N-[2-(6-Benzyloxy-1H-indol-3-yl)-ethyl]-succinamic acid | 215810-11-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: N-[2-(6-Benzyloxy-1H-indol-3-yl)-ethyl]-succinamic acid
• 英文别名: 4-oxo-4-[2-(6-phenylmethoxy-1H-indol-3-yl)ethylamino]butanoic acid
• CAS: 215810-11-0
• 化学式: C₂₁H₂₂N₂O₄
• 分子量: 366.417
• InChiKey: QZPGOKNVIGIHGY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  27
• 可旋转键数：
  9
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.24
• 拓扑面积：
  91.4
• 氢给体数：
  3
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  N-[2-(6-Benzyloxy-1H-indol-3-yl)-ethyl]-succinamic acid 在 钯 三氯氧磷 作用下， 反应 0.5h， 生成 7-hydroxy-β-carboline 1-propionic acid
  参考文献：
  名称：

  Nitrogen-containing compounds from the moss Fontinalis squamosa

  摘要：

  The alkaloid harmol and its hitherto unknown propionic acid derivative as well as a new amino acid derivative fontinalin were isolated from the watermoss Fontinalis squamosa. The structures have been elucidated spectroscopically and by independent chemical synthesis. (C) 1998 Elsevier Science Ltd. Ail rights reserved.

  DOI：

  10.1016/s0031-9422(97)01034-0
• 作为产物：
  描述：

  N-[2-(6-benzyloxy-indol-3-yl)-ethyl]-phthalimide 在 吡啶 、 盐酸 、 一水合肼 作用下， 反应 4.0h， 生成 N-[2-(6-Benzyloxy-1H-indol-3-yl)-ethyl]-succinamic acid
  参考文献：
  名称：

  Nitrogen-containing compounds from the moss Fontinalis squamosa

  摘要：

  The alkaloid harmol and its hitherto unknown propionic acid derivative as well as a new amino acid derivative fontinalin were isolated from the watermoss Fontinalis squamosa. The structures have been elucidated spectroscopically and by independent chemical synthesis. (C) 1998 Elsevier Science Ltd. Ail rights reserved.

  DOI：

  10.1016/s0031-9422(97)01034-0

文献信息

• Nitrogen-containing compounds from the moss Fontinalis squamosa
  作者：Rudolf F. Salm、Hans Dietmar Zinsmeister、Theophil Eicher

  DOI：10.1016/s0031-9422(97)01034-0

  日期：1998.10

  The alkaloid harmol and its hitherto unknown propionic acid derivative as well as a new amino acid derivative fontinalin were isolated from the watermoss Fontinalis squamosa. The structures have been elucidated spectroscopically and by independent chemical synthesis. (C) 1998 Elsevier Science Ltd. Ail rights reserved.