周亚兵 汪晓铭 杜芳 张建忠



摘 要 目的:改进苯磺顺阿曲库铵重要中间体R-四氢罂粟碱-N-乙酰-L-亮氨酸盐精制方法。方法:以3,4-二甲氧基苯乙胺、3,4-二甲氧基苯乙酸为起始物料,经缩合、环合、加氢得四氢罂粟碱,后经拆分、精制得R-四氢罂粟碱-N-乙酰-L-亮氨酸盐。结果:目标产物收率为24.0%以上,R对映体含量达99.5%以上。结论:本工艺操作简便,产品纯度和收率较高,适于大批量生产。
关键词 苯磺顺阿曲库铵 R-四氢罂粟碱-N-乙酰-L-亮氨酸盐 拆分精制工艺
中图分类号:O626.322 文献标志码:A 文章编号:1006-1533(2020)23-0105-05
Optimization of the refining process of R-tetrahydropapaverine-N-acetylL-leucine salt, an important intermediate of cisatracurium besylate*
ZHOU Yabing1**, WANG Xiaoming1, DU Fang1, ZHANG Jianzhong2***[1. SPH Dongying (Jiangsu) Pharmaceutical Co., Ltd., Jiangsu Nantong 226010, China; 2. Shanghai Pharmaceuticals Holding Co., Ltd., Shanghai 200020, China]
ABSTRACT Objective: To improve the refining method of R-tetrahydropapaverine-N-acetyl-L-leucine salt, an important intermediate of cisatracurium besylate. Methods: Using 3,4-dimethoxyphenethylamine and 3,4-dimethoxyphenylacetic acid as starting materials, tetrahydropapaverine is obtained by condensation, cyclization, and hydrogenation, which is resolved by a resolving agent. R-tetrahydropapaverine-N-acetyl-L-leucine salt is obtained after resolution and purification. Results: The yield of the target product is over 24.0%, and the content of R-enantiomer is over 99.5%. Conclusion: The process is easy to operate and suitable for mass production with high purity and yield.
KEy WORDS cisatracurium besylate; R-tetrahydropapaverine-N-acetyl-L-leucine salt; refining process
苯磺顺阿曲库铵是一起效快、作用强、恢复迅速、不释放组胺、对心血管影响小、代谢不依赖于肝肾功能,无蓄积、代谢产物无肌松效应也无毒性的理想的肌松药。目前已成为临床肌松药的主流,在中国、美国以及欧盟等重要国家和地区均有上市,且已收载入欧美主流国家及中国药典,安全有效性明确,临床优势明显[1]。在苯磺顺阿曲库铵的合成中,关键在于两次手性中心的形成,需要建立完善的控制体系对异构体进行控制。
R-四氢罂粟碱-N-乙酰-L-亮氨酸盐(Ⅰ),作为苯磺顺阿曲库铵重要中间体,是苯磺顺阿曲库铵第一个手性中心的形成,其对后续合成中手性的控制尤为重要。目前Ⅰ的合成方法的文献记载主要有3种:①手性Binol衍生磷酸催化剂负载在Merrified树脂上制成催化剂,并用该催化剂和Hantzsch酯为负氢供体,不对称还原3,4-二氢罂粟碱,该方法成本高,原料不易得[2-3];②以3,4-二甲氧基苯乙腈为起始原料,经还原、水解、酞化、脱水环化、还原等5步合成,该方法所得目标产物纯度96.0%左右,收率67.8%[4];……