FIELD: pharmaceuticals.
SUBSTANCE: proposed is a compound by the formula (II), a stereoisomer, prodrug or pharmacologically acceptable salt thereof, wherein X constitutes CH; R1 is selected from the group consisting of a C1-3 alkyl, a C5 cycloalkyl and a 4-6-membered heterocyclyl, optionally substituted with one or multiple additional substituents, R2 constitutes phenyl, pyridyl or pyrazolyl, optionally substituted with one or multiple additional substituents; R3 constitutes a methoxy; R4 is independently selected from the group consisting of H, F and Cl; R10 constitutes a C1 alkyl; R13 and R14 each independently constitute a C1 alkyl; r is 2; wherein, unless otherwise indicated, the heteroatom of heterocyclyl in the above substituents is selected from 1-2 nitrogen or oxygen atoms. Also proposed are a method for production and an application of a compound acting as an FGFR inhibitor for treating tumours, malignant neoplasms, myeloproliferative diseases, diseases of cells of bone and cartilaginous tissue, and hypophosphatemia.
EFFECT: production of heteroaromatic compounds applicable as an FGFR inhibitor.
9 cl, 10 ex, 2 tbl
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Authors
Dates
2022-05-05—Published
2019-07-23—Filed