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Updated: Oct 14, 2025

Facile Preparation of 4-Substituted Quinazoline Derivatives
Published on: February 15, 2016
Benzotriazoles and Triazoloquinones: Rearrangements to Carbazoles, Benzazirines, Azepinediones, and Fulvenimines
Jérémy Marchais1, Didier Bégué1, Alain Dargelos1
1CNRS/Université de Pau et des Pays de l'Adour/E2S UPPA, Institut des Sciences Analytiques et de Physicochimie pour l'Environnement et les Matériaux, UMR5254, Pau 64000, France.
Abstract:
The denitrogenative rearrangements of several types of benzotriazoles were investigated by DFT (B3LYP/6-311G(d,p)) and CASPT2(10,10)sp/6-311G(d,p) calculations. The Graebe-Ullmann synthesis of carbazoles 18 by pyrolysis or photolysis of 1-arylbenzotriazoles 14 proceeds without the involvement of benzazirines and without Wolff-type ring contraction to fulvenimines. However, 1-aryltetrahydrobenzotriazoles undergo both cyclization to tetrahydrocarbazole and ring contraction. Triazoloquinones like 34 undergo predominant ring contraction to aminofulvenediones like 38 and also ring expansion to azepinediones like 40 and cyclization to N-arylbenzaziridinediones 39, whereas carbazolediones are not formed. Denitrogenation of 1-methylbenzotriazole 64 results in a facile 1,2-H shift with formation of N-phenylmethanimine 67. 1-Cyanobenzotriazole 71 undergoes destructive pyrolysis with charring, and the calculations predict the occurrence of several low-activation energy reaction pathways.
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