SYNTHESIS OF <i>N</i>-(1-METHYLTETRAZOL-5-YL)TRINITROACETIMIDAMIDE

Authors

  • Владимир А. Заломленков Samara State Technical University, 244 Molodogvardeyskaya St., Samara 443100,
  • Владимир В. Бахарев Samara State Technical University, 244 Molodogvardeyskaya St., Samara 443100,
  • Александр А. Гидаспов Samara State Technical University, 244 Molodogvardeyskaya St., Samara 443100,
  • Виктор Е. Парфенов Samara State Technical University, 244 Molodogvardeyskaya St., Samara 443100,
  • Ольга В. Головина Samara State Technical University, 244 Molodogvardeyskaya St., Samara 443100,
  • Павел А. Слепухин I. Ya. Postovskii Institute of Organic Synthesis, Ural Branch of Russian Academy of Sciences, 22 S. Kovalevskoi / 20 Akademicheskaya St., Yekaterinburg 620219 Ural Federal University named after the first President of Russia B. N. Yeltsin, 19 Mir St., Yekaterinburg 620002

DOI:

https://doi.org/10.1007/3776

Keywords:

tetrazolо[1, 5-а][1, 3, 5]triazine, tetrazolyltrinitroacetimidamide, trinitromethyl-1, 5-triazine, hydrolysis, ring opening

Abstract

The reaction of 3-methyl-5-trinitromethyltetrazolо[1,5-а][1,3,5]triazin-7-one with water led to the opening of 1,3,5-triazine ring and preservation of trinitromethyl group in the product. The obtained N-(1-methyltetrazol-5-yl)trinitroacetimidamide is of interest as high-energy compound.

Authors: Vladimir A. Zalomlenkov, Vladimir V. Bakharev*, Alexander A. Gidaspov, Victor E. Parfenov, Olga V. Golovina, Pavel A. Slepukhin

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Published

2017-08-18

Issue

Vol. 53 No. 6/7 (2017): Heterocycle-based energetic materials

Section

Short Communications