6-N,N-dibenzylamino-6,8-dideoxy-1,2:3,4-di-O-isopropylidene-7-C-methyl-L-glycero-α-D-galacto-1,5-octopyranose | 1338819-31-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氧吡喃
• 英文名称: 6-N,N-dibenzylamino-6,8-dideoxy-1,2:3,4-di-O-isopropylidene-7-C-methyl-L-glycero-α-D-galacto-1,5-octopyranose
• CAS: 1338819-31-0
• 化学式: C₂₉H₃₉NO₆
• 分子量: 497.632
• InChiKey: ROYQJXPTOVQVEC-WQFLLUORSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.22
• 重原子数：
  36.0
• 可旋转键数：
  7.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.59
• 拓扑面积：
  69.62
• 氢给体数：
  1.0
• 氢受体数：
  7.0

反应信息

• 作为反应物：
  描述：

  6-N,N-dibenzylamino-6,8-dideoxy-1,2:3,4-di-O-isopropylidene-7-C-methyl-L-glycero-α-D-galacto-1,5-octopyranose 在 palladium 10% on activated carbon 、 氢气 作用下， 以 甲醇 为溶剂， 反应 32.0h， 以72%的产率得到6-amino-6,8-dideoxy-1,2:3,4-di-O-isopropylidene-7-C-methyl-L-glycero-α-D-galacto-1,5-octopyranose
  参考文献：
  名称：

  Efficient Synthesis of Direct Precursors of the Carbohydrate Moiety of New Antibacterials 6-Epi-VIC-105555 and 6-Epi-VIC-II

  摘要：

  In search for new antibiotics we have developed a novel route leading to direct precursors of the carbohydrate moieties of new promising antibacterial agents 6-epi-VIC-105555 and 6-epi-VIC-II. The presented synthetic strategy consists of using as starting material the readily available beta-dibenzylamino-alpha-ketoester and application of a sequence of chemical transformations on C-7: olefination or methylation, reduction, deoxygenation of the terminal alcohol, and finally hydrogenation. The desired molecules were obtained in a stereoselective fashion and with good overall yields.

  DOI：

  10.1080/07328303.2011.614982
• 作为产物：
  描述：

  isopropyl 6-deoxy-6-N,N-dibenzylamino-1,2:3,4-di-O-isopropylidene-7-C-methyl-D-threo-α-D-galacto-1,5-octopyranuronate 在 4-二甲氨基吡啶 、 lithium aluminium tetrahydride 、 三乙胺 作用下， 以 四氢呋喃 、 乙醚 、 二氯甲烷 为溶剂， 反应 72.0h， 生成 6-N,N-dibenzylamino-6,8-dideoxy-1,2:3,4-di-O-isopropylidene-7-C-methyl-L-glycero-α-D-galacto-1,5-octopyranose
  参考文献：
  名称：

  Efficient Synthesis of Direct Precursors of the Carbohydrate Moiety of New Antibacterials 6-Epi-VIC-105555 and 6-Epi-VIC-II

  摘要：

  In search for new antibiotics we have developed a novel route leading to direct precursors of the carbohydrate moieties of new promising antibacterial agents 6-epi-VIC-105555 and 6-epi-VIC-II. The presented synthetic strategy consists of using as starting material the readily available beta-dibenzylamino-alpha-ketoester and application of a sequence of chemical transformations on C-7: olefination or methylation, reduction, deoxygenation of the terminal alcohol, and finally hydrogenation. The desired molecules were obtained in a stereoselective fashion and with good overall yields.

  DOI：

  10.1080/07328303.2011.614982