FIELD: pharmaceuticals.
SUBSTANCE: invention relates to a compound of formula I or a pharmaceutically acceptable salt thereof, compounds specified in 6 claims, having FGFR activity inhibitor properties, pharmaceutical compositions based thereon, use thereof in preparing a drug for treating or preventing diseases, as well as a method of treating or preventing diseases mediated by FGFR. In general formula (I), rings A and R, each independently, are selected from a group consisting of substituted or unsubstituted 6-member heteroaryl groups with 1 to 2 nitrogen atoms, and in the presence of substitution, A or R can be substituted with one or two substituents in any position, and such substitute is independently selected from a group consisting of halogen, cyano, C1-C8 alkyl, -C(O)R1, -OR1 and - NR2R3, wherein said alkyl group is optionally substituted with one substitute selected from a group consisting of -OR4; X is NR7; Y is -C(O)-; R1, R2, R3 and R4, each independently selected from a group consisting of hydrogen and C1-C8 alkyl; R7 is C1-C8 alkyl.
EFFECT: heterocyclic compound used as FGFR inhibitor.
12 cl, 26 ex
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Authors
Dates
2021-02-08—Published
2017-06-13—Filed