(2R,3S,4S,5R)-1,6-bis(benzyloxy)-3,4-bis((methylsulfonyl)oxy)-N2,N5-ditosylhexane-2,5-diamine | 914982-47-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (2R,3S,4S,5R)-1,6-bis(benzyloxy)-3,4-bis((methylsulfonyl)oxy)-N2,N5-ditosylhexane-2,5-diamine
• CAS: 914982-47-1
• 化学式: C₃₆H₄₄N₂O₁₂S₄
• 分子量: 825.016
• InChiKey: FYRLALCVLOGXSE-CLLHQPRTSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.42
• 重原子数：
  54.0
• 可旋转键数：
  21.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  197.54
• 氢给体数：
  2.0
• 氢受体数：
  12.0

反应信息

• 作为反应物：
  描述：

  (2R,3S,4S,5R)-1,6-bis(benzyloxy)-3,4-bis((methylsulfonyl)oxy)-N2,N5-ditosylhexane-2,5-diamine 在 sodium hydride 作用下， 以 四氢呋喃 为溶剂， 反应 12.0h， 以88%的产率得到(2R,3R)-2-((benzyloxy)methyl)-3-((2R,3R)-3-((benzyloxy)methyl)-1-tosylaziridin-2-yl)-1-tosylaziridine
  参考文献：
  名称：

  Synthesis of enantiopure bis-aziridines, bis-epoxides, and aziridino-epoxides from d-mannitol

  摘要：

  A practical synthesis of enantiopure bis-aziridines 11 and 15, bis-epoxides 12 and 17, and aziridino-epoxides 27 and 30 is reported using inexpensive D-mannitol as the starting material. The key transformation involves the reductive cleavage of bis-benzylidene acetal 3 to form dimesylate 4, which was further converted to monoazides and diazides followed by reduction, mesylation, and cyclization to furnish the required compounds in good yields. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2006.08.035
• 作为产物：
  描述：

  3,5-diazido-1,6-di-O-benzyl-2,5-dideoxy-3,4-O-methylethylidene-L-iditol 在 Lindlar's catalyst 吡啶 、 氢气 、 三氯化铁 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 28.0 ℃ 、101.33 kPa 条件下， 反应 16.5h， 生成 (2R,3S,4S,5R)-1,6-bis(benzyloxy)-3,4-bis((methylsulfonyl)oxy)-N2,N5-ditosylhexane-2,5-diamine
  参考文献：
  名称：

  Synthesis of enantiopure bis-aziridines, bis-epoxides, and aziridino-epoxides from d-mannitol

  摘要：

  A practical synthesis of enantiopure bis-aziridines 11 and 15, bis-epoxides 12 and 17, and aziridino-epoxides 27 and 30 is reported using inexpensive D-mannitol as the starting material. The key transformation involves the reductive cleavage of bis-benzylidene acetal 3 to form dimesylate 4, which was further converted to monoazides and diazides followed by reduction, mesylation, and cyclization to furnish the required compounds in good yields. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2006.08.035