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嘧啶联吡唑甲酰胺类化合物的合成及除草活性

彭雪琴 史建俊 彭伟立 唐伟 谭成侠

农药学学报Issue(2):220-224,5.
农药学学报Issue(2):220-224,5.DOI:10.3969/j.issn.1008-7303.2015.02.15

嘧啶联吡唑甲酰胺类化合物的合成及除草活性

Synthesis and herbicidal activity of novel pyrimidine substituted pyrazolecarboxamides

彭雪琴 1史建俊 1彭伟立 2唐伟 2谭成侠1

作者信息

  • 1. 浙江工业大学 化学工程学院,杭州310014
  • 2. 浙江省化工研究院,国家南方农药创制中心浙江基地,杭州310023
  • 折叠

摘要

Abstract

A number of novel pyrimidine substituted pyrazolecarboxamides 5a-5o were synthesized, and their structures were confirmed by 1 H NMR and MS analysis. The preliminary herbicidal activity indicated that Stellaria media growth inhibition rate was over 90% for the compounds( R)-N-[1-(4-chlorophenyl ) ethyl ]-3-( difluoromethyl )-1-( 4 , 6-dimethoxypyrimidin-2-yl )-1 H-pyrazole-4-carboxamide ( 5 c ) , N-( 1-( 4-chlorophenyl ) ethyl )-1-( 4 , 6-dimethoxypyrimidin-2-yl )-N-methyl-3-( trifluoromethyl )-1 H-pyrazole-4-carboxamide ( 5 i ) and N-( 1-( 4-chlorophenyl ) ethyl )-1-( 4 , 6-dimethoxypyrimidin-2-yl)-3-( trifluoromethyl )-1 H-pyrazole-4-carboxamide ( 5 k ) by postemergence foliar spray processing at 150 g/hm2; and the compounds N-[ 1-( 4-chlorophenyl ) ethyl ]-3-( difluoromethyl )-1-( 4 , 6-dimethoxy-pyrimidin-2-yl )-1 H-pyrazole-4-carboxamide ( 5 b ) and 5 c showed inhibition rate of 100% against S. media by preemergence soil spray processing at the same dose. Compounds of this structure can be potentially used as lead compounds for herbicide.

关键词

嘧啶联吡唑甲酰胺/合成/除草活性

Key words

pyrimidine substituted pyrazolecarboxamides/synthesis/herbicidal activity

分类

化学化工

引用本文复制引用

彭雪琴,史建俊,彭伟立,唐伟,谭成侠..嘧啶联吡唑甲酰胺类化合物的合成及除草活性[J].农药学学报,2015,(2):220-224,5.

基金项目

“十二五”国家科技支撑计划项目(2011BAE06B03-01) (2011BAE06B03-01)

农药学学报

OA北大核心CSCDCSTPCD

1008-7303

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