Pharmaceutical salts N-(2-(2-(dimethylamino)ethoxy)-4-methoxy-5-((4-(1-methyl-1H-indol-3-yl)pyrimidin-2-yl)amino)phenyl)acrylamide and crystalline forms thereof
Crystalline forms of N-(2-(2-(dimethylamino)ethoxy)-4-methoxy-5-((4-(1-methyl-1H-indol-3-yl)pyrimidin-2-yl)amino)phenyl)acrylamide (1) and its pharmaceutically acceptable salts and compositions thereof useful for the treatment or prevention of diseases or medical conditions mediated through mutated forms of epidermal growth factor receptor (EGFR), such as various cancers, are disclosed.
1. A crystalline form of the compound of formula 1, namely N-(2-(2-(dimethylamino)ethoxy)-4-methoxy-5-((4-(1-methyl-1H-indol-3-yl)pyrimidin-2-yl)amino)phenyl)acrylamide (free base), having an X-ray powder diffraction pattern comprising the following 2θ values measured using CuKα radiation: 8.5°±0.2°, 16.7°±0.2°, and 25.2°±0.2°
2. The crystalline form of claim 1 , wherein the X-ray powder diffraction pattern further comprises two or more of the following 2θ values measured using CuKα radiation: 9.5°±0.2°, 12.2°±0.2°, 12.5°±0.2°, 15.7°±0.2°, 16.0°±0.2°, 19.4°±0.2°, 19.7°±0.2°, 20.0°±0.2°, 23.2°±0.2°, 24.4°±0.2°, and 28.5°±0.2°.
3. The crystalline form of claim 1 , having a melting point with an onset temperature at about 169.6° C. and/or a peak temperature at about 171.7° C. as measured by differential scanning calorimetry.
4. A crystalline form of N-(2-(2-(dimethylamino)ethoxy)-4-methoxy-5-((4-(1-methyl-1H-indol-3-yl)pyrimidin-2-yl)amino)phenyl)acrylamide methanesulfonate salt (formula 2) having a molar ratio of about 1:1 between methanesulfonic acid and free base, designated as Form 2A, having an X-ray powder diffraction pattern comprising the following 2θ values measured using CuKα radiation: 12.6°±0.2°, 15.5°±0.2°, 17.9°±0.2°, 22.1°±0.2°, and 25.2°±0.2°
5. The crystalline form of claim 4 , wherein the X-ray powder diffraction pattern further comprises two or more of the following 2θ values measured using CuKα radiation: 11.1°±0.2°, 13.8°±0.2°, 14.7°±0.2°, 16.7°±0.2°, 19.3°±0.2°, 20.9°±0.2°, 23.2°±0.2°, and 25.8°±0.2°.
6. The crystalline form of claim 4 , having a melting point with an onset temperature at about 233.3° C. and/or a peak temperature at about 238.1° C. as measured by differential scanning calorimetry.
7. A crystalline form of N-(2-(2-(dimethylamino)ethoxy)-4-methoxy-5-((4-(1-methyl-1H-indol-3-yl)pyrimidin-2-yl)amino)phenyl)acrylamide methanesulfonate salt (formula 2) having a molar ratio of about 1:1 between methanesulfonic acid and free base, designated as Form 2B, having an X-ray powder diffraction pattern comprising three or more of the following 2θ values measured using CuKα radiation: 9.7°±0.2°, 12.8°±0.2°, 15.7°±0.2°, 18.2°±0.2°, 20.3°±0.2°, 25.1°±0.2°, 25.6°±0.2°, and 26.8°±0.2°
8. A crystalline form of N-(2-(2-(dimethylamino)ethoxy)-4-methoxy-5-((4-(1-methyl-1H-indol-3-yl)pyrimidin-2-yl)amino)phenyl)acrylamide hydrochloride salt (formula 3) having a molar ratio of about 1:1 between hydrochloride acid and free base, having an X-ray powder diffraction pattern comprising three or more of the following 2θ values measured using CuKα radiation: 8.5°±0.2°, 11.2°±0.2°, 18.1°±0.2°, 22.4°±0.2°, 23.5°±0.2°, and 26.3°±0.2°.
9. The crystalline form of claim 8 , wherein the X-ray powder diffraction pattern further comprises two or more of the following 2θ values measured using CuKα radiation: 9.0°±0.2°, 12.7°±0.2°, 16.1°±0.2°, 17.3°±0.2°, 18.7°±0.2°, 20.6°±0.2°, 21.8°±0.2°, and 25.4°±0.2°.
10. The crystalline form of claim 8 , having a melting point with an onset temperature at about 266.6° C. and/or a peak temperature at about 269.5° C. as measured by differential scanning calorimetry.
11. A crystalline form of N-(2-(2-(dimethylamino)ethoxy)-4-methoxy-5-((4-(1-methyl-1H-indol-3-yl)pyrimidin-2-yl)amino)phenyl)acrylamide sulfate salt (formula 4) having a molar ratio of about 1:1 between sulfuric acid and free base, having an X-ray powder diffraction pattern comprising three or more of the following 2θ values measured using CuKα radiation: 5.6°±0.2°, 7.3°±0.2°, 11.0°±0.2°, 11.9°±0.2°, 14.3°±0.2°, 18.1°±0.2°, 19.0°±0.2°, 19.6°±0.2°, 19.9°±0.2°, 22.2°±0.2°, 24.9°±0.2°, and 26.3°±0.2°.
12. The crystalline form of claim 11 , having a melting point with an onset temperature at about 152.3° C. and/or a peak temperature at about 167.1° C. as measured by differential scanning calorimetry.
13. A crystalline form of N-(2-(2-(dimethylamino)ethoxy)-4-methoxy-5-((4-(1-methyl-1H-indol-3-yl)pyrimidin-2-yl)amino)phenyl)acrylamide p-toluenesulfonate (p-tosylate) salt (formula 5) having a molar ratio of about 1:1 between p-toluenesulfonic acid and free base, having an X-ray powder diffraction pattern comprising three or more of the following 2θ values measured using CuKα radiation: 6.8°±0.2°, 7.3°±0.2°, 10.3°±0.2°, 11.3°±0.2°, 13.1°±0.2°, 15.6°±0.2°, 18.2°±0.2°, 20.5°±0.2°, 19.9°±0.2°, 22.7°±0.2°, 23.3°±0.2°, 27.1°±0.2°, and 29.7°±0.2°.
14. The crystalline form of claim 13 , having a melting point with an onset temperature at about 152.3° C. and/or a peak temperature at about 167.1° C. as measured by differential scanning calorimetry.
15. A crystalline form of N-(2-(2-(dimethylamino)ethoxy)-4-methoxy-5-((4-(1-methyl-1H-indol-3-yl)pyrimidin-2-yl)amino)phenyl)acrylamide citrate salt (formula 6) having a molar ratio of about 1:1 between citric acid and free base, having an X-ray powder diffraction pattern comprising three or more of the following 2θ values measured using CuKα radiation: 5.9°±0.2°, 8.0°±0.2°, 13.2°±0.2°, 19.0°±0.2°, 25.6°±0.2°, and 26.5°±0.2°.
16. The crystalline form of claim 15 , wherein the X-ray powder diffraction pattern further comprises two or more of the following 2θ values measured using CuKα radiation: 12.6°±0.2°, 16.0°±0.2°, 16.6°±0.2°, 17.0°±0.2°, 18.5°±0.2°, 20.3°±0.2°, 23.2°±0.2°, and 25.8°±0.2°.
17. A pharmaceutical composition comprising a crystalline form of claim 4 , and a pharmaceutically acceptable carrier, adjuvant, diluent, and/or vehicle.
18. A pharmaceutical composition comprising a crystalline form of claim 1 , and a pharmaceutically acceptable carrier, adjuvant, diluent, and/or vehicle.
19. A pharmaceutical composition comprising a crystalline form of claim 7 , and a pharmaceutically acceptable carrier, adjuvant, diluent, and/or vehicle.
20. A pharmaceutical composition comprising a crystalline form of claim 8 , and a pharmaceutically acceptable carrier, adjuvant, diluent, and/or vehicle.
21. A pharmaceutical composition comprising a crystalline form of claim 11 , and a pharmaceutically acceptable carrier, adjuvant, diluent, and/or vehicle.
22. A pharmaceutical composition comprising a crystalline form of claim 13 , and a pharmaceutically acceptable carrier, adjuvant, diluent, and/or vehicle.
23. A pharmaceutical composition comprising a crystalline form of claim 15 , and a pharmaceutically acceptable carrier, adjuvant, diluent, and/or vehicle.