Potential Insensitive and High-Energy Materials Based on a Pyrazole-Triazine-Oxadiazole Skeleton

The pyrazole-triazine-oxadiazole skeleton was constructed via introducing an oxadiazole ring onto a pyrazole-triazine fused ring through the cyclization reaction of a hydroximoylamine group. A series of heat-resistant compounds, namely, 3-(5-amino-1,2,4-oxadiazol-3-yl)-4,7-diamino-8-nitropyrazolo-[5,1- c ][1,2,4]triazine ( 4 ) and 7-amino-3-(5-amino-1,2,4-oxadiazol-3-yl)-8-nitro-1 H -pyrazolo[5,1- c ][1,2,4]triazin-4-one ( 10 ), based on the pyrazole-triazine-oxadiazole skeleton were synthesized, exhibiting low sensitivity and high stability. Unexpectedly, oxidation of compound 4 afforded the ring-opened product 6, and the high-energy compound 3-(5-amino-1,2,4-oxadiazol-3-yl)-7-[(nitroamino)]-8-nitro-1 H,4 H -pyrazolo[5,1- c ][1,2,4]triazin-4-one ( 8 ) was synthesized via two distinct synthetic routes, with compounds 4 and 10 serving as the respective starting materials. Compared with the classic heat-resistant explosive HNS ( T d = 318 °C, D v = 7612 m·s –1, D p = 24.3 GPa), compounds 4 and 10 have higher thermal stability ( T d = 343 °C and T d = 325 °C, respectively) and superior detonation performance ( D v = 8317 m·s –1 and D v = 7937 m·s –1, respectively), thereby demonstrating great potential as alternatives to HNS . Compound 8 ( D v = 8736 m·s –1 ) performs comparably to RDX ( D v = 8795 m·s –1, IS = 7.4 J, FS = 120 N) in detonation velocity but outperforms it in both sensitivity (IS = 15 J, FS = 192 N) and thermal stability ( T d = 214 °C), indicating its potential as a high-energy explosive.