FIELD: pharmaceuticals.
SUBSTANCE: invention relates to compounds of general formula (I), stereoisomers or pharmaceutically acceptable salts thereof, where in formula (I) R1 and R2 each independently denotes H, C1-C8 alkyl, C1-C5 acyl, each of which is optionally substituted by at least one of halide, hydroxyl, C1-C5 alkoxy and C3-C6 heteroaryl, containing one or two nitrogen atoms in the ring optionally substituted with methyl; or R1 and R2 together with the nitrogen atom to which they are bonded, form 4–7-member saturated ring which optionally includes O, or 5-member aromatic ring, which contains N; R3 denotes H or linear C1-C8 alkyl optionally substituted with hydroxyl; or R1 or R2 together with R3 and a carbon atom and a nitrogen atom, with which each is bonded, form 5-member saturated ring, which optionally includes at least one of NH, O and C=O; R4 and R8 denote H; R5 denotes a halide or C1-C8 alkyl optionally substituted with at least one halogenide; R6 denotes C1-C8 alkyl, C5-C6 cycloalkyl or 4–6-member saturated heterocyclyl containing an oxygen atom in the ring; R7 denotes C1-C8 alkyl substituted with C3-C7 cycloalkyl. Invention also relates to specific compounds specified in the patent claim, to methods of inhibiting and a method of treating malignant diseases.
(I)
EFFECT: technical result is pyrazolopyrimidine derivatives of formula (I) as inhibitors of casein kinase I (CKI) and kinase 1 associated with interleukin-1 receptor (IRAK1).
40 cl, 3 tbl, 42 dwg
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Authors
Dates
2020-11-03—Published
2016-08-04—Filed