FIELD: pharmaceuticals.
SUBSTANCE: invention relates to a compound having formula (I), or a stereoisomer or a pharmaceutically acceptable salt thereof, which has RIP-1 kinase inhibitory activity. In formula (I), T1 is selected from N and CR1t; T2 is selected from N and CR2t; T3 is CR3t; T4 is CR4t; E1 is selected from C(R1e)2 and O; cycle A is selected from 1,2,4-triazolyl, where 1,2,4-triazolyl, optionally substituted with 1, 2 or 3 halogens or C1-3 alkyls; cycle B is selected from phenyl and L is selected from a single bond, O and C1-3 alkylene; R1 is selected from H and C1-3 alkyl, where C1-3 alkyl is optionally substituted with 1, 2 or 3 Rb substituents; R1t, R2t, R3t and R4t are each independently selected from H, F, Cl, Br, I, CN, C1-3 alkyl, COOH and -C(=O)NH2; R1e is each independently selected from H and C1-3 alkyl; R2 is each independently selected from H, F, Cl, Br, I, CN, C1-3 alkyl and C1-3 alkoxy, where C1-3 alkyl and C1-3 alkoxy are optionally substituted with 1, 2 or 3 substituents Rf; n is 1, 2, 3, 4 or 5; Rb and Rf are each independently selected from F, Cl, Br, I and D. The invention also relates to particular compounds and to the use of the said compounds in the manufacture of a medicinal product for the treatment of a disease associated with RIP-1 kinase.
EFFECT: obtaining bicyclic compound as RIP-1 kinase inhibitor.
16 cl, 8 tbl, 42 ex
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Authors
Dates
2023-07-25—Published
2020-05-29—Filed