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Synthesis of Energetic 7-Nitro-3,5-dihydro-4H-pyrazolo[4,3-d][1,2,3]triazin-4-one Based on a Novel Hofmann-Type Rearrangement.


ABSTRACT: Rearrangement reactions are efficient strategies in organic synthesis and contribute enormously to the development of energetic materials. Here, we report on the preparation of a fused energetic structure of 7-nitro-3,5-dihydro-4H-pyrazolo[4,3-d][1,2,3]triazin-4-one (NPTO) based on a novel Hofmann-type rearrangement. The 1,2,3-triazine unit was introduced into the fused bicyclic skeleton from a pyrazole unit for the first time. The new compound of NPTO was fully characterized using multinuclear NMR and IR spectroscopy, elemental analysis as well as X-ray diffraction studies. The thermal behaviors and detonation properties of NPTO were investigated through a differential scanning calorimetry (DSC-TG) approach and EXPLO5 program-based calculations, respectively. The calculation results showed similar detonation performances between NPTO and the energetic materials of DNPP and ANPP, indicating that NPTO has a good application perspective in insensitive explosives and propellants.

SUBMITTER: Bi FQ 

PROVIDER: S-EPMC8659268 | biostudies-literature | 2021 Dec

REPOSITORIES: biostudies-literature

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Synthesis of Energetic 7-Nitro-3,5-dihydro-4<i>H</i>-pyrazolo[4,3-<i>d</i>][1,2,3]triazin-4-one Based on a Novel Hofmann-Type Rearrangement.

Bi Fu-Qiang FQ   Luo Yi-Fen YF   Zhang Jun-Lin JL   Huo Huan H   Wang Bo-Zhou BZ  

Molecules (Basel, Switzerland) 20211202 23


Rearrangement reactions are efficient strategies in organic synthesis and contribute enormously to the development of energetic materials. Here, we report on the preparation of a fused energetic structure of 7-nitro-3,5-dihydro-4<i>H</i>-pyrazolo[4,3-<i>d</i>][1,2,3]triazin-4-one (NPTO) based on a novel Hofmann-type rearrangement. The 1,2,3-triazine unit was introduced into the fused bicyclic skeleton from a pyrazole unit for the first time. The new compound of NPTO was fully characterized using  ...[more]

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