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反相高效液相色谱分析克拉霉素合成工艺中区域选择性甲基化的关键中间体
引用本文:梁建华,姚国伟,郑少军. 反相高效液相色谱分析克拉霉素合成工艺中区域选择性甲基化的关键中间体[J]. 色谱, 2004, 22(3): 237-240
作者姓名:梁建华  姚国伟  郑少军
作者单位:北京理工大学生命科学与技术学院,北京,100081
基金项目:国家经贸委技术创新项目(01BK 009).
摘    要:采用反相高效液相色谱法对克拉霉素合成工艺中关键中间体E-2′,4″-双(三甲基硅)-红霉素A-9-(1-异丙氧环己基)肟、Z-2′,4″-双(三甲基硅)-红霉素A-9-(1-异丙氧环己基)肟和E-2′,4″-双(三甲基硅)-6-甲基红霉素A-9-(1-异丙氧环己基)肟、Z-2′,4″-双(三甲基硅)- 6-甲基红霉素A-9-(1-异丙氧环己基)肟及其相关的6种工艺杂质进行了分离、定性和定量分析。色谱柱为DIKMA公司的Inertsil ODS-3(150 mm×4.6 mm i.d., 5 μm);流动相

关 键 词:高效液相色谱法  硅烷化  甲基化  克拉霉素  醚化  区域选择性    异构体  
文章编号:1000-8713(2004)03-0237-04
修稿时间:2003-08-28

Analysis of the Key Intermediates for the Regioselectivity Control in the Methylation of the Manufacture of Clarithromycin by Reversed-Phase High Performance Liquid Chromatography
LIANG Jianhua,YAO Guowei,ZHENG Shaojun. Analysis of the Key Intermediates for the Regioselectivity Control in the Methylation of the Manufacture of Clarithromycin by Reversed-Phase High Performance Liquid Chromatography[J]. Chinese journal of chromatography, 2004, 22(3): 237-240
Authors:LIANG Jianhua  YAO Guowei  ZHENG Shaojun
Affiliation:School of Life Science and Technology, Beijing Institute of Technology, Beijing 100081, China. ljhbit@bit.edu.com
Abstract:2',4'-O-Bis(trimethylsilyl)erythromycin A-9-O-(1-isopropoxycyclohexyl)oxime (2',4'-TMS-EMIPCH) and 2',4'-O-bis(trimethylsilyl)-6-O-methylerythromycin A-9-O-(1-isopropoxycyclohexyl)oxime (2',4"-TMS-IPCH) are the key intermediates for manufacturing clarithromycin. A qualitative and quantitative method for baseline separation of E- and Z-isomers and related process substances has been established. A DIKMA-Inertsil ODS-3 column (150 mm x 4.6 mm i.d., 5 microm) was used. The column temperature was maintained at 40 degrees C. The mobile phase was CH3CN-H2O (95:5, v/v). The flow rate was 1.5 mL/min and the detection wavelength was UV 205 nm. Good linearities for E-2',4'-TMS-EMIPCH and E-2',4'-TMS-IPCH were obtained in the ranges of 6-60 microg (r = 0.9994) and 6-72 microg (r = 0.9998), respectively. The method described has also been demonstrated to work equally well on other 2',4'-O-bis(trimethylsilyl)erythromycin 9-oxime hydroxyl derivatives, which provided the criterion for optimizing the protective groups at 9-oxime hydroxyl position and the study of regioselectivity of methylation at the 6-OH position.
Keywords:high performance liquid chromatography  clarithromycin  oxime  etherification  silylation  methylation  isomer  regioselectivity
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