FIELD: organic chemistry; pharmaceuticals.
SUBSTANCE: group of inventions relates to an aminonorbornane derivative as an inhibitor of Bruton's tyrosine kinase with high selectivity towards the BTK(C481S) mutant. The following is disclosed: a compound of Formula I, or a pharmaceutically acceptable salt thereof, wherein Ring A, Ring B, Ring C and wherein the values of L, R1, R2 and R5 are as set forth in the claims. In addition, a specific compound selected from the group, the use of the above compounds in the production of a medicinal product, pharmaceutical compositions and compositions for preventing the development or treatment of a heteroimmune disease based on these compounds are disclosed. A method of preparing the presented compounds is also disclosed.
EFFECT: group of inventions provides effective inhibition of Bruton's tyrosine kinase with high selectivity towards the BTK(C481S) mutant, which provides treatment for a heteroimmune disease, autoimmune disease or cancer.
22 cl, 2 dwg, 4 tbl, 6 ex
Title | Year | Author | Number |
---|---|---|---|
AMIDE DERIVATIVES OF PYROSOL | 2015 |
|
RU2658827C2 |
CERTAIN PROTEIN KINASE INHIBITORS | 2015 |
|
RU2671494C2 |
CROSS-LINKED ARTIFICIAL NUCLEIC ACID ALNA | 2019 |
|
RU2820226C2 |
IMIDAZOPIRASOTHINES AS PDE1 INHIBITORS | 2016 |
|
RU2712219C2 |
HETEROCYCLIC SUBSTANCES-GPR119 AGONISTS | 2017 |
|
RU2734500C2 |
MODULATORS OF ATP-BINDING TRANSPORTERS | 2010 |
|
RU2552353C2 |
SUBSTITUTED BENZENE COMPOUNDS | 2012 |
|
RU2629118C2 |
2, 5, 6, 7-TETRAHYDRO-[1, 4]OXAZEPIN-3-YLAMINES OR 2, 3, 6, 7-TETRAHYDRO-[1, 4]OXAZEPIN-5-YLAMINES | 2011 |
|
RU2570796C2 |
1-PHENYL-2-PYRIDINYL ALKYL ALCOHOL DERIVATIVES AS PHOSPHODIESTERASE INHIBITORS | 2013 |
|
RU2655170C2 |
MACROCYCLIC COMPOUNDS AS TRK KINASE INHIBITORS | 2019 |
|
RU2778294C2 |
Authors
Dates
2023-12-07—Published
2019-07-05—Filed