研究简报

腐殖酸催化合成1,4-二氢吡啶类化合物

  • 魏振中 ,
  • 李江飞 ,
  • 王泽云 ,
  • 李品华 ,
  • 王永秋
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  • 淮北师范大学化学与材料科学学院 淮北 235000

收稿日期: 2016-12-22

  修回日期: 2017-03-13

  网络出版日期: 2017-04-10

基金资助

安徽省先进功能复合材料协同创新中心开放基金(No.20160804)资助项目.

Synthesis of 1,4-Dihydropyridine Compounds Catalyzed by Humic Acid

  • Wei Zhenzhong ,
  • Li Jiangfei ,
  • Wang Zeyun ,
  • Li Pinhua ,
  • Wang Yongqiu
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  • Department of Chemistry and Materials Science, Huaibei Normal University, Huaibei 235000

Received date: 2016-12-22

  Revised date: 2017-03-13

  Online published: 2017-04-10

Supported by

Project supported by the Open Fund of Anhui Collaborative Innovation Center for Advanced Function Composites (No.20160804).

摘要

芳醛、乙酰乙酸乙酯(甲酯)和乙酸铵为原料,用腐殖酸催化一锅法合成1,4-二氢吡啶类化合物.该法产率较高,操作简单.催化剂易于回收再利用,环境友好.

本文引用格式

魏振中 , 李江飞 , 王泽云 , 李品华 , 王永秋 . 腐殖酸催化合成1,4-二氢吡啶类化合物[J]. 有机化学, 2017 , 37(7) : 1835 -1838 . DOI: 10.6023/cjoc201612055

Abstract

A novel, efficient and straightforward method to synthesize 1,4-dihydropyridine compounds with excellent yields is reported through Hantzsch reaction of aldehydes, ammonium acetate and ethyl acetoacetate or methyl acetoacetate using humic acid as the catalyst. This method has high yield and less pollution. The catalyst is easy to recycle and environment friendly.

参考文献

[1] Goldmann, S.; Stoltefuss, J. Angew. Chem., Int. Ed. 1991, 30, 1559.
[2] Lu, L.-L.; Xu, H.; Zhou, P.; Yu, F.-C. Chin. J. Org. Chem. 2016, 36, 2858(in Chinese). (鲁玲玲, 许辉, 周攀, 余富朝, 有机化学, 2016, 36, 2858.)
[3] Soo-Jeong, C.; Joong-Heui, C.; Isak, I. Eur. J. Med. Chem. 2010, 45, 2578.
[4] Hilgroth, A.; Lilie, H. Eur. J. Med. Chem. 2003, 38, 495.
[5] Prashantha, K. B. R.; Pankaj, M.; Karthikeyan, E.; Ankur, B.; Suja, P. V. Med. Chem. Res. 2010, 19, 344.
[6] Samzadeh, K. A.; Shafaroodi, H.; Miri, R.; Mirkhani, H. Med. Chem. Res. 2009, 18, 112.
[7] Kharkar, P. S.; Desai, B.; Gaveria, H. J. Med. Chem. 2002, 45, 4858.
[8] Cooper, K.; Fray, M. J.; Parry, M. J. J. Med. Chem. 1992, 35, 3115.
[9] Nasr, M.; Hoseini, S.; Montazerozohori, M.; Mehrabi, R.; Nasrabadi, H. J. Mol. Catal. A:Chem. 2014, 382, 99.
[10] Bitaraf, M.; Ali, A.; Otokesh, S. J. Chin. Chem. Soc. 2016, 63, 336.
[11] Tamaddon, F.; Ghazi, S. Catal. Commun. 2015, 72, 63.
[12] Guo, S.-R.; Yuan, Y.-Q.; Zhang, C.-N.; Wu, X.-M.; Sun, C. Chin. J. Org. Chem. 2010, 28, 811(in Chinese). (郭圣荣, 袁艳琴, 张春牛, 吴香梅, 孙晨, 有机化学, 2010, 28, 811.)
[13] Li, J.-P.; Chou, J.-K.; Li, H.-J.; Zhang, G.-S. Chin. J. Org. Chem. 2011, 29, 511(in Chinese). (李建平, 仇记宽, 李会娟, 张贵生, 有机化学, 2011, 29, 511.)
[14] Wang, D.-L.; Dong, Z.; Liu Z.; Zhao W.; Yang, F.-F. Chin. J. Org. Chem. 2014, 34, 783(in Chinese). (王道林, 董哲, 刘忠, 赵伟, 杨菲菲, 有机化学, 2014, 34, 783.)
[15] Pei, W.; Wang, Q.; Li, X.-N.; Sun, C. Chin. J. Chem. 2010, 28, 483.
[16] Nikoorazm, M.; Ghorbani, C. A.; Khanmoradi, M. RSC Adv. 2016, 6, 56549.
[17] Ananda, K. T.; Mohan, C. V. S.; Satyanarayana, K. Synth. Commun. 2014, 44, 574.
[18] Tabassum, S.; Govindaraju, S.; Khan, R.; Pasha, M. A. RSC Adv. 2016, 6, 29802.
[19] Khaskel, A.; Barman, P. Heteroat. Chem. 2016, 27, 114.
[20] Zhang, Z.; Zeng, X.; Xie, D.; Chen, D.; Ding, L,; Wang, A.; Yang, L.; Zhong, G. Org. Lett. 2015, 17, 5052.
[21] Jiang, Y.-H.; Yan, C.-G. Chin. J. Chem. 2016, 34, 1255.
[22] Lin, W.; Zheng, Y.-X.; Huang, Z.-B.; Shi, D.-Q. Chin. J. Org. Chem. 2017, 37, 508(in Chinese). (林伟, 郑永祥, 黄志斌, 史达清, 有机化学, 2017, 37, 508.)
[23] Shabalala, N.; Maddila, S.; Jonnalagadda, S. B. New J. Chem. 2016, 40, 5107.
[24] Kumar, A.; Sharma, S. Green Chem. 2011, 13, 2017.
[25] Wang, R.; Liu, X.; Wu, R.; Yu, B.; Li, H. RSC Adv. 2016, 6, 11.
[26] Xu, Q.-J.; Zhou, D.-P.; Cui, Y.-C. Chin. J. Org. Chem. 2007, 27, 1520(in Chinese). (徐启杰, 周大鹏, 崔元臣, 有机化学, 2007, 27, 1520.)

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