Chem. J. Chinese Universities ›› 2004, Vol. 25 ›› Issue (12): 2259.

• Articles • Previous Articles     Next Articles

Synthesis and Biological Activity of New Phenylsulfonylurea Derivatives

MA Ning1,2, LI Peng-Fei1, LI Yong-Hong1, LI Zheng-Ming1, WANG Ling-Xiu1, WANG Su-Hua1   

  1. 1. State Key Laboratory of Elemento-Organic Chemistry, Institute of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, China;
    2. Department of Chemistry, School of Science, Tianjin University, Tianjin 300072, China
  • Received:2003-10-27 Online:2004-12-24 Published:2004-12-24

Abstract: In order to develop new herbicidal active structures and research the structure-activity relationship, on the basis of the known monosubstituted phenylsulfonylureas with a high activity we designed and synthesized 14 novel sulfonylurea compounds with a single substituting group, such as alkoxy, alkylthio and alkylamino in the pyrimidine ring. The structures of all compounds were confirmed by 1H NMR spectra data and elemental analysis. Herbicidal activitiy including IC50 was determined by rape root length experiment and pot experiment. The results show that the variation of 4- substituting group of the pyrimidine ring affects the activity of the compounds respectively. Herbicidal activity decreases in the sequence of alkoxy, alkylthio and alkylamino substituent.

Key words: Sulfonylurea, Herbicide, Synthesis, Pyrimidine

CLC Number: 

TrendMD: