FIELD: chemistry.
SUBSTANCE: present invention relates to a compound represented by the formula (I) or a pharmaceutically acceptable salt thereof,
In the compound of the formula (I): 1 or 2 of T1, T2, T3 and T4 constitute N, wherein the rest independently constitute CH; each R1 is independently selected from H, halogen, NH2 or C1-3alkyl optionally substituted with 1, 2 or 3 R; each R2 is independently selected from H, halogen or C1-3alkyl; n is selected from 0 and 1; m is selected from 0, 1 and 2; the ring A is selected from 5-10-membered heteroaryl; each "hetero" in the 5-10-membered heteroaryl is independently selected from N, S, and NH; the number of heteroatoms or heteroatomic groups in the 5-10-membered heteroaryl is independently selected from 1, 2 and 3; the ring B is selected from phenyl and 5-6-membered heteroaryl; each "hetero" in the 5-6-membered heteroaryl is independently selected from N, O, and S; the number of heteroatoms or heteroatomic groups in the 5-6-membered heteroaryl is independently selected from 1 and 2; R is selected from F, Cl, Br and I. Also proposed are specific compounds and application in manufacture of a medicinal product for treatment of a disease associated with the A2A receptor.
EFFECT: new organic compounds of the formula (I) constituting antagonists of an adenosine receptor A2A are proposed.
17 cl, 4 ex, 7 tbl
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Authors
Dates
2021-06-02—Published
2018-09-27—Filed