Hydrochloride salt forms of a sulfonamide structured kinase inhibitor
The present invention relates to novel hydrochloride salt forms of N-(2′,4′-difluoro-5-(5-(1-methyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-[1,1′-biphenyl]-3-yl)cyclopropanesulfonamide (I). Compound (I) is a selective inhibitor of FGFR/VEGFR kinase families and is useful in the treatment of cancer.
1. A compound which is hydrochloride salt of N-(2′,4′-difluoro-5-(5-(1-methyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-[1,1′-biphenyl]-3-yl)cyclopropanesulfonamide (I), wherein the compound is in crystalline form.
2. The compound according to claim 1 , wherein the compound is in crystalline form 1 and is characterized by a X-ray powder diffraction pattern comprising peaks at about 4.6, 9.6, 18.7, 19.2, 23.5, 25.0 and 26.9 degrees 2-theta.
3. The compound according to claim 1 , wherein the compound is in crystalline form 3 and is characterized by a X-ray powder diffraction pattern comprising peaks at about 7.2, 9.2, 11.6, 16.1, 18.5, 25.9 and 27.9 degrees 2-theta.
4. The compound according to claim 1 , wherein the compound is in crystalline form 5 and is characterized by a X-ray powder diffraction pattern comprising peaks at about 8.3, 9.5, 18.5, 19.8, 21.1, 23.9, 25.1 and 27.4 degrees 2-theta.
5. The compound according to claim 1 , wherein the compound is in crystalline form 8 and is characterized by a X-ray powder diffraction pattern comprising peaks at about 4.7, 14.2, 16.1, 18.0, 21.2, 23.5 and 26.5 degrees 2-theta.
6. The compound according to claim 5 , wherein the crystalline form is a monohydrate.
7. A method of preparing a compound according to claim 2 , comprising combining N-(2′,4′-difluoro-5-(5-(1-methyl-1H-pyrazol-4-yl) -1H-benzo[d]imidazol-1-yl)-[1,1′-biphenyl]-3-yl)cyclopropanesulfonamide with a mixture of aqueous hydrochloric acid and acetone, and isolating the crystalline product.
8. A method of preparing a compound according to claim 3 , comprising combining N-(2′,4′-difluoro-5-(5-(1-methyl-1H-pyrazol-4-yl) -1H-benzo[d]imidazol-1-yl)-[1,1′-biphenyl]-3-yl)cyclopropanesulfonamide with a mixture of aqueous hydrochloric acid and ethanol, and isolating the crystalline product.
9. A method of preparing a compound according to claim 4 , comprising grinding any crystalline form of hydrochloride salt of N-(2′,4′-difluoro-5-(5-(1-methyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-[1,1′-biphenyl]-3-yl)cyclopropanesulfonamide in the presence of water, and isolating the crystalline product.
10. A method of preparing a compound according to claim 5 , comprising:
(i) dissolving N-(2′,4′-difluoro-5-(5-(1-methyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-[1,1′-biphenyl]-3-yl)cyclopropanesulfonamide in a mixture of water and 2-propanol in the presence of hydrochloric acid and formic acid at elevated temperature,
(ii) cooling the mixture, and
(iii) isolating the crystalline product.
11. A pharmaceutical dosage form comprising a compound according to claim 1 and an excipient.
12. A method of treatment of treating cancer characterized by abnormal FGFR signalling, comprising administering a therapeutically effective amount of the compound according to claim 1 to a subject in need thereof.
13. The method according to claim 12 , wherein the cancer is multiple myeloma, gastric cancer, endometrial cancer, prostate cancer, breast cancer, cholangiocarcinoma, or uroepithelial carcinoma.
14. A method of preparing a compound according to claim 6 , comprising:
(i) dissolving N-(2′,4′-difluoro-5-(5-(1-methyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-[1,1′-biphenyl]-3-yl)cyclopropanesulfonamide in a mixture of water and 2-propanol in the presence of hydrochloric acid and formic acid at elevated temperature,
(ii) cooling the mixture, and
(iii) isolating the crystalline product.