研究论文

蚯蚓催化抗凝血药华法林及其衍生物的合成

  • 李志林 ,
  • 周海燕 ,
  • 官智
展开
  • a. 西南大学化学化工学院 重庆市应用化学重点实验室 重庆 400715;
    b. 西南大学生命科学学院 重庆 400715

收稿日期: 2016-12-11

  修回日期: 2017-01-11

  网络出版日期: 2017-02-08

基金资助

“国家级大学生创新创业训练计划”基金(No.201510635004)资助项目.

Synthesis of Anticogulant Warfarin and Its Derivatives by the Crude Earthwarm Extract

  • Li Zhilin ,
  • Zhou Haiyan ,
  • Guan Zhi
Expand
  • a. Key Laboratory of Applied Chemistry of Chongqing Municipality, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715;
    b. School of Life Sciences, Southwest University, Chongqing 400715

Received date: 2016-12-11

  Revised date: 2017-01-11

  Online published: 2017-02-08

Supported by

Project supported by the National Training Program of Innovation and Entrepreneurship for Undergraduates (No. 201510635004).

摘要

报道了蚯蚓粗提物作为生物催化剂催化华法林及其衍生物的合成.采用4-羟基香豆素与苄叉丙酮作为原料,探究了溶剂、催化剂的量、含水量、投料比、温度、反应时间对Michael反应合成华法林的影响.获得最佳反应条件为10%含水量,100 mg蚯蚓粗提物,50℃下反应48 h,4-羟基香豆素与苄叉丙酮投料比为1:3时华法林的最高收率为98%,其衍生物的收率为57%~99%,并有一定的对映选择性(达20%ee).对照实验表明蚯蚓粗提物中的酶催化了该反应.这项工作提供了一个很好的利用天然催化剂合成药物分子及其衍生物的例子.

本文引用格式

李志林 , 周海燕 , 官智 . 蚯蚓催化抗凝血药华法林及其衍生物的合成[J]. 有机化学, 2017 , 37(6) : 1494 -1500 . DOI: 10.6023/cjoc201612035

Abstract

This article describes the synthesis of warfarin and its derivatives by using the crude earthwarm extract as a biocatalyst. Warfarin, an effective anticogulant being used for half a century, has enormous clinic and commercial value. Warfarin and its derivatives are usually prepared through chemical catalysis while biocatalysis was rarely explored. Because biocatalysis is green, sustainable and usually under mild conditions, it is necessary to develop biocatalytic methods for these compounds. It is found that the crude extract of earthwarms is a fine biocatalyst. Earthwarms are harmless and abundant in nature. There are many hydrolases in the alimentary tract of earthwarms, and among of them, proteases are most thoroughly studied. The crude earthwarm extract from Eisenia foetida was prepared, and it was used as a cheap and ecologically friendly biocatalyst for the synthesis of warfarin and its derivatives. The procedure is simple and no additional cofactors and equipments are required. The best results were obtained using l00 mg of earthworm extract in DMSO/water (10% water, V/V) with 1:3 molar ratio of 4-hydroxycoumarin to benzylideneacetone at 50 ℃ for 48 h. Warfarin was obtained in an excellent yield of 98%, and its derivatives were achieved in yields of 57%~99% with some enantioselectivities (up to 20% ee). In addition, control experiments demonstrated that enzyme(s) in the crude extract of earthwarms catalyzed Michael addition reaction. This work provides an alternative method for the synthesis of warfarin and its derivatives by using an easily available natural catalyst.

参考文献

[1] Badran, N. W. DE 2535228, 1976[Chem. Abstr. 1976, 85, 5500].
[2] Hu, D.-Y.; Xu, J.-T. Chin. J. Med. Guide 2001, 3, 249 (in Chinese). (胡大一, 许俊堂, 中国医药导刊, 2001, 3, 249.)
[3] Kristensen, T. E.; Vestli, K.; Hansen, F. K.; Hansen, T. Eur. J. Org. Chem. 2009, 2009, 5185.
[4] Mei, R.-Q.; Xu, X.-Y.; Li, Y.-C.; Fu, J.-Y.; Huang, Q.-C.; Wang, L.-X.; Mei, R.-Q. Tetrahedron Lett. 2011, 52, 1566.
[5] Alexander, S. K.; Dmitry, E. S.; Albert, G. N.; Alexander, O. C.; Sergei, G. Z. Adv. Synth. Catal. 2012, 354, 3078.
[6] Young, J. L.; Dae, Y. K. Bull. Korean Chem. Soc. 2012, 33, 6.
[7] Dong, J.; Du, D.-M. Org. Biomol. Chem. 2012, 10, 8125.
[8] Alexander, S. K.; Vladislav, G. L.; Alexandr, O. C.; Sergei, G. Z. Eur. J. Org. Chem. 2014, 2014, 3808.
[9] Kim, H.; Yen, C.; Preston, P.; Chin, J. Org. Lett. 2006, 8, 23.
[10] Schoemaker, H. E.; Mink, D.; Wubbolts, M. G. Science 2003, 299, 1694.
[11] Sano, K.; Saito, S.; Hirose, Y.; Kohari, Y.; Nakano, H.; Seki, C.; Tokiwa, M.; Takeshita, M.; Uwai, K. Heterocycles 2013, 87, 6.
[12] Liu, W.-L.; Yang, N.-S.; Chen, Y.-T.; Stephen, L.; Wu, C.-Y.; Lin, C.-H.; Huang, H.-Y. Chem. Eur. J. 2015, 21, 115.
[13] Xie, B.-H.; Guan, Z.; He, Y.-H. J. Chem. Technol. Biotechnol. 2012, 87, 1709.
[14] Guan, Z.; Chen, Y.-L.; Yuan, Y.; Song, J.; Yang, D.-C. PLoS One 2014, 9, e105284.
[15] He, Y.-H.; Song, J.; Yang, D.-C.; Guan, Z. Tetrahedron 2015, 71, 5248.
[16] Nakajima, N.; Sugimoto, M.; Ishihara, K. J. Mol. Catal. B: Enzym. 2003, 23, 191.
[17] Liu, J.-F.; Wang, X.-Q.; Xu, L.; Zhang, J.-P.; Liang, D.-C.; Chang, W.-R. Chin. Sci. Bull. 2002, 47, 1718 (in Chinese). (刘俊峰, 王新泉, 徐磊, 张季平, 梁栋材, 常文瑞, 科学通报, 2002, 47, 1718.)
[18] Zhao, H.-Y.; Jing, T.-Y. J. Biochem. Mol. Biol. 1998, 14, 407 (in Chinese). (赵虹瑜, 静天玉, 中国生物化学与分子生物学报, 1998, 14, 407.)
[19] Luisetti, M.; Piccioni, P. D.; Dyne, K.; Donnini, M.; Bulgheroni, A.; Pasturenzi, L.; Donnetta, A. M.; Peona, V. Int. J. Tissue React. 1991, 4, 187.
[20] Zhang, J.; Zhao, L.-M.; Kang, L.-X. China Surfactant Deterg. Cosmet. 2012, 42, 192 (in Chinese). (张剑, 赵雷敏, 康林霞, 日用化学工业, 2012, 42, 192.)
[21] Szymczak, R. M.; Mlynarski, J. Tetrahedron: Asymmetry 2014, 25, 813.
[22] Liu, Y.; Kang, T.-R.; Liu, Q.-Z.; Chen, L.-M.; Wang, Y.-C.; Liu, J.; Xie, Y.-M.; Yang, J.-L.; He, L. Org. Lett. 2013, 15, 6090.
[23] Gladkowski, W.; Skrobiszewski, A.; Mazur, M.; Siepka, M.; Pawlak, A.; Mrukowicz, B. O.; Bialonska, A.; Poradowski, D.; Drynda, A.; Urbaniak, M. Tetrahedron 2013, 69, 10414.
[24] Yang, H.-M.; Li, L.; Jiang, K.-Z.; Jiang, J.-X.; Lai, G.-Q.; Xu, L.-W. Tetrahedron 2010, 66, 9708

文章导航

/