Prodigiosin synthesis with electron rich 2,2′-bipyrroles

Abstract

The prodigiosins possess a linear tripyrrolic scaffold with the A and B pyrrolic rings connected directly in a bipyrrole unit, and the B and C rings joined in a dipyrrin. These red streptomycete metabolites exhibit among other activities, antitumor, antimicrobial, and immunomodulating properties. A new prodigiosin synthesis has been developed that employs electron rich 2,2′-bipyrroles. In particular, undecylprodigiosin and PNU-156804 were synthesized by condensations of 4-methoxy and 4-benzyloxy 2,2′-bipyrroles, 20a and 20b, respectively, with 5-undecylpyrrole-2-carboxaldehyde in 75% and 83% yields. The 4-alkoxy-2,2′-bipyrroles were synthesized from 4-alkoxypyrrolyl butenyl ketones (15a and 15b), which were made by a novel one-pot process from 2-acyl-N-(PhF)pyrrolidin-4-one (13) [PhF = 9-(9-phenylfluorenyl)] using PhFNa in the presence of alkyl halide. A sequence of alkoxy pyrrole 15a and 15b protection, olefin oxidation, Paal–Knorr condensation, and deprotection gave the requisite 4-alkoxy-2,2′-bipyrroles (20). This route offers utility for making 4-alkoxybipyrroles as well as prodigiosins with diversity at the 6-position of the linear tripyrrolic skeleton.Key words: prodigiosin, pyrrole, bipyrrole, PNU-156804, undecylprodigiosin.