FIELD: pharmacology.
SUBSTANCE: invention relates to the deuterated phenylamino-pyrimidine of formula (I) or its pharmaceutically acceptable salts: . In the formula (I) R1, R2, R13, R14, R15, R16, R17, R18, R19, R20, R21 and R22 are each independently hydrogen or deuterium; R3, R4, R5, R6, R7, R8, R9, R10 and R11 are each independently hydrogen; R12 is hydrogen; Provided that at least one of R1, R2, R13, R14, R15, R16, R17, R18, R19, R20, R21 or R22 are deuterated or deuterium. The invention also relates to a pharmaceutical composition for inhibiting JAK kinase and to the use of compounds for the preparation of a pharmaceutical composition.
EFFECT: new compounds of formula (I) having the properties of a JAK kinase inhibitor have been obtained.
9 cl, 1 dwg, 4 tbl, 13 ex
Title | Year | Author | Number |
---|---|---|---|
THIAZOLPYRIMIDINES | 2012 |
|
RU2610840C2 |
NOVEL FUSED PYRIMIDINE DERIVATIVES FOR INHIBITION OF TYROSINE KINASE ACTIVITY | 2011 |
|
RU2598852C2 |
PHENYL AMINO PYRIMIDINE COMPOUND OR POLYMORPH OF SALT THEREOF | 2016 |
|
RU2712226C2 |
2-PHENYLAMINOPYRIMIDINE DERIVATIVES AS LEUCINE-RICH REPEAT KINASE 2 (LRRK2) MODULATORS FOR TREATMENT OF PARKINSON'S DISEASE | 2012 |
|
RU2661197C2 |
AMINOTRIAZOLOPYRIDINES AND USING THEM AS KINASE INHIBITORS | 2009 |
|
RU2552642C2 |
COMPOSITIONS AND METHODS FOR JAK PATH INHIBITION | 2011 |
|
RU2672100C2 |
DYETERED DIAMINOPYRIMIDINE COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS CONTAINING SUCH CONNECTIONS | 2014 |
|
RU2632907C2 |
DIAMINOTRIAZOLES, SUITABLE AS INHIBITORS OF PROTEIN KINASES | 2003 |
|
RU2350606C2 |
AZAINDOLYL PYRIDONE AND DIAZAINDOLYL PYRIDONE | 2018 |
|
RU2788659C2 |
PYRIDINAMINPYRIDONES AND PYRIMIDINAMINPYRIDONES | 2018 |
|
RU2804638C2 |
Authors
Dates
2017-10-17—Published
2014-01-28—Filed