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benzyl 2-benzyloxycarbonylamino-6-bromo-2,6-dideoxy-α-D-glucopyranoside | 154919-37-6

中文名称
——
中文别名
——
英文名称
benzyl 2-benzyloxycarbonylamino-6-bromo-2,6-dideoxy-α-D-glucopyranoside
英文别名
——
benzyl 2-benzyloxycarbonylamino-6-bromo-2,6-dideoxy-α-D-glucopyranoside化学式
CAS
154919-37-6
化学式
C21H24BrNO6
mdl
——
分子量
466.329
InChiKey
NFOKXFJKCIMRHW-WAPOTWQKSA-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):
    2.34
  • 重原子数:
    29.0
  • 可旋转键数:
    7.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    97.25
  • 氢给体数:
    3.0
  • 氢受体数:
    6.0

反应信息

  • 作为反应物:
    描述:
    benzyl 2-benzyloxycarbonylamino-6-bromo-2,6-dideoxy-α-D-glucopyranoside 在 palladium on activated charcoal sodium tetrahydroborate 、 sodium azide 、 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile氢气三正丁基氢锡sodium acetate 、 sodium hydride 、 氯化铵 、 nickel dichloride 、 1-(2,4,6-三异丙基苯基磺酰)咪唑 作用下, 以 乙醇甲苯 为溶剂, 反应 48.92h, 生成 2,4-diacetamido-3-O-acetyl-2,4,6-trideoxy-β-D-gulopyranose
    参考文献:
    名称:
    The synthesis of derivatives of 2,4-diamino-2,4,6-trideoxy-d-gulo- and l-altro-hexopyranoses
    摘要:
    Syntheses of two derivatives of two 2,4-diamino-2,4,6-trideoxyhexoses having the D-gulo (16) and L-altro (29) configuration have been described. Derivative 16 was obtained by two routes starting from benzyl 2-benzyloxycarbonylamino-2-deoxy-alpha-D-glucopyranoside. Derivative 29 was obtained from 3,4-di-O-acetyl-L-rhamnal in a 10-step reaction sequence.
    DOI:
    10.1016/0008-6215(95)00291-x
  • 作为产物:
    描述:
    benzyl-(2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranoside)吡啶四溴化碳三苯基膦 作用下, 反应 2.0h, 以55%的产率得到benzyl 2-benzyloxycarbonylamino-6-bromo-2,6-dideoxy-α-D-glucopyranoside
    参考文献:
    名称:
    The synthesis of derivatives of 2,4-diamino-2,4,6-trideoxy-d-gulo- and l-altro-hexopyranoses
    摘要:
    Syntheses of two derivatives of two 2,4-diamino-2,4,6-trideoxyhexoses having the D-gulo (16) and L-altro (29) configuration have been described. Derivative 16 was obtained by two routes starting from benzyl 2-benzyloxycarbonylamino-2-deoxy-alpha-D-glucopyranoside. Derivative 29 was obtained from 3,4-di-O-acetyl-L-rhamnal in a 10-step reaction sequence.
    DOI:
    10.1016/0008-6215(95)00291-x
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