期刊文献+

嘧啶双酰肼类化合物的合成及杀菌活性 被引量:1

Synthesis and fungicidal activity evaluation of diacylhydrazine derivatives containing pyrimidine moiety
下载PDF
导出
摘要 以氰基乙酰胺为原料,经过缩合、环化、水解、酯化、肼解、酰化等步骤,设计合成了一系列新型嘧啶双酰肼类化合物。通过IR,~1H NMR,^(13)C NMR,MS和元素分析进行确证其结构。对该类化合物的杀菌活性初步测试结果表明目标产物具有一定的杀菌活性。 Based on 2-cyanoacetamide as raw material,novel diacylhydrazine derivatives containing pyrimidine pharmacophore were designed and synthesized through several step reactions including condensation,cyclization,hydrolysis,esterification,and hydrazidation. The structures of these compounds were characterized by IR,~1H NMR,^(13) C NMR,MS and elemental analysis.Preliminary bioassay results showed that the target compounds had relatively fungicidalactivity.
出处 《化学研究与应用》 CSCD 北大核心 2017年第6期810-815,共6页 Chemical Research and Application
基金 贵阳学院人才引进基金项目资助 黔科合基础基金项目([2016]1006)资助 黔教合基金项目(KY字[2016]091)资助
关键词 嘧啶 双酰肼 杀菌 合成 pyrimidine diacylhydrazine fungicide synthesis
  • 相关文献

参考文献4

二级参考文献29

  • 1虞心红,汤建,温新民,毛庆华,沈永嘉.抗高血压新药奥美沙坦的合成[J].华东理工大学学报(自然科学版),2005,31(2):189-192. 被引量:9
  • 2魏太保,李满林,林奇,刘洪,张有明.芳醛-N-(1-苯基-1H-四唑-5-巯基)乙酰腙的微波合成及其晶体结构[J].有机化学,2006,26(4):477-481. 被引量:13
  • 3Dale A G, Hinds J, Mann J, et al. Symmetric bis-? benz- imidazoles are potent anti-staphylococcal agents with dual inhibitory mechanisms against DNA gyrase[J]. Biochemis- try,2012,51 (29) :5860-5871.
  • 4Steel H C, Tintinger G R, Anderson R. Comparison of the anti-inflammatory activities of imidazole antimycotics in re- lation to molecular structure [ J ]. Chem Biol Drug Des, 2008,72(3 ) :225-228.
  • 5Sorrenti V, Salerno L, Giacomo C D, et al. Imidole deriv- atives as antioxidants and selective inhibitors of nNOS [ J]. Nitric Oxide-Biol Ch,2006,14( 1 ) :45-50.
  • 6Yanagisawa H, Amemiya Y, Kanazaki T, et al. Nonpeptide angiotensin II receptor antagonists : synthesis, biological ac- tivities, and structure-activity relationships of imidazole-5- carboxylic acids bearing alkyl, alkenyl, and hydroxyalkyl substituents at the 4-position and their related compounds [ J]. J Med Chem, 1996,39( 1 ) :323-338.
  • 7Ajani, 0 O, Obafemi, C A, Nwinyi 0 C, et al. Microwave assisted synthesis and antimicrobial activity of 2-quinoxali- none-3-hydrazone derivatives [ J ]. Bioorg Med Chem, 2010,18( 1 ) :214-221.
  • 8Xia Y L, Cbuan-Dong F, Zhao B X, et al. Synthesis and structure-activity relationships of novel 1-arylmethyl-3-ar- yl-lH-pyrazole-5-carbohydrazide hydrazone derivatives as potential agents against A549 lung cancer ceils [ J ]. Eur J Med Chem ,2008,43 ( 11 ) :2347-2353.
  • 9Melnyk P, Leroux V, Serghergert C ,et al. Design, synthesis and in vitro antimalarial activity of an acylhydrazone li-brary[J].BioorgMedChemLett,2006,16(1):31-35.
  • 10Gupta P, Hameed S, Jain R. Ring-substituted imidazoles as a new class of anti-tuberculosis agents[ J]. Eur J Med Chem,2004 ,39( 9 ) :805-814.

共引文献15

同被引文献2

引证文献1

二级引证文献3

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