4-<2-(benzyloxycarbonylamino)ethyl>phenyl 3-O-(3-O-acetyl-4-O-benzyl-2-O-methyl-α-L-rhamnopyranosyl)-2,4-di-O-methyl-α-L-rhamnopyranoside | 146422-14-2

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 4-<2-(benzyloxycarbonylamino)ethyl>phenyl 3-O-(3-O-acetyl-4-O-benzyl-2-O-methyl-α-L-rhamnopyranosyl)-2,4-di-O-methyl-α-L-rhamnopyranoside
• 英文别名: [(2S,3R,4R,5S,6S)-2-[(2S,3S,4R,5R,6S)-3,5-dimethoxy-2-methyl-6-[4-[2-(phenylmethoxycarbonylamino)ethyl]phenoxy]oxan-4-yl]oxy-3-methoxy-6-methyl-5-phenylmethoxyoxan-4-yl] acetate
• CAS: 146422-14-2
• 化学式: C₄₀H₅₁NO₁₂
• 分子量: 737.844
• InChiKey: CQABYIACSCFPTB-QOPVYUHWSA-N

物化性质

• 沸点：
  800.5±65.0 °C(predicted)
• 密度：
  1.24±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.9
• 重原子数：
  53
• 可旋转键数：
  18
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  139
• 氢给体数：
  1
• 氢受体数：
  12

反应信息

• 作为反应物：
  描述：

  4-<2-(benzyloxycarbonylamino)ethyl>phenyl 3-O-(3-O-acetyl-4-O-benzyl-2-O-methyl-α-L-rhamnopyranosyl)-2,4-di-O-methyl-α-L-rhamnopyranoside 在 palladium on activated charcoal N-碘代丁二酰亚胺 、 三氟甲磺酸 、 MS 4 Angstroem 、 potassium tert-butylate 、 氢气 作用下， 以 甲醇 、 水 、 溶剂黄146 、 异丙醇 为溶剂， 反应 44.0h， 生成 4-(aminoethyl)phenyl 2,4-di-O-methyl-3-O-<2-O-methyl-3-O-(4-O-acetyl-2-O-methyl-α-L-fucopyranosyl)-α-L-rhamnopyranosyl>-α-L-rhamnopyranoside
  参考文献：
  名称：

  Iodonium ion assisted synthesis of a common inner core trisaccharide fragment corresponding to the cell-wall phenolic glycolipid of Mycobacterium kansasii

  摘要：

  The spacer containing trimer 4-(aminoethyl)phenyl 2,4-di-O-Me-3-O-[2-O-methyl-3-O-(4-O-acetyl-2-O-methyl-alpha-L-fucopyranosyl)-alpha-L-rhamnopyranosyl]-alpha-L-rhamnopyranoside (2) was prepared by stepwise extension of 4-[2-(benzyloxycarbonyl-amino)ethyl]phenyl 2,4-di-O-methyl-alpha-L-rhamnopyranoside (19) with property protected ethyl thioglycosides of L-rhamnose 8 and L-fucose 12 or 16 using iodonium ions as promotors. The resulting trimers 22 or 23 were deblocked in two steps to give homogeneous 2. Alternatively, fully protected trimer 22 was assembled by iodonium ion assisted condensation of the phenyl 1-thio-alpha-L-rhamnopyranoside 29 with 12 followed by extension of dimer 31 with 19.

  DOI：

  10.1016/s0040-4020(01)89043-8
• 作为产物：
  描述：

  苄基N-[2-(4-羟基苯基)乙基]氨基甲酸酯 在 N-碘代丁二酰亚胺 、 三氟甲磺酸 、 MS 4 Angstroem 、 potassium tert-butylate 作用下， 以 甲醇 、 乙醚 、 1,2-二氯乙烷 为溶剂， 反应 1.75h， 生成 4-<2-(benzyloxycarbonylamino)ethyl>phenyl 3-O-(3-O-acetyl-4-O-benzyl-2-O-methyl-α-L-rhamnopyranosyl)-2,4-di-O-methyl-α-L-rhamnopyranoside
  参考文献：
  名称：

  Iodonium ion assisted synthesis of a common inner core trisaccharide fragment corresponding to the cell-wall phenolic glycolipid of Mycobacterium kansasii

  摘要：

  The spacer containing trimer 4-(aminoethyl)phenyl 2,4-di-O-Me-3-O-[2-O-methyl-3-O-(4-O-acetyl-2-O-methyl-alpha-L-fucopyranosyl)-alpha-L-rhamnopyranosyl]-alpha-L-rhamnopyranoside (2) was prepared by stepwise extension of 4-[2-(benzyloxycarbonyl-amino)ethyl]phenyl 2,4-di-O-methyl-alpha-L-rhamnopyranoside (19) with property protected ethyl thioglycosides of L-rhamnose 8 and L-fucose 12 or 16 using iodonium ions as promotors. The resulting trimers 22 or 23 were deblocked in two steps to give homogeneous 2. Alternatively, fully protected trimer 22 was assembled by iodonium ion assisted condensation of the phenyl 1-thio-alpha-L-rhamnopyranoside 29 with 12 followed by extension of dimer 31 with 19.

  DOI：

  10.1016/s0040-4020(01)89043-8