FIELD: organic chemistry.
SUBSTANCE: group of inventions includes an isoindoline derivative of general formula (I), its pharmaceutically acceptable salt, stereoisomer, a method of production of a pharmaceutical composition based on it and its use. In Formula (I), R1 and R2 are each independently selected from H and halogen, provided that R1 and R2 are not both H; X represents O; each of X1, X2 is independently selected from C or N; each of X3, X4 and X5 represents C; each of R4, R5, R6, R7 and R8 is independently absent or selected from H, halogen, unsubstituted (C1-C12)alkyl or substituted with 1–3 halogens, unsubstituted (C1-C12)alkoxy group or substituted with 1–3 substituents selected from D, halogen or (C3-C6)cycloalkyl, unsubstituted (C3-C6)cycloalkyl, -CH=CH2, -C≡ CH, -CN, -OH, -NO2, or where each of R9 and R10 is independently selected from H or unsubstituted (C1-C12 )alkyl, provided that at least one of R4, R5, R6, R7 and R8 is selected from -CN, -NO2, -CH=CH2, -C≡ CH, (C1-C12)alkyl substituted with 1–3 halogens, (C1-C12)alkoxy group substituted with 1–3 halogens, or (C1-C12)alkoxy group substituted with 1–3 D.
EFFECT: obtaining isoindoline derivative of General formula (I), used for the treatment of multiple myeloma.
15 cl, 2 tbl, 29 ex
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Authors
Dates
2023-12-14—Published
2021-01-20—Filed