(4S,5R)-5-(2-methylprop-1-enyl)-1,3,4,5-tetrahydrobenzo[cd]indol-4-amine | 194346-09-3

• 分子结构分类: 有机化合物 - 生物碱及其衍生物
• 英文名称: (4S,5R)-5-(2-methylprop-1-enyl)-1,3,4,5-tetrahydrobenzo[cd]indol-4-amine
• CAS: 194346-09-3
• 化学式: C₁₅H₁₈N₂
• 分子量: 226.321
• InChiKey: BWSMORFTLCWFMD-OLZOCXBDSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  17.0
• 可旋转键数：
  1.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  41.81
• 氢给体数：
  2.0
• 氢受体数：
  1.0

反应信息

• 作为反应物：
  描述：

  (4S,5R)-5-(2-methylprop-1-enyl)-1,3,4,5-tetrahydrobenzo[cd]indol-4-amine 在 lithium aluminium tetrahydride 、 三乙胺 作用下， 以 四氢呋喃 为溶剂， 生成 (4S,5R)-N-methyl-5-(2-methylprop-1-enyl)-1,3,4,5-tetrahydrobenzo[cd]indol-4-amine
  参考文献：
  名称：

  Simple Total Syntheses of (-)-Ergot Alkaloids and Thier (+)-Enantiomers by a Common Synthesis Method Utilizing Optical Resolution

  摘要：

  The first and simple total syntheses of (-)-isochanoclavine-I ((-)-1b), (-)-agroclavine ((-)-3), (-)-agroclavine-I ((-)-4), and (-)-norchanoclavine-I ((-)-5C) and their (+)-enantiomers are achieved from indole-3-carboxaldehyde (8) by a common synthesis method utilizing optical resolution. Absolute configuration of (-)-agroclavine-I is determined to be 5R and 10S for the first time. Preparations of both enantiomers of chanoclavine-I (1c) are also included.

  DOI：

  10.3987/com-97-7821
• 作为产物：
  描述：

  (4S,5R)-5-(2-methylprop-1-enyl)-4-nitro-1,3,4,5-tetrahydrobenzo[cd]indole 在 盐酸 、 amalgamated zinc 作用下， 以 甲醇 为溶剂， 以95%的产率得到(4S,5R)-5-(2-methylprop-1-enyl)-1,3,4,5-tetrahydrobenzo[cd]indol-4-amine
  参考文献：
  名称：

  Simple Total Syntheses of (-)-Ergot Alkaloids and Thier (+)-Enantiomers by a Common Synthesis Method Utilizing Optical Resolution

  摘要：

  The first and simple total syntheses of (-)-isochanoclavine-I ((-)-1b), (-)-agroclavine ((-)-3), (-)-agroclavine-I ((-)-4), and (-)-norchanoclavine-I ((-)-5C) and their (+)-enantiomers are achieved from indole-3-carboxaldehyde (8) by a common synthesis method utilizing optical resolution. Absolute configuration of (-)-agroclavine-I is determined to be 5R and 10S for the first time. Preparations of both enantiomers of chanoclavine-I (1c) are also included.

  DOI：

  10.3987/com-97-7821

文献信息

• SOMEHI, MASANORI;YAMADA, FUMIO;MAKITA, JOGIXIKO
  作者：SOMEHI, MASANORI、YAMADA, FUMIO、MAKITA, JOGIXIKO

  DOI：——

  日期：——
• SOMEI, MASANORI;YAMADA, FUMIO;MAKITA, YOSHIHIKO, HETEROCYCLES, 26,(1987) N 1, 895-899
  作者：SOMEI, MASANORI、YAMADA, FUMIO、MAKITA, YOSHIHIKO

  DOI：——

  日期：——