FIELD: chemistry.
SUBSTANCE: described are compounds of formula I, where n is an integer from 0 to 3; each A is independently selected from the group consisting of N and CH; A1 represents N or C(R5); A2 represents N or C(R7); R1 and R2 each are independently selected from the group consisting of H, halogen and -ORa; R3 is a representative selected from the group consisting of H, C1-8 alkyl, C3-8 cycloalkyl, C2-8 alkenyl, C1-8 haloalkyl, -ORa, -NRaRb, phenyl and 5- or 6- member heteroaryl; R4 is a representative selected from the group consisting of H and C1-8 alkyl; R5, R6, R7 and R8 each are independently selected from the group consisting of H, halogen, C1-8 alkyl, C1-8 haloalkyl, C1-8 hydroxyalkyl abd 5- or 6- member heteroaryl; R9 is a representative selected from the group consisting of H and C1-8 alkyl; and each Ra and Rb are independently selected from the group consisting of hydrogen atom, C1-8 alkyl; where each heteroaryl has from one to five heteroatoms selected from the group consisting of N, O and S, or their pharmaceutically acceptable salts. Said compounds act as potential CCR1 receptor antagonists and have in vivo anti-inflammatory action. Also, the pharmaceutical composition comprising the compound of formula I is described, as well as the method for treating diseases by administering the compound of formula I. formula I.
EFFECT: diazole lactams are proposed.
28 cl, 2 tbl, 46 ex
Title | Year | Author | Number |
---|---|---|---|
AMIDE DERIVATIVES OF PYROSOL | 2015 |
|
RU2658827C2 |
ANTAGONISTS OF CHEMOKINE RECEPTORS | 2013 |
|
RU2646762C2 |
SUBSTITUTED HETEROCYCLIC SULPHONAMIDE COMPOUNDS USEFUL AS TRPA1 MODULATORS | 2014 |
|
RU2675792C2 |
SERINE/THREONINE KINASE INHIBITORS | 2013 |
|
RU2650501C2 |
PYRAZOLE COMPOUND AND ITS PHARMACEUTICAL USE | 2012 |
|
RU2617678C2 |
NOVEL IMIDAZOLIDINE-2,4-DIONE DERIVATIVES | 2013 |
|
RU2650678C2 |
BENZODIAZEPINE DERIVATIVES AS RSV INHIBITORS | 2016 |
|
RU2738232C2 |
PROCESS FOR THE PREPARATION OF (6R,7S,7AS)-6-((R)-1-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)ETHOXY)-7-(4-FLUOROPHENYL)HEXAHYDRO-3H-PYRROLISIN-3-ONE | 2022 |
|
RU2789599C1 |
SUBSTITUTED IMIDAZOPYRIDINES AS HDM2 INHIBITORS | 2013 |
|
RU2690663C2 |
PYRAZINE COMPOUNDS AND THEIR USE | 2019 |
|
RU2809631C2 |
Authors
Dates
2018-09-12—Published
2013-12-06—Filed