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高等学校化学研究 ›› 1997, Vol. 13 ›› Issue (1): 27-33.

• Articles • 上一篇    下一篇

Studies on Thiosemicarbazides and Related Heterocycles(ⅩⅩⅤⅠ) ——Synthesis of 3-[5'-amino-1'-(4" chlorophenyl)-1', 2', 3'-triazol-4 yl]-4-aryl-1, 2, 4-triazoline-5-thiones

ZHANG Zi-yi, DONG Heng-shan, GUAN Zuo-wu   

  1. National Laboratory of Applied Organic Chemistry, Department of Chemistry, Lanzhou University, Lanzhou 730000
  • 收稿日期:1996-03-08 出版日期:1997-01-24 发布日期:2011-08-17
  • 基金资助:

    Supported by the National Natural Science Foundation of China.

Studies on Thiosemicarbazides and Related Heterocycles(ⅩⅩⅤⅠ) ——Synthesis of 3-[5'-amino-1'-(4" chlorophenyl)-1', 2', 3'-triazol-4 yl]-4-aryl-1, 2, 4-triazoline-5-thiones

ZHANG Zi-yi, DONG Heng-shan, GUAN Zuo-wu   

  1. National Laboratory of Applied Organic Chemistry, Department of Chemistry, Lanzhou University, Lanzhou 730000
  • Received:1996-03-08 Online:1997-01-24 Published:2011-08-17
  • Supported by:

    Supported by the National Natural Science Foundation of China.

摘要: The treatment of 5-amino-1-(4'-chlorophenyl)-1, 2, 3-triazol-4-carbohydrazide with equimolecular aryl isothiocyanate gave new derivatives 1 a—l . Twelve title compounds were obtained in 42% to 87% yields when compounds 1a—l were respectively treated with sodium hydroxide aqueous solution(2 mol/L). The products of Dimroth rearrangement were not observed in the experiment. The structures of all the compounds were confirmed by means of IR, 1H NMR, MS and elementary analysis.

关键词: 1, 2, 3-Triazole, 1, 2, 4-Triazoline-5-thione, Heterocycle, Synthesis

Abstract: The treatment of 5-amino-1-(4'-chlorophenyl)-1, 2, 3-triazol-4-carbohydrazide with equimolecular aryl isothiocyanate gave new derivatives 1 a—l . Twelve title compounds were obtained in 42% to 87% yields when compounds 1a—l were respectively treated with sodium hydroxide aqueous solution(2 mol/L). The products of Dimroth rearrangement were not observed in the experiment. The structures of all the compounds were confirmed by means of IR, 1H NMR, MS and elementary analysis.

Key words: 1,2,3-Triazole, 1,2,4-Triazoline-5-thione, Heterocycle, Synthesis