阿加曲班杂质合成研究  

Study on the Synthesis of Impurities in Argatroban Anhydrous

作　　者：黎银波[1] 李剑峰 姚金成[1] 张贵赋 LI Yinbo;LI Jianfeng;YAO Jincheng;ZHANG Guifu(Hunan Center for Drug Evaluation and ADR Monitoring,Changsha,Hunan,China 410013;Hunan Sailong Pharmaceutical Co.,Ltd.,Yueyang,Hunan,China 414200)

机构地区：[1]湖南省药品审评认证与不良反应监测中心,湖南长沙410013 [2]湖南赛隆药业股份有限公司,湖南岳阳414200

出　　处：《中国药业》2019年第5期18-20,共3页China Pharmaceuticals

摘　　要：目的探讨阿加曲班起始原料3-甲基-8-喹啉磺酰氯中的异构体杂质来源与合成方法,为阿加曲班的质量控制提供依据和杂质对照品。方法杂质A以5-溴-3-甲基喹啉为起始物,依次进行Buchwald、脱保护基、与亚硝酸盐重氮化及Sandermeyer等反应制得;杂质B以5-溴-2-硝基苯甲醛为起始物,经铁粉还原、关环,再经Buchwald、脱保护基、重氮化及Sandermeyer等反应制得。结果该试验所合成的2个异构体杂质经液相色谱-质谱联用(LC-MS)及氢谱核磁共振(1H-NMR)进行结构确证,与目标化合物结构相符。结论该合成方法简单易行,合成的2个异构体杂质可作为杂质对照品,用于阿加曲班原料药的质量控制。Objective To investigate the source and synthesis method of isomer impurities in 3-methyl-8-quinoline sulfonyl chloride,the starting material of argatroban anhydrous,and to provide a basis and impurity reference materials for quality control of argatrobananhydrous. Methods The impurity A was prepared from 5-bromo-3-methylquinoline by reaction with Buchwald, off-protectinggroup,diazotization and Sandermeyer. The impurity B was prepared from 5-bromo-2-nitrobenzaldehyde by the reduction with iron powderand closure of the ring, and reaction of Buchwald, off-protecting group, azotization and Sandermeyer. Results The structures of thetwo isomers were confirmed by LC-MS and1 H-NMR, which were consistent with the target compounds. Conclusion The syntheticmethod is simple and feasible. The two synthesized isomer impurities can be used as impurity reference substances for the qualitycontrol of argatroban anhydrous.

关 键 词：阿加曲班 3-甲基-8-喹啉磺酰氯 异构体杂质 合成方法 

分 类 号：R973.2[医药卫生—药品] R917[医药卫生—药学]