FIELD: organic chemistry.
SUBSTANCE: invention relates to organic chemistry, namely to a compound of the formula 1 or its pharmaceutically acceptable salts, where, in the formula 1, W is selected from O and S; X1 is N; X2 is CR3; X3 is CR4; X4 is CR5; X5 is CR6; Y is -NRdRe, where Rd and Re are hydrogen; D is absent; R1 is C1-12-alkyl; R3, R4 and R5 each independently is selected from hydrogen; C1-12-alkyl; C2-12-alkynyl; halogen; C1-12-haloalkyl; C1-12-alkoxy; C1-12-alkylsulfonyl; ciano; tetrazolyl; -(CH2)m-(Z)n-(CO)-Rf and -(CH2)m-(Z)n-SO2-(NRg)n'-Rf, where m, n and n' each independently is 0 or 1; Z is O or NRg; Rf and Rg are hydrogen; R6 and R7 are hydrogen. The invention also relates to a compound 42 and its pharmaceutically acceptable salts, and to a pharmaceutical composition based on compounds of the formula 1 or the compound 42.
EFFECT: pyrimidine derivatives having inhibiting activity relatively to purinergic receptors P2X3 and/or P2X2/3 are obtained.
formula 1,
8 cl, 3 tbl, 49 ex
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Authors
Dates
2021-11-30—Published
2017-03-20—Filed