((7R,9aR)-9-Methyl-2,7,8,9,9a,10-hexahydro-pyrrolo[3',2':5,6]cyclohepta[1,2,3-cd]indol-7-yl)-methanol | 61771-50-4

• 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: ((7R,9aR)-9-Methyl-2,7,8,9,9a,10-hexahydro-pyrrolo[3',2':5,6]cyclohepta[1,2,3-cd]indol-7-yl)-methanol
• 英文别名: [(4R,7R)-6-methyl-6,11-diazatetracyclo[7.6.1.03,7.012,16]hexadeca-1(16),2,9,12,14-pentaen-4-yl]methanol
• CAS: 61771-50-4
• 化学式: C₁₆H₁₈N₂O
• 分子量: 254.332
• InChiKey: HNUDKJWEFHMGQE-IUODEOHRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  19
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  39.3
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  ((7R,9aR)-9-Methyl-2,7,8,9,9a,10-hexahydro-pyrrolo[3',2':5,6]cyclohepta[1,2,3-cd]indol-7-yl)-methanol 在 sodium tetrahydroborate 、 溴 、 三氯氧磷 作用下， 以 吡啶 、 溶剂黄146 、 二甲基亚砜 为溶剂， 反应 6.0h， 生成 (7R,9aR)-1,5-Dibromo-7,9-dimethyl-2,7,8,9,9a,10-hexahydro-pyrrolo[3',2':5,6]cyclohepta[1,2,3-cd]indole
  参考文献：
  名称：

  5(10→9)Abeo-ergoline derivatives: Synthesis, 5-HT1A-receptor affinity and selectivity

  摘要：

  The synthesis and the structure-affinity relationship (S.A.F.I.R.) study for the 5-HT1A receptor sites of a novel series of 5(10-->9)abeo-ergoline derivatives are presented. Most derivatives showed moderate to high affinity and selectivity for 5-HT1A receptor sites. The structure-affinity relationship pointed out the role of the substituent at position 8, and the outstanding importance of the reduction of the indole 2,3-double bond for achieving the highest 5-HT1A affinity and selectivity within the compounds presented. (C) Elsevier, Paris.

  DOI：

  10.1016/s0223-5234(98)80062-7
• 作为产物：
  描述：

  D-麦角酸甲酯 在 sodium hydroxide 、 吡啶盐酸盐 、 三氯氧磷 作用下， 以 吡啶 、 甲醇 为溶剂， 反应 9.0h， 生成 ((7R,9aR)-9-Methyl-2,7,8,9,9a,10-hexahydro-pyrrolo[3',2':5,6]cyclohepta[1,2,3-cd]indol-7-yl)-methanol
  参考文献：
  名称：

  5(10→9)Abeo-ergoline derivatives: Synthesis, 5-HT1A-receptor affinity and selectivity

  摘要：

  The synthesis and the structure-affinity relationship (S.A.F.I.R.) study for the 5-HT1A receptor sites of a novel series of 5(10-->9)abeo-ergoline derivatives are presented. Most derivatives showed moderate to high affinity and selectivity for 5-HT1A receptor sites. The structure-affinity relationship pointed out the role of the substituent at position 8, and the outstanding importance of the reduction of the indole 2,3-double bond for achieving the highest 5-HT1A affinity and selectivity within the compounds presented. (C) Elsevier, Paris.

  DOI：

  10.1016/s0223-5234(98)80062-7

文献信息

• Synthesis of 5(10Æ9)abeo-Ergolines
  作者：Sergio Mantegani、Emanuele Arlandini、Daniela Borghi、Enzo Brambilla、Mario Varasi

  DOI：10.3987/com-97-7788

  日期：——

  Reaction of the (5 R, 8 R)-ergoline derivative (6) with the couple CCl4/(Ph)(3)P unexpectedly resulted in the formation of the novel (5 S, 8 R)-5 (10-->9)abeo-ergoline derivative. A mechanism of this transposition process is proposed.
• 5(10→9)Abeo-ergoline derivatives: Synthesis, 5-HT1A-receptor affinity and selectivity
  作者：Sergio Mantegani、Luca Baumer、Enzo Brambilla、Carla Caccia、Maria Cioia Fornaretto、Robert Albert McArthur、Mario Varasi

  DOI：10.1016/s0223-5234(98)80062-7

  日期：1998.4

  The synthesis and the structure-affinity relationship (S.A.F.I.R.) study for the 5-HT1A receptor sites of a novel series of 5(10-->9)abeo-ergoline derivatives are presented. Most derivatives showed moderate to high affinity and selectivity for 5-HT1A receptor sites. The structure-affinity relationship pointed out the role of the substituent at position 8, and the outstanding importance of the reduction of the indole 2,3-double bond for achieving the highest 5-HT1A affinity and selectivity within the compounds presented. (C) Elsevier, Paris.