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methyl 2,3-di-O-benzyl-6-cyano-6-deoxy-4-O-methyl-α-D-glucopyranoside | 193287-58-0

中文名称
——
中文别名
——
英文名称
methyl 2,3-di-O-benzyl-6-cyano-6-deoxy-4-O-methyl-α-D-glucopyranoside
英文别名
——
methyl 2,3-di-O-benzyl-6-cyano-6-deoxy-4-O-methyl-α-D-glucopyranoside化学式
CAS
193287-58-0
化学式
C23H27NO5
mdl
——
分子量
397.471
InChiKey
PMNKLAANENFUOK-ZQGJOIPISA-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):
    3.46
  • 重原子数:
    29.0
  • 可旋转键数:
    9.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    69.94
  • 氢给体数:
    0.0
  • 氢受体数:
    6.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    methyl 2,3-di-O-benzyl-6-cyano-6-deoxy-4-O-methyl-α-D-glucopyranoside 在 palladium on activated charcoal 、 Rh/Al2O3 氢气 作用下, 以 甲醇二氯甲烷 为溶剂, 20.0 ℃ 、5.0 MPa 条件下, 反应 2.0h, 生成 N-(methyl 6,7-dideoxy-4-O-methyl-α-D-glucoheptopyranoside-7-ylaminocarbonyl)-L-aspartic acid dimethylester
    参考文献:
    名称:
    Synthesis of novel amino acid glycoside conjugates
    摘要:
    A new class of non-anomeric amino acid glycoconjugates can be prepared starting from either omega-amino- or omega-halodeoxyglucosides. Treatment of an ether-protected methyl 7-amino-6,7-dideoxy-alpha-D-glucoheptopyranoside with methyl aspartate isocyanate gave an urea-linked conjugate of methyl glucoheptopyranoside and aspartic acid. Nucleophilic displacement of the ether-protected methyl 6-chloro-6-deoxy-alpha-D-glucopyranoside with potassium succinimide followed by imide ring opening and amidation of the succinic acid monoamide with dimethyl iminodiacetate led to a conjugate of methyl 6-amino-6-deoxy-alpha-D-glucopyranoside and iminodiacetate bridged by succinate. (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0008-6215(97)00091-8
  • 作为产物:
    参考文献:
    名称:
    Synthesis of novel amino acid glycoside conjugates
    摘要:
    A new class of non-anomeric amino acid glycoconjugates can be prepared starting from either omega-amino- or omega-halodeoxyglucosides. Treatment of an ether-protected methyl 7-amino-6,7-dideoxy-alpha-D-glucoheptopyranoside with methyl aspartate isocyanate gave an urea-linked conjugate of methyl glucoheptopyranoside and aspartic acid. Nucleophilic displacement of the ether-protected methyl 6-chloro-6-deoxy-alpha-D-glucopyranoside with potassium succinimide followed by imide ring opening and amidation of the succinic acid monoamide with dimethyl iminodiacetate led to a conjugate of methyl 6-amino-6-deoxy-alpha-D-glucopyranoside and iminodiacetate bridged by succinate. (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0008-6215(97)00091-8
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