摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

O-<3,6-Di-O-acetyl-2-azido-2-desoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-glucopyranosyl>trichloracetimidat | 94715-60-3

中文名称
——
中文别名
——
英文名称
O-<3,6-Di-O-acetyl-2-azido-2-desoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-glucopyranosyl>trichloracetimidat
英文别名
2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-3,6-di-O-acetyl-2-azido-2-deoxy-β-D-glucopyranosyl trichloroacetimidate
O-<3,6-Di-O-acetyl-2-azido-2-desoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-glucopyranosyl>trichloracetimidat化学式
CAS
94715-60-3
化学式
C26H33Cl3N4O16
mdl
——
分子量
763.924
InChiKey
PLAYXADMYOTKBB-FHKWVZCOSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    1.72
  • 重原子数:
    49.0
  • 可旋转键数:
    12.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    267.33
  • 氢给体数:
    1.0
  • 氢受体数:
    18.0

反应信息

  • 作为反应物:
    描述:
    O-<3,6-Di-O-acetyl-2-azido-2-desoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-glucopyranosyl>trichloracetimidat 在 palladium on activated charcoal 吡啶三氟甲磺酸三甲基硅酯氢气sodium methylate 作用下, 以 甲醇二氯甲烷 为溶剂, -20.0 ℃ 、300.0 kPa 条件下, 反应 40.0h, 生成
    参考文献:
    名称:
    Synthesis of tetrasaccharides as possible metastatic inhibitors
    摘要:
    The synthesis is reported of the possible metastatic inhibitors - methyl beta-D-galactopyranosyl-(1 --> 4)-(2-acetamido-2-deoxy-alpha-D-glucopyranosyl)-(1 --> 6)-beta-D-galactopyranosyl-(1 --> 4)-beta-D-glucopyranoside (11) and methyl beta-D-galactopyranosyl-(1 --> 4)-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-(1 --> 6)-beta-D-galactopyranosyl-(1 --> 4)-beta-D-glucopyranoside (14) - by procedures for regio- and stereo-selective coupling, reduction of azido groups, N-acetylation, and O-deacetylation. (C) 1996 Elsevier Science Ltd.
    DOI:
    10.1016/s0008-6215(96)00244-3
  • 作为产物:
    描述:
    (2S,3R,4S,5S,6R)-2-(((2R,3S,4R,5R)-4-acetoxy-2-(acetoxymethyl)-5-azido-6-hydroxytetrahydro-2H-pyran-3-yl)oxy)-6-(acetoxymethyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate 、 三氯乙腈potassium carbonate 作用下, 以 二氯甲烷 为溶剂, 反应 6.0h, 以33%的产率得到(2S,3R,4S,5S,6R)-2-(((2R,3S,4R,5R,6R)-4-acetoxy-2-(acetoxymethyl)-5-azido-6-(2,2,2-trichloro-1-iminoethoxy)tetrahydro-2H-pyran-3-yl)oxy)-6-(acetoxymethyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate
    参考文献:
    名称:
    Synthesis of tetrasaccharides as possible metastatic inhibitors
    摘要:
    The synthesis is reported of the possible metastatic inhibitors - methyl beta-D-galactopyranosyl-(1 --> 4)-(2-acetamido-2-deoxy-alpha-D-glucopyranosyl)-(1 --> 6)-beta-D-galactopyranosyl-(1 --> 4)-beta-D-glucopyranoside (11) and methyl beta-D-galactopyranosyl-(1 --> 4)-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-(1 --> 6)-beta-D-galactopyranosyl-(1 --> 4)-beta-D-glucopyranoside (14) - by procedures for regio- and stereo-selective coupling, reduction of azido groups, N-acetylation, and O-deacetylation. (C) 1996 Elsevier Science Ltd.
    DOI:
    10.1016/s0008-6215(96)00244-3
点击查看最新优质反应信息

文献信息

  • Grundler, Gerhard; Schmidt, Richard R., Liebigs Annalen der Chemie, 1984, # 11, p. 1826 - 1847
    作者:Grundler, Gerhard、Schmidt, Richard R.
    DOI:——
    日期:——
查看更多