Articles

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).

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.

Cite this article

Li Zhilin , Zhou Haiyan , Guan Zhi . Synthesis of Anticogulant Warfarin and Its Derivatives by the Crude Earthwarm Extract[J]. Chinese Journal of Organic Chemistry, 2017 , 37(6) : 1494 -1500 . DOI: 10.6023/cjoc201612035

References

[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

Outlines

/