FIELD: chemistry.
SUBSTANCE: invention relates to compounds of formula (I), in which R1, R2 are independently selected from H and alkyl; R7 and R9 are independently selected from H and halogen; R8 and R11 together form -CH2-CH2-; R10 is H or R10 and R11 together form - (CH2)w-; A is -C(O)- or -S(O)2-; B is -C- or -N-; R12 is alkyl, cycloalkyl or substituted heteroaryl, where the substituted heteroaryl is a monovalent aromatic monocyclic ring system of 3-6 ring carbon atoms and 1 or 2 heteroatoms selected from N, where the substituted heteroaryl is substituted with one to three substitutes independently selected from H, alkyl and halogen; R13 is halogen, cyano or alkoxy; R14 is H; m and n are 0; p is from 0 and 1; w is 1, 2 or 3; and to their pharmaceutically acceptable salts. Invention also relates to a pharmaceutical composition inhibiting aldosterone synthase based on said compounds.
(I).
EFFECT: obtaining novel compounds and pharmaceutical compositions based thereon, which can be used in medicine for treating chronic renal disease, congestive heart failure, hypertension.
23 cl, 2 tbl, 49 ex
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Authors
Dates
2019-05-28—Published
2014-05-26—Filed