Pellicciari R, Cecchetti S, Natalini B, Roda A, Grigolo B, Fini A
J Med Chem. 1985 Feb;28(2):239-42. doi: 10.1021/jm00380a015.
The preparation of 3 alpha,7 beta-dihydroxy-22,23-methylene-5 beta-cholan-24-oic acid (2-sulfoethyl)amide (5) by the one-step EEDQ-induced conjugation between ursodeoxycholic acid "cyclopropylog" (4) and taurine is described. The presence of a cyclopropyl ring adjacent to the amide bond is shown to make it resistant to degradation by intestinal bacteria. This new cyclopropylog is neither deconjugated at the C-24 amide bond nor 7-dehydroxylated when incubated with human stools in anaerobic conditions.
描述了通过熊去氧胆酸“环丙基类似物”(4)与牛磺酸之间一步法EEDQ诱导的偶联反应制备3α,7β-二羟基-22,23-亚甲基-5β-胆烷-24-酸(2-磺基乙基)酰胺(5)的方法。结果表明,酰胺键相邻的环丙基的存在使其对肠道细菌的降解具有抗性。当在厌氧条件下与人粪便一起孵育时,这种新的环丙基类似物在C-24酰胺键处既不会发生去偶联反应,也不会发生7-脱羟基反应。