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β-D-糖基苯胺基硫脲的合成与表征

孙卫东1,2, 王小明2, 张锁秦2, 李耀先2, 郑吉富2, 袁宏3, 郭清焕3   

  1. 1. 赤峰学院 化学系, 内蒙古自治区 赤峰 024001; 2. 吉林大学 化学学院, 长春 130021; 3. 吉林化学集团公司, 吉林省 吉林 132021
  • 收稿日期:2005-06-06 修回日期:1900-01-01 出版日期:2006-01-26 发布日期:2006-01-26
  • 通讯作者: 张锁秦

Synthesis and Characterization of β-D-Glucopyranosyl Thiourea

SUN Wei-dong1,2, WANG Xiao-ming2, ZHANG Suo-qin2, LI Yao-xian2, ZHENG Ji-fu2, YUAN Hong3, GUO Qing-huan3   

  1. 1. Department of Chemistry, Chifeng College, Chifeng 024001, Inner Mongolia Autonomous Region,China; 2. College of Chemistry, Jilin University, Changchun 130021, China; 3. Jilin Chemical Combine Company, Jilin 132021, Jilin Province, China
  • Received:2005-06-06 Revised:1900-01-01 Online:2006-01-26 Published:2006-01-26
  • Contact: ZHANG Suo-qin

摘要: 从糖基异硫氰酸酯出发, 其与苯胺类化合物在乙腈回流条件下, 得到一类糖基硫脲化合物, 且收率较高. 所得化合物经元素分析,IR, MS和1H NMR核磁等谱学分析, 确定其结构为β构型.

关键词: 糖基异硫氰酸酯, 合成, 糖基硫脲

Abstract: 2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl thiourea compounds were synthesised from the reaction of aniline and 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate in acetonitrile under reflux. The 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate was synthesised from 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl bromine. The structures of the title compounds were confirmed by elemental analyses, IR, MS and 1H NMR spectra.

Key words: glycosyl isothiocyanate, synthesis, glucosyl thiourea

中图分类号: 

  • O626