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NOVEL VARIANTS OF THE MULTICOMPONENT REACTION FOR THE SYNTHESIS OF 1,2,4-TRIAZOLO[1,5-а]PYRIMIDINES AND PYRIDO[3,4-е][1,2,4]TRIAZOLO[1,5-а]PYRIMIDINES

Владимир А. Поликарчук, Юлия В. Чертова, Андрей Ю. Потапов, Ирина В. Леденёва, Евгения А. Кошелева, Михаил Ю. Крысин, Олег А. Козадёров, Геннадий В. Шаталов, Дмитрий Ю. Вандышев, Хидмет С. Шихалиев, Четти Прабхакар
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Abstract


A new multicomponent reaction for regioselective synthesis of substituted 1,2,4-triazolo[1,5-a]pyrimidines using aminotriazoles, β-ketoglutaric acid dimethyl ester, and dimethylformamide dimethyl acetal was implemented. The selective reduction of 1,2,4-triazolo[1,5-a]pyrimidines to dihydro derivatives and the use of triazolo pyrimidines as starting compounds in multicomponent synthesis of dihydropyrido[3,4-е][1,2,4]triazolo[1,5-a]pyrimidinecarboxylates was demonstrated.

Keywords


acetone-1,3-dicarboxylates; aminotriazoles; dihydropyrido[3,4-e]triazolo[1,5-a]pyrimidines; dimethylformamide dimethyl acetal; 1,2,4-triazolo[1,5-a]pyrimidines; high-resolution HPLC/MS; multicomponent reactions.

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