应用化学 ›› 2015, Vol. 32 ›› Issue (4): 399-404.DOI: 10.11944/j.issn.1000-0518.2015.04.140359

• 研究论文 • 上一篇    下一篇

含噻唑、硫醚结构的1,2,4-三唑类化合物的合成及生物活性

钱存卫a*, 黄海军b, 费正皓a, 张愉晴a, 王栋a, 宗乾收c   

  1. a盐城师范学院化学化工学院 江苏 盐城 224007
    b盐城利民农化有限公司 江苏 盐城 224005
    c嘉兴学院生物与化学工程学院 浙江 嘉兴314001
  • 收稿日期:2014-10-21 修回日期:2014-10-29 出版日期:2015-04-10 发布日期:2015-04-10
  • 通讯作者: 钱存卫,讲师; Tel:0515-88233662; Fax:0515-88231709; E-mail:qiancunwei@163.com; 研究方向:氮杂环化合物合成、结构和生物活性
  • 基金资助:
    2013年江苏省科技支撑(工业)项目基金(SBE201330457)江苏省高校自然科学基金(14JKD150009)资助

Synthesis and Bioactivity of New 1,2,4-Triazole Compounds Containing Thiazole and Thioether

QIAN Cunweia, *, HUANG Haijunb, FEI Zhenghaoa, ZHANG Yuqinga, WANG Donga, ZONG Qianshouc   

  1. aSchool of Chemistry and Chemical Engineering,Yancheng Teachers University,Yancheng,Jiangsu 224007,China
    bYancheng Limin Chemical Company Limited,Yancheng,Jiangsu 224005,China
    cCollege of Biology and Chemical Engineering,Jiaxing University,Jiaxing,Zhejiang 314001,China
  • Received:2014-10-21 Revised:2014-10-29 Published:2015-04-10 Online:2015-04-10
  • Contact: Corresponding author:QIAN Cunwei, lecturer; Tel:0515-88233662; Fax:0515-88231709; E-mail:qiancunwei@163.com; Research interests:synthesis, structure and biological activity of nitrogen heterocyclic compounds
  • Supported by:
    Supported by the Program of the Science and Technology Support Plan of Jiangsu Province(No.SBE201330457), the Natural Science Foundation of the Jiangsu Higher Education Institutions of China(No.14JKD150009)

摘要:

以三氟乙酰乙酸乙酯、磺酰氯、水合肼、异硫氰酸苯酯、碘代芳烃、氯乙酸等为原料,设计、合成了7种新型的含噻唑环、硫醚和三氟甲基的1,2,4-三氮唑类化合物,通过1H NMR、13C NMR、19F NMR和MS等技术手段对新化合物进行了结构表征。 杀菌活性测试表明,化合物6b、6d和6g在浓度为100 mg/L时对纹枯病菌(Rhizoctoniasolani)的抑制率分别为91%、92%和93%。

 

关键词: 噻唑, 三氮唑, 硫醚, 合成, 生物活性

Abstract:

Seven novel 1,2,4-triazole derivatives containing thioether and thiazole were designed and synthesized from ethyl 4,4,4-trifluoro-3-oxobutanoate, sulfonyl chloride, hydrazine hydrate, phenyl isothiocyanate, aryl iodides, chloroacetic acid as starting materials via substitution, hydrazinolysis, cyclization and Ullmann coupling. The structures of these compounds were characterized with 13C NMR, 1H NMR, 19F NMR and MS. Bactericidal activity test shows that Rhizoctoniasolani can be inhibited by compounds 6b, 6d, and 6g at a concentration of 100 mg/L with inhibition rates of 91%, 92% and 93%, respectively.

Key words: thioether, thiazole, triazole, synthesis, bioactivity

中图分类号: