FIELD: organic chemistry.
SUBSTANCE: invention relates to a heterocyclic compound of formula (III) and/or a pharmaceutically acceptable salt thereof, where J is N; J' is CR1, where R1 is hydrogen; Ar is phenyl substituted with three or four substitutes independently selected from C1-C6 alkoxy and halogen; R2 is C1-C6 alkyl, C2-C6 alkynyl, halogen-C1-C6 alkyl, C3-C6 cycloalkyl, optionally substituted with hydroxy-group; C3-C6 cycloalkyl-C1 alkyl, hydroxy-C1-C6 alkyl, C1-C6 alkoxy-C1-C6 alkyl, C4-C6 heterocyclyl containing one heteroatom selected from O; or C5-C6 heterocyclyl-C1-C2 alkyl containing one or two heteroatoms selected from N or O; Q represents C1-C3 alkylene or C1-C3 alkylene substituted with two methyl; and X represents a group of formula (a), wherein R3 represents hydrogen or C1-C6 alkyl; and R4 denotes hydrogen or C1-C6 alkyl; Y is -CO-; Rc is hydrogen or C1-C6 alkyl; and Rd is hydrogen. Invention also relates to specific compounds of formula (III) and a pharmaceutical composition based on the compound of formula (III).
EFFECT: obtaining novel heterocyclic compounds useful as fibroblast growth factor receptor (FGFR) inhibitor, and therefore also useful for treating cancer.
14 cl, 3 dwg, 2 tbl, 162 ex
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Authors
Dates
2020-05-21—Published
2015-02-04—Filed