EGFR inhibitor free base or acid salt polycrystalline form, preparation method therefor, and application
Disclosed are an EGFR inhibitor free base or acid salt polycrystalline form, a preparation method therefor, and an application thereof. The present invention specifically relates to an N-(5-((4-(1-cyclopropyl-1H-indol-3-yl)pyrimidin-2-yl)amino)-2-((2-(dimethylamino)ethyl)(methyl)amino)-4-methoxyphenyl)acrylamide free base or acid salt polycrystalline form, a preparation method therefor, and an application of the polycrystalline form in preparing a drug for treating an EGFR mutant activity-mediated disease. The present invention is used for inhibiting the activity of an L858R EGFR mutant, a T790M EGFR mutant and an exon 19 deletion activating mutant etc., may be widely applied in preventing and treating cancer, especially non-small cell lung cancer and other related diseases, and is expected to develop into a new generation of EGFR inhibitors.
1. A crystal form of a mesylate salt-of N-(5-((4-(1-cyclopropyl-1H-indol-3-yl)pyrimidin-2-yl)amino)-2-((2-(dimethylamino)ethyl)(methyl)amino)-4-methoxyphenyl)acrylamide (a compound of formula I), wherein the mesylate salt is selected from the group consisting of crystal form I of a mesylate salt, crystal form II of a mesylate salt, crystal form III of a mesylate salt, crystal form IV of a mesylate salt, crystal form V of a mesylate salt, and crystal form VI of a mesylate crystal, and wherein
an X-ray powder diffraction spectrum of crystal form I of the mesylate salt comprises peaks at diffraction angles (2θ) of 19.1±0.2°, 25.6±0.2°, 15.0±0.2° and 25.0±0.2°;
an X-ray powder diffraction spectrum of crystal form II of the mesylate salt comprises peaks at diffraction angles (2θ) of 24.3±0.2°, 20.1±0.2°, 11.0±0.2° and 20.6±0.2°;
an X-ray powder diffraction spectrum of crystal form III of the mesylate salt comprises peaks at diffraction angles (2θ) of 24.5±0.2°, 22.6±0.2°, 6.1±0.2° and 18.8±0.2°;
an X-ray powder diffraction spectrum of crystal form IV of the mesylate salt comprises peaks at diffraction angles (2θ) of 21.0±0.2°, 18.0±0.2°, 25.1±0.2° and 13.6±0.2°;
an X-ray powder diffraction spectrum of crystal form V of the mesylate salt comprises peaks at diffraction angles (2θ) of 24.6±0.2°, 23.3±0.2°, 14.9±0.2° and 20.1±0.2°; and
an X-ray powder diffraction spectrum of crystal form VI of the mesylate salt comprises peaks at diffraction angles (2θ) of 11.7±0.2°, 19.8±0.2°, 17.2±0.2° and 6.8±0.2°.
2. A pharmaceutical composition comprising a therapeutically effective amount of the crystal form of a mesylate salt according to claim 1 , and a pharmaceutically acceptable carrier.
3. Crystal form I of a mesylate salt of N-(5-((4-(1-cyclopropyl-1H-indol-3-yl)pyrimidin-2-yl)amino)-2-((2-(dimethylamino)ethyl)(methyl)amino)-4-methoxyphenyl)acrylamide, wherein an X-ray powder diffraction spectrum of crystal form I of the mesylate salt comprises peaks at diffraction angles (2θ) of 10.2±0.2°, 19.1±0.2°, 19.7±0.2°, 20.5±0.2°, 23.0±0.2°, 24.4±0.2°, 25.6±0.2°, 15.0±0.2° and 25.0±0.2°.
4. A pharmaceutical composition comprising a therapeutically effective amount of the crystal form of a mesylate salt according to claim 3 , and a pharmaceutically acceptable carrier.