1228047-83-3Relevant academic research and scientific papers
Thermal rearrangements of (arylimino)diaziridines by simultaneous cascades of pericyclic reactions
Quast, Helmut,Ross, Karl-Heinz,Philipp, Gottfried
, p. 2212 - 2217 (2010)
(Arylimino) diaziridines rearrange in several cascade reactions at temperatures 60-100 °C. Those that possess unoccupied ortho positions yield fluorescent: 3-amino-2H-indazoles and 2-amino-1H-benzimidazoles. If both ortho positions are blocked by methyl groups, indazoles are not formed and deeply yellow 2-imino-2,3-dihydro-3aH-benzimidazoles are formed, which partly dimerize through Diels-Alder reaction or regenerate the aromatic system, by formal loss of CH2. In addition, one of the methyl groups of 2,6-dimethylphenyl rings is involved in a [1,7] H shift affording orthoquinonoid intermediates which undergo 1,6-electrocyclization to furnish 2-amino-3,4-dihydroquinazolines. The formation of fivemembered ring heterocycles is interpreted in terms of valence isomerization by [1,3] N shift to yield elusive 1-ary 1-3iminodiaziridines as first step. These immediately experience triaza-Cope rearrangement to benzimidazole derivatives or electrocyclic opening of the N-C bond to generate conjugated azomethine imines (1,5-dipoles), followed by their 1,5electrocyclization to indazoles. First-order rate constants of the decay of (arylimino) diaziridines refer to the [1,3] N shifts as rate-determining steps. They are larger than the corresponding rate constants for alkylsubstituted iminodiaziridines.
