Claims for Patent: 10,266,523

Summary for Patent: 10,266,523

Title:	Crystaline forms of N-[6-(cis-2,6-dimethylmorpholine-4-yl)pyridine-3-yl]-2-Methyl-4′-(trifluoromethoxy) [1,1′-biphenyl]-3-Methanamide monophosphate, and process of preparation thereof
Abstract:	The present disclosure relates to novel crystalline forms of N-[6-(cis-2,6-dimethylmorpholine-4-yl)pyridine-3-yl]-2-methyl-4′-(trifluoromethoxy) [1,1′-biphenyl]-3-carboxamide monophosphate, and process of preparation thereof. The crystalline form of the monophosphate of a compound of formula (I) has low hygroscopicity, is convenient to store, has better stability than that of diphosphonate in prior art, can avoid the risk of crystal transformation in the development and production of the drug. The preparation method is simple, has low cost, and has important value for further optimization and development of the drug.
Inventor(s):	Minhua Chen, Yanfeng Zhang, Fei Lu, Xiaoyu Zhang
Assignee:	Sun Pharmaceutical Industries Ltd
Application Number:	US15/579,881
Patent Claims:	1. A monophosphate of formula (I): 2. A crystalline Form A of the monophosphate of formula (I) according to claim 1, wherein the X-ray powder diffraction pattern shows characteristic peaks at 2theta values of 17.5°±0.2°, 5.1°±0.2° and 13.0°±0.2°. 3. The crystalline Form A of the monophosphate of formula (I) according to claim 2, wherein the X-ray powder diffraction pattern further shows one or two or three of the characteristic peaks at 2theta values of 18.0°±0.2°, 16.3°±0.2° and 24.4°±0.2°. 4. The crystalline Form A of the monophosphate of formula (I) according to claim 2, wherein the X-ray powder diffraction pattern further shows one or two or three of the characteristic peaks at 2theta values of 20.5°±0.2°, 9.8°±0.2° and 13.9°±0.2°. 5. A process of preparing crystalline Form A of the monophosphate of formula (I) according to claim 2, comprising reacting the compound of formula (I) with concentrated phosphoric acid in water or solvents containing water, and drying the obtained solid at 100° C.-200° C. 6. The process of preparation according to claim 5, wherein said solvents containing water comprise solvents of alcohols, ketones, esters, aromatic hydrocarbons, halogenated hydrocarbons, nitriles, cyclic ethers, aliphatic hydrocarbons mixed with water. 7. A process of preparing crystalline Form A of the monophosphate of formula (I) according to claim 2, comprising adding the hydrochloride of compound of formula (I) into one or more solvents selected from the group of water, alcohols, ketones, acids, esters or nitriles, and then adding sodium hydroxide solution, stirring to obtain a solid, reacting the obtained solid with concentrated phosphoric acid in water or solvents containing water, then drying the obtained solid at the temperature of 100-200° C. 8. The process of preparing crystalline Form A according to claim 7, wherein said alcohol is methanol. 9. The process of preparing crystalline Form A according to claim 7, wherein said solvents contain water and comprise solvents of alcohols, ketones, esters, aromatic hydrocarbons, halogenated hydrocarbons, nitriles, cyclic ethers, or aliphatic hydrocarbons mixed with water. 10. A crystalline Form B of monophosphate of formula (I) according to claim 1, wherein the X-ray powder diffraction pattern shows characteristic peaks at 2theta values of 19.2°±0.2°, 9.7°±0.2° and 16.5°±0.2°. 11. The crystalline Form B according to claim 10, wherein the X-ray powder diffraction pattern further shows one or two or three of the characteristic peaks at 2theta values of 19.6°±0.2°, 29.6°±0.2° and 12.6°±0.2°. 12. The crystalline Form B according to claim 10, wherein the X-ray powder diffraction pattern further shows one or two or three of the characteristic peaks at 2theta values of 17.2°±0.2°, 15.4°±0.2° and 25.0°±0.2°. 13. A process of preparing crystalline Form B according to claim 10, comprising reacting the compound of formula (I) with concentrated phosphoric acid in water or solvents containing water, and drying the obtained solid at 50° C.-80° C. 14. The process according to claim 13, wherein said solvents containing water comprise solvents of alcohols, ketones, esters, aromatic hydrocarbons, halogenated hydrocarbons, nitriles, cyclic ethers, aliphatic hydrocarbons mixed with water. 15. A process of preparing crystalline Form B according to claim 10, comprising adding the hydrochloride of compound of formula (I) into one or more solvents selected from the group of water, alcohols, ketones, acids, esters or nitriles, then stirring and crystallizing at the temperature of 50-80° C. 16. The process according to claim 15, wherein said acid is acetic acid, said nitrile is acetonitrile, said ketone is acetone, and said alcohol is methanol. 17. A process of preparing crystalline Form B according to claim 10, comprising adding the hydrochloride of compound of formula (I) into one or more solvents selected from the group of water, alcohols, ketones, acids, esters or nitriles, then adding sodium hydroxide solution, stirring to obtain a solid, reacting the obtained solid with concentrated phosphoric acid in water or solvents containing water, then drying the obtained solid at the temperature of 50-80° C. 18. The process according to claim 17, wherein said alcohol is methanol. 19. The process according to claim 17, wherein said solvents containing water comprise solvents of alcohols, ketones, esters, aromatic hydrocarbons, halogenated hydrocarbons, nitriles, cyclic ethers, aliphatic hydrocarbons mixed with water. 20. A pharmaceutical composition comprising an effective amount of the the monophosphate of formula (I) according to claim 1 and a pharmaceutically acceptable carrier, diluent or excipient. 21. A pharmaceutical composition comprising an effective amount of the crystalline Form A of the monophosphate of formula (I) according to claim 2, and a pharmaceutically acceptable carrier, diluent or excipient. 22. A pharmaceutical composition comprising an effective amount of the crystalline Form B of the monophosphate of formula (I) according to claim 10, and a pharmaceutically acceptable carrier, diluent or excipient.