期刊文献+

1-脱氢松香酰基-3-取代硫脲以及5-(脱羧脱氢松香-4-基)-3-芳氨基-1H-1,2,4-三唑化合物的合成与生物活性 被引量:7

Synthesis and Biological Activities of 1-Dehydroabietoyl-3-substituted Thiourea and Related 4-Decarboxy-4-{3-[(un)substituted ani- lino]-1H-1,2,4-triazol-5-yl}dehydroabietic Acid Derivatives
原文传递
导出
摘要 以广西的优势资源松香为原料,脱氢松香酸与亚硫酰氯、硫氰化钾分别在回流条件下反应6h和1.5h,得到脱氢松香酰异硫氰酸酯,产率52%;然后与胺在加热回流条件下反应1.5h,得到11种1-脱氢松香酰基-3-取代硫脲4,产率63%~94%;4a~4f分别与水合肼在搅拌下回流反应3~6h,得到6种5-(脱羧脱氢松香-4-基)-3-芳氨基-1H-1,2,4-三唑化合物5,产率70%~94%;所有化合物的结构均经IR,1HNMR,13CNMR和元素分析确认.初步生物活性测试表明,4e,4f,4j,5b对枯草杆菌抑菌率较高,特别是4j在浓度为50mg/L时就达到较好效果;4b,4h,4i,5e在100mg/L时对大肠杆菌的抑菌效果较好. In an attempt to find novel bioactive compounds, a series of 1-dehydroabietoyl-3-substituted thiourea 4 and 4-decarboxy-4-{3-[(un)substituted anilino]-1H-1,2,4-triazol-5-yl}dehydroabietic acid 5 were synthesized from dehydroabietic acid. Compounds 4a~4k were obtained from the reaction of dehydroabietic acyl isothiocyanate with amines, and 5a~5f were prepared by the reaction of 4 with hydrazine hydrate. The structures of the title compounds were confirmed by IR, 1H NMR and 13C NMR. The preliminary biological tests display that some of the title compounds (4j, 4e, 4f and 5b) possess a fungicidal activity against B. subtilis at a test concentration (for 4j: 50 mg/L; for 4e, 4f, 5b: 100 mg/L); 4b, 4h, 4i and 5e possess a fungicidal activity against E. coli at a test concentration of 100 mg/L.
出处 《化学学报》 SCIE CAS CSCD 北大核心 2008年第24期2717-2724,共8页 Acta Chimica Sinica
基金 广西“新世纪十百千人才工程”专项基金(No.2004219) 广西科技开发计划应用基础研究专项基金(桂科基0731054) 广西师大博士科研启动基金 广西师大学科建设基金重点资助项目
关键词 脱氢松香酸 1-脱氢松香酰基-3-取代硫脲 5-(脱羧脱氢松香-4-基)-3-芳氨基-1H-1 2 4-三唑化合物 dehydroabietic acid 1-dehydroabietoyl-3-substituted thiourea 4-decarboxy-4-{3- [(un)substituted anilino]-1H-1 2 4-triazol-5-yl}dehydroabietic acid
  • 相关文献

参考文献21

二级参考文献81

共引文献107

同被引文献145

引证文献7

二级引证文献52

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