有机化学 ›› 2004, Vol. 24 ›› Issue (7): 797-801. 上一篇    下一篇

研究论文

1-[2-(2,4-二氯苯氧)乙酰基]-5-氨基-1H-吡唑衍生物的合成与生物活性

王宏青a,b, 刘惠a, 刘钊杰*,a   

  1. a华中师范大学有机合成研究所 武汉 430079
    b南华大学化学化工学院 衡阳 421001
  • 收稿日期:2003-09-15 修回日期:2003-11-25 接受日期:2004-02-12 发布日期:2022-09-20
  • 通讯作者: *E-mail: zhjliu@ccnu.edu.cn
  • 基金资助:
    科技部国家“九五”重点科技攻关(No. 97-563-02-05)资助项目

Synthesis and Biological Activity of 1-[2-(2,4-Dichlorophenoxyl)acetyl]- 5-amino-1H-pyrazole Derivatives

WANG, Hong-Qinga,b, LIU, Huia, LIU, Zhao-Jie*,a   

  1. a Institute of Organic Synthesis, Central China Normal University, Wuhan 430079
    b College of Chemistry & Chemical Engineering, Nanhua University, Hengyang 421001
  • Received:2003-09-15 Revised:2003-11-25 Accepted:2004-02-12 Published:2022-09-20

为寻求高效低毒的农药,设计、合成了一系列新的1-[2-(2,4-二氯苯氧)乙酰基]-5-氨基-1H-吡唑衍生物3a~3j和4a~4d.元素分析,1H NMR, IR和MS证实了它们的结构.初步的生物活性测试结果表明,在10 mg/L浓度下,化合物3a~3j和4a~4d对油菜的根茎均有很好的抑制作用,对油菜的根的抑制率为90.0%~98.7%;于100 mg/L浓度下,对稗草的根抑制率为84.0%~100%.

关键词: 1-[2-(2,4-二氯苯氧)乙酰基]吡唑, 合成, 除草活性

In an attempt to discover novel compounds with high activity and low toxicity, a series of new 1-[2-(2,4-dichlorophenoxyl)acetyl]-5-amino-1H-pyrazole derivatives 3a~3j and 4a~4d have beendesigned and synthesized by the reaction of 2,4-dichlorophenoxylacetyl chloridewith 5-amino-1H-pyrazole. The structures of all new compounds were confirmed by elemental analyses, 1H NMR, IR and MS spectroscopies. The results of preliminary bioassay indicate that compounds 3a~3j and 4a~4d possess high herbicidal activity against the root of rape and barnyard grass.

Key words: 1-[2-(2,4-dichlorophenoxyl)acetyl]pyrazole, synthesis, herbicide