FIELD: chemistry.
SUBSTANCE: invention relates to a compound represented by formula (I) or a pharmaceutically acceptable salt thereof. In formula (I), p is an integer from 0 to 3; q is an integer from 0 to 1; Z is N or CR5; every R1 independently represents a fluorine atom, a chlorine atom, a bromine atom, a cyano group, a methyl group, an ethyl group, an isopropyl group, a tert-butyl group, a vinyl group, a hydroxyethyl group, a cyclopropyl group, a difluoromethyl group, a trifluoromethyl group, a methoxy group, an ethoxyethyl group or an acetyl group, R2 represents a methyl group; every R3 independently represents a fluorine atom or a chlorine atom; R4 represents a phenyl group, a pyridyl group, a pyrolidinyl group or a morpholinyl group, moreover, the phenyl group, pyridyl group, pyrolidinyl group and morpholinyl group, which represent R4, are optionally substituted with one to two groups selected from a fluorine atom, a methyl group, a trifluoromethyl group, a methoxy group, and a methoxymethyl group; R5 represents a hydrogen atom, a fluorine atom; ring A, which is represented by partial structural formula (II), is a 5–6 membered monocyclic heteroaryl group, which has a structure in that the pyrazole ring is directly connected in position 4 to position α in relation to the nitrogen atom of a 5–6-membered monocyclic heteroaryl group, and selected from the group of heteroaryl specified in the claims; R6 represents a methyl group; and condensed ring B that is represented by partial structural formula (III). Also the invention relates to a compound represented by formula (Ib), a compound represented by formula (Id), to individual compounds, to pharmaceutical compositions, to an agent for preventing and / or treating at least one disease or condition associated with PDE10, to a PDE10 inhibitor, to a treatment method, to a compound represented by formula (I ').
EFFECT: technical result: new compounds with inhibitory action against phosphodiesterase 10 (PDE10) are obtained.
34 cl, 59 tbl, 181 ex
Title | Year | Author | Number |
---|---|---|---|
HETEROCYCLIC COMPOUNDS AS PESTICIDES | 2016 |
|
RU2724555C2 |
SUBSTITUTED THIOPHENECARBOXAMIDES AND ANALOGUES AS ANTIBACTERIAL AGENTS | 2019 |
|
RU2797316C2 |
SUBSTITUTED THIOPHENECARBOXAMIDES AND ANALOGUES AS ANTIBACTERIAL AGENTS | 2019 |
|
RU2799335C2 |
MULTI-SUBSTITUTED AROMATIC COMPOUNDS AS THROMBIN INHIBITORS | 2011 |
|
RU2639876C2 |
NOVEL HETEROARYLTRIAZOLE COMPOUNDS AS PESTICIDES | 2020 |
|
RU2824488C2 |
IDENTIFICATION OF LKB1 MUTATION AS PROGNOSTIC BIOMARKER OF SENSITIVITY TO TOR-KINASE INHIBITORS | 2011 |
|
RU2565034C2 |
NEW TETRAHYDROPYRIMIDINE CONNECTION OR ITS SALT | 2015 |
|
RU2636310C1 |
BICYCLIC LACTAMS AND METHODS FOR USE THEREOF | 2016 |
|
RU2716136C2 |
SUBSTITUTED THIOPHENECARBOXAMIDES AND ANALOGUES AS ANTIBACTERIAL AGENTS | 2019 |
|
RU2797513C2 |
PHENOXYMETHYL DERIVATIVES | 2016 |
|
RU2746481C1 |
Authors
Dates
2019-03-18—Published
2014-02-26—Filed