Abstract
Various synthetic methodologies to obtain 3,4-diaminoisocumarin nucleus have been reported and described. However, mechanistic analysis based on experimental evidence is lacking. Herein, we report the synthesis of the novel 3-amino-4-(diphenylamino)-1H-2-benzopyran-1-one using a two-step methodology with a new mechanistic proposal to explain the formation of the latter based on previously reported precursors and the established conditions. This compound was afforded in 80% yield.
Funder
Universidad Nacional de Colombia-Sede Bogotá and Dirección de Investigación y Extensión, Sede Bogotá for financial support
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry