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US 10,561,646 B2Granted
EGFR inhibitor and pharmaceutically acceptable salt and polymorph thereof, and use thereof
AssigneesShanghai Haiyan Pharmaceutical Technology Co., Ltd., Yangtze River Pharmaceutical Group Co., Ltd.
InventorsJiong Lan, Taotao Jiang, Daofei Li, Xing Liu
Life of this patent
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Abstract
Provided is an EGFR inhibitor and a pharmaceutically acceptable salt and a polymorph thereof, and a use thereof. In particular, provided is a polymorph, a pharmaceutically acceptable salt or a prodrug of N-(2-(4-(dimethylamino)piperid-1-yl)-5-(5-fluoro-4-(1-methyl-1H-pyrazol-4-yl) pyrimidin-2-ylamino)-4-methoxy phenyl) acrylamide. In addition, also provided is a pharmaceutical composition containing the inhibitor and a use thereof.
Claims15
A crystalline form of a compound of formula X:
- wherein the crystalline form is selected from the group consisting of:
- 1) crystalline form A of a hydrochloride salt of the compound of formula X, wherein the crystalline form A has an X-ray powder diffraction pattern with diffraction angle 2θ(°) values of the following group A1:
- 8.47±0.10, 20.32±0.10, 23.31±0.10 (the highest peak) and 25.98±0.10;
- 2) crystalline form B of a phosphate salt of the compound of formula X, wherein the crystalline form B has an X-ray powder diffraction pattern with diffraction angle 2θ(°) values of the following group B1:
- 11.94±0.10, 19.92±0.10 (the highest peak), 22.27±0.10, 23.93±0.10;
- 3) crystalline form C-1 of a maleate salt of the compound of formula X, wherein the crystalline form C-1 has an X-ray powder diffraction pattern with diffraction angle 2θ(°) values of the following group C-1-1:
- 8.73±0.10, 13.37±0.10, 18.08±0.10 and 25.55±0.10 (the highest peak);
- 4) crystalline form C-2 of the maleate salt of the compound of formula X, wherein the crystalline form C-2 has an X-ray powder diffraction pattern with diffraction angle 2θ(°) values of the following group C-2-1:7.48±0.10 (the highest peak), 8.60±0.10, 20.63±0.10 and 23.27±0.10;
- 5) crystalline form D of a L-malate salt of the compound of formula X, wherein the crystalline form D has an X-ray powder diffraction pattern with diffraction angle 2θ(°) values of the following group D1:7.47±0.10, 18.75±0.10, 22.69±0.10 (the highest peak) and 24.39±0.10;
- 6) crystalline form E of an adipate salt of the compound of formula X, wherein the crystalline form E has an X-ray powder diffraction pattern with diffraction angle 2θ(°) values of the following group E1:
- 7.43±0.10, 18.45±0.10, 21.64±0.10 (the highest peak) and 24.22±0.10;
- 7) crystalline form I of the compound of formula X, wherein the crystalline form I has an X-ray powder diffraction pattern with diffraction angle 2θ(°) values of the group I-1:
- 8.74±0.10, 9.80±0.10, 15.63±0.10, and 21.38±0.10 (the highest peak);
- 8) crystalline form II of the compound of formula X, wherein the crystalline form II has an X-ray powder diffraction pattern with diffraction angle 2θ(°) values of the group II-1:
- 9.47±0.10 (the highest peak), 17.34±0.10, 18.87±0.10, and 23.89±0.10;
- 9) crystalline form III of the compound of formula X, wherein the crystalline form III has an X-ray powder diffraction pattern with diffraction angle 2θ(°) values of the group III-1:
- 9.72±0.10, 18.41±0.10, 23.89±0.10 (the highest peak) and 28.02±0.10;
- 10) crystalline form IV of the compound of formula X, wherein the crystalline form IV has an X-ray powder diffraction pattern with diffraction angle 2θ(°) values of the group IV-1:
- 7.69±0.10 (the highest peak), 18.90±0.10;
- and
- 11) crystalline form V of the compound of formula X, wherein the crystalline form V has an X-ray powder diffraction pattern with diffraction angle 2θ(°) values of the group V-1:
- 8.28±0.10, 8.89±0.10 (the highest peak), 9.44±0.10, 17.76±0.10.
19 more elements
A process for preparing a crystalline form of a salt of a compound of formula X:
- comprising:
- 1a) contacting the compound of formula X in a free base form with a solution comprising an organic solvent and an acid to form a turbid solution;
- 2a) stirring the turbid solution for a period of 1-72 hours;
- 3a) isolating a solid from the turbid solution;
- and
- 4a) drying the solid to provide a crystalline form,
- wherein the acid is selected from the group consisting of hydrochloric acid, phosphoric acid, maleic acid, L-malic acid, and adipate acid;
- the organic solvent is selected from the group consisting of methanol, ethanol, propanol, isopropanol, butanol, acetone, acetonitrile, tetrahydrofuran, propylene glycol, and mixtures thereof;
- the molar ratio of the acid to the compound of formula X is (1-2):1;
- steps 1a) and 2a) are conducted at a temperature of 5-30° C.;
- and
- the crystalline form is selected from the group consisting of crystalline form A of a hydrochloride salt of the compound of formula X, crystalline form B of a phosphate salt of the compound of formula X, crystalline form C-1 of a maleate salt of the compound of formula X, crystalline form D of a L-malate salt of the compound of formula X, and crystalline form E of an adipate salt of the compound of formula X
- or
- 1b) contacting a solution comprising the compound of formula X in a free base form and an organic solvent with maleic acid at a reflux temperature to form a mixture comprising a precipitate;
- 2b) cooling the mixture to a temperature of 5-15° C. over a period of 1-10 hours;
- 3b) isolating the precipitate;
- and
- 4b) drying the precipitate to provide crystalline form C-1 of a maleate salt of the compound of formula X,
- wherein the organic solvent is selected from the group consisting of methanol, ethanol, propanol, isopropanol, butanol, acetone, acetonitrile, tetrahydrofuran, propylene glycol, and mixtures thereof;
- and
- the molar ratio of the maleic acid to the compound of formula X is (1-3):1.
18 more elements
A process for preparing crystalline form C-2 of a maleate salt of a compound of formula X:
- comprising:
- 1) dissolving crystalline form C-1 of a maleate salt of the compound of formula X with dichloromethane in a reaction vessel, which is then sealed and punctured with small holes;
- and
- 2) placing the reaction vessel under ventilation to allow slow natural volatilization to provide the crystalline form C-2 of the maleate salt of the compound of formula X.
1 more element
Dependencies are inferred from the claim text.