Investigation into a Conformationally Locked (Z)-Azidoxime

• Published in: Journal of organic chemistry Vol. 88; no. 20; pp. 14404 - 14412
• Main Authors: Cleveland, Alexander H., Davis, Jack V., Imler, Gregory H., Byrd, Edward F. C., Snyder, Christopher J., Chavez, David E., Parrish, Damon A.
• Format: Journal Article
• Language: English
• Published: American Chemical Society 20-10-2023
• ISSN: 0022-3263; 1520-6904
• DOI: 10.1021/acs.joc.3c01324

High nitrogen compounds find wide use in the development of new propellants and explosives as well as pharmaceutical chemistry as bioisosteres, bacterial stains, and antifungal agents. A class of underexplored high-nitrogen materials includes azidoximes and their 1-hydroxytetrazole isomers. Azidoximes possess an energetic azide group and are quite sensitive to impact, spark, and friction. Therefore, these materials are generated in situ and cyclized under mild acidic conditions to their 1-hydroxytetrazole isomers. Recently, we synthesized a novel 1,2,4-triazine-derived azidoxime; however, upon subjecting this material to established cyclization conditions, no reaction was observed, even after prolonged reaction times with heating. Additional 1,2,4-triazine-derived azidoximes also displayed a similar lack of reactivities. This observation led us to probe the reactivity of these materials with both a DFT investigation and crystallographically based electrostatic potential mapping. In all, the lack of reactivity toward cyclization was found to be due to an inability of 1,2,4-triazine-based azidoximes to isomerize into the reactive (E)-conformation, requiring an activation energy of 26.4 kcal mol–1.