研究论文

新型吡嗪氨基脲类化合物的合成及除草活性

  • 马青森 ,
  • 刘幸海 ,
  • 翁建全 ,
  • 李永曙 ,
  • 张旻 ,
  • 张向阳 ,
  • 谭成侠
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  • 浙江工业大学化学工程与材料学院 杭州 310014

收稿日期: 2013-02-27

  修回日期: 2013-04-02

  网络出版日期: 2013-04-12

基金资助

“十二五”国家科技支撑计划(No. 2011BAE06B03-01);浙江省创新团队(No. 2010R50018)资助项目.

Synthesis and Herbicidal Activity of New Pyrazine Derivative

  • Ma Qingsen ,
  • Liu Xinghai ,
  • Weng Jianquan ,
  • Li Yongshu ,
  • Zhang Min ,
  • Zhang Xiangyang ,
  • Tan Chengxia
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  • College of Chemical Engineering and Materials Science, Zhejiang University of Technology, Hangzhou 310014

Received date: 2013-02-27

  Revised date: 2013-04-02

  Online published: 2013-04-12

Supported by

Project supported by the National Key Technologies R&D Program (No. 2011BAE06B03-01), and the Key Innovation Team of Science and Technology in Zhejiang Province (No. 2010R50018).

摘要

为寻求具有较高生物活性的农药新品种, 根据亚活性拼接原理, 将吡嗪环和氨基脲结构进行亚活性结构拼接, 设计并合成了26个未见文献报道的吡嗪氨基脲类化合物, 其结构均经1H NMR, FTIR和MS确证, 同时对化合物进行了初步除草活性测试. 活性测试结果表明, 在浓度为150 gai/ha时, 4m对反枝苋、鳢肠的芽后抑制率达到80%.

本文引用格式

马青森 , 刘幸海 , 翁建全 , 李永曙 , 张旻 , 张向阳 , 谭成侠 . 新型吡嗪氨基脲类化合物的合成及除草活性[J]. 有机化学, 2013 , 33(08) : 1749 -1754 . DOI: 10.6023/cjoc201301061

Abstract

To find new pesticidal lead compounds with high bioactivity, 26 new pyrazines emicarbazide derivatives were designed and synthesized by combining with the pyrazine ring and semicarbazide. Their structures were confirmed by 1H NMR, FTIR and MS techniques. The herbicidal activities of these compounds were evaluated. The bioassay results showed that the post-emergence inhibitory rate of 4m reached 80% on Amaranthus retroflexus and Eclipta prostrata at 150 gai/ha.

参考文献

[1] Liu, X.-H.; Chen, P.-Q.; Wang, B.-L.; Li, Y.-H.; Wang, S.-H.; Li, Z.-M. Bioorg. Med. Chem. Lett. 2007, 17, 3784.
[2] Liu, X.-H.; Zhang, C.-Y.; Guo, W.-C.; Li, Y.-H.; Chen, P.-Q.; Wang, T.; Dong, W. L.; Sun, H. W.; Li, Z. M. J. Enzyme Inhib. Med. Chem. 2009, 24, 545.
[3] Liu, X.-H.; Shi, Y.-X.; Ma, Y.; Zhang, C.-Y.; Dong, W.-L.; Li, P.; Wang, B.-L.; Li, B.-J.; Li, Z.-M. Eur. J. Med. Chem. 2009, 44, 2782.
[4] Liu, X.-F.; Liu, X.-H. Acta Crystallogr., Sect. E 2011, 67, O202~U3145.
[5] Song, B.-A.; Wu, J. New Heterocyclic Pesticide (Herbicide), Chemical Industry Press, Beijing, 2011. pp. 143~150 (in Chinese).
(宋宝安, 吴剑, 新杂环农药(除草剂), 化学工业出版社, 北京, 2011. pp. 143~150.)
[6] Elsevier Ltd. Tuberculosis 2008, 88(2), 141.
[7] Zhou, L.-Y.; Feng, Y.-Q.; Qu, H.-M. Chem. Prop. Polym. Mater. 2002, 88(4), 4.
[8] Fischer, G. C. US 4742167, 1988[Chem. Abstr. 1988, 109, 73476].
[9] Merce, B.; Jesus, A.; Jaume, P.; Ramon, C. J. Agric. Food Chem. 2000, 48(1), 83.
[10] Allison, C. G.; Chambers, R. D. GB 1342598, 1974[Chem. Abstr. 1974, 80, 133478].
[11] Gulbenk, A. H.; Johnstou, H. US 3746707, 1973[Chem. Abstr. 1973, 79, 105301].
[12] Johnston, D. B. US 4518599, 1985[Chem. Abstr. 1985, 103, 87908].
[13] Krumkalns, E. V. EP 109299, 1984[Chem. Abstr. 1984, 101, 110960].
[14] Allison, C. G.; Chambers, R. D. GB 1342598, 1974 [Chem. Abstr. 1974, 80, 133470].
[15] John, L. M. US 4160834, 1979[Chem. Abstr. 1979, 91, 140598].
[16] Tumova, L.; Gallova, K.; Rimakova, J. Acta Physiol. Plant. 2005, 27(3B), 357.
[17] Zhang, X.-Y.; Li, Y.-S.; Weng, J.-Q.; Tan, C.-X. Chin. J. Org. Chem. 2011, 31(8), 1295 (in Chinese).
(张向阳, 李永曙, 翁建全, 谭成侠, 有机化学, 2011, 31(8), 1295.)
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