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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

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

CLC Number: 

  • O626