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1-(吡唑-5-酰基)-1H-取代吡唑的合成及生物活性
引用本文:谭成侠,沈德隆,翁建全,欧晓明,樊德方.1-(吡唑-5-酰基)-1H-取代吡唑的合成及生物活性[J].农药学学报,2005,7(1):69-72.
作者姓名:谭成侠  沈德隆  翁建全  欧晓明  樊德方
作者单位:1.浙江大学 农业与生物技术学院,浙江 杭州 310029
基金项目:浙江省教育厅资助项目(20030145).
摘    要:为了寻求新的含吡唑双杂环先导化合物,用4-取代-1-甲基-3-乙基-5-吡唑甲酰氯与3-甲基-5-吡唑酮、3-乙基-5-吡唑甲酸乙酯等含氮杂环反应得到了8个新的含吡唑环的双杂环类化合物。经IR、1H NMR、MS和元素分析对化合物的结构进行了表征。初步生物活性实验结果表明:在25 μg/mL浓度下, 5d 对水稻稻瘟病菌Pyricularia oryzae的抑制率为45.6%;在500 μg/mL浓度下, 5c 对稻黑尾叶蝉Nephotettix cincticeps的死亡率为53.9%。

关 键 词:吡唑    双杂环    含氮杂环    生物活性
文章编号:1008-7303(2005)01-0069-04
收稿时间:2004/6/24 0:00:00
修稿时间:2004年6月24日

Synthesis of 1H-Substituted 1- pyrazole, and their Biological Activities
TAN Cheng-xi,SHEN De-long,WENG Jian-quan,OU Xiao-ming and FAN De-fang.Synthesis of 1H-Substituted 1- pyrazole, and their Biological Activities[J].Chinese Journal of Pesticide Science,2005,7(1):69-72.
Authors:TAN Cheng-xi  SHEN De-long  WENG Jian-quan  OU Xiao-ming and FAN De-fang
Institution:1.College of Agric & Biotech, Zhejiang University, Hangzhou 310029, China2.College of Chemical Engineering & Materials, Zhejiang University of Technology, Hangzhou 310014, China3.Bioassay Department, Hunan Branch of National Southern Pesticide Research Centre, Changsha 410007, China
Abstract:In order to search for the new pyrazolyl-heterocycles lead compounds, eight pyrazolyl-heterocycles were synthesized from 3-ethyl-1-methyl- 4-substituted-5-pyrazolecarboxylic acid chloride and nitrogen heterocyclic rings such as 3-methyl-5-pyrazolone, 1H-3-ethyl-5-pyrazole carboxylic ethyl ester, etc. The structures of the new compounds were confirmed by 1H NMR, IR, MS and elementary analysis. The results of pretiminary biological tests indicated that compound 5d showed inhibitory activities (45.6%) against Pyricularia oryzae at 25 μg/mL. 5c showed inhibitory activities (53.9%) against Nephotettix cincticeps at 500 μg/mL.
Keywords:pyrazole  bis-heterocycles  nitrogen heterocyclic rings  biological activity
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