Crystalline form of (S)-7-(1-acryloylpiperidin-4-yl)-2-(4-phenoxyphenyl)-4,5,6,7-tetra-hydropyrazolo[1,5-a]pyrimidine-3-carboxamide, preparation, and uses thereof
The present invention relates to a crystalline form of (S)-7-(1-acryloylpiperidin-4-yl)-2-(4-phenoxyphenyl)-4,5,6,7-tetra-hydropyrazolo[1,5-a]pyrimidine-3-carboxamide for inhibiting Btk, methods of preparation thereof and pharmaceutical compositions, and use of the crystalline form above in the treatment of a disease, or in the manufacturing of a medicament for the treatment of a disease.
1. A crystalline form of Compound 1,
wherein the crystalline form exhibits an X-ray powder diffraction pattern comprising diffraction peaks having 2 θ angle values at 14.8±0.2°, 15.6±0.2°, 16.4±0.2° and 21.4±0.2°.
2. The crystalline form of claim 1 , wherein the crystalline form is an anhydrate.
3. The crystalline form of claim 1 , having an X-ray powder diffraction pattern:
a) further comprising diffraction peaks having 20 angle values at 12.2±0.2°, 12.9±0.2°;
b) further comprising diffraction peaks having 20 angle values at 12.2±0.20, 12.9±0.2°, 17.7±0.2°, 18.5±0.2° and 20.7±0.2°; or
c) substantially similar to FIG. 1 .
4. The crystalline form of claim 2 , wherein the crystalline form has a melting point of 139±2° C. (onset temperature) or wherein the crystalline form has a differential scanning calorimetry thermogram substantially similar to FIG. 2 .
5. A method of preparing the crystalline form of claim 2 , comprising the steps of:
a) dissolving Compound 1 in EtOAc, adding hexane, and obtaining the crystalline form of Compound 1;
b) dissolving Compound 1 in an organic solvent, adding water and obtaining the crystalline form of Compound 1, wherein the organic solvent is selected from acetone or DMAc (N,N-dimethylacetaminde);
c) dissolving the crystalline form of claim 1 in an organic solvent, adding water, and obtaining the crystalline form of Compound 1, wherein the organic solvent is selected from acetone or DMAc;
d) dissolving Compound 1 in an organic solvent, adding n-heptane, and obtaining the crystalline form of Compound 1, wherein the organic solvent is selected from EtOAc, DCM, toluene or 2-MeTHF (2-methyltetrahydrofuran);
e) dissolving the crystalline form of claim 1 in an organic solvent, adding n-heptane, and obtaining the crystalline form of Compound 1, wherein the organic solvent is selected from EtOAc, DCM, toluene or 2-MeTHF;
f) dissolving Compound 1 in acetone or EtOAc to obtain a solution, placing the solution into n-heptane, evaporating at room temperature, and obtaining the crystalline form of Compound 1; or
g) dissolving the crystalline form of claim 1 in acetone or EtOAc to obtain a solution, placing the solution into n-heptane, evaporating at room temperature, and obtaining the crystalline form of Compound 1.
6. A pharmaceutical composition comprising a therapeutically effective amount of the crystalline form of claim 1 , and a pharmaceutically acceptable excipient.