One-Pot Synthesis of Seven-Membered Heterocyclic Derivatives of Diazepines Involving Copper-Catalyzed Rearrangement Cascade Allyl-Amination

A novel and efficient method has
been proposed for the synthesis
of 1,4-benzodiazepine-5-ones from o-nitrobenzoic N-allylamides by using molybdenyl acetylacetonate and copper­(II)
trifluoromethanesulfonate as catalysts in the presence of triphenylphosphine.
This synthesis process involves nitrene formation, C–H bond
insertion, CC bond rearrangement, and C–N bond formation
cascade reactions via copper- and molybdenum-catalyzed mediation.
The method features a wide substrate scope and a moderate to high
yield (up to 90%), exhibiting the possibility for practical applications.