methyl (1S,2S,4R)-N-benzoyl-2-aminomethyl-7-azabicyclo[2.2.1]heptane-1-carboxylate | 869195-17-5

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: methyl (1S,2S,4R)-N-benzoyl-2-aminomethyl-7-azabicyclo[2.2.1]heptane-1-carboxylate
• 英文别名: methyl (1S,2S,4R)-2-(aminomethyl)-7-benzoyl-7-azabicyclo[2.2.1]heptane-1-carboxylate
• CAS: 869195-17-5
• 化学式: C₁₆H₂₀N₂O₃
• 分子量: 288.346
• InChiKey: SERGPLSOWUSXDZ-ZENOOKHLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  21
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  72.6
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  methyl (1S,2S,4R)-N-benzoyl-2-aminomethyl-7-azabicyclo[2.2.1]heptane-1-carboxylate 在 间氯过氧苯甲酸 作用下， 以 1,2-二氯乙烷 为溶剂， 以32 mg的产率得到methyl (1S,2S,4R)-N-benzoyl-2-nitromethyl-7-azabicyclo[2.2.1]heptane-1-carboxylate
  参考文献：
  名称：

  New enantiopure 7-azanorbornane β-substituted prolines by SN2 displacements at the Cγ of the side chain

  摘要：

  Continuing our work on building new beta-substituted prolines in en antiomerically pure form as new surrogates to be incorporated into model peptides, we describe functional group conversions and carbon-carbon bond forming reactions by S(N)2 displacements at the gamma-position of the alpha-amino acid side chain of an azanorbornane derivative. This work extends efforts on the elaboration of the side arm at carbon C2 of the 7-azabicyclo[2.2.1]heptane core. (C) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2005.08.003
• 作为产物：
  描述：

  methyl (1S,2R,4R)-N-benzoyl-2-bromomethyl-7-azabicyclo[2.2.1]heptane-1-carboxylate 在 palladium on activated charcoal sodium azide 、 氢气 作用下， 以 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 8.0h， 生成 methyl (1S,2S,4R)-N-benzoyl-2-aminomethyl-7-azabicyclo[2.2.1]heptane-1-carboxylate
  参考文献：
  名称：

  New enantiopure 7-azanorbornane β-substituted prolines by SN2 displacements at the Cγ of the side chain

  摘要：

  Continuing our work on building new beta-substituted prolines in en antiomerically pure form as new surrogates to be incorporated into model peptides, we describe functional group conversions and carbon-carbon bond forming reactions by S(N)2 displacements at the gamma-position of the alpha-amino acid side chain of an azanorbornane derivative. This work extends efforts on the elaboration of the side arm at carbon C2 of the 7-azabicyclo[2.2.1]heptane core. (C) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2005.08.003

文献信息

• New enantiopure 7-azanorbornane β-substituted prolines by SN2 displacements at the Cγ of the side chain
  作者：Ana M. Gil、Ester Orús、Verónica López-Carrillo、Elena Buñuel、Carlos Cativiela

  DOI：10.1016/j.tetasy.2005.08.003

  日期：2005.9

  Continuing our work on building new beta-substituted prolines in en antiomerically pure form as new surrogates to be incorporated into model peptides, we describe functional group conversions and carbon-carbon bond forming reactions by S(N)2 displacements at the gamma-position of the alpha-amino acid side chain of an azanorbornane derivative. This work extends efforts on the elaboration of the side arm at carbon C2 of the 7-azabicyclo[2.2.1]heptane core. (C) 2005 Elsevier Ltd. All rights reserved.