Unusual formation of 4-diazo-3-nitriminopyrazoles upon acid nitration of pyrazolo[3,4-<em>d</em>][1,2,3]triazoles

Nitration of 6-R-4-phenylpyrazolo[3,4-<em>d</em>][1,2,3]triazoles at the phenyl substituent is accompanied by the triazole ring opening to give new 3-R-4-diazo-1-(di)nitrophenylpyrazole- 5-nitrimines. Chemical and physicochemical properties of the prepared compounds are reported.

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Publication Details

Journal
Mendeleev Communications
Published
2025-01-01
DOI
https://doi.org/10.71267/mencom.7628
Primary Topic
Synthesis and Biological Evaluation
Type
article
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article

Unusual formation of 4-diazo-3-nitriminopyrazoles upon acid nitration of pyrazolo[3,4-d][1,2,3]triazoles

Igor L. Dalinger, Алла Н. Пивкина, Kyrill Yu. Suponitsky, T. E. Khoranyan et al.
Mendeleev Communications
Synthesis and Biological Evaluation
article

Unusual formation of 4-diazo-3-nitriminopyrazoles upon acid nitration of pyrazolo[3,4-d][1,2,3]triazoles

Igor L. Dalinger, Алла Н. Пивкина, Kyrill Yu. Suponitsky, T. E. Khoranyan, Alexandr V. Kormanov
article en

Abstract

Nitration of 6-R-4-phenylpyrazolo[3,4-<em>d</em>][1,2,3]triazoles at the phenyl substituent is accompanied by the triazole ring opening to give new 3-R-4-diazo-1-(di)nitrophenylpyrazole- 5-nitrimines. Chemical and physicochemical properties of the prepared compounds are reported.

Mendeleev CommunicationsVol. 35(3)
Semenov Institute of Chemical Physics (RU), N.D. Zelinsky Institute of Organic Chemistry (RU)
Openalex Percentile: Top 95%
Synthesis and Biological Evaluation
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