STEREOSPECIFIC SYNTHESIS AND 2-DIMENSIONAL H-1-NMR INVESTIGATION OF ISOURSOCHOLIC ACID

This report describes the chemical synthesis of isoursocholic acid (3-beta,7-beta,12-alpha-trihydroxy-5-beta-cholanoic acid) from its corresponding 3-alpha-analog. The method consists of refluxing a mixture of ursocholic acid, triphenylphosphine, and diethyl azodicarboxylate in benzene solution with an acid such as formic acid. The sterically pure ester (3-beta-formate) so formed after saponification with LiOH-aqueous methanol then allowed an easy access to the epimer of the starting acid. Large scale preparative separation and purification of the final product and synthetic intermediates were accomplished by flash column chromatography of their methyl ester derivatives. Structural assignment of the isoursocholic acid molecule was confirmed by complete analysis of proton NMR spectra using 2-D NMR correlation experiments which rigorously established the (3-beta/3-alpha) and (7-beta/7-alpha) hydroxyl configurations in the isoursocholic and ursocholic acids. It is suggested that the isoursocholic acid will be useful as a reference compound and as a substrate in studies dealing with the hepatic inversion of the 3-beta-hydroxy group.