Quaterpyrroles as Building Blocks for the Synthesis of Expanded Porphyrins

Abstract

A new family of quaterpyrroles and their application as building blocks for the synthesis of macrocycles is reported. The preparation of these quaterpyrroles consisted of two synthetic steps: bromination of 2,2′-bipyrroles bearing two electron-withdrawing groups followed by Suzuki coupling with 1-(<i>tert</i>-butoxy­carbonyl)­pyrrole-2-boronic acid. The resulting quaterpyrroles have been used to prepare an octaphyrin and a substituted cyclo[8]­pyrrole. Additionally, the synthesis of a new macrocycle containing the quaterpyrrole and 2,5-di­(1<i>H</i>-pyrrol-2-yl)­thio­phene moieties is presented