SYNTHESIS OF NEW 2-SUBSTITUTED 6,8-DINITRO[1,2,4]TRIAZOLO[1,5-<i>a</i>]PYRIDINES

Authors

  • Maxim A. Bastrakov N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Ave., Moscow 119991, Russia
  • Alexey M. Starosotnikov N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Ave., Moscow 119991, Russia
  • Ivan V. Fedyanin N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Ave., Moscow 119991, Russia
  • Igor L. Dalinger N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Ave., Moscow 119991, Russia

DOI:

https://doi.org/10.1007/6013

Keywords:

nitro compounds, nitrogen heterocycles, [1, 2, 4]triazolo[1, 5-a]pyridines, N-bridged fused ring systems.

Abstract

A number of new 2-substituted 6,8-dinitro[1,2,4]triazolo[1,5-a]pyridines containing explosophoric groups or their precursors were synthesized based on reactions of the commercially available 2-chloro-3,5-dinitropyridine with 5-(hetaryl)tetrazoles or through modification of aryl substituent to 2-aryl-6,8-dinitrotriazolo[1,5-a]pyridine.

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Published

2021-01-26

Issue

Vol. 57 No. 1 (2021)

Section

Short Communications