The Synthesis of 4-Deoxypyrido[L’,2’-L,2]Imidazo[5,4-C]Rifamycin Sv Derivatives

Abstract

Two series of new semisynthetic rifamycin SV derivatives have been prepared. One of them bears a quaternary ammonium salt at C3 (1 ~ 5), and the other a pyridoimidazo system condensed at C3 and C4 (6~11). While compounds 1~5 had poor antibacterial activity in vitro, compounds 6~11 were found to be highly active in vitro but poorly absorbed in vivo. They could thus have potential as agents in the therapy of intestinal infections. The synthesis and the 1H NMR structure determination of these new compounds are reported. © 1984, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.