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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2024, том 34, выпуск 5, страницы 706–708 (Mi mendc227)

Communications

An alternative synthesis of 7-amino-6-nitro-substituted azolo[1,5-a]pyrimidines

I. I. Butorina, O. A. Konovalovaa, P. A. Slepukhinb, S. K. Kotovskayaa, V. L. Rusinova

a Institute of Chemical Engineering, Ural Federal University, Ekaterinburg, Russian Federation
b I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation


Аннотация: New 7-amino-6-nitro-substituted [1,2,4]triazolo- and pyrazolo[1,5-a]pyrimidines were synthesized by an alternative strategy based on amino azoles and 2-nitro-3-(p-tolylamino)acrylonitrile. Unexpectedly, 3,5-dinitro-N-(p-tolyl)pyridine-2,6-diamine was formed when the starting 5-amino-1,2,4-triazoles contained NO2 or CF3 substituents.

Ключевые слова: [1,2,4]triazolo[1,5-a]pyrimidines, pyrazolo[1,5-a]pyrimidines, nitro synthons, dinitropyridines, acrylonitrile, DFT.

Язык публикации: английский

DOI: 10.1016/j.mencom.2024.09.026



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