Cleavage of the CN Bond in Carbodiimides via Release of High Ring Strain: A New Strategy for the Selective Synthesis of 2‐Aminoaryl Alkynyl Imines

Abstract

A novel pattern of the cleavage and reorganization of C=N bond in the multicomponent reaction (MCR) of terminal alkynes or haloalkynes, carbodiimides, and benzynes is achieved for the first time to construct efficiently 2-aminoaryl alkynyl imines. The selective formation and ring-opening of the azetine intermediate with the high ring strain is essential for this reaction. Further transformation of 2-aminoaryl alkynyl imines via the Cu-catalyzed cycloisomerization is explored to provide steroselectively the bi-, tri-, and tetracyclic fused pyrrolines.