期刊文献+

新型邻吡唑甲酰胺基苯甲酰胺化合物设计、合成与生物活性研究

Design, synthesis and biological activities of a novel o-pyrazole formamidobenzamide derivative
原文传递
导出
摘要 近年来,已经有多种具备广泛生物活性的邻吡唑甲酰胺基苯甲酰胺类杀虫剂被研制出来。为了开发高效、低毒和环境友好型绿色生态杀虫剂,以邻氨基苯甲酸和2-(3-氯-2-吡啶基)-5-氧代-3-吡唑烷羧酸乙酯为主要原料合成了一种新颖邻吡唑甲酰胺基苯甲酰胺化合物,并通过NMR和元素分析确认。初步的生物活性测定结果表明,该化合物对小菜蛾和甜菜夜蛾的生物活性在10mg/kg下均达到100%。 In recent years, many o-pyrazole formamidobenzamide insecticides with extensive biological activities have been developed.In order to develop green insecticides with high bioactivity, low toxicity and environment friendly, a novel o-pyrazole formamidobenzamide derivative was synthesized with o-aminobenzoic acid and ethyl 2-(3-chloro-2-pyridyl)-5-oxo-3-pyrazolidane carboxylate as the main starting materials, which was confirmed by NMR and elemental analysis.Preliminary bioassay results showed that the bioactivity of the compound to both plutella xylostella and asparagus caterpillar reached 100% at 10mg/kg.
作者 唐蜜 刘少华 周红生 李娟 周玮 赵亮 TANG Mi;LIU Shao-hua;ZHOU Hong-sheng;LI Juan;ZHOU Wei;ZHAO Liang(North China Pharmaceutical Co.,Ltd.,Shijiazhuang 050015,China;Hebei Chengxin Co.,Ltd.,Shijiazhuang 051130,China;Hebei Innovation Center of Cyanide Derivatives Technology,Shijiazhuang 051130,China;Hebei Institute of Fine Chemical Industry Technology,Shijiazhuang 051130,China)
出处 《精细与专用化学品》 CAS 2024年第10期32-35,54,共5页 Fine and Specialty Chemicals
关键词 邻吡唑甲酰胺基苯甲酰胺 设计 合成 杀虫活性 o-pyrazole formamidobenzamide design synthesis insecticidal activity
  • 相关文献

参考文献4

二级参考文献44

  • 1杨桂秋,童怡春,杨辉斌,于海波,李斌.新型杀虫剂氯虫苯甲酰胺研究概述[J].世界农药,2012,34(1):31-34. 被引量:54
  • 2Tohnishi, M.; Nakao, H.; Furuya, T.; Seo, A.; Kodama, H.; Tsubata,K.; Fujioka, S.; Kodama, H.; Hirooka, T.; Nishimatsu, T. J. Pestic. Sci. 2005, 30, 354.
  • 3Ebbinghaus-Kintscher, U.; Luemmena, P.; Lobitz, N.; Schulte, T.; Funke, C.; Fischer, R.; Masaki, T.; Yasokawa, N.; Tohnishi, M. Cell Calcium 2006, 39, 21.
  • 4Gewehr, M.; Puhl, M.; Dickhaut, J.; Bastiaans, H. M. M.; Anspaugh, D. D.; Kuhn, D. G.; Oloumi-Sadeghi, H.; Armes, N. WO 2007082841, 2007 [Chem. Abstr. 2007, 147, 159937].
  • 5Muehlebach, M.; Jeanguenat, A.; Hall, R. G. WO 2007080131, 2007 [Chem. Abstr. 2007, 147, 553327].
  • 6Cordova, D.; Benner, E. A.; Sacher, M. A.; Rauh, J. J.; Sopa, J. S.; Lahm, G. P.; Selby, T. P.; Stevenson, T. M.; Flexner, L.; Gutteridge, S.; Rhoades, D. F.; Wu, L.; Smith, R. M.; Tao, Y. Pestic. Biochem. Physiol. 2006, 84, 196.
  • 7Clark, D. A.; Lahm, G. P.; Smith, B. K.; Berry, J. D.; Clagg, D. G. Bioorg. Med. Chem. 2008, 16, 3163.
  • 8Lahm, G. P.; Stevenson, T. M.; Selby, T. P.; Freudenberger, J. H.; Cordova, D.; Flexner, L.; Bellin, C. A.; Dubas, C. M.; Smith, B. K.; Hughes, K. A.; Hollingshaus, J. G.; Clark, C. E.; Benner, E. A. Bioorg. Med Chem. Lett. 2007, 17, 6274.
  • 9Sun, L.; Wang, T.; Ye, S. Chin. J. Chem. 2012, 30, 190.
  • 10Smart, B. E. J. Fluorine Chem. 2001, 109, 3.

共引文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部