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

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 deri...

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Veröffentlicht in:Chemistry of heterocyclic compounds (New York, N.Y. 1965) N.Y. 1965), 2020-08, Vol.56 (8), p.1054-1061
Hauptverfasser: Polikarchuk, Vladimir А., Chertova, Yuliya V., Potapov, Andrei Yu, Ledenyova, Irina V., Kosheleva, Yevgeniya А., Krysin, Mikhail Yu, Kozadyorov, Oleg А., Shatalov, Gennadiy V., Vandyshev, Dmitriy Yu, Shikhaliev, Khidmet S., Prabhakar, Chetti
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Sprache:eng
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Zusammenfassung: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.
ISSN:0009-3122
1573-8353
DOI:10.1007/s10593-020-02773-7