有机化学 ›› 2018, Vol. 38 ›› Issue (10): 2731-2735.DOI: 10.6023/cjoc201804029 上一篇    下一篇

研究简报

2-取代苯基-3-(N,N-二甲基甲酰胺基)-4-甲基-1,5-苯并硫氮杂(艹卓)的合成及抑菌活性

许同绣a, 王岩a, 田克情c, 王冉冉a, 闫静怡b, 张萍a   

  1. a 河北师范大学化学与材料科学学院 石家庄 050024;
    b 河北师范大学生命科学学院 石家庄 050024;
    c 河北化工医药职业技术学院化学与环境工程系 石家庄 050026
  • 收稿日期:2018-04-16 修回日期:2018-05-31 发布日期:2018-06-22
  • 通讯作者: 张萍,E-mail:zhangpingp@sina.com E-mail:zhangpingp@sina.com
  • 基金资助:

    河北省自然科学基金(No.B2017205100)资助项目.

Synthesis and Antimicrobial Activity of 2-Substituted-phenyl-3-(N, N-dimethylformamido)-4-methyl-1,5-benzothiazepine

Xu Tongxiua, Wang Yana, Tian Keqingc, Wang Ranrana, Yan Jingyib, Zhang Pinga   

  1. a College of Chemistry and Materials Science, Hebei Normal University, Shijiazhuang 050024;
    b College of Life Science, Hebei Normal University, Shijiazhuang 050024;
    c Environment and Chemical Engineering, Hebei Chemical and Pharmaceutical College, Shijiazhuang 050026
  • Received:2018-04-16 Revised:2018-05-31 Published:2018-06-22
  • Contact: 10.6023/cjoc201804029 E-mail:zhangpingp@sina.com
  • Supported by:

    Project supported by the Natural Science Foundation of Hebei Province (No. B2017205100).

将N,N-二甲基甲酰胺基引入1,5-苯并硫氮杂(艹卓),设计合成了6个2-取代苯基-3-(N,N-二甲基甲酰胺基)-4-甲基-1,5-苯并硫氮杂(艹卓)化合物,研究了它们的合成反应条件,发现其为动力学控制产物.生物活性研究表明,目标化合物对真菌和细菌都有明显的抑制作用,尤其是对新生隐球菌和大肠杆菌有突出的抑制效果.

关键词: 1,5-苯并硫氮杂(艹卓), 动力学控制产物, 热力学控制产物, 抑菌活性

By introducing N,N-dimethylformamido into 1,5-benzothiazepine, 6 compounds of 2-substituted-phenyl-3-(N,N-dimethylformamido)-4-methyl-1,5-benzothiazepine 3a~3f were designed and synthesized, Studies on the synthesis conditions of 3a~3f revealed that 3a~3f were dynamic control products. 3a~3f had obvious inhibitory effect on fungi and bacteria especially for Cryptococcus neoformans and Escherichia coli.

Key words: 1,5-benzothiazepine, dynamic control product, thermodynamic control product, antimicrobical activity