used instead of 1-(3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4-isopropylpiperazine (Intermediate 8a). 1H NMR(400MHz,DMSO-d6)δ 8.36(d,1H),8.26(d,1H),8.09(d,1H),7.62-7.51(m,2H),7.37-7.28(m,2H),7.09(s,2H),4.55(d,1H),3.70(dq,1H),3.44 -3.34(m,2H),3.03(d,1H),2.75(s,2H),2.29-2.06(m,2H),1.87-1.68(m,5H),1.42-1.17(m,5H),1.06(t,6H).(UPLC-MS)t R 0.48 min; ESI-MS 423[M+H] + .

[0188] Intermediate 12a: 1-isopropyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine The title compound was prepared in a similar manner to 1-(3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4-isopropylpiperazine (Intermediate 8a), except that 3-(4-bromophenyl)-1-isopropylpyrrolidine (Intermediate 12b) was used instead of 1-(4-bromo-3-fluorophenyl)-4-isopropylpiperazine (Intermediate 8b). (UPLC-MS)t R 0.79 min;ESI-MS 316[M+H] + .

[0189] Intermediate 12b: 3-(4-bromophenyl)-1-isopropylpyrrolidine The title compound was prepared in a similar manner to 1-(4-bromo-3-fluorophenyl)-4-isopropylpiperazine (Intermediate 8b), except that 3-(4-bromophenyl)pyrrolidine hydrochloride was used instead of 1-(4-bromo-3-fluorophenyl)piperazine (Intermediate 8c). (UPLC-MS)t R 0.62 min;ESI-MS 269[M+H] + .

[0190] Example 13: 2-Amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 5), except 4-(2-bromoethyl)morpholine was used instead of 4-(3-bromopropyl)morpholine. 1H NMR(400MHz,DMSO-d6)δ 8.38(d,1H),8.31(d,1H),8.11(d,1H),7.59(d,2H),7.22(d,2H),7.12(s,2H),4.59(d,1H),3.84-3.67(m,1H),3.63-3.51(m,4H) (UPLC-MS)t R 0.49 min;ESI-MS 506[M+H] + .

[0191] Example 14: 2-amino-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared by using 2-amino-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 14a) instead of 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c). Prepared in a similar manner as (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b) except trans-4-amino-1-methylcyclohexanol was used instead of trans-4-aminocyclohexanol. The crude product was purified by prepHPLC (Method 1a) to give the title compound as the TFA salt. 1H NMR(400MHz,DMSO-d6)δ 8.53(d,1H),8.46(d,1H),8.35(s,1H),7.72(d,2H),7.71(bs,2H),7.41(d,2H),4.06(dd,1H),3.98(dd,2H),3.85-3.43(m,5H), 3.27(t,2H),2.26(dd,1H),1.99(d,2H),1.83-1.76(m,4H),1.68-1.56(m,3H),1.51-1.45(m,5H),1.21-1.13(m,5H).(UPLC-MS)t R 0.51 min;ESI-MS 491[M+H] + .

[0192] Intermediate 14a: 2-amino-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (TFA salt) To a solution of methyl 2-amino-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate (Intermediate 14b, 1.30 g, 2.97 mmol) in anhydrous THF (16 mL) was added a 2M aqueous solution of LiOH (4.46 mL, 8.92 mmol) at room temperature. The reaction mixture was stirred at 65° C. for 140 min and then concentrated under reduced pressure. The residue was purified by reverse phase chromatography (Method 3b). Pure fractions were concentrated and lyophilized to give the title compound as an off-white TFA salt. (UPLC-MS)t R 0.40 min;ESI-MS 380[M+H] + .

[0193] Intermediate 14b: Methyl 2-amino-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate To a solution of methyl 5-(4-((1R,5S)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-aminonicotinate hydrochloride (intermediate 14c, 1.18 g, 3.28 mmol) in DCM (16 mL) was added dihydro-2H-pyran-4(3H)-one (0.33 mL, 3.60 mmol) and AcOH (0.38 mL, 6.55 mmol) at room temperature. The reaction mixture was stirred at 45° C. for 30 min. Sodium triacetoxyborohydride (1.74 g, 8.19 mmol) was added at room temperature and the reaction mixture was stirred at 45° C. for 1 h. The reaction mixture was then diluted with a saturated solution of NaHCO3 and mixed with EtOAc. After phase separation, the aqueous layer was extracted again with EtOAc. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound, which was used without further purification. (UPLC-MS) R 0.67 minutes;ESI-MS 394[M+H]+.

[0194] Intermediate 14c: Methyl 5-(4-((1R,5S)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-aminonicotinate hydrochloride To a solution of (1R,5S)-tert-butyl-1-(4-(6-amino-5-(methoxycarbonyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1d, 1.50 g, 3.66 mmol) in dioxane (25 mL) was added a 4 M solution of HCl in dioxane (3.66 mL, 14.7 mmol) at room temperature. The reaction mixture was stirred at 60° C. for 3 h and then concentrated under reduced pressure to give the title compound as the hydrochloride salt. (UPLC-MS)t R 0.58 min; ESI-MS 310[M+H] + .

[0195] Example 15: 2-Amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was synthesized by using 2-amino-5-(4-((1R,5S)-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 15a) instead of 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c) in trans-4 This was prepared in a similar manner to (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b), except that 4-aminobicyclo[2.2.2]octan-1-ol hydrochloride was used instead of 1R,5S)-aminocyclohexanol. The crude product was purified first by prepHPLC (Method 1a) and then by reverse-phase flash chromatography (Method 3a) to give the title compound as a colorless solid. 1H NMR(400MHz,DMSO-d6)δ 8.34(d,1H),7.98(d,1H),7.79(s,1H),7.56(d,2H),7.21(d,2H),6.92(s,2H),4.31(s,1H),3.58-3.56(m,4H),3.09(d,1H),2.64 -2.62(m,2H),2.59-2.41(m,9H),2.07-2.04(m,6H),1.82-1.79(m,1H),1.65-1.61(m,6H),1.31(t,1H),0.75(dd,1H).(UPLC-MS)t R 0.53 min;ESI-MS 532[M+H] + .

[0196] Intermediate 15a: 2-amino-5-(4-((1R,5S)-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 2c), except that methyl 2-amino-5-(4-((1R,5S)-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate (Intermediate 15b) was used instead of (1R,5S)-tert-butyl 1-(4-(6-amino-5-(methoxycarbonyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1d). (UPLC-MS)t R 0.39 min;ESI-MS 409[M+H] + .

[0197] Intermediate 15b: Methyl 2-amino-5-(4-((1R,5S)-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate The title compound was prepared in a similar manner to methyl 2-amino-5-(4-((1S,5R)-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-aminonicotinate hydrochloride (Intermediate 7b), except that methyl 5-(4-((1R,5S)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-aminonicotinate hydrochloride (Intermediate 14c) was used instead of methyl 5-(4-((1S,5R)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-aminonicotinate hydrochloride (Intermediate 7c) and 4-(2-bromoethyl)morpholine was used instead of 1-bromo-2-methoxyethane. (UPLC-MS)t R 0.62 min;ESI-MS 423[M+H] + .

[0198] Example 16: 2-amino-N-(3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide (Example 2), except that 2-amino-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 9a) was used instead of 2-amino-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid TFA salt (Intermediate 2a) and (3-aminobicyclo[1.1.1]pentan-1-yl)methanol (Intermediate 16a) was used instead of trans-4-aminocyclohexanol hydrochloride. 1H NMR(400MHz,DMSO-d6)δ 9.05(s,1H),8.41(d,1H),8.18(d,1H),7.61(d,2H),7.48(dd,1H),7.33-7.17(m,4H),4.55(t,1H),3.51(d,3H) ),3.31(s,2H),3.08(s,2H),2.07-1.99(m,1H),1.41-1.22(m,3H),1.17-0.98(m,9H),0.79(d,1H).(UPLC-MS)t R 0.54 min;ESI-MS 433[M+H] + .

[0199] Intermediate 16a: (3-aminobicyclo[1.1.1]pentan-1-yl)methanol To a solution of methyl 3-aminobicyclo[1.1.1]pentane-1-carboxylate HCl salt (218 mg, 1.23 mmol) in THF (7 mL) was added LiAlH4 (140 mg, 3.68 mmol) in small portions at 0° C. The reaction mixture was stirred at room temperature for 2 h, quenched with a mixture of THF and water at 0° C., then filtered through a pad of Celite and concentrated under reduced pressure to give the title compound as a yellow oil, which was used without further purification. FIA-MS114 [M+H] + .

[0200] Example 17: 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(3,3,3-trifluoropropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 5), except that 3,3,3-trifluoropropyl trifluoromethanesulfonate was used instead of 4-(3-bromopropyl)morpholine, and the reaction mixture was stirred at room temperature for 60 minutes. 1H NMR(400MHz,DMSO-d6)δ 8.39(d,1H),8.31(d,1H),8.12(d,1H),7.60(d,2H),7.23(d,2H),7.12(s,2H),4.59(d,1H),3.79-3.66(m, (UPLC-MS)t R 0.59 min;ESI-MS 489[M+H] + .

[0201] Example 18: 2-Amino-N-((1r,4r)-4-hydroxycyclohexyl)-5-(4-(pyrrolidin-3-yl)phenyl)nicotinamide [ka] To a solution of tert-butyl 3-(4-(6-amino-5-(((1r,4r)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)pyrrolidine-1-carboxylate (Intermediate 18a, 120 mg, 0.140 mmol) in dioxane (3 mL) was added 4N HCl in dioxane (0.210 mL, 0.839 mmol) at room temperature under nitrogen atmosphere, and the resulting mixture was stirred for 4 h. After concentration under reduced pressure, the crude product was purified by reverse phase chromatography (Method 3a). Pure fractions were partitioned between a saturated aqueous solution of NaHCO3 and EtOAc. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound as a mixture of diastereomers. 1H NMR(400MHz,DMSO-d6)δ 8.26(d,1H),8.09(d,1H),7.57(d,2H),7.35-7.29(m,2H),7.09(s,2H),4.55(d,1H),3.77-3.69(m,2H),3.22-3. 15(m,2H),3.12-2.91(m,2H),2.74-2.62(m,2H),2.24-2.07(m,1H),1.83(dd,4H),1.42-1.16(m,5H).(UPLC-MS)t R 0.42 min;ESI-MS 381[M+H] + .

[0202] Intermediate 18a: tert-Butyl 3-(4-(6-amino-5-(((1r,4r)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)pyrrolidine-1-carboxylate The title compound was prepared in a similar manner to 2-amino-5-(2-fluoro-4-(4-isopropylpiperazin-1-yl)phenyl)-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide (Example 8), except that tert-butyl 3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine-1-carboxylate (Intermediate 18b) was used instead of 1-(3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4-isopropylpiperazine (Intermediate 8a). (UPLC-MS)t R 0.95 min; ESI-MS 481[M+H] + .

[0203] Intermediate 18b: tert-Butyl 3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine-1-carboxylate The title compound was prepared in a similar manner to 1-(3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4-isopropylpiperazine (Intermediate 8a), except that tert-butyl 3-(4-bromophenyl)pyrrolidine-1-carboxylate (Intermediate 18c) was used instead of 1-(4-bromo-3-fluorophenyl)-4-isopropylpiperazine (Intermediate 8b). (UPLC-MS)t R 1.43 minutes; ESI-MS 374[M+H] + .

[0204] Intermediate 18c: tert-Butyl 3-(4-bromophenyl)pyrrolidine-1-carboxylate To a solution of 3-(4-bromophenyl)pyrrolidine (200 mg, 0.885 mmol) in DCM (7 mL) was added di-tert-butyl dicarbonate (0.308 mL, 1.327 mmol) and TEA (0.247 mL, 1.769 mmol) at room temperature under nitrogen atmosphere. The reaction mixture was stirred for 2 h. The reaction mixture was then diluted with a saturated aqueous solution of NaHCO3 and mixed with DCM. After phase separation, the aqueous layer was extracted again with DCM. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound as a colorless oil, which was used without further purification. (UPLC-MS)t R 1.33 minutes; ESI-MS 270[M+H] + .

[0205] Example 19: 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(1-(methylsulfonyl)piperidin-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide (Example 1), except dihydro-2H-pyran-4(3H)-one was used instead of 1-(methylsulfonyl)piperidin-4-one. 1H NMR(400MHz,DMSO-d6)δ 8.39(s,1H),8.31(d,1H),8.12(d,1H),7.62(dd,2H),7.25(s,2H),7.12(s,2H),4.59(d,1H),3.97-3.63 (m,4H),3.40(m,2H),3.31(m,2H),3.19-3.03(m,2H),1.99-1.65(m,8H),1.51-1.16(m,8H).(UPLC-MS)t R 0.48 min; ESI-MS 477[M+H] + .

[0206] Example 20: 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 5), except that 1-bromo-2-methoxyethane was used instead of 4-(3-bromopropyl)morpholine, and the reaction mixture was stirred at 60° C. for 4 h. 1H NMR(400MHz,DMSO-d6)δ 8.38(s,1H),8.11(s,1H),7.59(d,2H),7.22(d,2H),7.13(s,2H),4.60(d,1H),3.73(d,1H),3.54 -3.36(m,4H),3.27(s,3H),2.64(m,4H),1.87(m,6H),1.40-1.27(m,6H),0.76(s,1H).(UPLC-MS)t R 0.49 min;ESI-MS 451[M+H] + .

[0207] Example 21: 2-amino-N-((1R,3S,4R)-3-fluoro-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared by using 2-amino-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 14a) instead of 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c) to obtain the trans-4-amino Prepared in a similar manner to (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b) except that (1R,2S,4R)-4-amino-2-fluorocyclohexanol hydrochloride (Intermediate 21a) was used instead of 2-fluorocyclohexanol. The crude product was purified by prep HPLC (Method 1a) to give the title compound as the TFA salt. 1H NMR(400MHz,DMSO-d6)δ 9.60(bs,1H),8.42(s,1H),8.35(d,1H),8.12(s,1H),7.64(bs,2H),7.36(bs,2H),7.14(s,2H),4.94(t,1H),4.80(d,1H),4.16-3.82(m,4H) ),3.81-3.45(m,4H),3.30-3.25(m,4H),2.15(bs,1H),1.88-1.85(m,2H),1.65-1.59(m,5H),1.76-1.27(m,3H),1.18(bs,1H).(UPLC-MS)t R 0.48 min; ESI-MS 495[M+H] + .

[0208] Intermediate 21a: (1R,2S,4R)-4-amino-2-fluorocyclohexanol hydrochloride To a solution of benzyl ((1R,3S,4R)-3-fluoro-4-hydroxycyclohexyl)carbamate (Intermediate 21b, 376 mg, 1.41 mmol) in EtOH (20 mL) was added palladium on charcoal (10%) (80 mg, 0.075 mmol) under nitrogen atmosphere. The reaction vessel was purged three times with nitrogen and then twice with hydrogen. After stirring at room temperature for 17 h, the reaction mixture was passed through a Celite pad and the filter cake was washed with EtOH to give a colorless solution. Hydrochloric acid (1.25 M in EtOH, 14 mL, 17.5 mmol) was added slowly and the mixture was stirred at room temperature for 5 h. Concentration under reduced pressure afforded the title compound as an off-white hygroscopic solid. FIA ESI-MS 134[M+H] + .

[0209] Intermediate 21b: Benzyl ((1R,3S,4R)-3-fluoro-4-hydroxycyclohexyl)carbamate To a solution of benzyl ((1R,3S)-3-fluoro-4-oxocyclohexyl)carbamate (Intermediate 21c, 768 mg, 2.90 mmol) in MeOH (15 mL) was added NaBH4 (274 mg, 7.24 mmol) in small portions at 0°C. After stirring for 30 min at 0°C, the reaction mixture was diluted with a saturated aqueous solution of NH4Cl and allowed to warm to room temperature. The solvent was removed under reduced pressure and DCM and water were added. After phase separation, the aqueous layer was extracted three times with DCM. The combined organic layers were washed with brine, dried over anhydrous MgSO4, filtered and concentrated under reduced pressure to give a white solid. The crude product was purified by normal phase chromatography (Method 2b) to give the title compound as a colorless solid. (UPLC-MS)t R 0.76 min; ESI-MS 268[M+H] + The absolute configuration shown was confirmed by X-ray crystallography.

[0210] Intermediate 21c: Benzyl ((1R,3S)-3-fluoro-4-oxocyclohexyl)carbamate To a solution of benzyl ((1R,3S,4S)-3-fluoro-4-hydroxycyclohexyl)carbamate (Intermediate 21d, 710 mg, 2.66 mmol) in DCM (26 mL) was added pyridinium chlorochromate (859 mg, 3.98 mmol). The reaction mixture was stirred at room temperature for 6 h. Another portion of pyridinium chlorochromate (573 mg, 2.66 mmol) was added and the reaction mixture was stirred for another 18 h. After addition of DCM and saturated aqueous NaHCO3 solution, both phases were separated, the aqueous layer was extracted twice with DCM, and the combined organic layers were washed with brine, dried over anhydrous MgSO4, filtered and concentrated under reduced pressure. The residue was purified by normal phase chromatography (Method 2b) to give the title compound as a colorless oil. (UPLC-MS)t R 0.82 min; ESI-MS 266[M+H] + .

[0211] Intermediate 21d: Benzyl ((1R,3S,4S)-3-fluoro-4-hydroxycyclohexyl)carbamate A vial was charged with benzyl (1R,3R,6S)-7-oxabicyclo[4.1.0]heptan-3-ylcarbamate (Intermediate 21e, 1.50 g, 6.07 mmol) and TEA trihydrofluoride (4.94 mL, 30.3 mmol) was added. The vial was sealed and stirred at 100 °C for 2 h. After cooling, the reaction mixture was slowly poured into a stirred solution of K2CO3 (5.87 g, 42.5 mmol) in water (400 mL) and extracted three times with DCM. The combined organic layers were washed with water and brine, dried over anhydrous MgSO4, filtered and concentrated under reduced pressure. The crude was purified by normal phase chromatography (Method 2b) to give a mixture of regioisomers, which were separated by preparative chiral HPLC (column: ChiralPak AD, 20 μm, 50 × 5 cm; flow rate: 90 mL / min; detection wavelength: 220 nm; mobile phase: 90:10 n-heptane:EtOH until t = 52 min, 85:15 until t = 69 min, then 80:20). The title compound was isolated as a colorless oil and characterized by UPLC-MS (SQ13, column: Acquity HSS T3 1.8 μm, 2.1 × 50 mm, 60 °C; eluent A: water + 0.05% formic acid + 3.75 mM NH4OAc; eluent B: acetonitrile + 0.04% formic acid; gradient: 5 to 98% B in 1.4 min; flow rate 1.0 mL / min; t R 0.81 min; ESI-MS 268[M+H] + ).

[0212] Intermediate 21e: (1R,3R,6S)-7-oxabicyclo[4.1.0]heptan-3-ylcarbamate Syn-benzyl (7-oxabicyclo[4.1.0]heptan-3-yl) carbamate (prepared as described by Gomez-Sanchez et al, Tetrahedron 2005,61(5),1207-1219) was separated by preparative chiral HPLC (column: ChiralPak AY, 10 μm, 25×5 cm; flow rate: 30 mL / min; detection wavelength: 214 nm; mobile phase: 80:20 n-heptane:isopropanol). The title compound was isolated as a colorless oil and purified by chiral HPLC (ChiralPak AY-H, 5 μm, 15×0.46 cm; flow rate: 1 mL / min; detection wavelength: 214 nm; mobile phase: 70:30 hexane:isopropanol; t R 2.24 min; 99.2% ee). R 0.90 min; ESI-MS 248[M+H] + .

[0213] Example 22: 2-Amino-N-((1s,4S)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared by using 2-amino-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 14a) instead of 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c). Prepared in a similar manner to (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b) except using 1,2-dihydro-3,4-trimethylphenyl-2,4-tetrahydrofuran-2-yl (TFA) and 1,2-dihydro-3,4-trimethylphenyl-2 ... 1H NMR(400MHz,DMSO-d6)δ 9.50(bs,1H),8.41-8.33(m,2H),8.17(d,1H),7.62(bs,2H),7.26(bs,2H),7.14(s,1H),4.42(d,1H),4.05-3.79(m,5H), 3.34-3.24(m,4H),3.11(bs,1H),2.70-2.50(m,1H),1.83-1.71(m,7H),1.62-1.47(m,7H),1.35-1.29(m,1H).(UPLC-MS)t R 0.52 min;ESI-MS 477[M+H] + .

[0214] Example 23: 5-(4-(2-azaspiro[3.3]heptan-2-ylmethyl)phenyl)-2-amino-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(2-fluoro-4-(4-isopropylpiperazin-1-yl)phenyl)-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide (Example 8), except that 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-2-azaspiro[3.3]heptane (Intermediate 23a) was used instead of 1-(3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4-isopropylpiperazine (Intermediate 8a). 1H NMR(400MHz,DMSO-d6)δ 8.40(d,1H),8.30(d,1H),8.14(d,1H),7.61(d,2H),7.33(d,2H),7.14(s,2H),4.58(d,1H),3.79-3.66(m, 1H),3.55(s,2H),3.41(dt,1H),3.14(s,3H),2.07(t,4H),1.94-1.72(m,6H),1.47-1.20(m,5H)(UPLC-MS)t R 0.51 min; ESI-MS 421 [M+H] + .

[0215] Intermediate 23a: 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-2-azaspiro[3.3]heptane To a solution of 2-(4-(bromomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (300 mg, 1.01 mmol) in acetonitrile (8 mL) was added 2-azaspiro[3.3]heptane (148 mg, 1.11 mmol) and cesium carbonate (428 mg, 1.31 mmol) at room temperature under nitrogen atmosphere. The reaction mixture was stirred for 60 min and then diluted with a saturated aqueous solution of NaHCO3 and EtOAc. After phase separation, the aqueous layer was extracted with EtOAc and the combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound, which was used without further purification (UPLC-MS)t R 0.82 min; ESI-MS 314[M+H] + .

[0216] Example 24: 2-amino-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide (Example 2), except that trans-4-amino-1-methylcyclohexanol was used instead of trans-4-aminocyclohexanol hydrochloride. 1H NMR(400MHz,DMSO-d6)δ 8.43(d,1H),8.34(d,1H),8.16(d,1H),7.68(d,2H),7.39(d,2H),4.06(dd,1H),3.86-3.41(m,9H), 2.26(dt,1H),1.78(d,2H),1.68-1.55(m,2H),1.47(t,4H),1.33(dd,6H),1.18(s,4H).(UPLC-MS)t R 0.53 min;ESI-MS 449[M+H] + .

[0217] Example 25: 2-amino-5-(4-((1R,5S)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(1-(methylsulfonyl)piperidin-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide (Example 1), except that 4,4-difluorocyclohexanone was used instead of 1-(methylsulfonyl)piperidin-4-one. 1H NMR(400MHz,DMSO-d6)δ 8.38(d,1H),8.32(d,1H),8.11(d,1H),7.59(d,2H),7.23(d,2H),7.13(s,2H),4.59(d,1H),3.73(d,1H),3.39(d,2H),3.09 (d,1H),2.68-2.55(m,2H),2.37(d,2H),2.00(s,2H),1.84(d,8H),1.64(d,2H),1.46-1.16(m,5H),0.78(s,1H).(UPLC-MS)t R 0.56 min;ESI-MS 511[M+H] + .

[0218] Example 26: 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(oxetan-3-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] To a solution of 5-(4-((1S,5R)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide TFA salt (intermediate 5a, 70 mg, 0.138 mmol) in DCM (4 mL) was added oxetan-3-one (12.0 mg, 0.166 mmol) and AcOH (0.012 mL, 0.207 mmol) at room temperature under nitrogen atmosphere. The reaction mixture was stirred at 45° C. for 30 min. Sodium triacetoxyborohydride (58.6 mg, 0.276 mmol) was added at room temperature and the reaction mixture was stirred at 45° C. for 3 h. The reaction mixture was then diluted with a saturated aqueous solution of NaHCO3 and mixed with EtOAc. After phase separation, the aqueous layer was extracted again with EtOAc. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The crude product was purified first by prepHPLC (Method 1a) and then by reverse-phase flash chromatography (Method 3a) to give the title compound as a colorless solid. (UPLC-MS)t R 0.48 min;ESI-MS 449[M+H] + .

[0219] Example 27: 2-amino-5-(4-((1S,5R)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(oxetan-3-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide (Example 26), except that 4,4-difluorocyclohexanone was used instead of oxetan-3-one. After purification, the title compound was obtained as a TFA salt. 1H NMR(400MHz,DMSO-d6)δ 9.50(bs,1H),8.38(d,1H),8.32(d,1H),8.11(d,1H),7.59(d,2H),7.23(d,2H),7.13(s,2H),4.59(d,1H),4.12(bs,1H),3.73(d,1H) ),3.39(d,2H),3.09(d,1H),2.68-2.55(m,2H),2.37(d,2H),2.00(s,2H),1.84(d,8H),1.64(d,2H),1.46-1.16(m,5H).(UPLC-MS)t R 0.56 min;ESI-MS 511[M+H] + .

[0220] Example 28: 2-amino-N-(3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)-5-(4-((1S,5R)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was synthesized by using 2-amino-5-(4-((1S,5R)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 28a) instead of 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c) to obtain the trans-4- Prepared in a similar manner as (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b) except that (3-aminobicyclo[1.1.1]pentan-1-yl)methanol (Intermediate 16a) was used instead of aminocyclohexanol. The crude product was purified first by prepHPLC (Method 1a) and then by reversed-phase flash chromatography (Method 3a) to give the title compound as a colorless solid. 1H NMR (400 MHz, DMSO-d6) δ 9.35(bs,1H),9.06(s,1H),8.44(s,1H),8.19(s,1H),7.68(d,2H),7.37(d, 2H),7.26(bs,2H),4.57(t,1H),4.12(d,1H),3.97(bs,1H),3.80-3.56(m,2H ),3.51(d,2H),3.35-3.20(m,6H),2.29-2.23(m,1H),2.11-2.05(m,1H),1. 99(bs,1H),1.97(s,6H),1.67-1.61(m,1H),1.19-1.14(bs,1H).(UPLC-MS)t R 0.50 min;ESI-MS 475[M+H] + .

[0221] Intermediate 28a: 2-amino-5-(4-((1S,5R)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 2c), except that methyl 2-amino-5-(4-((1S,5R)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate (Intermediate 28b) was used instead of (1R,5S)-tert-butyl 1-(4-(6-amino-5-(methoxycarbonyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1d). (UPLC-MS)t R 0.37 min;ESI-MS 380[M+H] + .

[0222] Intermediate 28b: Methyl 2-amino-5-(4-((1S,5R)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate The title compound was prepared in a similar manner to methyl 2-amino-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-aminonicotinate hydrochloride (Intermediate 14b), except that methyl 5-(4-((1R,5S)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-aminonicotinate hydrochloride (Intermediate 7c) was used instead of methyl 5-(4-((1R,5S)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-aminonicotinate hydrochloride (Intermediate 14c). (UPLC-MS)t R 0.62 min; ESI-MS 394[M+H] + .

[0223] Example 29: 2-amino-5-(2-fluoro-4-(piperazin-1-yl)phenyl)-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-((1r,4r)-4-hydroxycyclohexyl)-5-(4-(pyrrolidin-3-yl)phenyl)nicotinamide (Example 18), except that tert-butyl 4-(4-(6-amino-5-(((1r,4r)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)-3-fluorophenyl)piperazine-1-carboxylate (Intermediate 29a) was used instead of 3-(4-(6-amino-5-(((1r,4r)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)pyrrolidine-1-carboxylate (Intermediate 18a). 1H NMR(400MHz,DMSO-d6)δ 8.29-8.16(m,2H),7.95(d,1H),7.38(t,1H),7.06(s,2H),6.88-6.75(m,2H),4.54(d,1H),3.69(m,1) H),3.42-3.32(m,2H),3.17(dd,4H),2.92(dt,4H),1.88-1.73(m,4H),1.43-1.15(m,4H).(UPLC-MS)t R 0.42 min; ESI-MS 414[M+H] + .

[0224] Intermediate 29a: tert-Butyl 4-(4-(6-amino-5-(((1r,4r)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)-3-fluorophenyl)piperazine-1-carboxylate The title compound was prepared in a similar manner to 1-(3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4-isopropylpiperazine (Example 8), except that tert-butyl 4-(3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperazine-1-carboxylate (Intermediate 29b) was used instead of 1-(3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4-isopropylpiperazine (Intermediate 8a). The reaction mixture was stirred at 80° C. for 60 min and purified by normal phase chromatography (Method 2b) to give the title compound as a brownish solid. (UPLC-MS)t R 0.96 min;ESI-MS 514[M+H] + .

[0225] Intermediate 29b: tert-Butyl 4-(3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperazine-1-carboxylate The title compound was prepared in a similar manner to tert-butyl 4-(3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperazine-1-carboxylate (Intermediate 8a), except that tert-butyl 4-(4-bromo-3-fluorophenyl)piperazine-1-carboxylate was used instead of 1-(4-bromo-3-fluorophenyl)piperazine (Intermediate 8b). (UPLC-MS)t R 1.38 minutes; ESI-MS 407[M+H] + .

[0226] Example 30: 2-amino-N-(3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was synthesized by using 2-amino-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 14a) instead of 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c) to obtain the trans-4- Prepared in a similar manner as (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b) except that (3-aminobicyclo[1.1.1]pentan-1-yl)methanol (Intermediate 16a) was used instead of aminocyclohexanol. The crude product was purified first by prepHPLC (Method 1a) and then by reverse phase flash chromatography (Method 3a) to give the title compound as a colorless solid. 1H NMR(400MHz,DMSO-d6)δ 9.05(s,1H),8.41(d,1H),8.18(d,1H),7.61(d,2H),7.24-7.22(m,4H),4.55(t,1H),3.87-3.84(m,2H),3.51(d,2H),3.48- 3.25(m,2H),3.10(bs,1H),2.56-2.47(m,4H),1.97(s,6H),1.96-1.74(m,3H),1.39-0.30(m,3H),0.77(bs,1H).(UPLC-MS)t R 0.51 min; ESI-MS 475[M+H] + .

[0227] Example 31: 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(2-fluoro-4-(4-isopropylpiperazin-1-yl)phenyl)-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide (Example 8), except that (R)-(4-((2-methylpyrrolidin-1-yl)methyl)phenyl)boronic acid (Intermediate 31a) was used instead of 1-(3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4-isopropylpiperazine (Intermediate 8a). Purification was carried out by normal phase chromatography (Method 2b) to give the title compound as a yellow solid. 1H NMR(400MHz,DMSO-d6)δ 8.75(d,1H),8.65(d,1H),8.48(d,1H),7.81(dd,2H),7.63(d,2H),4.52(dd,1H),4.18(dd,1H),3.69(ddt,1H),3.5 1-3.31(m,2H),3.25-3.04(m,3H),2.19(ddt,1H),1.82(td,6H),1.64-1.52(m,1H),1.39-1.15(m,7H).(UPLC-MS)t R 0.44 min;ESI-MS 409[M+H] + .

[0228] Intermediate 31a: (R)-(4-((2-methylpyrrolidin-1-yl)methyl)phenyl)boronic acid To a solution of (4-(bromomethyl)phenyl)boronic acid (125 mg, 0.582 mmol) in acetonitrile (4 mL) was added K2CO3 (161 mg, 1.164 mmol) and (R)-2-methylpyrrolidine (54.5 mg, 0.640 mmol) at room temperature under nitrogen atmosphere. The reaction mixture was stirred for 60 min and then filtered through a pad of Celite. The filtrate was concentrated under reduced pressure to give the title compound as an off-white solid, which was used without further purification. (UPLC-MS)t R 0.33 min; ESI-MS 220[M+H] + .

[0229] Example 32: 2-amino-N-((1r,4S)-4-hydroxy-4-methylcyclohexyl)-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide (Example 2), except that 2-amino-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid TFA salt (Intermediate 9a) was used instead of 2-amino-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid TFA salt (Intermediate 2a) and trans-4-amino-1-methylcyclohexanol was used instead of trans-4-aminocyclohexanol hydrochloride. 1H NMR(400MHz,DMSO-d6)δ 8.43(d,1H),8.34(d,1H),8.16(d,1H),7.68(d,2H),7.39(d,2H),4.06(dd,1H),3.86-3.41(m,9H), 2.26(dt,1H),1.78(d,2H),1.68-1.55(m,2H),1.47(t,4H),1.33(dd,6H),1.18(s,4H).(UPLC-MS)t R 0.50 min;ESI-MS 449[M+H] + .

[0230] Example 33: 2-amino-5-(4-((1S,5R)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(oxetan-3-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide (Example 26), except dihydro-2H-pyran-4(3H)-one was used instead of oxetan-3-one. 1H NMR(400MHz,DMSO-d6)δ 8.39(s,1H),8.31(d,1H),8.12(d,1H),7.62(dd,2H),7.25(s,2H),7.12(s,2H),4.59(d,1H),3.97-3.63 (m,4H),3.40(m,2H),3.31(m,2H),3.19-3.03(m,2H),1.99-1.65(m,8H),1.51-1.16(m,8H).(UPLC-MS)t R 0.47 min;ESI-MS 477[M+H] + .

[0231] Example 34: 2-Amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide (also referred to herein as Compound A) [ka] To a solution of 2-amino-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid TFA salt (Intermediate 14a, 4.10 g, 8.14 mmol) and 4-aminobicyclo[2.2.2]octan-1-ol hydrochloride (2.17 g, 12.2 mmol) in anhydrous DMF (60 mL) was added N-methylmorpholine (2.24 mL, 20.4 mmol) and HATU (4.64 g, 12.2 mmol) at room temperature under nitrogen atmosphere. The reaction mixture was stirred for 2 h, then diluted with a saturated aqueous solution of NaHCO3 and extracted three times with EtOAc. The combined organic extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The crude product was purified by reverse phase chromatography (Method 3b). The pure fractions were treated with saturated aqueous NaHCO3 solution and extracted three times with EtOAc. The combined organic extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound as an off-white solid. The absolute configuration shown was confirmed by X-ray crystallography of the title compound in complex with the ALK-2 kinase domain. 1H NMR (400 MHz, DMSO-d6) δ 8.34(d,1H), 7.98(d,1H), 7.79(s,1H), 7.57(d,2H), 7.23(d,2H), 6.92(s,2H), 4.31(s,1H), 3.91-3.78(m,2H), 3.40(bs,1H), 3.33-3.24(m,2H), 3.11(d,1H), 2.57 (bs,1H),2.50-2.34(m,1H),2.34(bs,1H),2.12-1.94(m,6H),1.90-1.72(m,3H), 1.71-1.51(m,6H),1.51-1.34(m,2H),1.31(t,1H),0.82-0.68(m,1H).(UPLC-MS)t R 0.54 min;ESI-MS 503[M+H] + .Chiral HPLC (ChiralPakId, 5 μm, flow rate: 1 mL / min; detection wavelength: 270 nm; mobile phase: 60:40 heptane:isopropanol (+0.1% diethylamine)); R 18.7 mins; 92.3% ee.

[0232] Alternative Example 34A: To a solution of 2-amino-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid hydrochloride (1 kg, 1.683 mol) and 4-aminobicyclo[2.2.2]octan-1-ol hydrochloride (343.9 g, 1.935 mol) in DMF (3500 mL) was added Et3N (681.2 g, 6.732 mol) and HATU (767.9 g, 2.019 mol) at room temperature. The reaction mixture was stirred at room temperature for 1 h. The mixture was heated to IT=45° C. and 5% NH3·H2O solution (5200 g) was added. Stirred for about 30 min and another 5% NH3·H2O solution (1800 g) was added. The mixture was heated at IT=45°C for 2 h. The mixture was cooled to IT=22°C. It was filtered and the wet cake was washed with H2O (1500 mL x 3). The wet cake was dried under vacuum at 45°C for 24 h. The crude product was dissolved in acetone (3000 mL) and then filtered to remove some undissolved solids. The filtrate was heated to IT=50°C. H2O (2000 mL) was added. The mixture was stirred at IT=50°C for 30 min until a white precipitate formed. H2O (4000 mL) was added slowly. The mixture was stirred at IT=50°C for 2 h. The mixture was cooled at IT=22°C for 2 h, filtered and the wet cake was washed with acetone:H2O=1:2 (v / v, 1000 mL x 2). The wet cake was dried under vacuum at 45° C. for 24 hours to give a total of 760 g of white solid (89% yield, 99.4% ee). 1H NMR(DMSO-d6)δ: 8.32(d,J=2.3 Hz,1H),7.97(d,J=2.3 Hz,1H),7.77(s,1H),7.54(d,J=8.3 Hz,2H),7.20(d,J=8.4 Hz,2H),6.90(s,2H),4.31(s,1H),3.82(m,2H),3.29(m,2H),3.07(d,J=8.5 Hz,1H),2.54(d,J=8.3 Hz,1H),2.44(dd,J=8.5,3.5 Hz,1H),2.37(m,1H),2.31(td,J=10.2,5.0 Hz,1H),2.04(m,6H),1.80(dt,J=7.9,3.8 Hz,1H),1.71(d,J=12.3 Hz,1H),1.65(d,J=11.5 Hz,1H),1.62(m,6H),1.38(m,1H),1.34(m,1H),1.29(t,J=3.9 Hz,1H),0.73(dd,J=7.9,3.6 Hz,1H). 13 C NMR(DMSO-d6)δ: 167.80,157.69,148.28,141.27,134.91,134.79,126.40,125.66,123.53,111.01,6 6.22,65.59,59.10,55.46,52.04,33.72,31.92,31.77,30.59,29.61,24.14,17.20. MS(ESI-TOF):503.3018[M+H]+.

[0233] The starting material (hydrochloride salt) was obtained as follows: Methyl 2-amino-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid dihydrochloride (10 g, 19.5 mmol, 1.0 equiv) was suspended in MeOH (31.7 g). A solution of NaOH (2.9 g, 72.2 mmol, 3.7 equiv) in HO (10 g) was then added. The reaction mixture was heated to 45±5° C. and stirred for not less than 3 h to give a suspension. To a separate flask containing acetone (200 g) was added 5-6N HCl in i-PrOH (14.8 g, 97.6 mmol, 5 equiv). The solution was heated to 47±3°C. The above MeOH suspension was then added dropwise to the mixture and stirred at 47±3°C for 3 h. The mixture was cooled to 23±3°C and stirred for 3 h. After filtration, the wet cake was washed with acetone (40 g). The wet cake was dried under vacuum at 55°C for 8 h. 2-Amino-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid hydrochloride (12.3 g, 99.3% HPLC purity, 62.1% assay yield) was obtained as an off-white solid. 1 H NMR(DMSO-d6)δ: 11.53(br s,1H),8.64(br s,1H),8.54(br s,1H),7.72-8.42(m,2H),7.64(br d,J=7.9 Hz,2H),7.38(br d,J=7.8 Hz,2H),3.85-4.04(m,3H),3.40-3.73(m,4H),3.15-3.33(m,2H),2.18(br d,J=3.9 Hz,1H),1.95-2.12(m,4H),1.88(br d,J=10.0 Hz,1H),1.05(br t,J=6.4 Hz,1H). 13 C NMR(DMSO-d6)δ: 167.2,155.8,144.3,142.0,139.6,133.8,127.7,126.3,124.1,110.0,65.8,62.5,55.7,53.2,29.9,28.8,28.7,23.5,16.6. MS(ESI-TOF):380.1974[M+H]+.

[0234] The starting material, 2-amino-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid dihydrochloride, was obtained as follows: A 500 mL round bottom flask was charged with 1R,5S)-1-(4-bromophenyl)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-3-ium chloride (20 g, 1 equiv.), EA (200 mL), and 25% K2CO3 (62 g). The mixture was stirred for 30 min until all solids were dissolved. After phase separation, the organic layer was concentrated. 2-Methyl-2-butanol (48 g, 60 mL) was added. The organic layer was concentrated. 2-Methyl-2-butanol (144 g, 180 mL) was added. The mixture was transferred to a 500 mL Redlay. K2CO3 (18.8 g, 2.5 eq.) and methyl 2-amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (16.8 g, 1.04 eq.; see intermediate 1e) were added. The mixture was degassed with N2 three times. The mixture was heated at IT=50±5°C within 1 h. Pd(dppf)Cl2 (1.2 g, 0.03 eq.) was added. The mixture was heated at IT=70±3°C and stirred for 2 h. After cooling to 22°C, H2O (120 g) and EA (180 g) were added and stirred for 30 min. MCC (6 g) was added and the mixture was filtered through MCC. The cake was washed with EA (54 g). After phase separation, the organic layer was washed with 5% NaCl (124 g). Quadrasil MP (heavy metal scavenger from Johnson Matthey, 6 g) was then added to the organic layer. The mixture was heated at IT=55°C for 8 h, filtered through MCC and washed with EA (54 g). Quadrasil MP (2 g) was added to the organic layer. The mixture was heated at IT=55°C for 6 h, filtered through CMC and washed with EA (54 g). The organic layer was concentrated. Acetone (158 g, 200 mL) was added. After stirring for 30 min at IT=22±3°C, the mixture was heated to IT=40±3°C. 15.5% HCl (38.4 g) was added dropwise at IT<50°C. The mixture was stirred at IT=45±3°C for 1 h. The mixture was cooled to 22±3°C. The mixture was stirred at 22±3°C for 1 h and filtered. The cake was washed with acetone (32 g x 2). The wet cake was dried under vacuum at 50° C. for at least 8 hours. The starting material was obtained as 22.5 g white solid (97.1% HPLC purity, 5.2% water content, 87% assay yield). 1H NMR(DMSO-d6)δ: 11.43(br d,J=5.7 Hz,1H),8.62-8.80(m,2H),7.85-8.58(m,2H),7.67(d,J=8.3 Hz,2H),7.39(d,J=8.4 Hz,2H),3.85-4.06(m,6H),3.60-3.69(m,2H),3.50-3.59(m,1H),3.44(br d,J=7.7 Hz,1H),3.14-3.31(m,2H),2.21(dt,J=8.4,4.2 Hz,1H),1.94-2.12(m,4H),1.76-1.93(m,1H),1.07(br t,J=7.1 Hz,1H). 13 C NMR(DMSO-d6)δ: 165.0,154.0,143.5,142.0,140.1,132.8,127.7,126.5,124.2,110.7,65.8,62.5,55.6,53.3,53.3,29.9,28.9,28.8,23.6,16.8. MS(ESI-TOF):394.2071[M+H]+.

[0235] The starting material, 1R,5S)-1-(4-bromophenyl)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-3-ium chloride, was obtained as follows: A 1L Redlay was charged with (1R,5S)-1-(4-bromophenyl)-3-azabicyclo[3.1.0]hexan-3-ium chloride (30 g, 1 equiv), dihydro-2H-pyran-4(3H)-one (13.13 g, 1.2 equiv) and THF (300 mL). The mixture was stirred at IT = 22 ± 5 °C for 1 h. NaBH(OAc)3 (30.1 g, 1.3 equiv) was added in small portions while maintaining an IT < 30 °C. The mixture was stirred at IT = 22 ± 5 °C for 2 h. 6.2% HCl (93 g, 90 ml, 1.5 equiv) was added while maintaining an IT < 30 °C and pH < 2. The mixture was stirred for 10 min. 25% K2CO3 (259 g, 210 mL) was added to adjust the pH = 8-9. IPAc (300 mL) was added. The mixture was stirred for 10 min. After phase separation, H2O (150 g) was added to the organic layer. The mixture was stirred for 10 min. After phase separation, the organic layer was concentrated under vacuum (50-100 mbar, 50 °C water bath). IPA (120 g, 150 mL) was added. The organic layer was concentrated under vacuum (50-100 mbar, 50 °C water bath). IPA (144 g, 180 mL) was added. The mixture was filtered through CMC. The cake was washed with IPA (24 g x 2). H2O (5 g) was added to the organic layer. 31% HCl (19.3 g) was added dropwise at IT < 35 °C. The mixture was stirred at IT = 22 ± 5 °C for 2 h and filtered. The cake was washed with IPA (48 g x 2). The wet cake was dried under vacuum at 50 °C for at least 6 h. The desired product was obtained as a white solid (31.4 g, 98% HPLC purity, 78% yield). 1 H NMR (DMSO-d6 and D2O) δ: 7.46(br d,J=8.4 Hz,2H),7.15(br d,J=8.4 Hz,2H),3.90(br d,J=7.8 Hz,3H),3.62(br s,1H),3.51(br s,2H),3.16-3.38(m,3H),2.05-2.21(m,1H),1.93(br s,2H),1.49-1.71(m,2H),1.05-1.30(m,1H). 13C NMR(DMSO-d6)δ: 138.3,131.9,129.2,120.4,65.5,62.3,56.2,53.9,29.1,28.9,24.8,23.0. MS(ESI-TOF): 322.0761[M+H]+

[0236] The complete method for the preparation of Alternative Example 34A is shown below in Reaction Scheme 34A: [ka]

[0237] The first compound A1 of this scheme can be obtained as follows: Steps 1-2 Synthesis of 1c and 1d Scheme 34A1 [ka]

[0238] Reaction procedure (see also Xu, Feng et al., Org. Lett. Vol 8, No. 17, 2006, pp. 3885-3888): NaHMDS (2.0 M in THF, 19.2 L, 38.4 mol, 2.5 equiv.) was added dropwise over 5 h to a solution of 1a (3.00 kg, 15.3 mol, 1.0 equiv., available, for example, from Sigma-Aldrich) and 1b (1.80 kg, 19.47 mmol, 1.27 equiv.; available, for example, from Sigma-Aldrich) in THF (30 L) at −15 to 20° C. under N2. The reaction mixture was stirred at −15° C. for an additional 3 h, then gradually warmed to room temperature and stirred for 16 h. HPLC showed that 4-bromophenylacetonitrile was completely consumed.

[0239] BF3·Et2O (4.74 kg, 15.3 mol, 1.0 equiv) was added slowly at 20-40 °C. After the addition, BH3·DMS (19.2 L, 38.4 mol, 2.5 equiv) was added slowly at 20-40 °C. After the addition, the mixture was stirred at 50-55 °C for 16 h. HPLC showed that the intermediate was completely consumed.

[0240] The mixture was cooled to -5-0°C and AcOH (4.5 kg, 74.4 mol, 4.86 equiv) was added slowly. After the addition, 3N HCl (36 kg) was added slowly. The mixture was stirred for 1 h and most of the THF was removed under vacuum at 40-45°C. The residue was then extracted with MTBE (3 x 10 L). The MTBE phase was washed with 3N HCl (4 x 5 L). The combined aqueous layers were cooled to 0°C. The aqueous layer was then neutralized to pH > 10 with 30% NaOH, extracted with IPAc (3 x 15 kg), washed with brine (5 L) and evaporated under vacuum to give crude compound 1d (3.71 kg), which was used directly in the subsequent step.

[0241] Steps 3-4 Synthesis of 1e and 1f Scheme 34A2 [ka]

[0242] Reaction Procedure: IPAc (12 L) was cooled to 0° C. and SOCl2 (5.46 kg, 45.9 mol, 1.5 equiv.) was added while maintaining the temperature between 0-4° C. After the addition, a solution of crude compound 1d (7.46 kg, two batches combined from 6 kg of 1a) in IPAc (24 L) was added slowly. After the addition, the mixture was stirred at 0° C. for 1 h, then warmed to RT and stirred for 4 h. HPLC showed the intermediate was completely consumed.

[0243] The mixture was cooled to −5 to 0° C., quenched with water (30 L), then 30% NaOH aqueous solution was added slowly to adjust the pH to 8.5 to 9, and stirred overnight at 0 to 5° C. HPLC showed that the intermediate was completely consumed.

[0244] The pH was adjusted to 11-12 at 0-10 °C by slow addition of 30% NaOH aqueous solution and stirred at room temperature for 30 min. The phases were separated, the aqueous layer was extracted with IPAc (10 kg), and the combined organic phase was washed with brine (5 L), dried over Na2SO4, and filtered. The filtrate was then cooled to 0-5 °C. 4M HCl\IPA (8.0 kg, 151 mol) was slowly added at 0-5 °C. After addition, the reaction mixture was stirred at 0-5 °C for 4 h. The mixture was filtered, the solid was collected, washed with MTBE (6 L), and dried under vacuum to give compound 1f (3.10 kg, assay 98%, yield 37%).

[0245] Alternative Example 34B: Starting material A5 of Scheme 34A may alternatively be obtained as follows (Reaction Scheme 34B) and then used as shown in Alternative Example 34A above: [ka]

[0246] In detail, the steps are as follows: [ka] In a 100 ml three-neck flask, a solution of (1R,5S)-1-(4-bromophenyl)-3-tetrahydropyran-4-yl-3-azabicyclo[3.1.0]hexane (5.00 g, 15.52 mmol, 1.00 equiv) in anhydrous THF (50.00 mL) was cooled to −78° C. under N2. n-BuLi (2.5 M in hexane, 7.45 mL, 1.20 equiv) was added dropwise at −78° C. and stirred at −78° C. for 1 h. A solution of trimethylborate (4.84 g, 46.56 mmol, 5.26 mL, 3.00 equiv) in anhydrous THF (10.00 mL) was added dropwise at −78° C. After the addition, the reaction mixture was allowed to warm to 25° C. and stirred at 25° C. for 16 h. After complete consumption of the starting material, monitoring by LC-MS was continued and 74.23% of the target compound was observed. The reaction mixture was cooled to 0°C under ice bath and quenched with saturated NH4Cl solution (50 mL). The pH of the mixture was adjusted to 12-13 with NaOH solution (1M) and extracted with EtOAc (30 mL x 3). The aqueous layer was concentrated under reduced pressure to give a residue (18 g). The residue was purified by preparative HPLC (TFA condition) to give [4-[(1R,5S)-3-tetrahydropyran-4-yl-3-azabicyclo[3.1.0]hexan-1-yl]phenyl]boronic acid (4.60 g, 11.47 mmol, 73.88% yield, TFA salt) as a white solid. 1 H NMR(400 MHz,DMSO-d6)δ: 7.72(d,2H),7.24(d,2H),4.13(d,1H),4.06-4.03(m,2H),3.86(d,1H),3.70-3.67(m,2H),3. 45-3.32(m,3H),2.26-2.23(m,1H),2.11-2.05(m,2H),1.81-1.77(m,2H),1.34-1.20(m,2H). ESI-MS 288[M+H] + .

[0247] [ka] A mixture of [4-[(1R,5S)-3-tetrahydropyran-4-yl-3-azabicyclo[3.1.0]hexan-1-yl]phenyl]boronic acid (500.00 mg, 1.25 mmol, 1.00 equiv, TFA salt), methyl 2-amino-5-bromo-pyridine-3-carboxylate (433.22 mg, 1.88 mmol, 1.50 equiv), Pd(dppf)Cl2 (91.46 mg, 0.125 mmol, 0.10 equiv) and K2CO3 (518.29 mg, 3.75 mmol, 3.00 equiv) in dioxane (5.00 mL) and HO (1.00 mL) was heated to 100 °C under N2 and stirred at 100 °C for 16 h. The reaction mixture was cooled to 30 °C and concentrated under reduced pressure. The residue was purified by preparative HPLC (neutral conditions) to give methyl 2-amino-5-[4-[(1R,5S)-3-tetrahydropyran-4-yl-3-azabicyclo[3.1.0]hexan-1-yl]phenyl]pyridine-3-carboxylate (100.00 mg, 20.02% yield, 98.47% HPLC purity) as a brown solid. 1 H NMR(400 MHz,DMSO-d6)δ: 8.49(d,1H),8.35(d,1H),7.46(d,2H),7.24(d,2H),4.01-3.98(m,2H),3.94(s,3H),3.47-3.41(m,3H),3.19(d,1H),2.65 (d,1H),2.50-2.55(m,1H),2.45-2.35(m,1H),1.81-1.76(m,3H),1.64-1.46(m,2H),1.45-1.40(m,1H),0.86-0.83(m,1H). ESI-MS 394[M+H] + .

[0248] Example 35: 2-amino-5-(4-((1S,5R)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide [ka] The title compound was synthesized by the synthesis of tranexamin using 2-amino-5-(4-((1S,5R)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 35a) instead of 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c). Prepared in a similar manner to (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b) except that 4-aminobicyclo[2.2.2]octan-1-ol hydrochloride was used instead of 1R,5S)-4-aminocyclohexanol. The crude product was purified by prepHPLC (Method 1a) to give the title compound as the TFA salt. 1H NMR(400MHz,DMSO-d6)δ 9.05(bs,1H),8.42(d,1H),8.22(s,1H),8.02(s,1H),7.69(d,2H),7.50(bs,2H),7.39(d,2H),4.83(bs,1H),4.08(dd,1H),3.80-3. 25(m,6H),2.31-2.09(m,4H),2.09-1.99(m,6H),1.98-1.71(m,4H),1.70-1.56(m,6H),1.42-1.40(m,1H),1.10(t,1H).(UPLC-MS)t R 0.62 min;ESI-MS 537[M+H] + .

[0249] Intermediate 35a: 2-amino-5-(4-((1S,5R)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 2c), except that methyl 2-amino-5-(4-((1S,5R)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate (Intermediate 35b) was used instead of (1R,5S)-tert-butyl 1-(4-(6-amino-5-(methoxycarbonyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1d). (UPLC-MS)t R 0.46 min;ESI-MS 414[M+H] + .

[0250] Intermediate 35b: Methyl 2-amino-5-(4-((1S,5R)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate The title compound was prepared in a similar manner to methyl 2-amino-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-aminonicotinate hydrochloride (Intermediate 14b), except that methyl 5-(4-((1R,5S)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-aminonicotinate hydrochloride (Intermediate 7c) was used instead of methyl 5-(4-((1R,5S)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-aminonicotinate hydrochloride (Intermediate 14c) and 4,4-difluorocyclohexanone was used instead of dihydro-2H-pyran-4(3H)-one. (UPLC-MS)t R 0.73 min;ESI-MS 428[M+H] + .

[0251] Example 36: 2-amino-N-(3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide (Example 2), except that (3-aminobicyclo[1.1.1]pentan-1-yl)methanol (Intermediate 16a) was used instead of trans-4-aminocyclohexanol hydrochloride. 1H NMR(400MHz,DMSO-d6)δ 9.05(s,1H),8.41(d,1H),8.18(d,1H),7.61(d,2H),7.48(dd,1H),7.33-7.17(m,4H),4.55(t,1H),3.51(d,3H) ),3.31(s,2H),3.08(s,2H),2.07-1.99(m,1H),1.41-1.22(m,3H),1.17-0.98(m,9H),0.79(d,1H).(UPLC-MS)t R 0.54 min;ESI-MS 433[M+H] + .

[0252] Example 37: 2-amino-5-(4-((1S,5R)-3-(but-2-yn-1-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 5), except that 1-bromobut-2-yne was used instead of 4-(3-bromopropyl)morpholine, and the reaction mixture was stirred at room temperature for 30 minutes. 1H NMR(400MHz,DMSO-d6)δ 8.38(s,1H),8.31(d,1H),8.12(d,1H),7.59(d,2H),7.21(s,2H),7.13(s,2H),4.60(d1H),3.72(s,1H), 3.39(s,3H),3.21(s,1H),2.98-2.58(m,3H),1.84(dd,8H),1.49-1.17(m,5H),0.78(s,1H).(UPLC-MS)t R 0.54 min;ESI-MS 445[M+H] + .

[0253] Example 38: 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(oxetan-3-ylmethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 5), except that 3-(iodomethyl)oxetane was used instead of 4-(3-bromopropyl)morpholine, and the reaction mixture was stirred at 60° C. for 60 min. 1H NMR(400MHz,DMSO-d6)δ 8.39(d,1H),8.30(d,1H),8.11(d,1H),7.59(d,2H),7.22(d,2H),7.12(s,2H),4.73-4.61(m,2H),4.58(d,1H),4.29(s,2H),3.84-3.67 (m,1H),3.52-3.38(m,2H),3.27-3.12(m,2H),2.94(d,1H),2.80(s,2H),1.95-1.76(m,5H),1.54-1.14(m,6H),0.76(s,1H).(UPLC-MS)t R 0.49 min;ESI-MS 463[M+H] + .

[0254] Example 39: 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(1-(2,2,2-trifluoroethyl)piperidin-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(1-(methylsulfonyl)piperidin-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide (Example 1), except that 1-(2,2,2-trifluoroethyl)piperidin-4-one was used instead of 1-(methylsulfonyl)piperidin-4-one. 1H NMR(400MHz,DMSO-d6)δ 8.38(d,1H),8.31(d,1H),8.11(d,1H),7.58(d,2H),7.23(d,2H),7.12 (s,2H),4.55(bs,1H),3.80-3.62(m,1H),3.20-3.04(m,3H),2.88(d,2 (UPLC-MS)t R 0.62 min;ESI-MS 558[M+H] + .

[0255] Example 40: 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1S,5R)-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared by using 5-(4-((1S,5R)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide HCl salt (intermediate) instead of 5-(4-((1S,5R)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (intermediate 5a). Prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (example 5), except that 40a) was used and 4-(2-bromoethyl)morpholine was used instead of 4-(3-bromopropyl)morpholine, and the reaction mixture was stirred at 60° C. for 3 h. 1H NMR(400MHz,DMSO-d6)δ 8.34(d,1H),7.98(d,1H),7.79(s,1H),7.57(d,2H),7.21(d,2H),6.92(s,2H),4.32(s,1H),3.65-3.49(m,4H),3.08(d,1H),2. 61(t,2H),2.59-2.39(m,9H),2.15-1.98(m,6H),1.85-1.73(m,1H),1.70-1.54(m,6H),1.31(t,1H),0.75(dd,1H).(UPLC-MS)t R 0.52 min;ESI-MS 532[M+H] + .

[0256] Intermediate 40a: 5-(4-((1S,5R)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide The title compound was prepared by the reaction of (1S,5R)-tert-butyl 1-(4-(6-amino-5-(((1r,4S)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 5b) with (1S,5R)-tert-butyl 1-(4-(6-amino-5-((4-hydroxybicyclo[2.2.2]octadecyl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate. 5-(4-((1S,5R)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Intermediate 5a) was prepared in a similar manner to 5-(4-((1S,5R)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Intermediate 5a), except that 5-(4-((1S,5R)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Intermediate 5a) was used. One fraction of the title compound was obtained as the hydrochloride salt after evaporation of dioxane; another fraction was obtained as the TFA salt after further purification by prepHPLC (Method 1a). (UPLC-MS)t R 0.48 min;ESI-MS 419[M+H] + .

[0257] Intermediate 40b: (1S,5R)-tert-butyl 1-(4-(6-amino-5-((4-hydroxybicyclo[2.2.2]octan-1-yl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate The title compound was synthesized by the trans-method using 2-amino-5-(4-((1S,5R)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 5c) instead of 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c). -Prepared in a similar manner to (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b), except that 4-aminobicyclo[2.2.2]octan-1-ol hydrochloride was used instead of 4-aminocyclohexanol. (UPLC-MS)t R 1.05 minutes;ESI-MS 519[M+H] + .

[0258] Example 41: 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(2-(2,2,2-trifluoroethoxy)ethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 6), except that 2-(2,2,2-trifluoroethoxy)ethyl trifluoromethanesulfonate (Intermediate 41a) was used instead of 1,3-difluoropropan-2-yl trifluoromethanesulfonate (Intermediate 6a). After purification, the title compound was obtained as a TFA salt. 1H NMR(400MHz,DMSO-d6)δ 9.15(bs,1H),8.40(s,1H),8.31(d,1H),8.12(d,1H),7.63(d,2H),7.23(s,2H),7.13(s,2H),4.59(d,1H),4 .11(s,2H),3.80-3.63(m,3H),3.40(m,4H),2.75-2.60(m,3H),1.86(m,5H),1.51-1.15(m,6H).(UPLC-MS)t R 0.60 min;ESI-MS 519[M+H] + .

[0259] Intermediate 41a: 2-(2,2,2-trifluoroethoxy)ethyl trifluoromethanesulfonate The title compound was prepared in a similar manner to 1,3-difluoropropan-2-yl trifluoromethanesulfonate (Intermediate 6a), except that 2-(2,2,2-trifluoroethoxy)ethanol was used instead of 1,3-difluoropropan-2-ol, and was obtained as a crude oil that was used without further purification.

[0260] Example 42: 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1S,5R)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared by mixing 5-(4-((1S,5R)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide HCl salt (Figure 1A) instead of 5-(4-((1R,5S)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Intermediate 1a). Prepared in a similar manner to 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(1-(methylsulfonyl)piperidin-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide (Example 1), except that intermediate 40a) was used and dihydro-2H-pyran-4(3H)-one was used instead of 1-(methylsulfonyl)piperidin-4-one. After purification, the title compound was obtained as a TFA salt. 1H NMR (400 MHz, DMSO-d6) δ 9.62(bs,1H),8.38(d,1H),7.98(d,1H),7.81(s,1H),7.65(d,2H),7.37(d,2 H),6.95(s,2H),4.33(s,1H),4.06-3.97(m,3H),3.75-3.43(m,4H),3.29-3.2 6(m,2H),2.28-2.19(m,1H),2.07-2.03(m,6H),2.03-1.96(m,2H),1.75-1.63 (m,1H),1.63-1.61(m,6H),1.63-1.61(m,1H),1.25-1.17(m,1H).(UPLC-MS)t R 0.52 min;ESI-MS 503[M+H] + .

[0261] Example 43: 2-Amino-N-cyclohexyl-5-(4-(3-(piperidin-1-yl)propoxy)phenyl)nicotinamide [ka] To a solution of 2-amino-5-bromo-N-cyclohexylnicotinamide (Intermediate 43a, 50 mg, 0.168 mmol) in 2 ml of DMF / EtOH / water (2:1:1) was added 1-(3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)propyl)piperidine (60.9 mg, 0.168 mmol), K2CO3 (69.5 mg, 0.503 mmol), and PdCl2(PPh3)2 (11.8 mg, 0.017 mmol). The reaction mixture was stirred at 80 °C for 15 min, then cooled and diluted with 5 ml of EtOAc and filtered over a pad of Na2SO4. After concentration under reduced pressure, the crude product was purified by prepHPLC (Method 1a) to give the title compound as a colorless solid. 1H NMR(400MHz,DMSO-d6)δ 8.34(d,1H),8.33(d,1H),8.09(d,1H),7.59(d,2H),7.06(s,2H),7.01(d,2H),4.03(t,2H),3.75(s,1H),2.50-2 .22(m,6H),1.95-1.65(m,6H),1.62(d,1H),1.52-1.48(m,4H),1.46-1.34(m,6H),1.32-1.15(m,1H).(HPLC-MS)t R 1.46 min; APCI-MS 437.3 [M+H] + .

[0262] Intermediate 43a: 2-amino-5-bromo-N-cyclohexylnicotinamide The title compound was prepared in a similar manner to (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b), except that 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c) was used instead of 2-amino-5-bromonicotinic acid and cyclohexanamine was used instead of trans-4-aminocyclohexanol. The crude product was used without further purification. (HPLC-MS)tR 0.98 min;ESI-MS 208 / 300[M+H] + .

[0263] Example 44: 2-amino-5-(4-((1R,5S)-3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(1-(methylsulfonyl)piperidin-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide (Example 1), except that dihydro-2H-thiopyran-4(3H)-one 1,1-dioxide was used instead of 1-(methylsulfonyl)piperidin-4-one. 1H NMR(400MHz,DMSO-d6)δ 8.39(d,1H),8.31(d,1H),8.12(d,1H),7.59(d,2H),7.24(d,2H),7.12(s,2H),4.58(d,1H),3.82-3.65(m,1H),3.48-3.35(m, (UPLC-MS)t R 0.48 min; ESI-MS 525[M+H] + .

[0264] Example 45: 2-Amino-N-cyclohexyl-5-(4-(4-methylpiperazine-1-carbonyl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-cyclohexyl-5-(4-(3-(piperidin-1-yl)propoxy)phenyl)nicotinamide (Example 43), except that (4-methylpiperazin-1-yl)(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanone was used instead of 1-(3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)propyl)piperidine. 1H NMR(400MHz,DMSO-d6)δ 8.46(d,1H),8.37(s,1H),8.21(d,1H),7.76(d,2H),7.47(d,2H),7.22(s,2H),3.82-3.55(m,1H),3.35(t,4H),2.31-2.22(t, (HPLC-MS)t R 1.29 min; APCI-MS 422 [M+H] + .

[0265] Example 46: 2-amino-5-(3-fluoro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide [ka] A microwave vial was charged with 2-amino-5-bromo-N-((1r,4r)-4-hydroxy-4-methylcyclohexyl)nicotinamide (Intermediate 59b, 33 mg, 0.10 mmol), (R)-2-(3-fluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione (Intermediate 46a, 38.3 mg, 0.11 mmol) and XPhosPd (7.39 mg, 0.01 mmol). Dioxane (1 mL) was added followed by a 3N aqueous solution of K3PO4 (0.10 ml, 0.30 mmol). The reaction mixture was purged with a stream of nitrogen for 5 min and then irradiated in a microwave reactor at 120 °C for 30 min. After cooling, the reaction mixture was concentrated under reduced pressure and purified by prepHPLC (Method 1b) to give the title compound. UPLC-HRMSt R 3.21 min; ESI441.26 [M+H] + .

[0266] Intermediate 46a: (R)-2-(3-fluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione A solution of 2-fluoro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzaldehyde (Intermediate 46b, 112 mg, 0.40 mmol), (R)-(2)-methylpyrrolidine (37.5 mg, 0.44 mmol), and acetic acid (2.4 mg, 0.040 mmol) in THF (2 mL) was shaken at room temperature for 2 h and sodium triacetoxyborohydride (110 mg, 0.52 mmol) was added. The resulting reaction mixture was shaken for 18 h and then filtered through an SPE carbonate cartridge followed by a wash with THF. The filtrate and washings were concentrated under reduced pressure to give the title compound, which was used without further purification. ESI-MS 349 [M+H] + .

[0267] Intermediate 46b: 2-Fluoro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzaldehyde A solution of (3-fluoro-4-formylphenyl)boronic acid (67 mg, 0.40 mmol) and N-methyliminodiacetic acid (65 mg, 0.44 mmol) in DMF (2 mL) was stirred at 90° C. for 18 h. The reaction mixture was cooled and filtered through an SPE carbonate cartridge, followed by three washes with acetonitrile. The filtrate and washings were concentrated under reduced pressure to give the title compound, which was used without further purification. ESI-MS 558 [2M+H] + .

[0268] Example 47: 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(3,3,3-trifluoropropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 6), except that 3,3,3-trifluoropropyl trifluoromethanesulfonate was used instead of 1,3-difluoropropan-2-yl trifluoromethanesulfonate (Intermediate 6a). 1H NMR(400MHz,DMSO-d6)δ 8.39(s,1H),8.31(d,1H),8.12(d,1H),7.60(d,2H),7.23(d,2H),7.13(s,2H),4.59(d,1H),3.74(m,1H) ,3.40(m,3H),3.09(m,1H),2.72-2.64(m,4H),1.86(m,5H),1.49-1.14(m,6H),0.78(s,1H).(UPLC-MS)t R 0.60 min;ESI-MS 489[M+H] + .

[0269] Example 48: 2-amino-5-(4-((1R,5S)-3-(2-fluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 6), except that 1-bromo-2-fluoroethane was used instead of 1,3-difluoropropan-2-yl trifluoromethanesulfonate (Intermediate 6a), and the reaction mixture was stirred at 60° C. for 3 hours. After purification, the title compound was obtained as a TFA salt. 1H NMR(400MHz,DMSO-d6)δ 9.95(bs,1H),8.41(s,1H),8.32(d,1H),8.13(d,1H),7.70-7.57(m,2H),7.36(bs,2H),7.16(s,2H),4.80-4.62(m,2H),4. 59(d,1H),4.08(bs,1H),3.77-3.52(m,4H),3.51-3.35(m,3H),2.24(bs,1H),1.87(t,4H),1.59-1.13(m,6H).(UPLC-MS)t R 0.46 min;ESI-MS 439[M+H] + .

[0270] Example 49: 2-Amino-N-cyclohexyl-5-(4-morpholinophenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-cyclohexyl-5-(4-(3-(piperidin-1-yl)propoxy)phenyl)nicotinamide (Example 43), except 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)morpholine was used instead of 1-(3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)propyl)piperidine. 1H NMR(400MHz,DMSO-d6)δ 8.35(d,1H),8.34(s,1H),8.08(d,1H),7.55(d,2H),7.03(d,2H),7.03(s,2H),3.85-3.65(m,1H),3.77(t,4H),3. 14(t,4H),1.90-1.80(m,2H),1.80-1.70(m,2H),1.80(dd,1H),1.38-1.20(m,4H),1.19-1.05(m,1H).(HPLC-MS)t R 1.60 min; APCI-MS 381 [M+H] + .

[0271] Example 50: 2-amino-5-(4-((1R,5S)-3-(2,2-difluoropropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 6), except that 2,2-difluoropropyl trifluoromethanesulfonate was used instead of 1,3-difluoropropan-2-yl trifluoromethanesulfonate (Intermediate 6a), and the reaction mixture was stirred at room temperature for 60 minutes. 1H NMR(400MHz,DMSO-d6)δ 8.39(s,1H),8.33(s,1H),8.14(s,1H),7.59(d,2H),7.32-7.11(m,4H),4.58(bs,1H),3.74(bs,1H),3. 11(bs,1H),3.00-2.66(m,5H),1.86(bs,5H),1.63(t,3H),1.48-1.18(m,6H),0.81(bs,1H).(UPLC-MS)t R 0.81 min;ESI-MS 471[M+H] + .

[0272] Example 51: 2-amino-5-(4-((1S,5R)-3-(2-cyanoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 5), except that 3-bromopropanenitrile was used instead of 4-(3-bromopropyl)morpholine, and the reaction mixture was stirred at 60° C. for 24 h. 1H NMR(400MHz,DMSO-d6)δ 8.39(d,1H),8.30(d,1H),8.12(d,1H),7.60(d,2H),7.23(d,2H),7.12(s,2H),4.59(d,1H),3.73(d,1H),3. 18(d,1H),3.09(d,1H),2.81-2.62(m,6H),1.99-1.78(m,5H),1.48-1.18(m,6H),0.80(dd,1H).(UPLC-MS)t R 0.50 min;ESI-MS 446[M+H] + .

[0273] Example 52: 2-Amino-N-cyclohexyl-5-(4-(3-morpholinopropoxy)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-cyclohexyl-5-(4-(3-(piperidin-1-yl)propoxy)phenyl)nicotinamide (Example 43), except 4-(3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)propyl)morpholine was used instead of 1-(3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)propyl)piperidine. 1H NMR(400MHz,DMSO-d6)δ 8.35(d,1H),8.34(s,1H),8.10(d,1H),7.59(d,2H),7.06(s,2H),7.01(d,2H),4.04(t,2H),3.82-3.68(m,1H),3.58(t,4H) ,2.50-2.22(m,6H),1.90-1.78(m,4H),1.78-1.69(m,2H),1.63(dd,1H),1.38-1.20(m,4H),1.19-1.05(m,1H).(HPLC-MS)t R 1.40 min; APCI-MS 439 [M+H] + .

[0274] Example 53: 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(prop-2-yn-1-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(3-morpholinopropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide (Example 5), except 3-bromoprop-1-yne was used instead of 4-(3-bromopropyl)morpholine. 1H NMR(400MHz,DMSO-d6)δ 8.38(d,1H),8.31(d,1H),8.12(d,1H),7.59(d,2H),7.21(d,2H),7.13(s,2H),4.59(d,1H),3.73(d,1H),3.52-3.38(m,2H),3. 21(d,1H),2.93(d,1H),2.83(d,1H),2.72(d,1H),2.40(s,3H),1.95-1.75(m,4H),1.44-1.19(m,5H),0.80(dd,1H).(UPLC-MS)t R 0.49 min;ESI-MS 431[M+H] + .

[0275] Example 54: 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(prop-2-yn-1-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 6), except that 3-bromoprop-1-yne was used instead of 1,3-difluoropropan-2-yl trifluoromethanesulfonate (Intermediate 6a). 1H NMR(400MHz,DMSO-d6)δ 8.39(d,1H),8.31(d,1H),8.12(d,1H),7.59(d,2H),7.21(d,2H),7.12(s,2H),4.59(d,1H),3.76-3.70(m,1H),3.46(s,2H),3.45-3. 37(m,1H),3.22(d,1H),2.83(d,1H),2.72(d,1H),2.71-2.69(m,2H),1.92-1.77(m,5H),1.51-1.17(m,5H),0.80(dd,1H).(UPLC-MS)t R 0.52 min;ESI-MS 431[M+H] + .

[0276] Example 55: 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)-2-chlorophenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 3), except that (R)-6-(1-(4-bromophenyl)ethyl)-2-oxa-6-azaspiro[3.3]heptane (Intermediate 55a) was used instead of (R)-6-(1-(4-bromophenyl)ethyl)-2-oxa-6-azaspiro[3.3]heptane (Intermediate 3b). 1H NMR(400 MHz,DMSO-d6)δ 8.17(m,2H),8.00(s,1H),7.42-7.44(m,2H),7.40(m,1H),7.34(bs,2H),4.62(s,3H),4.55 -4.57(m,1H),3.72(m,1H),3.35-3.54(m,4H),3.20-3.24(m,2H),3.15(bs,1H),1.78-1.88(m,4H),1.20-1.41(m,4H),1.11(bs,3H).(UPLC-MS)t R 0.47 min;ESI-MS 471 / 473[M+H] + .

[0277] Intermediate 55a: (R)-6-(1-(4-bromo-3-chlorophenyl)ethyl)-2-oxa-6-azaspiro[3.3]heptane The title compound was prepared in a similar manner to (R)-6-(1-(4-bromophenyl)ethyl)-2-oxa-6-azaspiro[3.3]heptane (Intermediate 3b), except that (R)-1-(4-bromo-3-chlorophenyl)ethanamine was used instead of (R)-1-(4-bromophenyl)ethanamine. (UPLC-MS)t R 0.63 min;ESI-MS 316 / 318[M+H] + .

[0278] Example 56: 2-amino-5-(2-fluoro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(3-fluoro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide (Example 46), except that (R)-2-(2-fluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione (Intermediate 56a) was used instead of (R)-2-(3-fluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione (Intermediate 46a). UPLC-HRMSt R 3.22 min; ESI441.26 [M+H] + .

[0279] Intermediate 56a: (R)-2-(2-fluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione The title compound was prepared in a similar manner to (R)-2-(3-fluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione (Intermediate 46a), except that 3-fluoro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocane-2-yl)benzaldehyde (Intermediate 56b) was used instead of 2-fluoro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocane-2-yl)benzaldehyde (Intermediate 46b). ESI-MS 349[M+H] + .

[0280] Intermediate 56b: 3-Fluoro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzaldehyde The title compound was prepared in a similar manner to 2-fluoro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzaldehyde (Intermediate 46b), except that (2-fluoro-4-formylphenyl)boronic acid was used instead of (3-fluoro-4-formylphenyl)boronic acid. ESI-MS 576 [2M+H2O+H] + .

[0281] Example 57: 2-amino-5-(4-((1R,5S)-3-(2-fluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide [ka] The title compound was prepared by using 5-(4-((1R,5S)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide HCl salt (Intermediate 34) instead of 5-(4-((1R,5S)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Intermediate 1a). Prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 6), except that intermediate 6a was used and 1-bromo-2-fluoroethane was used instead of 1,3-difluoropropan-2-yl trifluoromethanesulfonate (Intermediate 6a). After purification, the title compound was obtained as a TFA salt. 1H NMR(400MHz,DMSO-d6)δ 10.00(bs,1H),8.38(d,1H),8.04(d,1H),7.85(s,1H),7.77(d,2H),7.35(d,2H),7.08(s,2H),4.83(td,2H),4.74(bs,1H),4.08(bs (UPLC-MS)t R 0.53 min;ESI-MS 465[M+H] + .

[0282] Example 58: 2-amino-5-(4-((1S,5R)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxy-4-methylcyclohexyl)nicotinamide [ka] The title compound was synthesized by using 2-amino-5-(4-((1S,5R)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 35a) instead of 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c). Prepared in a similar manner as (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b) except trans-4-amino-1-methylcyclohexanol was used instead of trans-4-aminocyclohexanol. The crude product was purified by prepHPLC (Method 1a) and passed through an ion exchange cartridge (PL-HCO3) for desalting to give the title compound. 1H NMR(400MHz,DMSO-d6)δ 8.39(d,1H),8.29(d,1H),8.10(d,1H),7.59(d,2H),7.25(d,2H),7.10(s,2H),4.33(s,1H),3.81(bs,1H),3.39(d,2H),2.62-2.56(m, (UPLC-MS)t R 0.61 min;ESI-MS 525[M+H] + .

[0283] Example 59: 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 3), except that (6-amino-5-(((1r,4r)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)boronic acid (Intermediate 59a) was used instead of (6-amino-5-(((1r,4r)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)boronic acid (Intermediate 3a). 1H NMR(400MHz,DMSO-d6)δ 8.38(s,1H),8.25(bs,1H),8.11(d,1H)7.71-7.54(m,2H),7.49-7.28(m,2H),7.12(bs,2H),4.61(bs,4H),4.31(s,1H),3.89-3.68(m,2H) ),3.31(s,15H),3.27-2.99(m,2H),1.86-1.69(m,2H),1.66-1.52(m,2H),1.51-1.35(m,5H),1.16(s,1H),1.30-0.95(m,2H).(UPLC-MS)t R 0.47 min;ESI-MS 451[M+H] + .

[0284] Intermediate 59a: (6-amino-5-(((1r,4r)-4-hydroxy-4-methylcyclohexyl)carbamoyl)pyridin-3-yl)boronic acid The title compound was prepared in a similar manner to (6-amino-5-(((1r,4r)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)boronic acid (Intermediate 3a), except that 2-amino-5-bromo-N-((1r,4r)-4-hydroxy-4-methylcyclohexyl)nicotinamide (Intermediate 59b) was used instead of 2-amino-5-bromo-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide (Intermediate 3c). (UPLC-MS)t R 0.33 min;ESI-MS 394[M+H] + .

[0285] Intermediate 59b: 2-amino-5-bromo-N-((1r,4r)-4-hydroxy-4-methylcyclohexyl)nicotinamide The title compound was prepared in a similar manner to 2-amino-5-bromo-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide (Intermediate 3c), except that trans-4-amino-1-methylcyclohexanol was used instead of trans-4-aminocyclohexanol. (UPLC-MS)t R 0.68 min;ESI-MS 328 / 330[M+H] + .

[0286] Example 60: 2-amino-5-(4-((1R,5S)-3-(but-2-yn-1-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 6), except that 1-bromobut-2-yne was used instead of 1,3-difluoropropan-2-yl trifluoromethanesulfonate (Intermediate 6a). 1H NMR(400MHz,DMSO-d6)δ 8.39(d,1H),8.31(d,1H),8.12(d,1H),7.59(d,2H),7.21(d,2H),7.12(s,2H),4.58(d,1H),3.77-3.71(m,1H),3.43- 3.37(m,3H),3.22(d,1H),2.92(d,1H),2.80(d,1H),1.93-1.78(m,8H),1.44-1.19(m,6H),0.79(dd,1H).(UPLC-MS)t R 0.54 min;ESI-MS 445[M+H] + .

[0287] Example 61: 2-amino-N-cyclohexyl-5-(4-(piperidin-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-cyclohexyl-5-(4-(3-(piperidin-1-yl)propoxy)phenyl)nicotinamide (Example 43), except 4-(piperidin-1-yl)phenylboronic acid was used instead of 1-(3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)propyl)piperidine. 1H NMR(400MHz,DMSO-d6)δ 8.33(d,1H),8.33(s,1H),8.08(d,1H),7.51(d,2H),7.01(s,2H),7.00(d,2H),3.82-3.68(m,1H),3.17(t,4H) ),1.90-1.78(m,2H),1.78-1.69(m,2H),1.68-1.49(m,7H),1.38-1.20(m,4H),1.19-1.05(m,1H).(HPLC-MS)t R 1.40 min; APCI-MS 379 [M+H] + .

[0288] Example 62: 2-amino-N-(3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)-5-(4-((1S,5R)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared by using 2-amino-5-(4-((1S,5R)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 28a) instead of 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c). Prepared in a similar manner as (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b), except that trans-4-amino-1-methylcyclohexanol was used instead of trans-4-aminocyclohexanol. The crude product was purified first by prepHPLC (Method 1a) and then by reverse-phase flash chromatography (Method 3a) to give the title compound as a colorless solid. 1H NMR(400MHz,DMSO-d6)δ 8.92(d,1H),8.46(s,1H),8.22(s,1H),7.61(d,2H),7.25(d,2H),7.18(s,2H),4.15-4.09(m,1H),3.88-3.82(m,2H), 3.42-3.36(m,3H),3.10(bs,1H),2.65-2.34(m,12H),1.85-1.75(m,3H),1.45-1.31(m,6H),0.77(bs,1H).(UPLC-MS)t R 0.49 min;ESI-MS 491[M+H] + .

[0289] Example 63: 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1S,5R)-3-(oxetan-3-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound is 5-(4-((1S,5R)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide instead of 5-(4-((1R,5S)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (intermediate 1a). Prepared in a similar manner to 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(1-(methylsulfonyl)piperidin-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide (Example 1), except that the HCl salt (Intermediate 40a) was used and oxetan-3-one was used instead of 1-(methylsulfonyl)piperidin-4-one. 1H NMR(400MHz,DMSO-d6)δ 8.34(d,1H),7.98(d,1H),7.80(s,1H),7.57(d,2H),7.22(d,2H),6.92( s,2H),4.61-4.56(m,2H),4.52-4.48(m,2H),4.32(s,1H),3.80-3.74(m, 1H),3.03(d,1H),2.57-2.51(m,3H),2.14-1.98(m,6H),1.88-1.85(m,1 H),1.71-1.55(m,6H),1.45-1.35(m,1H),0.83-0.80(m,1H).(UPLC-MS)t R 0.51 min; ESI-MS 475[M+H] + .

[0290] Example 64: 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(oxetan-3-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound is 5-(4-((1R,5S)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide instead of 5-(4-((1R,5S)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (intermediate 1a). Prepared in a similar manner to 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(1-(methylsulfonyl)piperidin-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide (Example 1), except that the HCl salt (Intermediate 34a) was used and oxetan-3-one was used instead of 1-(methylsulfonyl)piperidin-4-one. 1H NMR(400MHz,DMSO-d6)δ 8.34(d,1H),7.98(d,1H),7.80(s,1H),7.57(d,2H),7.22(d,2H),6.92( s,2H),4.61-4.56(m,2H),4.52-4.48(m,2H),4.31(s,1H),3.81-3.76(m, 1H),3.03(d,1H),2.57-2.51(m,3H),2.07-2.03(m,6H),1.88-1.85(m,1 H),1.65-1.61(m,6H),1.45-1.35(m,1H),0.83-0.80(m,1H).(UPLC-MS)t R 0.55 min; ESI-MS 475[M+H] + .

[0291] Example 65: 2-Amino-N-cyclohexyl-5-(4-((2-(4-methylpiperazin-1-yl)ethyl)carbamoyl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b), except that 4-(6-amino-5-(cyclohexylcarbamoyl)pyridin-3-yl)benzoic acid (Intermediate 65a) was used instead of 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c) and 2-(4-methylpiperazin-1-yl)ethanamine was used instead of trans-4-aminocyclohexanol. The crude product was purified by normal phase chromatography (Method 2c) to give the title compound as an off-white solid. 1H NMR (400 MHz, DMSO-d6) δ 8.50(d,1H),8.42(t,1H),8.37(d,1H),8.23(d,1H),7.91(d,2H),7.80(d,2 H),7.25(s,2H),3.82-3.65(m,1H),3.40(q,2H),3.32-3.13(m,3H),2.99-2 .83(m,1H),2.43-2.31(m,6H),2.17(s,3H),1.90-1.80(m,2H),1.80-1.70( m,2H),1.70-1.55(m,1H),1.40-1.25(m,4H),1.20-1.10(m,1H).(HPLC-MS)t R 1.28 min; APCI-MS 465 [M+H] + .

[0292] Intermediate 65a: 4-(6-amino-5-(cyclohexylcarbamoyl)pyridin-3-yl)benzoic acid The title compound was prepared in a similar manner to 2-amino-N-cyclohexyl-5-(4-(3-(piperidin-1-yl)propoxy)phenyl)nicotinamide (Example 43), except that 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid was used instead of 1-(3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)propyl)piperidine. The crude product was triturated with 2-propanol to give a brownish solid, which was purified by prepHPLC (Method 1a). The pure fractions were collected and concentrated under reduced pressure, then basified with Na2CO3, whereupon the title compound precipitated as a colorless solid, which was filtered and dried under reduced pressure. (HPLC-MS)t R 1.52 minutes; ESI-MS 340[M+H] + .

[0293] Example 66: 2-amino-5-(4-((1S,5R)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 5), except that 1,3-difluoropropan-2-yl trifluoromethanesulfonate (Intermediate 6a) was used instead of 4-(3-bromopropyl)morpholine. 1H NMR(400MHz,DMSO-d6)δ 8.39(d,1H),8.31(d,1H),8.12(d,1H),7.59(d,2H),7.24(d,2H),7.12(s,2H),4.68(t,2H),4.57(dd,3H),3.81-3.65(m,1H) ,3.46-3.35(m,2H),3.08(d,1H),2.93(d,1H),2.83(dd,1H),2.05-1.76(m,5H),1.53-1.16(m,6H),0.78(dd,1H).(UPLC-MS)t R 0.68 min;ESI-MS 471[M+H] + .

[0294] Example 67: 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(2,2,2-trifluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 5), except that 2,2,2-trifluoroethyl trifluoromethanesulfonate was used instead of 4-(3-bromopropyl)morpholine. 1H NMR(400MHz,DMSO-d6)δ 8.46-8.31(m,2H),8.18(bs,1H),7.59(d,2H),7.29(bs,1H),7.23(d,2H),3.83-3.54(m,1H),3.51-3.24(m,5H),3.11(d,1H),2 .92(d,1H),2.86(m,1H),1.92-1.77(m,5H),1.29-1.21(m,1H),1.42-1.18(m,4H),1.14(bs,1H),0.85-0.79(m,1H).(UPLC-MS)t R 1.04 minutes;ESI-MS 475[M+H] + .

[0295] Example 68: 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1r,3R)-3-hydroxyadamantan-1-yl)nicotinamide [ka] The title compound was prepared in a similar manner to 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 3), except that (6-amino-5-(((1r,4r)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)boronic acid (Intermediate 3a) was replaced with (6-amino-5-(((1r,3r)-3-hydroxyadamantan-1-yl)carbamoyl)pyridin-3-yl)boronic acid (Intermediate 68a). 1H NMR(400MHz,DMSO-d6)δ 8.65(bs,1H),8.49(s,1H),8.35(s,1H),7.87(d,2H),7.59(d,2H),4.73(dd,2H),4.65-4.54(m,4H),4.45-4.39(m,1H),4. 16-4.10(m,1H),3.98(s,1H),3.90(bs,1H),2.21(s,2H),2.04-1.94(m,6H),1.60(bs,2H),1.49-1.43(m,3H).(UPLC-MS)t R 0.56 min;ESI-MS 489[M+H] + .

[0296] Intermediate 68a: 6-amino-5-(((1r,3r)-3-hydroxyadamantan-1-yl)carbamoyl)pyridin-3-yl)boronic acid The title compound was prepared in a similar manner to (6-amino-5-(((1r,4r)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)boronic acid (Intermediate 3a), except that 2-amino-5-bromo-N-((1r,3r)-3-hydroxyadamantan-1-yl)nicotinamide (Intermediate 68b) was used instead of 2-amino-5-bromo-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide (Intermediate 3c). (UPLC-MS)t R 0.47 min;ESI-MS 332[M+H] + .

[0297] Intermediate 68b: 2-amino-5-bromo-N-((1r,3r)-3-hydroxyadamantan-1-yl)nicotinamide The title compound was prepared in a similar manner to 2-amino-5-bromo-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide intermediate 3c), except that 3-amino-1-adamantanol was used instead of trans-4-aminocyclohexanol. (UPLC-MS)t R 0.82 minutes; ESI-MS 366 / 368[M+H] + .

[0298] Example 69: 2-amino-N-cyclohexyl-5-(4-(morpholine-4-carbonyl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-cyclohexyl-5-(4-(3-(piperidin-1-yl)propoxy)phenyl)nicotinamide (Example 43), except 4-(morpholine-4-carbonyl)phenylboronic acid was used instead of 1-(3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)propyl)piperidine. 1H NMR(400 MHz,DMSO-d6)δ 8.47(d,1H),8.42(s,1H),8.30(d,1H),7.78(d,2H),7.51(d,2H),7.49(s,2H),3.85-3.70(m,1H),3.70 -3.50(m,8H),1.90-1.80(m,2H),1.80-1.70(m,2H),1.70-1.55(m,1H),1.35-1.29(m,4H),1.28-1.05(m,1H).(HPLC-MS)t R 1.51 min; APCI-MS 409 [M+H] + .

[0299] Example 70: 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(oxetan-3-ylmethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 6), except that oxetan-3-ylmethyl trifluoromethanesulfonate (Intermediate 70a) was used instead of 1,3-difluoropropan-2-yl trifluoromethanesulfonate (Intermediate 6a), and the reaction mixture was stirred at 60° C. for 3 hours. 1H NMR (400 MHz, DMSO-d6) δ 8.38(d,1H),8.30(d,1H),8.11(d,1H),7.58(d,2H),7.21(d,2H),7.12(s,2 H),4.66(dt,2H),4.58(d,1H),4.28(t,2H),3.90-3.66(m,1H),3.43-3.35( m,1H),3.25(dd,1H),3.19-3.09(m,1H),2.97(d,1H),2.79(d,2H),2.62-2. 51(m,2H),1.98-1.75(m,5H),1.48-1.13(m,5H),0.75(dd,1H).(UPLC-MS)t R 0.46 min;ESI-MS 463[M+H] + .

[0300] Intermediate 70a: Oxetan-3-ylmethyl trifluoromethanesulfonate The title compound was prepared in a similar manner to 1,3-difluoropropan-2-yl trifluoromethanesulfonate (Intermediate 6a), except that oxetan-3-ylmethanol was used instead of 1,3-difluoropropan-2-ol, and was obtained as a crude oil that was used without further purification.

[0301] Example 71: 2-amino-N-((1s,4R)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b), except that 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c) was used instead of 2-amino-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 71a) and cis-4-aminocyclohexanol hydrochloride was used instead of trans-4-aminocyclohexanol. The crude product was purified by prepHPLC (Method 1a) to give the title compound as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ 8.49-8.34 (m, 2H), 8.17 (s, 1H), 7.67 (s, 2H), 7.36 (s, 2H), 7.16 (s, 2H), 4.43 (d, 1H), 3.81 (s, 2H), 3.81-3.59 (m, 4H), 1.88-1.62 (m, 5H), 1.61-1.44 (m, 5H), 1.35 (s, 6H), 1.16 (s, 2H). (UPLC-MS) t R 0.52 min; ESI-MS 435[M+H] + .

[0302] Intermediate 71a: 2-amino-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c), except that methyl 2-amino-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate (Intermediate 71b) was used instead of (1R,5S)-tert-butyl 1-(4-(6-amino-5-(methoxycarbonyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1d). (UPLC-MS)t R 0.40 min;ESI-MS 338[M+H] + .

[0303] Intermediate 71b: Methyl 2-amino-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate The title compound was prepared in a similar manner to methyl 2-amino-5-(4-((1S,5R)-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate (Intermediate 7b), except that 2-iodopropane was used instead of 1-bromo-2-methoxyethane. (UPLC-MS)t R 0.65 min; ESI-MS 352[M+H] + .

[0304] Example 72: 2-amino-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)-5-(4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)nicotinamide [ka] To a solution of (4-(bromomethyl)phenyl)boronic acid (73.1 mg, 0.340 mmol) in acetonitrile (2 mL), (R)-2-methylpyrrolidine (29.0 mg, 0.340 mmol) and K2CO3 (78 mg, 0.567 mmol) were added at room temperature under nitrogen atmosphere, and the resulting white suspension was stirred at 60 °C for 2 h. Water (1 mL) was added at room temperature, followed by the addition of 2-amino-5-bromo-N-((1r,4r)-4-hydroxy-4-methylcyclohexyl)nicotinamide (Intermediate 59b, 150 mg, 0.283 mmol) in acetonitrile (2 mL). PdCl2(dppf) (10.37 mg, 0.014 mmol) was then added, and the reaction mixture was stirred at 90 °C for 60 min. After filtration through a celite pad and concentration under reduced pressure, the crude product was diluted with a saturated aqueous solution of NaHCO3 and EtOAc. After phase separation, the aqueous layer was extracted with EtOAc and the combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The resulting crude product was purified first by prepHPLC (Method 1a) and then by normal phase flash chromatography (Method 2b) to give the title compound as a colorless solid. 1H NMR(400MHz,DMSO-d6)δ 9.75(d,1H),8.52(t,1H),8.41(d,1H),8.27(d,1H),7.85(d,2H),7.66( d,2H),7.38(bs,2H),4.67-4.53(m,1H),4.25(dd,1H),3.85(s,1H),3.58 -3.49(m,1H),3.37-3.18(m,3H),2.29(m,1H),2.06-1.88(m,2H),1.83(s ,2H),1.65(dd,2H),1.51(d,4H),1.39(dd,3H),1.22(d,3H).(UPLC-MS)t R 0.47 min;ESI-MS 423[M+H] + .

[0305] Example 73: 2-amino-5-(4-((1S,5R)-3-(2-fluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide [ka] The title compound was prepared by mixing 5-(4-((1S,5R)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide HCl salt (Intermediate 5a) instead of 5-(4-((1S,5R)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Intermediate 5b). Prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (example 5), except that compound 40a) was used and 1-bromo-2-fluoroethane was used instead of 4-(3-bromopropyl)morpholine, and the reaction mixture was stirred at 60° C. for 3 hours. 1H NMR(400MHz,DMSO-d6)δ 8.35(d,1H),7.98(d,1H),7.79(s,1H),7.57(d,2H),7.22(d,2H),6.92 (s,2H),4.55(td,2H),4.31(s,1H),3.38(d,1H),3.10(d,1H),2.84(t, (UPLC-MS)t R 0.51 min;ESI-MS 465[M+H] + .

[0306] Example 74: 2-amino-5-(2,3-difluoro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(3-fluoro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide (Example 46), except that (R)-2-(2,3-difluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione (Intermediate 74a) was used instead of (R)-2-(3-fluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione (Intermediate 46a). (UPLC-MS)t R 0.76 min;ESI-MS 459[M+H] + .

[0307] Intermediate 74a: (R)-2-(2,3-difluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione The title compound was prepared in a similar manner to (R)-2-(3-fluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione (Intermediate 46a), except that 2,3-difluoro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocane-2-yl)benzaldehyde (Intermediate 74b) was used instead of 2-fluoro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocane-2-yl)benzaldehyde (Intermediate 46b). ESI-MS 367[M+H] + .

[0308] Intermediate 74b: 2,3-difluoro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzaldehyde The title compound was prepared in a similar manner to 2-fluoro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzaldehyde (Intermediate 46b), except that (2,3-difluoro-4-formylphenyl)boronic acid was used instead of (3-fluoro-4-formylphenyl)boronic acid. ESI-MS 595[2M+H] + .

[0309] Example 75: 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 6), except that 1-bromo-2-methoxyethane was used instead of 1,3-difluoropropan-2-yl trifluoromethanesulfonate (Intermediate 6a), and the reaction mixture was stirred at 60° C. for 3 hours. After purification, the title compound was obtained as a TFA salt. 1H NMR(400MHz,DMSO-d6)δ 9.70(bs,1H),8.41(s,1H),8.31(d,1H),8.12(d,1H),7.66-7.60(m,2H),7.30(bs,2H),7.14(s,2H),4.5 9(d,1H),3.81-3.38(m,8H),3.31(s,3H),2.75-2.25(m,4H),1.86(t,4H),1.50-1.21(m,6H).(UPLC-MS)t R 0.48 min;ESI-MS 451[M+H] + .

[0310] Example 76: 2-amino-5-(4-((1S,5R)-3-(2,2-difluoropropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 5), except that 2,2-difluoropropyl trifluoromethanesulfonate was used instead of 4-(3-bromopropyl)morpholine. 1H NMR(400MHz,DMSO-d6)δ 8.39(d,1H),8.33(d,1H),8.14(d,1H),7.60(d,2H),7.32-7.09(m,4H),4.59(bs,1H),3.74(bs,1H),3.11 (d,1H),2.98-2.63(m,5H),1.89-1.83(m,5H),1.63(t,3H),1.42-1.25(m,6H),0.81(bs,1H).(UPLC-MS)t R 0.82 min;ESI-MS 471[M+H] + .

[0311] Example 77: 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(2,2,2-trifluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (Example 6), except that 2,2,2-trifluoroethyl trifluoromethanesulfonate was used instead of 1,3-difluoropropan-2-yl trifluoromethanesulfonate (Intermediate 6a), and the reaction mixture was stirred at 60° C. for 1 hour. 1H NMR(400MHz,DMSO-d6)δ 8.39(d,1H),8.32(d,1H),8.13(d,1H),7.60(d,2H),7.24(d,2H),7.16(s,2H),4.58(s,1H),3.73(dt,1H),3.41( m,4H),3.13(d,1H),2.93(d,1H),2.84(dd,1H),1.92-1.77(m,5H),1.51-1.15(m,5H),0.84(dd,1H).(UPLC-MS)t R 1.03 minutes;ESI-MS 475[M+H] + .

[0312] Example 78: 2-amino-N-((1r,4S)-4-hydroxycyclohexyl-4-d)-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was prepared by using 2-amino-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 71a) instead of 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c) to obtain the trans-4-aminocyclopropanediol (Eq. 1). Prepared in a similar manner as (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b) except that trans-4-aminocyclohexan-1-d-1-ol hydrochloride (Intermediate 78a) was used instead of hexanol. The crude product was purified first by prepHPLC (Method 1a) and then by reverse phase flash chromatography (Method 3a) to give the title compound as a colorless solid. 1H NMR(400MHz,DMSO-d6)δ 8.38(d,1H),8.31(d,1H),8.11(d,1H),7.58(d,2H),7.22(d,2H),7.12(s,2H),4.56(s,1H),3.73(dt,1H),3.37(s,1H) ,3.06(d,1H),2.57(d,1H),2.49-2.41(m,2H),1.93-1.73(m,5H),1.31(m,5H),1.04(dd,6H),0.74(dd,1H).(UPLC-MS)t R 0.50 min;ESI-MS 436[M+H] + .

[0313] Intermediate 78a: trans-4-aminocyclohexan-1-d-1-ol hydrochloride Deuterated aminocyclohexyl starting materials can be prepared using methods similar to those known in the art (e.g., Quirante, J. et al, J. Org. Chem. 67(7):2323-2328(2002)). For example, tert-butylbenzyl(4-oxocyclohexyl)-carbamate can be reduced with NaBD4 to give deuterated tert-butylbenzyl((1r,4r)-4-hydroxy-cyclohexyl)carbamate, which can be incorporated by the synthetic methods described herein after deprotection of the tert-butyloxycarbonyl and benzyl protecting groups.

[0314] Example 79: 2-amino-N-((1s,4s)-4-hydroxycyclohexyl)-5-(4-(4-methylpiperazine-1-carbonyl)phenyl)nicotinamide TFA salt [ka] The title compound was prepared in a similar manner to 2-amino-N-cyclohexyl-5-(4-(3-(piperidin-1-yl)propoxy)phenyl)nicotinamide (Example 43), except that 2-amino-5-bromo-N-((1s,4s)-4-hydroxycyclohexyl)nicotinamide (Intermediate 79a) was used instead of 2-amino-5-bromo-N-cyclohexylnicotinamide (Intermediate 43a) and (4-methylpiperazin-1-yl)(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanone was used instead of 1-(3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)propyl)piperidine. The reaction was carried out in a microwave reactor (irradiation time of 15 min at 80° C.). The title compound was obtained as a TFA salt. 1H NMR(400MHz,DMSO-d6)δ 10.01(s,2H),8.56(d,1H),8.51(d,1H),8.43(d,1H),7.85(d,2H),7.57(d,2H),3.86-3.55(m,3H),3.55-3.20 (m,4H),3.40-3.15(m,3H),2.85(s,3H),1.85-1.70(m,2H),1.70-1.65(m,2H),1.65-1.40(m,4H).(HPLC-MS)t R 0.35 min; ESI-MS 438[M+H] + .

[0315] Intermediate 79a: 2-amino-5-bromo-N-((1s,4s)-4-hydroxycyclohexyl)nicotinamide The title compound was prepared in a similar manner to 2-amino-5-bromo-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide (Intermediate 3c), except that cis-4-aminocyclohexanol was used instead of trans-4-aminocyclohexanol. (UPLC-MS)t R 0.53 min;ESI-MS 314 / 316[M+H] + .

[0316] Example 80: 2-amino-5-(4-((1R,5S)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide [ka] The title compound is 5-(4-((1R,5S)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide HCl salt instead of 5-(4-((1R,5S)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide (intermediate 1a). Prepared in a similar manner to 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(1-(methylsulfonyl)piperidin-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide (Example 1), except using (Intermediate 34a) and using 4,4-difluorocyclohexanone instead of 1-(methylsulfonyl)piperidin-4-one. 1H NMR(400MHz,DMSO-d6)δ 8.32(d,1H),7.95(d,1H),7.76(s,1H),7.55(d,2H),7.21(d,2H),6.88(s,2H),4.28(s,1H),3.36(s,1H),3.07(s,1H),2.55 (s,1H),2.45(s,1H),2.32(d,1H),2.30-1.95(m,8H),1.77(d,5H),1.70-1.32(m,8H),1.27(t,1H),0.75(s,1H).(UPLC-MS)t R 0.63 min;ESI-MS 537[M+H] + .

[0317] Example 81: 2-amino-5-(2-chloro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide TFA salt [ka] The title compound was prepared in a similar manner to 2-amino-5-(3-fluoro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide (Example 46), except that (R)-2-(2-chloro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione (Intermediate 81a) was used instead of (R)-2-(3-fluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione (Intermediate 46a). UPLC-HRMSt R 3.45 minutes 457.24 / 459.24[M+H] + .

[0318] Intermediate 81a: (R)-2-(2-chloro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione The title compound was prepared in a similar manner to (R)-2-(3-fluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione (Intermediate 46a), except that 3-chloro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocane-2-yl)benzaldehyde (Intermediate 81b) was used instead of 2-fluoro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocane-2-yl)benzaldehyde (Intermediate 46b). ESI-MS 365 / 367[M+H] + .

[0319] Intermediate 81b: 3-chloro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzaldehyde The title compound was prepared in a similar manner to 2-fluoro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzaldehyde (Intermediate 46b), except that (2-chloro-4-formylphenyl)boronic acid was used instead of (3-fluoro-4-formylphenyl)boronic acid. ESI-MS 313 / 315 [M+H2O+H] + .

[0320] Example 82: 2-amino-5-(4-((1R,5S)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide [ka] The title compound was synthesized by using 2-amino-5-(4-((1R,5S)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 82a) instead of 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c). Prepared in a similar manner to (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b) except trans-4-amino-1-methylcyclohexanol was used instead of trans-4-aminocyclohexanol. The crude product was purified by prepHPLC (Method 1a) to give the title compound, which was obtained as the TFA salt. 1H NMR(400MHz,DMSO-d6)δ 8.37(s,1H),8.26(d,1H),8.09(d,1H),7.57(d,2H),7.23(d,2H),7.08(s,2H),4.33(s,1H),3.81(bs,1H),3.39(d,2H),2.62-2.56( (UPLC-MS)t R 0.61 min;ESI-MS 525[M+H] + .

[0321] Intermediate 82a: 2-amino-5-(4-((1R,5S)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid The title compound was prepared in a similar manner to 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 2c), except that methyl 2-amino-5-(4-((1R,5S)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate (Intermediate 82b) was used instead of (1R,5S)-tert-butyl 1-(4-(6-amino-5-(methoxycarbonyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1d). (UPLC-MS)t R 0.46 min;ESI-MS 414[M+H] + .

[0322] Intermediate 82b: Methyl 2-amino-5-(4-((1R,5S)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate The title compound was prepared in a similar manner to methyl 2-amino-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinate (Intermediate 14b), except that 4,4-difluorocyclohexanone was used instead of dihydro-2H-pyran-4(3H)-one. (UPLC-MS)t R 0.72 min; ESI-MS 428[M+H] + .

[0323] Example 83: 2-amino-N-(3-(2-hydroxypropan-2-yl)bicyclo[1.1.1]pentan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide [ka] The title compound was synthesized by the synthesis of trans-4-aminocyclohexane using 2-amino-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 14a) instead of 2-amino-5-(4-((1R,5S)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinic acid (Intermediate 1c). Prepared in a similar manner to (1R,5S)-tert-butyl 1-(4-(6-amino-5-(((1r,4R)-4-hydroxycyclohexyl)carbamoyl)pyridin-3-yl)phenyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (Intermediate 1b) except that 2-(3-aminobicyclo[1.1.1]pentan-1-yl)propan-2-ol hydrochloride (Intermediate 83a) was used instead of dihydrohexanol. The crude product was purified by prepHPLC (Method 1a) to give the title compound. 1H NMR(400MHz,DMSO-d6)δ 8.98(s,1H),8.37(s,1H),8.15(s,1H),7.57(d,2H),7.20(d,2H),7.18(s,2H),4.15(s,1H),3.85-3.79(m,2H),3.38(bs,1H) ,3.08(bs,1H),2.55-2.25(m,5H),1.90(s,6H),1.89-1.71(m,3H),1.39-1.22(m,3H),1.06(s,6H),0.75(bs,1H).(UPLC-MS)t R 0.59 min;ESI-MS 503[M+H] + .

[0324] Intermediate 83a: 2-(3-aminobicyclo[1.1.1]pentan-1-yl)propan-2-ol hydrochloride tert-Butyl (3-(2-hydroxypropan-2-yl)bicyclo[1.1.1]pentan-1-yl)carbamate (Intermediate 83b, 298 mg, 1.235 mmol) was stirred in HCl saturated ethanolic solution (3.8 mL) at room temperature for 29 h. The reaction mixture was concentrated under reduced pressure to give the title compound as the crude hydrochloride salt, which was used without further purification. 1H-NMR (400 MHz, DMSO-d6) δ 8.51 (s, 3H), 1.78 (s, 6H), 1.03 (s, 6H).

[0325] Intermediate 83b: tert-Butyl (3-(2-hydroxypropan-2-yl)bicyclo[1.1.1]pentan-1-yl)carbamate To a solution of methyl 3-((tert-butoxycarbonyl)amino)bicyclo[1.1.1]pentane-1-carboxylate (679 mg, 2.81 mmol) in anhydrous THF was added dropwise 3M methylmagnesium bromide in THF (4.13 mL, 12.4 mmol) at −78° C. under argon atmosphere. The reaction mixture was allowed to warm to room temperature, stirred for 4 h, and then slowly diluted with 2 mL of MeOH under temperature control. The mixture was concentrated under reduced pressure and the crude product was purified by normal phase chromatography (Method 2a) to give the title compound. (UPLC-MS)t R 0.22 min;ESI-MS 142[M+H] + indicates loss of a BOC group under ionizing conditions.

[0326] Example 84: 2-amino-N-cyclohexyl-5-(3-(morpholine-4-carbonyl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-cyclohexyl-5-(4-(3-(piperidin-1-yl)propoxy)phenyl)nicotinamide (Example 43), except 3-(morpholine-4-carbonyl)phenylboronic acid was used instead of 1-(3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)propyl)piperidine. 1H NMR(400MHz,DMSO-d6)δ 8.45(s,1H),8.38(d,1H),8.18(s,1H),7.78(d,1H),7.71(s,1H),7.52(t,1H),7.34(d,1H),7.20(s,2H),3.85-3.70(m,1H),3.70 -3.50(m,8H),1.90-1.80(m,2H),1.80-1.70(m,2H),1.70-1.55(m,1H),1.35-1.29(m,4H),1.28-1.05(m,1H).(HPLC-MS)t R 1.52 min; APCI-MS 409 [M+H] + .

[0327] Example 85: 2-amino-5-(3-chloro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(3-fluoro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide (Example 46), except that (R)-2-(3-chloro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione (Intermediate 85a) was used instead of (R)-2-(3-fluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione (Intermediate 46a). (UPLC-MS)t R0.79 min;ESI-MS 457 / 459[M+H] + .

[0328] Intermediate 85a: (R)-2-(3-chloro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione The title compound was prepared in a similar manner to (R)-2-(3-fluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione (Intermediate 46a), except that 2-chloro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocane-2-yl)benzaldehyde (Intermediate 85b) was used instead of 2-fluoro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocane-2-yl)benzaldehyde (Intermediate 46b). ESI-MS 365 / 367[M+H] + .

[0329] Intermediate 85b: 2-chloro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzaldehyde The title compound was prepared in a similar manner to 2-fluoro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzaldehyde (Intermediate 46b), except that (3-chloro-4-formylphenyl)boronic acid was used instead of (3-fluoro-4-formylphenyl)boronic acid. ESI-MS 591 [2M+H] + .

[0330] Example 86: 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1r,4R)-4-hydroxy-1-methylcyclohexyl)nicotinamide [ka] To a solution of 2-amino-5-bromo-N-((1r,4r)-4-hydroxy-1-methylcyclohexyl)nicotinamide (Intermediate 86a, 100 mg, 0.152 mmol) in dioxane (3 mL) was added (R)-6-(1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl)-2-oxa-6-azaspiro[3.3]heptane (Intermediate 86b, 100 mg, 0.152 mmol), PdCl2(dppf) (5.57 mg, 7.62 μmol), and 2N aqueous NaOH (0.152 mL, 0.305 mmol) at room temperature under nitrogen atmosphere. The reaction mixture was stirred at 80° C. for 2 h and then diluted with EtOAc and water. After two extractions with EtOAc, the combined organic layers were washed with a saturated aqueous solution of NaHCO3 and brine, respectively. After drying over MgSO4, filtration, and concentration under reduced pressure, the crude product was purified by normal phase chromatography (Method 2b) to give the title compound. 1H NMR(400MHz,DMSO-d6)δ 8.37(s,1H),8.05(bs,1H),7.70(s,1H),7.62(bs,2H),7.38(bs,2H),6.92(bs,2H),4.62(s,4H),4.47(s,1H),3.4 8-3.42(m,1H),3.40-3.35(m,4H),3.27-3.20(m,2H),3.15(bs,1H),1.60(m,2H),1.65-1.16(m,13H).(UPLC-MS)t R 0.52 min;ESI-MS 451[M+H] + .

[0331] Intermediate 86a: 2-amino-5-bromo-N-((1r,4r)-4-hydroxy-1-methylcyclohexyl)nicotinamide. The title compound was prepared in a similar manner to 2-amino-5-bromo-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide intermediate 3c), except that trans-4-amino-4-methylcyclohexanol was used instead of trans-4-aminocyclohexanol. (UPLC-MS)t R 0.70 min;ESI-MS 328 / 330[M+H] + .

[0332] Intermediate 86b: (R)-6-(1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl)-2-oxa-6-azaspiro[3.3]heptane The title compound was prepared in a similar manner to 1-(3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4-isopropylpiperazine (Intermediate 8a), except that (R)-6-(1-(4-bromophenyl)ethyl)-2-oxa-6-azaspiro[3.3]heptane (Intermediate 3b) was used instead of 1-(4-bromo-3-fluorophenyl)-4-isopropylpiperazine (Intermediate 8b). (UPLC-MS)t R 0.70 min;ESI-MS 330[M+H] + .

[0333] Example 87: 2-amino-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)-5-(2-methyl-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-5-(3-fluoro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide (Example 46), except that (R)-6-methyl-2-(2-methyl-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-1,3,6,2-dioxazaborocane-4,8-dione (Intermediate 87a) was used instead of (R)-2-(3-fluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione (Intermediate 46a). (UPLC-MS)t R 0.65 min; ESI-MS 437[M+H] + .

[0334] Intermediate 87a: (R)-6-methyl-2-(2-methyl-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-1,3,6,2-dioxazaborocane-4,8-dione The title compound was prepared in a similar manner to (R)-2-(3-fluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione (Intermediate 46a), except that 3-methyl-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocane-2-yl)benzaldehyde (Intermediate 87b) was used instead of 2-fluoro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocane-2-yl)benzaldehyde (Intermediate 46b). ESI-MS 345 [M+H] + .

[0335] Intermediate 87b: 3-Methyl-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzaldehyde The title compound was prepared in a similar manner to 2-fluoro-4-(6-methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzaldehyde (Intermediate 46b), except that (4-formyl-2-methylphenyl)boronic acid was used instead of (3-fluoro-4-formylphenyl)boronic acid. ESI-MS 568 [2M+H2O+H] + .

[0336] Example 88: 2-amino-N-cyclohexyl-5-(3-(4-(2-hydroxyethyl)piperazine-1-carbonyl)phenyl)nicotinamide [ka] The title compound was prepared in a similar manner to 2-amino-N-cyclohexyl-5-(4-(3-(piperidin-1-yl)propoxy)phenyl)nicotinamide (Example 43), except 3-(4-(2-hydroxyethyl)piperazine-1-carbonyl)phenylboronic acid was used instead of 1-(3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)propyl)piperidine. 1H NMR(400MHz,DMSO-d6)δ 8.44(s,1H),8.38(d,1H),8.17(s,1H),7.77(d,1H),7.68(s,1H),7.51 (t,1H),7.31(d,1H),7.19(s,2H),4.44(t,1H),3.85-3.70(m,1H),3.70 -3.58(m,2H),3.58-3.48(m,2H),3.48-3.35(m,2H),2.50-2.32(m,6H),1.90-1.80(m,2H) ,1.80-1.70(m,2H),1.70-1.55(m,1H),1.35-1.29(m,4H),1.28-1.05(m,1H).(HPLC-MS)t R 1.31 min; APCI-MS 452 [M+H] + .

[0337] Example 89 Salts, amorphous forms and crystalline polymorphs and polymorphs of the compound of Example 34: A) Free form modified H A800 g of 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide free form was dissolved in 3 liters of acetone. The resulting solution was stirred at 50° C. and 2 liters of water were added slowly. The mixture was stirred at 50° C. for 30 minutes and then 4 liters of water were added slowly. The mixture was stirred at 50° C. for 2 hours and cooled to 22° C. over 2 hours. The solid was separated by suction filtration, washed twice with 1 liter of 1:2 acetone:water and dried at 45° C. without vacuum for 24 hours. Approximately 660 g of 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide free form modified H A was obtained as a white solid. A is the monohydrate.

[0338] FIG. 3 shows the free form modified H A The XRPD diagram of

[0339] The corresponding peaks and their 2θ values ​​("angles") along with their relative intensities are detailed in Table A below (all 2θ values ​​are ±0.2):

[0340] [Table 1]

[0341] FIG. 4 shows the free form modified H A 1 shows an empty pan differential scanning calorimetry (DSC) diagram of 1H-HEX-1, ... A The second endothermic peak corresponds to the melting of the anhydrous form resulting from dehydration.

[0342] FIG. 5 shows the free form modified H A4 shows a thermogravimetric analysis (TGA) diagram of the above.

[0343] The TGA results show that the free form modified H A contains about 3.5% water by weight, which corresponds to about one water molecule.

[0344] FIG. 6 shows the free form modified H A The FT-IR diagram of the above. The peaks observed are as follows: wave numbers (cm -1 Units): 3481(w), 3328(m), 2931(m), 2886(w), 2863(w), 2787(w), 1632(s), 1617(m), 1584(w), 1524(s), 1459(s), 1242(m), 1090(m), 885(m), 769(m). (s=strong, m=moderate, w=weak)

[0345] B) Free form modification A: 0.5 g of 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide free form modification H A was added to 3.5 ml of acetone. The mixture was stirred at 40° C. for 1 hour and cooled to 22° C. The solid was filtered and dried at 40° C. for 12 hours. Approximately 0.4 g of educt form modified A was obtained as a white solid.

[0346] FIG. 7 shows the XRPD diagram of the free form modification A.

[0347] In Table B below, the corresponding peaks and their 2θ values ​​("angles") are detailed along with their relative intensities (all 2θ values ​​are ±0.2):

[0348] [Table 2]

[0349] FIG. 8 shows an empty pan differential scanning calorimetry (DSC) diagram of free form modification A.

[0350] Figure 9 shows the thermogravimetric analysis (TGA) diagram of the free form modification A. The TGA results suggest that the free form modification A is anhydrous.

[0351] Figure 10 is the FT-IR diagram of the free form modified A. The peaks seen are as follows: wave numbers (cm -1 Units): 3480(w), 3436(w), 3401(w), 3301(m), 2944(w), 2864(w), 2805(w), 1644(s), 1615(m), 1583(w), 1520(s), 1459(m), 1247(m), 1098(m), 883(m), 801(m). (s=strong, m=moderate, w=weak)

[0352] C) Free form anhydrous: 100 mg 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide Free form modified H A was exposed to N2 atmosphere at 25°C for 6 hours. The resulting solid was characterized by XRPD under N2 protection. The solid is the free form anhydrous 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide.

[0353] FIG. 18 shows the XRPD diagram of this anhydrous form.

[0354] D) Free form trihydrate: 100 mg 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide free form modified H Awas exposed to 80% relative humidity overnight at 25° C. The solid was characterized by XRPD at 25° C. and 80% relative humidity. The solid is the free form trihydrate of 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide.

[0355] FIG. 19 shows the XRPD diagram of the trihydrate form.

[0356] E) Fumarate-modified H A To 3.03 g of 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide free form was added 30 ml of acetone:water (80:20, v / v). The mixture was stirred at 50° C. for 0.5 h to obtain a clear solution. To the solution was slowly added a solution of 708.4 mg of fumaric acid in 15 ml of acetone:water (80:20, v / v). The resulting suspension was gradually cooled to 25° C. and stirring was continued for 12 h. The solid was separated by suction filtration, washed once with 10 mL of acetone, and exposed to ambient environment (approximately 25° C., 50% RH) overnight. 3.3 g of 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide fumarate modified H A was obtained as a white solid. A is a dihydrate.

[0357] FIG. 11 shows the fumarate-modified H A The XRPD diagram of

[0358] In Table C below, the corresponding peaks and their 2θ values ​​("angles") are detailed along with their relative intensities (all 2θ values ​​are ±0.2):

[0359] [Table 3]

[0360] FIG. 12 shows the fumarate-modified H A The DSC diagram of the fumarate-modified H A It corresponds to dehydration.

[0361] FIG. 13 shows fumarate-modified H A The thermogravimetric analysis (TGA) diagram of the fumarate-modified H A contains about 5.9% water by weight, which corresponds to about two water molecules.

[0362] FIG. 14 shows fumarate-modified H A The FT-IR diagram of the above. The peaks observed are as follows: wave numbers (cm -1 Units): 3241(m), 2951(w), 2867(w), 1669(m), 1538(m), 1456(w), 1355(m), 1249(m), 1087(w), 979(w), 885(w), 797(w). (s=strong, m=moderate, w=weak)

[0363] FIG. 15 shows fumarate-modified H A The DVS diagram of the fumarate-modified H A However, it can be estimated to be physically stable at least from 0% to 90% RH at 25°C.

[0364] FIG. 16 shows the fumarate-modified H A The DVS diagram of the fumarate-modified H A However, it can be estimated to be physically stable at 40°C and at least 10% to 90% RH.

[0365] Fumarate-modified H AIt should be noted that the free form polymorph is more stable over a wider humidity range than the free form polymorph (data not shown).

[0366] F) Fumarate Amorphous Form (Variant 1): 500 mg of 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide fumarate modified H A was added to 10 ml of ethanol at 25° C. to form a clear solution. 3 mL of heptane was then added to the solution. A white solid precipitated out. The solid was isolated by suction filtration and dried overnight under vacuum at 40° C. 380 mg of the fumarate salt amorphous form of 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide was obtained as a white solid. The amorphous form exhibits a glass transition of about 143° C. when analyzed by modulated DSC at a heating rate of 2 K / min and an amplitude temperature of 1 K for 60 seconds.

[0367] G) Fumarate Amorphous Form (Variant 2): 2-Amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide Fumarate Modification H A was heated to 150° C. at 10 K / min and then cooled to −20° C. at 20 K / min by DSC. The resulting material is 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide fumarate amorphous form, which is a white solid and shows a glass transition at about 78° C. when analyzed by DSC at a heating rate of 10 K / min.

[0368] H) Phosphate salt: 3.01 g of 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide free form was added with 30 mL of acetone:water (75:25, v / v). The resulting mixture was stirred at 50° C. for 0.5 h to obtain a clear solution. To the solution was slowly added a solution of 695.2 mg in 10 mL of acetone:water (95:5, v / v). The resulting suspension was gradually cooled to 25° C. and stirring was continued for 24 h. 1.5 mL of water was added to the suspension. The mixture was continued to stir at 50° C. for 12 h and slowly cooled to 25° C. The solid was isolated by suction filtration, washed once with 10 mL of acetone:water (90:10, v / v), and exposed to ambient conditions (approximately 25° C., 50% RH) overnight to obtain 2.7 g of 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide phosphate as a white solid.

[0369] FIG. 17 shows the XRPD diagram of the phosphate salt.

[0370] In Table D below, the corresponding peaks and their 2θ values ​​("angles") are detailed along with their relative intensities (all 2θ values ​​are ±0.2):

[0371] [Table 4]

[0372] I) Fumarate-modified H A (F) above) is in free form in several aqueous buffers. A Shows better solubility than

[0373] [Table 5]

[0374] [Table 6]

[0375] [Table 7]

[0376] [Table 8]

[0377] [Table 9]

[0378] J) The lactate, tartrate, and malate salts of Compound A may be obtained by methods similar to those described above.

[0379] K) Various solvates can be obtained from many of the salts and salt forms of Compound A above (details not shown).

[0380] Where noted in the preceding examples, XRPD, TGA, DSC, FT-IR, and DVS data were obtained using the following methods:

[0381] a) TGA method Equipment:TA Discovery,TA Discovery,New Castle,DE,USA Temperature range: 30~300℃ Scanning speed: 10°C / min Nitrogen flow rate: 20mL / min Sample mass: approx. 2 to 10 mg

[0382] b) DSC method Equipment: TA Discovery Temperature range: 30~250 or 300℃ Scanning speed: 10°C / min Nitrogen flow rate: 50mL / min Sample mass: approx. 2 mg

[0383] c) XRPD Method: All XRPD diagrams were obtained in reflectance mode.

[0384] (i) XRPD Method 1 (Figures 3, 11, 17) Equipment: Bruker D8 Advance (Bruker, Bruchsal, Germany) Detector: LYNXEYE (1D mode), Opening angle: 1.996° Irradiation: CuKα (0.15406nm) Monochromator: Nickel filter X-ray generator power: 40kV, 40mA Step size: Resolution 0.041 degrees Scanning range: 2°~45°(2θ value) Scan time: 36 minutes Primary slit: fixed illumination sample size 5mm, secondary slit: 5mm, axial solar 2.5°

[0385] (ii) XRPD Method 2 (Figure 7) Equipment:Bruker D8 Advance Detector: LYNXEYE (1D mode), Opening angle: 1.996° Irradiation: CuKα (0.15406nm) Monochromator: Nickel filter X-ray generator power: 40kV, 40mA Step size: Resolution 0.041 degrees Scanning range: 2°~45°(2θ value) Scan time: 330 seconds Primary slit: fixed illumination sample size 5mm, secondary slit: 5mm, axial solar 2.5

[0386] XRPD Method 3 (Figures 18 and 19) Equipment: Bruker D8 Advance XRPD equipped with a Cryo-RH chamber (Bruker, Bruchsal, Germany) Detector: VANTEC-1 (1D detector) Irradiation: CuKα (0.15406nm) Monochromator: Nickel filter X-ray generator power: 40kV, 40mA Step size, resolution 0.0165 degrees Scanning range: 2°~45°(2θ value) Scan time: 17 minutes Slits: Branch slit: V12, Anti-scattering slit: 10.0mm, Detection slit: 17.43mm, Primary Soller slit: 2.5°, secondary Soller slit: 2.5°

[0387] d) DVS Equipment: Advantage (Surface Measurement Systems, London, UK) Sample mass: approx. 10 mg Temperature: 25℃ dm / dt:0.002% / min

[0388] e) FT-IR Thermo Fisher Nicolet 6700 equipped with attenuated total reflectance (ATR), Thermo Fisher Scientific, Waltham, MA, USA

[0389] Biochemical Assays (Examples 90 and 91) For all biochemical assays, human recombinant proteins were expressed in baculovirus-transfected insect cells and purified. Constructs comprised the GS and kinase domains of wild-type ALK2 (aa172-499), ALK2FOP mutant (aa172-499R206H), ALK3 (aa198-525), ALK5 (aa162-503), and ALK6 (aa168-495).

[0390] Example 90: In vitro enzyme inhibition using a biochemical autophosphorylation assay (luminescence-based ADPGlo kinase activity assay) - "ADPGlo Assay" A kinase selectivity panel was set up for wild-type ALK2 (aa172-499) and ALK3 (aa198-525) measuring autophosphorylation using the ADP-Glo™ Kinase Assay (Promega, V9101).

[0391] Assays were performed in 384-well low volume microtiter assay plates in a final reaction volume of 6 μl. Dose-response curves were generated by incubating 10 nM of each kinase in 50 mM Hepes pH 7.5, 0.02% Tween 20, 0.02% BSA, 1 mM DTT, 10 μm Na3VO4, 10 mM ss-glycerol phosphate, 1 mM MgCl2, 12 mM MnCl2, and 15 μm ATP for 60 min at 32° C. in the presence or absence of compounds diluted in DMSO. The amount of ADP produced is a measure of kinase activity and is quantified using the ADP-Glo™ Kinase Assay (Promega) according to the manufacturer's instructions. ADP is converted to ATP by adding 3 μl of ADP-Glo™ Reagent and incubating for 60 min at 32° C. Subsequently, ATP is converted to a bioluminescence signal by adding 6 μl of luciferase assay reagent (kinase detection buffer + kinase detection substrate (Promega)) and further incubating for 60 min at 32 °C. For the measurement of luminescence, a PHERAstar™ Multilabel Reader was used (optical module for luminescence measurement in the wavelength range of 230 nm to 750 nm) with a measurement interval time of 0.1 s. The luminescence signal is positively correlated with the kinase activity.

[0392] The specific activities are shown in the table below.

[0393] [Table 10]

[0394] [Table 11]

[0395] [Table 12]

[0396] Example 91: In vitro enzyme inhibition using a biochemical peptide phosphorylation assay - "Caliper Assay" A kinase selectivity panel was set up to measure the phosphorylation of a substrate peptide for wild-type ALK2 (aa172-499), ALK2FOP mutant (aa172-499R206H), ALK1 (aa166-493), ALK5 (aa162-503), and ALK6 (aa168-495). The technique used in the described assay is based on the separation and quantification of substrates and products in an electric field. In the course of the kinase reaction, the peptide substrate is phosphorylated by the kinase. The transfer of the phosphate residue also causes the introduction of two additional negative charges, thus causing a change in the net charge of the phosphopeptide compared to the non-phosphorylated peptide. Due to this charge difference, the phosphorylated and non-phosphorylated peptides migrate at different rates in an electric field.

[0397] In the applied method, this separation occurs in a chip containing a complex capillary system that analyzes 12 samples simultaneously ("12-sipper chip", Caliper Technologies Corp., Mountain View, USA). To allow detection and quantification of the peptides in the capillary system, the peptides carry a fluorescent label (fluorescein). This label allows the peptides to be quantified by fluorescence intensity through the laser and detection system of the instrument (LC3000, Caliper Life Sciences).

[0398] Assays were performed in 384-well low-volume microtiter assay plates in a final reaction volume of 9 μl. Dose-response curves were generated by incubating 10 nM of each kinase with 2 μM of fluorescently labeled substrate peptide 5-Fluo-Ahx-KKYQAEEN-T-YDEYENKK-amid (10 mM stock solution in DMSO) for 60 min at 30°C in 50 mM Hepes pH 7.5, 0.02% Tween 20, 0.02% BSA, 1 mM DTT, 10 μM Na3VO4, 10 mM ss-glycerol phosphate, 1 mM MgCl2, 12 mM MnCl2 (ALK1 and ALK6 7 mM), and 15 μM ATP in the presence or absence of compounds diluted in DMSO.

[0399] The kinase reaction was stopped by adding 15 μl of STOP buffer (100 mM HEPES pH 7.5, 5% DMSO, 0.1% Caliper coating reagent, 10 mM EDTA, and 0.015% Brij35).

[0400] The plates with stopped kinase reactions were transferred to a Caliper LC3000 workstation (Caliper Technologies Corp. Mountain View USA) for reading. The relative amount of phosphorylated peptide, r, was calculated using the height of the substrate peak, s, and the product peak, p: r=p / (p+s). The specific activity is shown in the table below.

[0401] [Table 13]

[0402] [Table 14]

[0403] [Table 15]

[0404] [Table 16]

[0405] Example 92: BMP signaling reporter gene assay A human liver hepatocellular carcinoma cell line (HuH7) stably transfected with a reporter plasmid consisting of a BMP response element (BRE) derived from the Id1 promoter fused to a luciferase reporter gene was generated by lentiviral transduction.

[0406] Cells were maintained at 37°C, 5% CO2 in DMEM (GIBCO #41965 high glucose supplemented L-glutamine), 10% FCS (Amimed #2-01F10-I), 1% Pen / Strp (Amimed #4-01F00), and 5ug / ml Blastidicin (InvivoGen #ant-bl-1). Assays were performed in 384-well flat-bottom polystyrene microtiter plates (cell culture treated) with sterile lids. 16 hours prior to the assay, cells were starved by medium change in medium without blasticidin and FCS. Prior to the assay, cells were detached from stock flasks using trypsin / EDTA and counted. A cell suspension in the same medium, without blasticidin and FCS, was prepared. 2x10 cells were added in a total volume of 40ul to each well of the plate already containing serial dilutions of each compound in DMSO (final DMSO concentration 0.5%). 4 Cells were added. Cells and compounds are incubated for 1 hour at 37° C., 5% CO2 before stimulation with 5 μl / well of recombinant BMP6 (R&D Systems #507-BP / CF) at a final concentration of 100 ng / ml. Assay plates are incubated for an additional 5 hours at 37° C., 5% CO2 before measuring luciferase levels.

[0407] The amount of expressed luciferase is quantified using the Steady-Glo® Luciferase Assay System (Promega #E2520). 5 μl of Steady-Glo® Reagent is added to each well and mixed by vigorously shaking the plate before measuring luminescence 1 sec / well in a PHERAstar® Multilabel Reader (optical module for luminescence measurement in the wavelength range of 230 nm to 750 nm).

[0408] Further specific activities of the compounds of the invention are set forth in the table below.

[0409] [Table 17]

[0410] [Table 18]

[0411] Example 93: In vivo efficacy in a pediatric FOP (fibrodysplasia ossificans progressiva) mouse model Ubiquitous heterozygous expression of the FOP causing BMP type I receptor Alk2 R206H mutant in mice results in perinatal lethality ( Chakkalakal et al., 2012 ).

[0412] To study the postnatal role of Alk2(R206H) in young organisms as a preclinical mouse model of FOP, inducible Alk2(R206H) mutant mice (Prof. D. Goldhamer, UConn, ASBMR abstract, 2013) are needed, which carry a floxed stop cassette inserted upstream of the mutant exon that makes the expression of the mutant allele Cre-recombinase dependent. They were crossed with Rosa26-CreERt2 mice, allowing for a temporally and spatially defined heterozygous expression of Alk2(R206H).

[0413] Here, ubiquitously inducible Alk2(R206H) heterozygous mice were used together with tamoxifen (tam)-inducible CreER-loxP technology. Successful induction of Alk2(R206H) expression is achieved following tamoxifen administration to 1-week-old male and female Alk2(R206H);Rosa26-CreERt2 mice.

[0414] FOP flare-ups are induced through deep muscle injury by local intramuscular (i.m.) injection of cardiotoxin (CTX) and concomitant i.m. injection of adenovirus, which produces an Alk2(R206H)-dependent local FOP flare-up. CTX induces injury in skeletal muscle through inhibition of Ca / Mg-ATPase in the plasma membrane and induction of calcium release from the sarcoplasmic reticulum.

[0415] One-week-old male and female Alk2(R206H);Rosa26-CreERt2 mice were weighed at the start of the experiment and daily thereafter. All pups were treated subcutaneously (sc.) with 20 mg / kg tamoxifen (tamoxifen-free base (Sigma T5648), dissolved at 8 mg / ml in 10% ethanol absolute + 90% sunflower oil (Sigma S5007)) once daily for 10 days starting at 1 week of age.

[0416] On the third day after tamoxifen injection, all pups were subjected to a local muscle injury by a single intramuscular injection of 100 μl of adenovirus plus cardiotoxin (CTX) into the gastrocnemius muscle of the right hind limb, taking care not to inject into any blood vessels and not to touch the bone with the needle. To this end, 90 μl of adenovirus (Ad-GFP-2A-iCre, catalog number 1772, Vector Biolabs; titer: 1 × 10 10PFU (plaque forming units) / mL were mixed with 10 μl of 100 μm cardiotoxin stock solution (Cardiotoxin, Cat. No. L8102, Latoxan or Cardiotoxin, Cat. No. C9759, Sigma, prepared using sterile saline. Animals were anesthetized with low dose isoflurane inhalation, the right hind limb was shaved, and the skin was disinfected with betaseptic prior to slow, careful intramuscular injection with an insulin syringe.

[0417] Therapeutic twice-daily oral treatment of Alk2(R206H) heterozygous mice was started 3 days after muscle injury and administered 2, 5, 10, and 25 mg / kg of compound A (compound of Example 34=2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide) or corresponding vehicle for 6 weeks. All mice were evaluated for heterotopic ossification every two weeks by whole body and hind limb X-ray (Faxitron device) and in vivo micro-computed tomography (μCT) imaging, starting 2 weeks after Ad / CTX application.

[0418] At necropsy, the right hindlimb was collected for ex vivo microCT imaging to determine the total extent of HO. The entire right hindlimb with attached muscles was dissected as quickly as possible and transferred to 70% ethanol at 4°C. After 24 hours, the sample was transferred to fresh 70% ethanol for high-resolution μCT imaging using a μCT40 instrument from Scanco Medical (voxel size: 16 μm, integration time: 250 ms, medium resolution, 55E (kVp), 145 μA, mode: cone beam continuous rotation, threshold 275, Gaussian filter: sigma 0.7, support 1). The total bone mass (mm3) of the ectopic bone of the hindlimb was determined. The results are shown in Figure 1. The figure shows that compound A (compound of Example 34) suppresses bone mass of the right hindlimb in vitro.

[0419] To examine the effect of compound A (compound of Example 34) on the progression of ectopic bone formation after the process has started, Alk2 (R206H) heterozygous mice were similarly injected with 100 μl adenovirus + cardiotoxin (CTX) and ectopic bone was allowed to develop for 2.5 weeks. After 2 weeks, when HO formation was confirmed, pups were randomized based on HO presence, genetic background, and sex. Treatment began 2.5 weeks after injury with vehicle or 10 mg / kg twice daily compound A and continued for 6 weeks. All mice were evaluated for ectopic bone formation every two weeks by whole body and hind limb radiography (Faxitron device) and in vivo micro-computed tomography (μCT) imaging, starting 2 weeks after Ad / CTX application.

[0420] At necropsy, the right hindlimb was collected for ex vivo microCT imaging to determine the full extent of HO. The entire right hindlimb with attached muscles was dissected as quickly as possible and transferred to 70% ethanol at 4 °C. After 24 h, samples were transferred to fresh 70% ethanol for high-resolution μCT imaging using a μCT40 instrument from Scanco Medical (voxel size: 16 μm, integration time: 250 ms, medium resolution, 55E (kVp), 145 μA, mode: cone beam continuous rotation, threshold 275, Gaussian filter: sigma 0.7, support 1). Total bone volume (mm) of the ectopic bone in the hindlimb was determined. 3 ) was determined. The results are shown in Figure 2. The results show that Compound A (the compound of Example 34) prevents the progression of bone mass in the right hind paw in vitro.

[0421] The results shown in Figures 1 and 2 demonstrate that a compound of the present invention (Compound A) inhibits heterotopic ossification when administered early after muscle injury and prevents further progression of heterotopic ossification in ALK2(R206H) mouse pups when administered after heterotopic ossification has already begun.

[0422] Example 94: Heterotopic ossification induced by midpoint Achilles tendon detachment in rats To test whether the compounds of the present invention can prevent trauma-induced heterotopic ossification (HO) of soft tissues, therapeutic efficacy in a rat model of unilateral Achilles midpoint tenotomy can be used (Rooney et al., Matrix 12:274-281, 1992). To this end, the left Achilles tendon of 8-week-old female Wistar rats (body weight 190-265 g) is completely dissected using a sterile scalpel (blade number 11) under isoflurane inhalation anesthesia, followed by analgesic treatment with 0.03 mg / kg buprenorphine applied subcutaneously every 10-12 hours for 48 hours. Prophylactic oral treatment with the compounds of the present invention (10 mg / kg q.d.) or vehicle (sodium carboxymethylcellulose:water:Tween 80, 0.5:99:0.5) is given for 10 weeks starting on the day of surgery (n=11-12 rats per group). Rats are housed individually for 3-4 days after surgery, then housed in groups of 2 animals per cage on a 12 h:12 h light:dark cycle at 25 °C and fed a standard rodent chow (3890, Provimi Kliba SA) containing 18.2% protein and 3.0% fat with an energy content of 15.8 MJ / kg, with food and water available ad libitum. Treatment efficacy is assessed longitudinally by taking radiographs (Faxitron LX-60 system) of the operated distal lower limb at 4 and 10 weeks after surgery. Ectopic bone volume is quantified in vivo by micro-computed tomography (micro-CT) (vivaCT40 device, Scanco Medical AG; 17.5 μm resolution) under isoflurane inhalation anesthesia at 6 and 9 weeks after surgery.

Claims

1. Formula (I), in free form or in pharma- ceutically acceptable salt form: 【Chemistry 1】 (In the formula, L is a bond, (CH ２ ) ｎ , -CH(CH ３ ) -, -O-(CH ２ ) ｎ -, -C(O)-, -C(O)-NH-(CH ２ ) ｎ - and n is 1, 2, 3; R １ is hydroxyl, halogen, C １ ~C ３ C optionally substituted one or more times with substituents independently selected from alkyl ３ ~C ７ Cycloalkyl; Hydroxyl, Hydroxy C １ ~C ３ a bridge C optionally substituted one or more times with substituents independently selected from alkyl; ５ ~C １０ cycloalkyl; R ２ and R ３ is H, halogen, C １ ~C ３ independently selected from alkyl; R ４ is R ７ an N-containing heterocyclic non-aromatic ring optionally comprising one or more additional heteroatoms selected from N, O or S, optionally substituted one or more times with R ７ is C １ ~C ３ Alkyl, Hydroxy C １ ~C ３ Alkyl, haloC １ ~C ３ Alkyl, C １ ~C ３ Alkoxy C １ ~C ３ Alkyl, haloC １ ~C ３ Alkoxy C １ ~C ３ Alkyl, C ２ ~C ４ Alkynyl, Cyano C １ ~C ３ Alkyl, (CH ２ ) ｍ -R ８ are independently selected from; m is 0, 1, 2 or 3; R ８ , oxo, SO ２ C １ ~C ３ Alkyl, haloC １ ~C ３ a 4-, 5-, or 6-membered saturated or unsaturated non-aromatic heterocycle comprising one or more heteroatoms selected from N, O, or S, optionally substituted one or more times with substituents independently selected from alkyl; or C optionally substituted one or more times with halo ３ ~C ６ Cycloalkyl (selected from Compound.

2. A compound of formula (I) according to claim 1 in free form or in pharma- ceutically acceptable salt form, In the formula, R ４ But, N.R. ５ R ６ ;R ７ an N-containing 5-membered heterocyclic non-aromatic ring optionally comprising one or more additional heteroatoms selected from N, O, or S, optionally substituted one or more times with and attached to the remainder of the molecule via a ring carbon atom; or R ７ and optionally comprising one or more additional heteroatoms selected from N, O, or S, attached to the remainder of the molecule via a carbon atom; R ５ and R ６ together with the N atoms to which they are attached, R ７ a 5-membered ring optionally comprising one additional heteroatom selected from N, O or S, optionally substituted one or more times with R ７ a 6-membered ring optionally comprising one additional heteroatom selected from N, O or S, optionally substituted one or more times with R ７ A seven-membered ring optionally comprising one additional heteroatom selected from N, O or S, optionally substituted one or more times with Forming a compound.

3. R ２ and R ３ is hydrogen; L is a bond; R ４ is an N-containing 6-membered heterocyclic non-aromatic bicycle optionally comprising one or more additional heteroatoms selected from N, O, or S, said ring being ７ and said ring is attached to the remainder of the molecule via a ring carbon atom; R ７ However, (CH ２ ) ｍ -R ８ and m is 0, 1, 2 or 3; R ８ But, oxo, SO ２ C １ ~C ３ Alkyl, haloC １ ~C ３ is a 6-membered saturated or unsaturated non-aromatic heterocycle comprising one or more heteroatoms selected from N, O or S, optionally substituted one or more times with substituents independently selected from alkyl; 3. A compound of formula (I) according to claim 1 or 2, in free form or in a pharma- ceutically acceptable salt form.

4. R １ The compound of formula (I), in free form or in a pharma- ceutically acceptable salt form, according to any one of claims 1 to 3, wherein is cyclohexyl substituted once with hydroxyl.

5. R １ The compound of formula (I), in free form or in a pharma- ceutically acceptable salt form, according to any one of claims 1 to 3, wherein is bicyclo[2.2.2]octanyl substituted with hydroxyl.

6. R １ The compound of formula (I), in free form or in a pharma- ceutically acceptable salt form, according to any one of claims 1 to 3, wherein is bicyclo[1.1.1]pentanyl substituted with hydroxymethyl.

7. 2-amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(1-(methylsulfonyl)piperidin-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 5-(4-(-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-(-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(3-morpholinopropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-(-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-(-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(2-fluoro-4-(4-isopropylpiperazin-1-yl)phenyl)-N-(-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-(-3-(2-fluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-(-4-hydroxycyclohexyl)-5-(4-(1-isopropylpyrrolidin-3-yl)phenyl)nicotinamide; 2-amino-N-(-4-hydroxy-4-methylcyclohexyl)-5-(4-(-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-(-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)-5-(4-(-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(3,3,3-trifluoropropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(-4-hydroxycyclohexyl)-5-(4-(pyrrolidin-3-yl)phenyl)nicotinamide; 2-amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(3-fluoro-4-hydroxycyclohexyl)-5-(4-(-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 5-(4-(2-azaspiro[3.3]heptan-2-ylmethyl)phenyl)-2-amino-N-(-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-(-4-hydroxy-4-methylcyclohexyl)-5-(4-(-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-(-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(oxetan-3-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)-5-(4-(-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(2-fluoro-4-(piperazin-1-yl)phenyl)-N-(-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-(-4-hydroxycyclohexyl)-5-(4-((2-methylpyrrolidin-1-yl)methyl)phenyl)nicotinamide; 2-amino-N-(4-hydroxycyclohexyl)-5-(4-(3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-(3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-(-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide; 2-amino-5-(4-(-3-(but-2-yn-1-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(oxetan-3-ylmethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(1-(2,2,2-trifluoroethyl)piperidin-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(2-(2,2,2-trifluoroethoxy)ethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-cyclohexyl-5-(4-(3-(piperidin-1-yl)propoxy)phenyl)nicotinamide; 2-amino-5-(4-(-3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(-4-hydroxycyclohexyl)nicotinamide; 2-Amino-N-cyclohexyl-5-(4-(4-methylpiperazine-1-carbonyl)phenyl)nicotinamide 2-amino-5-(3-fluoro-4-(2-methylpyrrolidin-1-yl)methyl)phenyl)-N-(-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-amino-N-cyclohexyl-5-(4-morpholinophenyl)nicotinamide; 2-amino-5-(4-(-3-(2,2-difluoropropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(-4-hydroxycyclohexyl)nicotinamide; 2-amino-5-(4-(-3-(2-cyanoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-cyclohexyl-5-(4-(3-morpholinopropoxy)phenyl)nicotinamide; 2-amino-N-(4-hydroxycyclohexyl)-5-(4-(3-(prop-2-yn-1-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 5-(4-(-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)-2-chlorophenyl)-2-amino-N-(-4-hydroxycyclohexyl)nicotinamide; 2-amino-5-(2-fluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-N-(-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-amino-5-(4-(-3-(2-fluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide; 2-amino-5-(4-(-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(-4-hydroxy-4-methylcyclohexyl)nicotinamide; 5-(4-(-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-(-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-amino-N-cyclohexyl-5-(4-(piperidin-1-yl)phenyl)nicotinamide; 2-amino-N-(4-hydroxy-4-methylcyclohexyl)-5-(4-(3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-(-3-(oxetan-3-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-cyclohexyl-5-(4-((2-(4-methylpiperazin-1-yl)ethyl)carbamoyl)phenyl)nicotinamide; 2-amino-N-(-4-hydroxycyclohexyl)-5-(4-(-3-(2,2,2-trifluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 5-(4-(-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-(-3-hydroxyadamantan-1-yl)nicotinamide; 2-amino-N-cyclohexyl-5-(4-(morpholine-4-carbonyl)phenyl)nicotinamide; 2-amino-N-(-4-hydroxy-4-methylcyclohexyl)-5-(4-((2-methylpyrrolidin-1-yl)methyl)phenyl)nicotinamide; 2-amino-5-(2,3-difluoro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-N-(-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-amino-N-(-4-hydroxycyclohexyl-4-d)-5-(4-(-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(-4-hydroxycyclohexyl)-5-(4-(4-methylpiperazine-1-carbonyl)phenyl)nicotinamide; 2-amino-5-(2-chloro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-N-(-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-amino-N-(3-(2-hydroxypropan-2-yl)bicyclo[1.1.1]pentan-1-yl)-5-(4-(-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-cyclohexyl-5-(3-(morpholine-4-carbonyl)phenyl)nicotinamide; 2-amino-5-(3-chloro-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)-N-(-4-hydroxy-4-methylcyclohexyl)nicotinamide; 5-(4-(-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-(-4-hydroxy-1-methylcyclohexyl)nicotinamide; 2-amino-N-(-4-hydroxy-4-methylcyclohexyl)-5-(2-methyl-4-((2-methylpyrrolidin-1-yl)methyl)phenyl)nicotinamide; and 2-Amino-N-cyclohexyl-5-(3-(4-(2-hydroxyethyl)piperazine-1-carbonyl)phenyl)nicotinamide 2. The compound of claim 1, in free form or in pharma- ceutically acceptable salt form, selected from:

8. 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(1-(methylsulfonyl)piperidin-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide; 5-(4-((S)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(3-morpholinopropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-((1R,5S)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1S,5R)-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(2-fluoro-4-(4-isopropylpiperazin-1-yl)phenyl)-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-((1S,5R)-3-(2-fluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-((1r,4r)-4-hydroxycyclohexyl)-5-(4-(1-isopropylpyrrolidin-3-yl)phenyl)nicotinamide; 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(3,3,3-trifluoropropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1r,4r)-4-hydroxycyclohexyl)-5-(4-(pyrrolidin-3-yl)phenyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1R,3S,4R)-3-fluoro-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1s,4S)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 5-(4-(2-azaspiro[3.3]heptan-2-ylmethyl)phenyl)-2-amino-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-((1R,5S)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(oxetan-3-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-((1S,5R)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-(3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)-5-(4-((1S,5R)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-Amino-5-(2-fluoro-4-(piperazin-1-yl)phenyl)-N-((1r,4r)-4-hydroxycyclohexyl)nicotinamide 2-amino-N-(3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)nicotinamide; 2-amino-N-((1r,4S)-4-hydroxy-4-methylcyclohexyl)-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-((1S,5R)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide; 2-amino-N-(3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)-5-(4-((1R,5S)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-((1S,5R)-3-(but-2-yn-1-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(oxetan-3-ylmethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(1-(2,2,2-trifluoroethyl)piperidin-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1S,5R)-3-(2-morpholinoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(2-(2,2,2-trifluoroethoxy)ethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1S,5R)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-((1R,5S)-3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide; 2-amino-5-(3-fluoro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(3,3,3-trifluoropropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-((1R,5S)-3-(2-fluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide; 2-amino-5-(4-((1R,5S)-3-(2,2-difluoropropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide; 2-amino-5-(4-((1S,5R)-3-(2-cyanoethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(prop-2-yn-1-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(prop-2-yn-1-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)-2-chlorophenyl)-2-amino-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide; 2-amino-5-(2-fluoro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-amino-5-(4-((1R,5S)-3-(2-fluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide; 2-amino-5-(4-((1S,5R)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxy-4-methylcyclohexyl)nicotinamide; 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-amino-5-(4-((1R,5S)-3-(but-2-yn-1-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-((1r,4S)-4-hydroxy-4-methylcyclohexyl)-5-(4-((1S,5R)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1S,5R)-3-(oxetan-3-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(oxetan-3-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-cyclohexyl-5-(4-((2-(4-methylpiperazin-1-yl)ethyl)carbamoyl)phenyl)nicotinamide; 2-amino-5-(4-((1S,5R)-3-(1,3-difluoropropan-2-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-((1r,4S)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-(2,2,2-trifluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1R,3R)-3-hydroxyadamantan-1-yl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(oxetan-3-ylmethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1s,4R)-4-hydroxycyclohexyl)-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)-5-(4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)nicotinamide; 2-amino-5-(4-((1S,5R)-3-(2-fluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide; 2-amino-5-(2,3-difluoro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(2-methoxyethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(4-((1S,5R)-3-(2,2-difluoropropyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4S)-4-hydroxycyclohexyl)nicotinamide; 2-amino-N-((1r,4R)-4-hydroxycyclohexyl)-5-(4-((1R,5S)-3-(2,2,2-trifluoroethyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1r,4S)-4-hydroxycyclohexyl-4-d)-5-(4-((1S,5R)-3-isopropyl-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-N-((1s,4s)-4-hydroxycyclohexyl)-5-(4-(4-methylpiperazine-1-carbonyl)phenyl)nicotinamide; 2-amino-5-(4-((1R,5S)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)nicotinamide; 2-amino-5-(2-chloro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-amino-5-(4-((1R,5S)-3-(4,4-difluorocyclohexyl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide; 2-amino-N-(3-(2-hydroxypropan-2-yl)bicyclo[1.1.1]pentan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide; 2-amino-5-(3-chloro-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)nicotinamide; 5-(4-((R)-1-(2-oxa-6-azaspiro[3.3]heptan-6-yl)ethyl)phenyl)-2-amino-N-((1r,4R)-4-hydroxy-1-methylcyclohexyl)nicotinamide; and 2-Amino-N-((1r,4R)-4-hydroxy-4-methylcyclohexyl)-5-(2-methyl-4-(((R)-2-methylpyrrolidin-1-yl)methyl)phenyl)nicotinamide 2. The compound of claim 1, in free form or in pharma- ceutically acceptable salt form, selected from:

9. In the free form, in the fumarate form or in the phosphate form, especially in the free form modified H Ａ or as A, amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide.

10. in fumarate form or in phosphate form, especially fumarate-modified H Ａ Amino-N-(4-hydroxybicyclo[2.2.2]octan-1-yl)-5-(4-((1R,5S)-3-(tetrahydro-2H-pyran-4-yl)-3-azabicyclo[3.1.0]hexan-1-yl)phenyl)nicotinamide as the compound of formula (I).

11. 11. A pharmaceutical composition comprising a therapeutically effective amount of a compound according to any one of claims 1 to 10, or a pharma- ceutically acceptable salt thereof, and one or more pharma- ceutically acceptable carriers.

12. 11. A method of inhibiting ALK-2 receptor activity in a subject, comprising the step of administering to the subject a therapeutically effective amount of a compound according to any one of claims 1 to 10, or a pharma- ceutically acceptable salt thereof.

13. 11. A method for treating a disorder or disease selected from heterotopic ossification or fibrodysplasia ossificans progressiva, comprising the step of administering to said subject a therapeutically effective amount of a compound according to any one of claims 1 to 10 or a pharma-ceutical acceptable salt thereof.

14. A compound according to any one of claims 1 to 10 or a pharma- ceutically acceptable salt thereof for use as a medicament.

15. 11. A compound according to any one of claims 1 to 10, or a pharma- ceutically acceptable salt thereof, for use in the treatment of a disorder or disease selected from heterotopic ossification or fibrodysplasia ossificans progressiva.

16. 13. Use of a compound according to any one of claims 1 to 10, or a pharma- ceutically acceptable salt thereof, in the manufacture of a medicament for treating a disorder or disease selected from heterotopic ossification or fibrodysplasia ossificans progressiva.

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