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Annulation-Triggered Denitrogenative Transformations of 2-(5-Iodo-1,2,3-triazolyl)benzoic Acids.

Vladislav A VoloshkinYury N KotovshchikovGennadij V LatyshevNikolay V LukashevIrina P Beletskaya
Published in: The Journal of organic chemistry (2022)
The ability of [1,2,3]triazolobenzoxazinones to act as a source of "hidden" diazo group was discovered. These diazo precursors can be easily prepared by the intramolecular cyclization of 2-(5-iodo-1,2,3-triazolyl)benzoic acids. The Cu-catalyzed capture of the hidden diazo group allows for further functionalization through the denitrogenative pathway. The transformations proceed via the formation of either diazoimine or diazoamide intermediates. Novel routes to various anthranilamides as well as thiolated benzoxazinones were developed using the one-pot cyclization/diazo capture procedure.
Keyphrases
  • minimally invasive
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  • aqueous solution
  • metal organic framework
  • ionic liquid