蚯蚓催化抗凝血药华法林及其衍生物的合成
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
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).
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
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.
Key words: biocatalysis; the crude extract of earthworms; warfarin; Michael reaction
[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
/
| 〈 |
|
〉 |