FIELD: organic chemistry. SUBSTANCE: invention describes compounds of the formula (I) where R4 and R5 - independently hydrogen, halogen, CF3, CN, NO2 or group SO2NR1R2 where R1 - hydrogen or C1-C6-alkyl that can be branched or cyclic; R2 - hydrogen or C1-C6-alkyl that can be normal, branched or cyclic or where R1 and R2 form together group -(CH2)n-A-(CH2)m where A - O, S, CH2 or NRI where RI - H, C1-C6-alkyl that can be normal, branched or cyclic; n = 0, 1, 2, 3, 4, 5 and m = 0, 1, 2, 3, 4, 5; Q - NOH or O; Z - O, S, N-RII, , N-QIV-C(O)-N-RV-, where RII,RIII,RIV,RV - independently - hydrogen, benzyl, C1-C6-acyl, C1-C6-alkoxyl that can be branched or cyclic, or C1-C6-alkyl that can be branched or cyclic; X - -(CH2) where o = 0, 1, 2 or 3; Y - -(CH2)p where p = 0, 1, 2 or 3; α и β - addition points. Invention describes pharmaceutical composition showing activity associated with blockade of glutamic and aspartic acid receptors using the synthesized compounds. EFFECT: improved method of synthesis. 9 cl
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Authors
Dates
1998-07-10—Published
1992-08-27—Filed