Chinese Journal of Organic Chemistry ›› 2020, Vol. 40 ›› Issue (8): 2547-2554.DOI: 10.6023/cjoc202004050 Previous Articles     Next Articles


赵宇, 刘鑫磊, 李益豪, 许磊川, 苏彦豪, 蒋家珍, 王明安   

  1. 中国农业大学应用化学系 农药创新研究中心 北京 100193
  • 收稿日期:2020-04-29 修回日期:2020-05-10 发布日期:2020-05-29
  • 通讯作者: 王明安
  • 基金资助:

Synthesis and Unexpected Insecticidal Activity of (E)-3-(1-Imino-ethyl)-5,5-disubstituted-4-(methylamino)furan-2(5H)-one

Zhao Yu, Liu Xinlei, Li Yihao, Xu Leichuan, Su Yanhao, Jiang Jiazhen, Wang Ming'an   

  1. Innovation Center of Pesticide Research, Department of Applied Chemistry, China Agricultural University, Beijing 100193
  • Received:2020-04-29 Revised:2020-05-10 Published:2020-05-29
  • Supported by:
    Project supported by the National Natural Science Foundation of China (No. 21772229).

In order to improve the fungicidal activity against phytopathogens and enlarge the constructed molecular library, eighteen novel (E)-3-(1-iminoethyl)-5,5-disubstituted-4-(methylamino)-furan-2(5H)-ones were designed and synthesized based on the diversity-oriented synthesis strategy when the C-4 phenyl group of 3-(1-iminoethyl)-5,5-disubstituted-4-phenylfuran-2(5H)-one was replaced with the methylamino group. Their structures were characterized by 1H NMR, 13C NMR, HR-MS spectral data. The crystal structure of (E)-3-(1-((4-methoxybenzyloxy)imino)ethyl)-4-(methylamino)-1-oxaspiro[4.5]dec-3-en-2-one (5O) was determined by X-ray diffraction analysis. The bioassay results indicated that all compounds did not exhibit significant in vivo fungicidal activities against phytopathogens, but some of them showed good insecticidal activities against Plutella xylostella, Mythimna seprata and Myzus persicae with 100% mortality at the concentration of 600 μg/mL.

Key words: (E)-3-(1-iminoethyl)-5,5-disubstituted-4-(methylamino)furan-2(5H)-one, diversity-oriented synthesis, oxime ether scaffold, insecticidal activity