Chin. J. Org. Chem. ›› 2006, Vol. 26 ›› Issue (08): 1106-1110. Previous Articles     Next Articles

Reports

N-取代苯基-2-取代-1,3-噻唑烷-3-甲酰胺的合成、结构及生物活性

翁建全*,1,沈德隆1,谭成侠1,欧晓明2   

  1. (1浙江工业大学化学工程与材料学院 杭州 310032)
    (2国家南方农药创制中心湖南基地生测部 长沙 410007)
  • 收稿日期:2005-11-17 修回日期:2006-02-17 发布日期:2006-07-26
  • 通讯作者: 翁建全

Synthesis, Structure and Biological Activities of N-Arylaminocarbonyl-2-oxo/thio-thiazolidine

WENG Jian-Quan*,1,SHEN De-Long1,TAN Cheng-Xia1,OU Xiao-Ming2   

  1. (1 College of Chemical Engineering and Materials Science, Zhejiang University of Technology, Hangzhou 310032)
    (2 Bioassay Department, Hunan Branch of National Southern Pesti-cide Research Centre, Changsha 410007)
  • Received:2005-11-17 Revised:2006-02-17 Published:2006-07-26
  • Contact: WENG Jian-Quan

In order to find new thiazole-heterocycle lead compounds, seventeen N-arylaminocarbonyl-2- oxo/thio-thiazolidine derivatives were synthesized from a coupling reaction of 2-oxo/thio-thiazolidine and aryl isocyanates catalyzed by Et3N. Their structures were confirmed by 1H NMR, IR, MS spectra and elemental analysis. The crystal structure of N-anilinocarbonyl-2-oxothiazolidine was determined by X-ray diffraction analysis. The preliminary bioassay showed that some of them exhibited certain fungicidal and insecticidal activities.

Key words: substituted phenyl isocyanate, biological activity, synthesis, structure, 2-oxo/thio-thiazolidine