FIELD: pharmaceutics.
SUBSTANCE: invention relates to a compound of formula (I) or a pharmaceutically acceptable salt thereof, where R1 is independently selected from C1-6 alkyl, where C1-6 alkyl is optionally substituted with C6 aryl or C5-6 heteroaryl; where C5-6 heteroaryl contains 1 or 2 heteroatoms independently selected from nitrogen or sulfur; R2 is independently selected from H or C1-6 alkyl; Q is -CH2-or -NH-, where -CH2- is optionally substituted with C1-6 alkyl; X is C6 aryl, where C6 aryl is optionally substituted with halogen, halogen-C1-6 alkyl, C1-6 alkyl, C1-6 alkoxy, C1-6 alkylthio, C1-6 alkoxycarbonyl or C1-6 alkyl-SO2-; where Y is Invention also relates to the crystalline form of 6-methyl-4-(2-methyl-1-(4-(trifluoromethyl)benzyl)-1H-imidazo[4,5-b]pyrazin-6-yl)-1H-pyrrolo [2,3-c]pyridin-7(6H)-one, pharmaceutical composition as bromodomain-containing protein 4 (BRD4) inhibitor based on said compounds.
EFFECT: novel compounds which can be used in medicine for treating BET-mediated diseases, such as cancer, are obtained.
22 cl, 3 dwg, 9 tbl, 70 ex
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Authors
Dates
2024-05-02—Published
2018-12-20—Filed