摘要
2,3,4-三-O-乙酰基-β-D-糖基异硫氰酸酯分别与1,4,5,6-四氢-6-哒嗪酮-3-甲酰肼1和1,6-二氢-6-哒嗪酮-3-甲酰肼2反应,制得4种硫脲,再将硫脲用氧化汞在CHCl3/H2O作用下脱硫化氢,制得新化合物糖基哒嗪酮碳二亚胺1c-1d和2c-2d.化合物的结构经1HNMR,IR确定.
By the reaction of 2,3,4-tri-O-acetyl-β-D-glucosyl isothiocyanate with 1,4,5,6-tetrahydro-6- pyridazinone-3-carboxylic acid hydrazides 1 and 1,6-dihydro-6-pyridazinone-3-Carboxylic acid hydrazides 2 furnished four thioureas. Then these thioureas were desulfurated and transformed into the corresponding glucosyl carbodiimides lc-ld and 2c-2d using HgO in CHCl3/H2O at room temperature. The structures of all compounds have been established by ^1H NMR and IR.
出处
《伊犁师范学院学报(自然科学版)》
2009年第3期31-33,共3页
Journal of Yili Normal University:Natural Science Edition
基金
伊犁师范学院科研基金资助项目(2008YB031)
关键词
硫脲
糖基异硫氰酸脂
碳二亚胺
thiourea
glycosyl isothiocyanate
carbodiimmide