Chemical Research in Chinese Universities ›› 2012, Vol. 28 ›› Issue (3): 424-429.

• Articles • Previous Articles     Next Articles

Synthesis and Antibacterial Activities of 1,4-Disubstituted Phenyl-5-(halo-2-hydroxyphenyl)imino-1,2,3-triazole

ZHAO Xu1, LU Jun-rui1, XIN Chun-wei1, LU Bo-wei2, BAO Xiu-rong1, LI Jian-fa1, LIU Ya1, YANG Xu-yun1, YUAN Yi1   

  1. 1. College of Chemistry and Chemical Engineering, Tianjin University of Technology, Tianjin 300384, P. R. China;
    2. College of Chemistry, Nankai University, Tianjin 300071, P. R. China
  • Received:2011-11-24 Revised:2011-12-12 Online:2012-05-25 Published:2012-05-03
  • Contact: LU Jun-rui E-mail:lujunrui@tjut.edu.cn
  • Supported by:

    Supported by the National Natural Science Foundation of China(Nos.20976135, 21176194).

Abstract: According to the superposition principle of reinforcement of biological activities, 24 novel 1,4- disubstituted phenyl-5-(halo-2-hydroxyphenyl)imino-1,2,3-triazoles was synthesized and characterized by 1H NMR, 13C NMR, elemental analysis and IR. All the target compounds were screened for their antibacterial potential in vitro against Monilia albican, Escherichia coli and Staphylococcus aureus. It was shown that all the compounds possessed efficient antibacterial activities at a concentration of 0.1 mg/mL, even at a concentration of 0.01 mg/mL, some of the compounds still exhibited antibacterial activities against Escherichia coli and Monilia albican. At last, the structure- activity relationship was discussed based on the antibacterial results.

Key words: 1,4-Disubstituted phenyl-5-(halo-2-hydroxyphenyl)imino-1,2,3-triazole, Antibacterial activity, Structureactivity relationship