Claims for Patent: 9,181,223

Summary for Patent: 9,181,223

Title:	2-aminopyrimidin-6-ones and analogs exhibiting anti-cancer and anti-proliferative activities
Abstract:	Described are compounds of Formula I which find utility in the treatment of cancer, autoimmune diseases and metabolic bone disorders through inhibition of c-FMS (CSF-1R), c-KIT, and/or PDGFR kinases. These compounds also find utility in the treatment of other mammalian diseases mediated by c-FMS, c-KIT, or PDGFR kinases.
Inventor(s):	Michael D. Kaufman, Daniel L. Flynn, Yumi AHN, Lakshminarayana Vogeti, Timothy Malcolm Caldwell
Assignee:	Deciphera Pharmaceuticals LLC
Application Number:	US14/214,171
Patent Claims:	1. A compound of Formula I, or a pharmaceutically acceptable salt, enantiomer, stereoisomer, or tautomer thereof, wherein A is taken from the group consisting of —N(R2)R3 and G; G is selected from the group consisting of and wherein the symbol (**) is the point of attachment to the pyrimidine ring; each G moiety may be further substituted with one, two, or three R4 moieties; W is C5-C6heteroaryl, phenyl, —NHC(O)R6, —NHC(O)R7, —NHC(O)N(R8)R9 or —C(O)N(R8)R9, and wherein each C5-C6heteroaryl or phenyl is optionally substituted by one, two, or three R5 moieties; X1 and X2 are individually and independently hydrogen or C1-C6 alkyl; R1 is hydrogen, C1-C6 alkyl, deutero-C1-C6 alkyl wherein the alkyl chain is partially or completely deuterated, or branched C3-C8 alkyl; R2 is hydrogen, C1-C6 alkyl, deutero-C1-C6 alkyl wherein the alkyl chain is partially or completely deuterated, branched C3-C8 alkyl, C3-C8 cycloalkyl, fluoroC1-C6alkyl wherein the alkyl is fully or partially fluorinated, —(CH2)m—OR8, or a 3-8 membered heterocyclic ring, wherein each alkylene is optionally substituted with C1-C4 alkyl; R3 is hydrogen, C1-C6 alkyl, deutero-C1-C6 alkyl wherein the alkyl chain is partially or completely deuterated, branched C3-C8 alkyl, C3-C8 cycloalkyl, fluoroC1-C6alkyl wherein the alkyl is fully or partially fluorinated or a 3-8 membered heterocyclic ring; each R4 is individually and independently hydrogen, halogen, C1-C6 alkyl, fluoro-C1-C6 alkyl wherein the alkyl chain is partially or completely fluorinated, branched C3-C8 alkyl, C3-C8 cycloalkyl, —(CH2)m—OR8, —(CH2)m—NR8(R9), —(CH2)m—R7, or cyano, wherein each alkylene is optionally substituted with C1-C4 alkyl; each R5 is individually and independently hydrogen, C1-C6 alkyl, deutero-C1-C6 alkyl wherein the alkyl chain is partially or completely deuterated, branched C3-C8 alkyl, halogen, cyano, fluoro-C1-C6 alkyl wherein the alkyl chain is partially or completely fluorinated, —(CH2)m—C(O)NR8(R9), —(CH2)m—C(O)R7, —(CH2)m—OR8, —(CH2)m—NR8(R9), or —(CH2)m—R7, wherein each alkylene is optionally substituted with C1-C4 alkyl; Each R6 is individually and independently hydrogen, C1-C6 alkyl, branched C3-C8 alkyl, C3-C8 cycloalkyl, —(CH2)m—CN, —(CH2)m—OR8, —(CH2)m—NR8(R9), or —(CH2)m—R7, wherein each alkylene is optionally substituted with C1-C4 alkyl; each R7 is independently and individually selected from the group consisting of and wherein the symbol (##) is the point of attachment to respective W, R5 or R6 moieties containing a R7 moiety; each R7 is optionally substituted with —(R10)p; each R8 and R9 is individually and independently hydrogen, C1-C6 alkyl, fluoro-C1-C6 alkyl wherein the alkyl chain is partially or completely fluorinated, or branched C3-C8 alkyl; each R10 is individually and independently C1-C6 alkyl, —(CH2)m—CN, —(CH2)m—OR3, —(CH2)m—NR8(R9), or —(CH2)m—C(O)—R6, wherein each alkyl or alkylene is optionally substituted with one or two C1-C6 alkyl; wherein each alkylene is optionally substituted with C1-C4 alkyl each m is individually and independently 0, 1, 2, or 3; and each p is 0, 1, 2, or 3. 2. The compound of claim 1 wherein the compound is a compound of Formula Ia, or a pharmaceutically acceptable salt, enantiomer, stereoisomer, or tautomer thereof. 3. The compound of claim 2 wherein R3 is hydrogen. 4. The compound of claim 3 wherein the compound is a compound of Formula Ib, 5. The compound of claim 4 wherein one of X1 and X2 is C1-C6alkyl and the other is hydrogen. 6. The compound of claim 5, wherein R1 is hydrogen. 7. The compound of claim 5, wherein R1 is C1-C6alkyl. 8. The compound of claim 1 wherein the compound is a compound of Formula Ic, or a pharmaceutically acceptable salt, enantiomer, stereoisomer, or tautomer thereof. 9. The compound of claim 8 wherein the compound is a compound of Formula Id, 10. The compound of claim 9 wherein one of X1 and X2 is C1-C6alkyl and the other is hydrogen. 11. The compound of claim 10, wherein R1 is hydrogen. 12. The compound of claim 10, wherein R1 is C1-C6alkyl. 13. A compound selected from the group consisting of 2-(ethylamino)-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one, 2-(dimethylamino)-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one, 2-(isopropylamino)-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one, 2-(ethylamino)-5-(6-methyl-5-((6′-methyl-[2,3′-bipyridin]-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one, 2-(ethylamino)-5-(6-methyl-5-((2-(4-methyl-1H-imidazol-1-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one, 2-((2-methoxyethyl)amino)-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one, 5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)-2-(methylamino)pyrimidin-4(3H)-one, 2-(ethylamino)-5-(5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one, 5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)-2-(pyrrolidin-1-yl)pyrimidin-4(3H)-one, 2-(isopropylamino)-3-methyl-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one, 4-((6-(2-(isopropylamino)-6-oxo-1,6-dihydropyrimidin-5-yl)pyridin-3-yl)oxy)-N-methylpicolinamide, 5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)-2-morpholinopyrimidin-4(3H)-one, 5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)-2-(piperidin-1-yl)pyrimidin-4(3H)-one, 2-(cyclopropylamino)-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one, 2-(cyclopentylamino)-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one, 3-methyl-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)-2-(pyrrolidin-1-yl)pyrimidin-4(3H)-one, 2-(cyclopropylamino)-3-methyl-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one, 2-(isopropylamino)-5-(4-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one, N-(4-((6-(2-(isopropylamino)-6-oxo-1,6-dihydropyrimidin-5-yl)-2-methylpyridin-3-yl)oxy)pyridin-2-yl)acetamide, 5-(4-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)-2-(pyrrolidin-1-yl)pyrimidin-4(3H)-one, 5-(5-((2-(1-ethyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)-6-methylpyridin-2-yl)-2-(isopropylamino)pyrimidin-4(3H)-one, (R)-2-((1-methoxypropan-2-yl)amino)-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one, (R)-2-(2-(methoxymethyl)pyrrolidin-1-yl)-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one, (S)-2-(3-(dimethylamino)pyrrolidin-1-yl)-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one, 2-(ethylamino)-3-methyl-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one, 2-((2-methoxyethyl)amino)-3-methyl-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one, 5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)pyrimidin-4(3H)-one, 2-(tert-butylamino)-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one, 5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)-2-(neopentylamino)pyrimidin-4(3H)-one, and 2-(3,3-difluoropyrrolidin-1-yl)-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one. 14. A pharmaceutical composition, comprising a compound of claim 13 and a pharmaceutically acceptable carrier. 15. The compound 2-(ethylamino)-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one. 16. A pharmaceutical composition, comprising the compound of claim 15 and a pharmaceutically acceptable carrier. 17. The composition of claim 16 further comprising an additive selected from adjuvants, excipients, diluents, or stabilizers. 18. The compound 2-(isopropylamino)-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one. 19. A pharmaceutical composition, comprising the compound of claim 18 and a pharmaceutically acceptable carrier. 20. The composition of claim 19 further comprising an additive selected from adjuvants, excipients, diluents, or stabilizers. 21. The compound 2-(isopropylamino)-3-methyl-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one. 22. A pharmaceutical composition, comprising the compound of claim 21 and a pharmaceutically acceptable carrier. 23. The composition of claim 22 further comprising an additive selected from adjuvants, excipients, diluents, or stabilizers. 24. A pharmaceutical composition, comprising a compound of claim 1 and a pharmaceutically acceptable carrier. 25. The composition of claim 24 further comprising an additive selected from adjuvants, excipients, diluents, or stabilizers. 26. A method of treating gastrointestinal stromal tumors, melanomas, glioblastomas, ovarian cancer, pancreatic cancer, prostate cancer, lung cancers, breast cancers, renal cancers, hepatic cancers, osteosarcomas, multiple myelomas, cervical carcinomas, cancers that are metastatic to bone, papillary thyroid carcinoma, non-small cell lung cancer, colonic cancers, rheumatoid arthritis, osteoarthritis, autoimmune nephritis, lupus, Crohn's disease, asthma, chronic obstructive pulmonary disease, osteoporosis, mastocytosis, or mast cell leukemia, the method comprising administering to a human patient in need thereof an effective amount of a compound of claim 1, or a pharmaceutically acceptable salt, enantiomer, stereoisomer, or tautomer thereof. 27. A method of treating glioblastomas, breast cancers, pancreatic cancers, or cancers that are metastatic to bone, the method comprising administering to a human patient in need thereof an effective amount of a compound of claim 1, or a pharmaceutically acceptable salt, enantiomer, stereoisomer, or tautomer thereof. 28. The method of claim 26, wherein the compound is administered orally, parenterally, by inhalation, or subcutaneously. 29. The method of claim 27, wherein the compound is administered orally, parenterally, by inhalation, or subcutaneously.