DERIVATIVES OF [1,2,4]-TRIAZOLO-[4,3-A]-QUINOXALINONE OR THEIR PHARMACEUTICALLY ACCEPTABLE SALTS, METHOD OF THEIR SYNTHESIS, PHARMACEUTICAL COMPOSITION AND METHOD OF INHIBITION OF AMPA- -RECEPTORS Russian patent published in 2000 - IPC

Abstract RU 2149162 C1

FIELD: organic chemistry, pharmacy. SUBSTANCE: invention proposes derivatives of [1,2,4]-triazolo-[4,3-a] of the general formula (I) where R1 means linear or branched C1-6-alkyl, substituted COX' or POX'X'' where X' and X'' means independently hydroxyl- or alkoxy-group; R6 and R9 mean hydrogen atom; R7 means CF3 and R8 means imidazolyl, piperidino- or morpholino-group being their rings are optionally substituted with one or two substituents taken among phenyl and C1-6-alkyl, or their pharmaceutically acceptable salts. Compounds of the formula (I) show antagonistic activity with respect to AMPA-receptors and are useful for treatment of patients with symptoms of hyperactivity of exciting neuromediators. Invention proposes also method of synthesis of compounds of the formula (I), pharmaceutical composition based on said and method of inhibition of AMPA-receptors activity. EFFECT: improved method of synthesis, valuable pharmacological properties. 8 cl, 1 tbl, 13 ex

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RU 2 149 162 C1

Authors

Nel'Sen Flemming Ehl'Melund

Dates

2000-05-20Published

1995-09-12Filed