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.
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The study was carried out with a grant from the Russian Science Foundation (project No. 18-74-10097).
The results of the study were partially obtained using the equipment of the Center for Collective Use of the Voronezh State University.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, 2020, 56(8), 1054–1061
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Polikarchuk, V.А., Chertova, Y.V., Potapov, A.Y. et al. 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. Chem Heterocycl Comp 56, 1054–1061 (2020). https://doi.org/10.1007/s10593-020-02773-7
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DOI: https://doi.org/10.1007/s10593-020-02773-7