史海健, 王忠义, 史好新. 3-芳基/芳氧甲基-6-芳基-1,2,4-三唑并[3,4-b]-1,3,4-噻二唑衍生物的合成及生物活性J. 药学学报, 1999, 34(2): 151-152.
引用本文: 史海健, 王忠义, 史好新. 3-芳基/芳氧甲基-6-芳基-1,2,4-三唑并[3,4-b]-1,3,4-噻二唑衍生物的合成及生物活性J. 药学学报, 1999, 34(2): 151-152.
Shi Haijian , Shi Haoxin, Wang Zhongyi, . SYNTHESIS AND BIOLOGICAL ACTIVITIES OF DERIVATIVES OF 3-ARYL/ARYLOXYMETHYL-6-ARYL-1,2,4-TRIAZOLO[3,4-B]-1,3,4-THIADIAZOLESJ. Acta Pharmaceutica Sinica, 1999, 34(2): 151-152.
Citation: Shi Haijian , Shi Haoxin, Wang Zhongyi, . SYNTHESIS AND BIOLOGICAL ACTIVITIES OF DERIVATIVES OF 3-ARYL/ARYLOXYMETHYL-6-ARYL-1,2,4-TRIAZOLO[3,4-B]-1,3,4-THIADIAZOLESJ. Acta Pharmaceutica Sinica, 1999, 34(2): 151-152.

3-芳基/芳氧甲基-6-芳基-1,2,4-三唑并[3,4-b]-1,3,4-噻二唑衍生物的合成及生物活性

SYNTHESIS AND BIOLOGICAL ACTIVITIES OF DERIVATIVES OF 3-ARYL/ARYLOXYMETHYL-6-ARYL-1,2,4-TRIAZOLO[3,4-B]-1,3,4-THIADIAZOLES

  • Abstract: AIM: To synthesize a number of novel heterocyclic compounds and screen for their biological activities. Sixteen title compounds were prepared. METHODS: These novel compounds were prepared by the reaction of 3-aryl/aryloxymethyl-4-amino-5-mercapto-1,2,4-triazoles with aryl carboxylic acids in the presence of phosphorus oxychloride. The structures of these compounds were confirmed by elemental analysis, IR, 1HNMR and MS. The reaction conditions for the synthesis had been investigated. All the compounds were screened for antimicrobial activity against bacteria S.aureus, E.coli and B.subilis. The concentration of the test compounds was 0.002%. The antibacterial activities of the test compounds were compared with those of penicillin and gentamicin. RESULTS: The results display that some of them possess strong biological activities.CONCLUSION: Syntheses of these novel heterocyclic compounds and study on their biological activities are very important and valuable in medicine.

     

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