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有机化学
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有机化学 ›› 1994, Vol. 14 ›› Issue (5): 553-557. 上一篇    

研究论文

5-[5-(3-吡啶)-2H-四唑亚甲基]-2-芳酰氨基-1,3,4-噻二唑的合成

张自义;杨丰科   

  1. 兰州大学化学系;兰州大学应用有机化学国家重点实验室
  • 发布日期:1994-10-25

Syntheses of 5-[5-(3-pyridinyl)-2H-tetrazolymethylene]-2- aroylamino-1,3,4-thiadiazoles

ZHANG ZIYI;YANG FENGKE   

  • Published:1994-10-25

被引次数

22

本文首先用5-(3-吡啶)-2H-四唑乙酰基酰肼与芳酰基异硫氰酸盐反应制备成化合物1-[5-(3-吡啶)-2H-四唑乙酰基]-4-芳酰氨基硫脲化合物1a～j, 然后用冰醋酸回流处理1a～j得到一系列化合物5-[5-(3-吡啶)-2H-四唑亚甲基]-2-芳酰氨基-1,3,4-噻二唑2a～j . 化合物1a～b在强碱介质中首先发生降解, 然后进行环化反应 .

关键词: 硫脲类, 噻二唑 P, 杂环化合物

A series of new 5-[5-(3-pyridinyl)-2H-tetrazolymethylene]- 2-aroylamino-1,3,4-thiadiazoles 2a～j were obtained by refluxing 1-[5-(3-pyridinyl)-2H-tetrazolylacetyl]-4- aroylthiosemicabazides 1a～j in glacial acetic acid. The compounds 1a～j were prepared by the reaction of 5-(3-pyridinyl)-2H-tetrazolylacetic hydrazide with aroyl isothiocyanates. It is suggested that compounds 1a～b representatives are degraded first and followed by a cyclization in the presence of alkaline medium.

Key words: THIADIAZOLE P, SULFOCARBAMIDES, HETEROCYCLIC COMPOUNDS

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