Rao P N, Damodaran K M
Steroids. 1984 Mar;43(3):343-50. doi: 10.1016/0039-128x(84)90052-7.
Starting from 11 beta-hydroxytestosterone, we achieved the synthesis of a strategic precursor, C-9 (11) unsaturated 5 alpha-androstane-3 alpha, 17 beta-diol 17-glucuronide (9a), for the preparation of 9 alpha,11 alpha-tritiated 5 alpha-androstane-3 alpha, 17 beta-diol 17-glucuronide. We optimized the reaction conditions for catalytic reduction employing hydrogen and subsequent base hydrolysis followed by purification on Amberlite XAD-2 resin to obtain the saturated 5 alpha-androstane-3 alpha, 17 beta-diol 17-glucuronide.
从11β-羟基睾酮开始,我们成功合成了一种关键前体,即C-9(11)不饱和5α-雄甾烷-3α,17β-二醇17-葡糖醛酸苷(9a),用于制备9α,11α-氚代5α-雄甾烷-3α,17β-二醇17-葡糖醛酸苷。我们优化了使用氢气进行催化还原的反应条件,随后进行碱水解,再通过Amberlite XAD-2树脂纯化,以获得饱和的5α-雄甾烷-3α,17β-二醇17-葡糖醛酸苷。