FIELD: chemistry.
SUBSTANCE: invention relates to the field of organic chemistry, namely to a derivative of quinoline pyrrolidine-2-one by the formula (I), an isomer or a pharmacologically acceptable salt thereof, where E is selected from -N(R5)-, -O- and -C(R6)(R7)-; R1 is selected from a C1-3 alkyl and a C3-6 cycloalkyl; R 2 constitutes H; R 3 is selected from H, F, Cl; R4 is selected from a C1-6 alkyl and N(Rc)(Rd); R5 is selected from H, a C1-6 alkyl, a C3-6 cycloalkyl, a C1-6 alkyl-C=O-, a C1-6 alkyl-O-C=O- and a C3-6 cycloalkyl-C=O-, wherein said C1-6 alkyl is optionally substituted with 1, 2 or 3 Re; each of R6 and R7 is independently selected from H, F, OH, a C1-6 alkyl and a C1-6 alkoxy; L1 is selected from a single bond and -(CH2)m-O-; m is selected from 1, 2 and 3; ring B constitutes a 5-6-membered heteroaryl; each of Rc and Rd is independently selected from a C1-3 alkyl and a C3-6 cycloalkyl; or Rc and Rd jointly with the N atom whereto they are attached form a 5-6-membered heterocycloalkyl, optionally substituted with 1 R; Re constitutes F; R constitutes F; and each of said 5-6-membered heteroaryl and 5-6-membered heterocycloalkyl independently comprises 1 or 2 heteroatoms independently selected from -NH- and N. The invention also relates to a specific derivative of quinoline pyrrolidine-2-one and an application thereof for producing a medicinal product capable of inhibiting ATM kinase.
EFFECT: production of new heterocyclic compounds useful in treatment of diseases associated with inhibition of ATM kinase.
19 cl, 2 dwg, 5 tbl, 38 ex
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Authors
Dates
2022-04-29—Published
2019-09-27—Filed