9,10-Dioxa-1,2-diaza-anthracene derivatives from tetrafluoropyridazine

Abstract

Reaction of tetrafluoropyridazine with catechol gives a tricyclic 9,10-dioxa-1,2-diaza-anthracene system by a sequential nucleophilic aromatic substitution ring annelation process, further extending the use of perfluoroheteroaromatic derivatives for the synthesis of unusual polyfunctional heterocyclic architectures. The tricyclic scaffold reacts with amines and sodium ethoxide providing a short series of functional 9,10-dioxa-1,2-diaza-anthracene systems.

Keywords

• benzodioxinopyridazine
• 9,10-dioxa-1,2-diaza-anthracene
• heterocyclic synthesis
• nucleophilic aromatic substitution
• perfluoroheteroaromatic
• tetrafluoropyrazine