DBU mediated one-pot synthesis of triazolo triazines via Dimroth type rearrangement?

RSC Advances Pub Date: 2022-01-12 DOI: 10.1039/D1RA07749J

Abstract

Herein we report an efficient one-pot synthesis of [1,2,4]triazolo[1,5 a][1,3,5]triazines from commercially available substituted aryl/heteroaryl aldehydes and substituted 2-hydrazinyl-1,3,5-triazines via N-bromosuccinimide (NBS) mediated oxidative C–N bond formation. Isomerisation of [1,2,4]triazolo[4,3-a][1,3,5]triazines to [1,2,4]triazolo[1,5-a][1,3,5]triazines is driven by 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) affording both isomers with good to excellent yields (70–96%).

Graphical abstract: DBU mediated one-pot synthesis of triazolo triazines via Dimroth type rearrangement
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