Salts of an epidermal growth factor receptor kinase inhibitor
The present invention provides a salt form and compositions thereof, which are useful as an inhibitor of EGFR kinases and which exhibits desirable characteristics for the same.
1. A process for preparing Compound 2:
wherein:
n is 1 or 2; and
X is benzenesulfonic acid, camphor sulfonic acid, 1,2-ethane disulfonic acid, hydrobromic acid, hydrochloric acid, maleic acid, methanesulfonic acid, naphthalene-2-sulfonic acid, 1,5-naphthalene disulfonic acid, oxalic acid, 4-toluenesulfonic acid or 2,4,6-trihydroxybenzoic acid;
comprising a step of combining Compound 1:
with at least one equivalent of an acid selected from benzenesulfonic acid, camphor sulfonic acid, 1,2-ethane disulfonic acid, hydrobromic acid, hydrochloric acid, maleic acid, methanesulfonic acid, naphthalene-2-sulfonic acid, 1,5-naphthalene disulfonic acid, oxalic acid, 4-toluenesulfonic acid and 2,4,6-trihydroxybenzoic acid to form Compound 2.
2. The process of claim 1 , wherein the acid is hydrobromic acid.
3. The process of claim 2 , wherein the step comprises combining Compound 1 with one equivalent of hydrobromic acid.
4. The process of claim 3 , further comprising a step of precipitating from a solvent a crystalline solid form of Compound 2.
5. The process of claim 4 , wherein the crystalline solid form of Compound 2 is Form I hydrobromic acid salt characterized by one or more peaks in a powder X-ray diffraction pattern selected from those at about 17.39, about 19.45, about 21.41, about 23.56 and about 27.45 degrees 2-theta.
6. The process of claim 4 , wherein the crystalline solid form of Compound 2 is a Form III hydrobromic acid salt characterized by one or more peaks in a powder X-ray diffraction pattern selected from those at about 6.79, about 13.36, about 19.93, about 20.89, about 21.90, about 22.70, about 22.91 and about 26.34 degrees 2-theta.
7. The process of claim 4 , wherein the solvent comprises 1,4-dioxane.
8. The process of claim 7 , wherein the crystalline solid form of Compound 2 is a Form IV hydrobromic acid salt characterized by one or more peaks in a powder X-ray diffraction pattern selected from those at about 6.45, about 12.96, about 19.38, about 19.79, about 21.37 and about 21.58 degrees 2-theta.
9. The process of claim 4 , wherein the solvent comprises dimethylformamide.
10. The process of claim 9 , wherein the crystalline solid form of Compound 2 is a Form V hydrobromic acid salt characterized by one or more peaks in a powder X-ray diffraction pattern selected from those at about 6.17, about 6.99, about 12.50, about 14.14, about 17.72 and about 23.12 degrees 2-theta.
11. The process of claim 4 , wherein the solvent comprises dimethylsulfoxide.
12. The process of claim 11 , wherein the crystalline solid form of Compound 2 is a Form VI hydrobromic acid salt characterized by one or more peaks in a powder X-ray diffraction pattern selected from those at about 8.38, about 9.38, about 18.93, and about 21.58 degrees 2-theta.
13. The process of claim 11 , wherein the crystalline solid form of Compound 2 is a Form VII hydrobromic acid salt characterized by one or more peaks in a powder X-ray diffraction pattern selected from those at about 15.91, about 19.10, about 19.53, about 20.24, about 22.64 and about 25.58 degrees 2-theta.
14. The process of claim 4 , wherein the solvent comprises acetone and water.
15. The process of claim 14 , wherein the crystalline solid form of Compound 2 is a Form VIII hydrobromic acid salt characterized by one or more peaks in a powder X-ray diffraction pattern selected from those at about 8.79, about 11.13, about 19.97, about 21.31, about 21.56, about 25.30 and about 26.65 degrees 2-theta.
16. The process of claim 2 , wherein the step comprises combining Compound 1 with two equivalents of hydrobromic acid.
17. The process of claim 1 , wherein the acid is benzenesulfonic acid.
18. The process of claim 17 , wherein the step comprises combining Compound 1 with one equivalent of benzenesulfonic acid.
19. The process of claim 17 , wherein the step comprises combining Compound 1 with two equivalents of benzenesulfonic acid.
20. The process of claim 19 , further comprising a step of precipitating from a solvent a crystalline solid form of Compound 2.
21. The process of claim 20 , wherein the solvent comprises acetone.
22. The process of claim 21 , wherein the crystalline solid form of Compound 2 is a bis-benzenesulfonic acid salt characterized by one or more peaks in a powder X-ray diffraction pattern selected from those at about 10.68, about 16.10, about 18.44 and about 22.36 degrees 2-theta.