FIELD: pharmaceuticals.
SUBSTANCE: invention relates to a compound of formula (I) or a pharmaceutically acceptable salt thereof, a pharmaceutical composition based on it for the treatment of a disease associated with the CRBN protein, its use for the preparation of a medicinal product for the treatment of a disease associated with the CRBN protein, as well as a method of treating a disease associated with the CRBN protein. In the general formula (I), n is selected from the group consisting of 0, 1 and 2; each R1 is independently selected from the group consisting of F, Cl, Br, OH, NH2, C1-6-alkyl, C3-6-cycloalkyl, C1-6-alkoxy, C1-6-alkylamino, C2-6-alkenyl, , -S(=O)2NH2, -NHS(=O)2-C1-6-alkyl, -N[S(=O)2-C1-6-alkyl]2, -NHC(=O)-C1-6-alkyl and -C(=O)NH2, where NH2, C1-6-alkyl, C1-6-alkoxy, , -S(=O)2NH2 and -C(=O)NH2 are optionally substituted with 1 or 2 Ra; ring A is selected from the group consisting of 5–6-membered heteroaryl, phenyl and 5–6-membered heterocycloalkenyl; ring B is selected from the group consisting of phenyl; each Ra is independently selected from the group consisting of F, Cl, Br, OH, NH2, C1-6-alkyl, C1-6-alkoxy, C1-6-alkylamino, -NHC(=O)-C1-6-alkyl, C3-6-cycloalkylamino, 4–6-membered heterocycloalkyl, 5–6-membered heterocycloalkylamino and 5–6-membered heterocycloalkyl substituted with one carbonyl, where NH2, C1-6-alkyl, C1-6-alkylamino, C3-6-cycloalkylamino, 4–6-membered heterocycloalkyl and 5–6-membered heterocycloalkylamino are optionally substituted with 1 or 2 R; each R is independently selected from the group consisting of C1-3-alkyl, C1-3-alkoxy, C3-5-cycloalkyl, -C(=O)-C1-3-alkyl, -C(=O) OC1-6-alkyl, -S(=O)2-C1-3-alkyl, and ; each of 5–6-membered heteroaryl, 4–6-membered heterocycloalkyl, 5–6-membered heterocycloalkylamino and 5–6-membered heterocycloalkyl substituted with one carbonyl contains 1 or 2 heteroatoms or heteroatomic groups independently selected from the group consisting of -NH-, -O- and N.
EFFECT: obtaining tricyclic compounds affecting CRBN proteins.
20 cl, 3 dwg, 4 tbl, 84 ex
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Authors
Dates
2023-08-01—Published
2019-09-09—Filed