Chin. J. Org. Chem. ›› 2008, Vol. 28 ›› Issue (07): 1227-1232. Previous Articles     Next Articles

Original Articles

3-取代苄氧基-6-(取代-1H-吡唑-1-基)哒嗪的合成与生物活性

胡方中*; 张桂峰; 邹小毛*; 刘 斌; 朱有全; 杨华铮   

  1. (南开大学元素有机化学国家重点实验室 元素有机化学研究所 天津 300071)

  • 收稿日期:2007-07-19 修回日期:2007-12-07 发布日期:2008-07-28
  • 通讯作者: 胡方中;邹小毛

Synthesis and Biological Activity of 3-(Substituted benzyloxy)- 6-[(un)substituted 1H-prazol-1-yl]pyridazines

HU, Fang-Zhong*; ZHANG, Gui-Feng; ZOU, Xiao-Mao*; LIU, Bin ;
ZHU, You-Quan; YANG, Hua-Zheng
  

  1. (State Key Laboratory of Elemento-Organic Chemistry, Institute of Elemento-Organic Chemistry,
    Nankai University, Tianjin 300071)
  • Received:2007-07-19 Revised:2007-12-07 Published:2008-07-28
  • Contact: HU, Fang-Zhong*; ZOU, Xiao-Mao*;

A series of novel 3-(substituted benzyloxy)-6-[(un)substituted 1H-pyrazol-1-yl]pyridazine derivatives were synthesized through the condensation of various substituted benzyl alcohols with 3-chloro-6-(3,5-dimethyl-1H-pyrazole-1-yl)pyridazine (2) or 3-chloro-6-(1H-pyrazol-1-yl)pyridazine (4). 2 and 4 were obtained from the cyclization of 3-chloro-6-hydrazinylpyridazine with acetoacetone and/or 3-dimethylamino acrolein. The structures of the title compounds were identified by 1H NMR, IR spectra and elemental analysis. Preliminary bioassay showed that all of them possessed some extent herbicidal activity against Brassica campestris and Echinochloa crusgalli.

Key words: synthesis, herbicidal activity, pyridazine