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新型吡唑双酰肼类化合物的合成及除草活性
引用本文:何海琴,戴志猛,谢旭峰,刘幸海,谭成侠.新型吡唑双酰肼类化合物的合成及除草活性[J].农药学学报,2016,18(1):113-118.
作者姓名:何海琴  戴志猛  谢旭峰  刘幸海  谭成侠
作者单位:1.浙江工业大学化学工程学院, 杭州 310014
基金项目:十二五国家科技支撑计划资助项目(2011BAE06B02-04);浙江省重点科技创新团队资助项目(2010R50018).
摘    要:为了寻找具有较高除草活性的农药先导化合物,将吡唑环与双酰肼结构进行拼接,设计合成了13个未见报道的含吡唑环的双酰肼类目标化合物6a~6m,其结构均通过核磁共振氢谱及高分辨质谱确认。培养皿法测定结果表明:在200 mg/L下,化合物N'-(2-(2,4-二氯苯氧基)乙酰基)-3-(二氟甲基)-1-甲基-1H-吡唑-4-甲酰肼(6i)对小麦Triticum aestivum、油菜Brassicacampestris、高粱Sorghum bicolor、萝卜Raphanus sativus和黄瓜Cucumis sativus根、茎的抑制率均达80%以上。盆栽试验表明:在有效成分150 g/hm2剂量下,采用苗后茎叶喷雾处理,化合物6i对反枝苋Amaranthus retroflexus和鳢肠Eclipta prostrata的抑制率均达80%;相同剂量下采用苗前土壤喷雾处理,6i对反枝苋A. retroflexus的抑制率也达80%。

关 键 词:吡唑    双酰肼    合成    除草活性
收稿时间:2015/10/30 0:00:00

Synthesis and herbicidal activity evaluation of novel diacylhydrazine derivatives containing pyrazolyl moiety
HE Haiqin,DAI Zhimeng,XIE Xufeng,LIU Xinghai and TAN Chengxia.Synthesis and herbicidal activity evaluation of novel diacylhydrazine derivatives containing pyrazolyl moiety[J].Chinese Journal of Pesticide Science,2016,18(1):113-118.
Authors:HE Haiqin  DAI Zhimeng  XIE Xufeng  LIU Xinghai and TAN Chengxia
Institution:1.College of Chemical Engineering, Zhejiang University of Technology, Hangzhou 310014, China2.Lanxi Baigao Chemical Co. Ltd., Jinhua 310000, Zhejiang Province, China
Abstract:In order to discover pesticide lead compounds with high herbicidal activity, 13 novel diacylhydrazine derivatives containing pyrazolyl pharmacophore were designed and synthesized by introducing the pyrazolyl pharmacophore into the diacylhydrazine scaffold. Their structures were confirmed by 1H NMR and HRMS. The herbicidal activity of these compounds was evaluated. The dish test results indicated that the growth inhibition rates of the roots and stems of Triticum aestivum, Brassica campestris, Sorghum bicolor and Cucumi sativus were up to 80% for N'-(2-(2,4-dichlorophenoxy) acetyl)-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carbohydrazide (6i) at the dosage of 200 mg/L. The pot test results showed that the growth inhibition rate of Amaranthus retroflexus and Eclipta prostrate for compound 6i were 80% by postemergence foliar spray processing at the dose of 150 g/hm2; and compound 6i also demonstrated inhibition rate of 80% against A. retroflexus by preemergence soil spray processing at the same dose.
Keywords:pyrazole  diacylhydrazine  synthesis  herbicidal activity
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