Synthesis of deuterium-labeled 17-hydroxyprogesterone suitable as an internal standard for isotope dilution mass spectrometry
作者:Kyutaro Shimizu、Nobuo Yamaga、Hiromi Kohara
DOI:10.1016/0039-128x(88)90019-0
日期:1988.3
12,12,23,23(-2)H]lithocholic acid (V). The Meystre-Miescher degradation of the side chain of V yielded 3 alpha-hydroxy-5 beta-[11,11,12,12(-2)H]pregnan-20-one (X). Oxidation of the 3,20-enol-diacetate of X with perbenzoic acid followed by saponification afforded 3 alpha,17-dihydroxy-5 beta-[11,11,12,12(-2)H]pregnan-20-one (XI). Oxidation of XI with N-bromoacetamide yielded 17-hydroxy-5 beta-[11,11
据报道,合成了 17-羟基孕酮,在 C 环上用四个氘原子标记,适合用作同位素稀释质谱法的内标。3 α-乙酰氧基-12-氧代胆酸甲酯 (III) 与 2H2O 的碱催化平衡,然后使用 [2H] 二甘醇和 [2H] 水合肼通过改进的 Wolff-Kisher 方法还原 12-氧代基团得到[11,11,12,12,23,23(-2)H]石胆酸(V)。V 侧链的 Meystre-Miescher 降解产生了 3 alpha-hydroxy-5 beta-[11,11,12,12(-2)H]pregnan-20-one (X)。X 的 3,20-烯醇-二乙酸酯用过苯甲酸氧化,然后皂化得到 3 α,17-二羟基-5β-[11,11,12,12(-2)H]pregnan-20-one (XI )。XI 用 N-溴乙酰胺氧化产生 17-羟基-5β-[11,11,12,12(-2)H]pregnane-3,20-dione