FIELD: pharmaceuticals.
SUBSTANCE: invention relates to a compound of formula I or a pharmaceutically acceptable salt thereof, wherein R1 and R2 are each independently selected from hydrogen and halogen and both R1 and R2 are not hydrogen; R3 and R4 are each independently hydrogen; R5 and R6 are each independently hydrogen; L1 is missing; Cy1 is a group which is unsubstituted or substituted by one or more Ra shown in the general formula (A-1), (A-2), (A-3), (a), (b) or (c) below:
m is an integer which is either 1 or 2 and n is 0; Y1, Y2, Y3 and Y4 are each independently selected from CH2, CH, NH and C=O; X1, X2, X3, X4, X9 and X10 are each independently selected from CH, N, O and C=O; X5, X6, X7 and X8 are each independently selected from CH and N and at least one of X1, X2 and X3 is N; each Ra is independently selected from cyano, halogen, C1-6 alkyl, C1-6 alkoxy C1-6 alkyl, C1-6 alkylaminocarbonyl, aminocarbonyl, di(C1-6 alkyl)aminocarbonyl, Cy2-, Cy2-C1-6 alkyl, Cy2-carbonyl and Cy2-aminocarbonyl, unsubstituted or substituted with one to three Rb, Cy2 is a 3–6 membered cycloalkyl, 4–6 membered heterocyclyl, which refers to non-aromatic a cyclic group formed by substitution of cyclic carbon atoms from 1 to 2 heteroatoms selected from O and N, or phenyl; each Rb is independently selected from halogen, C1-6 alkyl and C1-6 alkoxy; with the proviso that when Cy1 corresponds to a group of formula (c), the group of formula (c) is substituted with one or more Ra; with the proviso that when Cy1 corresponds to formula (b), X1, X2, X3, X9 and X10 do not represent C=O; denotes a single bond or a double bond; and denotes a double bond, optionally present in the ring structure. The invention also relates to a pharmaceutical composition based on the said compound.
EFFECT: new compounds and a pharmaceutical composition based on them have been obtained, which can be used in medicine in the manufacture of a drug for the prevention and/or treatment of a disease associated with the SSAO/VAP-1 protein.
11 cl, 5 tbl, 48 ex
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Authors
Dates
2023-04-07—Published
2020-01-10—Filed