FIELD: chemistry; pharmaceutics.
SUBSTANCE: invention relates to a compound of formula I or a pharmaceutically acceptable salt thereof. In formula IW is selected from hydrogen and , where Ring A is selected from phenyl or 6-member monocyclic heteroaryl with one ring heteroatom selected from N; each X and Y is independently selected from CR1 and N; Z is selected from phenyl, 5- or 6-membered monocyclic heteroaryl with 1–2 ring heteroatoms independently selected from N, O and S, 6-membered monocyclic partially unsaturated heterocyclyl with one ring heteroatom selected from N; where each of phenyl, monocyclic heteroaryl and monocyclic heterocyclyl is independently substituted with 0–2 groups RC; L is selected from bond, -(C(R2)(R2))m-, -(C2-C6 alkynylene)-, -O-, -S- and -S(O)2-; each RA and RB is independently selected from halogen, C1-C6 alkyl and C1-C6 hydroxyalkyl; each RC is independently selected from C1-C6 alkyl, C1-C6 alkoxy, halogen, C1-C6 hydroxyalkyl, C3-C7 cycloalkyl, 4-member heterocyclyl with one ring heteroatom selected from O, (6-member heterocyclyl with 2 ring heteroatoms selected from N, O)-C1-C6 alkyl, cyano, -C(O)OR2 and -C(O)-N(R2)(R2); each RD and RF is independently selected from hydrogen and -N (R2) (R2); each R1 is hydrogen; each R2 is independently selected from hydrogen, hydroxyl, -NR "R", C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, C1-C6 hydroxyalkyl, C3-C7 cycloalkyl, or 2 R2 together with atoms, to which they are bonded, form 4-member heterocyclyl ring with 1 ring atom selected from O; each R "is hydrogen or C1-C6 alkyl; and m, p and q – each independently represent 0, 1, 2, 3 or 4. Invention also relates to individual compounds, to a pharmaceutical composition, to methods of treatment.
I.
EFFECT: technical result is obtaining novel compounds of formula I, having modulating activity on KIT and/or PDGFRα.
25 cl, 2 dwg, 3 tbl, 7 ex
Title | Year | Author | Number |
---|---|---|---|
SUBSTITUTED 1,2-DIHYDRO-3H-PYRAZOLO[3,4-D]PYRIMIDIN-3-ONES | 2019 |
|
RU2812726C2 |
BENZAMIDE COMPOUNDS | 2019 |
|
RU2801647C2 |
COMPOSITIONS AND METHODS OF TREATING KIT- AND PDGFRα-MEDIATED DISEASES | 2020 |
|
RU2817354C2 |
PYRIMIDINE DERIVATIVES | 2002 |
|
RU2320658C2 |
KINASE INHIBITORS APPLICABLE FOR TREATING MYELOPROLIFERATIVE DISEASES AND OTHER PROLIFERATIVE DISEASES | 2007 |
|
RU2482112C2 |
INHIBITORS JAK2 AND ALK2 AND METHODS OF USE THEREOF | 2014 |
|
RU2693480C2 |
PROTEINKINASE INHIBITORS, METHOD FOR OBTAINING THEREOF AND MEDICAL APPLICATION | 2016 |
|
RU2749437C2 |
BICYCLIC DIHYDROPYRIMIDINECARBOXAMIDE DERIVATIVES AS RHO-KINASE INHIBITORS | 2017 |
|
RU2778478C2 |
NOVEL COMPOUNDS THAT ARE ERK INHIBITORS | 2013 |
|
RU2660429C2 |
OXAZOLIDINONE COMPOUNDS AND METHODS OF THEIR APPLICATION AS ANTIBACTERIAL AGENTS | 2016 |
|
RU2794494C2 |
Authors
Dates
2019-11-15—Published
2014-10-15—Filed