FIELD: chemistry.
SUBSTANCE: invention relates to a compound of formula (I), including stereoisomers or tautomeric forms thereof, or a pharmaceutically acceptable salt thereof. In formula (I): R1 is represented by formula (g-1), R2, R3, R4, R5, R7 and R11 are H; R6 is selected from H, halogen, C1-4alkyl and C1-4alkyl substituted with one or more F atoms; R8 and R9 are independently selected from H and C1-6alkyl, wherein each of C1-6alkyl is optionally substituted with one or more substitutes selected from C1-4alkyl, OH, OCH3, -CO2H, -CO2C1-4alkyl and C3-6heterocycle containing one heteroatom N, where C3-6heterocycle is optionally substituted with one or more substitutes selected from oxo; provided that R8 and R9 do not simultaneously represent H; or where R8 and R9 are joined together to form a C3-6heterocycle containing one N heteroatom, optionally substituted with one or more substitutes selected from OH and CO2H; R10 is selected from H, CN, halogen and heteroaryl containing three N heteroatoms; X is N or CR12; R12 is selected from H, F, Cl, CN. Also disclosed is a method of producing said compound and a pharmaceutical composition containing said compound.
EFFECT: disclosed compounds are PD-L1 inhibitors and can be used in treating infectious diseases and cancer.
22 cl, 2 tbl, 3 ex
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Authors
Dates
2024-08-06—Published
2020-06-05—Filed