Citation:
Liu Weiwei, Cheng Fengchang, Yin Long, Li Quxiang. Syntheses of D-Glucosamine Acylthiourea Derivatives[J]. Chemistry,
;2016, 79(1): 77-82,76.
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Twelve kinds of D-glucosamine acylthiourea derivatives were synthesized from acyl isothiocyanate and 1,3,4,6-tetra-O-acetyl-2-deoxy-β-D-glucosamine hydrochloride prepared from D-glucosamine hydrochloride by protection of amino group followed by acetylation of hydroxyl group, and deprotection of the amino group. The optimal conditions for the coupling reaction were the molar ratio of acyl isothiocyanate and 1,3,4,6-tetra-O-acetyl-2-deoxy-β-D-glucosamine 1:1.2 in dichloromethane at 40℃ for 6 hours. The products were characterized by IR, 1H NMR and 13C NMR.
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Keywords:
- D-glucosamine,
- Acylthiourea,
- Synthesis
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