2,2,4-trimethyl-3-phenyl-1,2,3,4-tetrahydrocyclopenta[b]indole | 848623-58-5

• 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: 2,2,4-trimethyl-3-phenyl-1,2,3,4-tetrahydrocyclopenta[b]indole
• 英文别名: 2,2,4-Trimethyl-3-phenyl-1,2,3,4-tetrahydrocyclopenta[b]indole；2,2,4-trimethyl-3-phenyl-1,3-dihydrocyclopenta[b]indole
• CAS: 848623-58-5
• 化学式: C₂₀H₂₁N
• 分子量: 275.393
• InChiKey: AIEIUDMBWFNIJA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5
• 重原子数：
  21
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  4.9
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为反应物：
  描述：

  2,2,4-trimethyl-3-phenyl-1,2,3,4-tetrahydrocyclopenta[b]indole 在 间氯过氧苯甲酸 作用下， 以 二氯甲烷 为溶剂， 反应 0.33h， 以76%的产率得到1,4,4-trimethyl-3-phenyl-4,5-dihydro-1H,3H-benzo[b]azocine-2,6-dione
  参考文献：
  名称：

  Incorporation of an indole-containing diarylbutylamine pharmacophore into furo[2,3-a]carbazole ring systems

  摘要：

  Due to concurrent oxidation of the indole moiety in the starting carbazole alkenol, an epoxidation route aiming at incorporation of a conformationally constrained diarylbutylamine failed to give the desired furo[2,3-a]carbazole ring system. Instead, an indole epoxide intermediate was generated, which underwent rearrangement involving participation of a vicinal OH group. The required furo[2,3-a]2 carbazole could, however, be accessed via a Hg2+-induced cyclisation of a carbazole alkynol. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2004.12.049
• 作为产物：
  描述：

  2,2,4-trimethyl-3-phenyl-1,2,3,4-tetrahydrocyclopenta[b]indol-3-ol 在 对甲苯磺酸 作用下， 以 甲苯 为溶剂， 反应 1.0h， 以52%的产率得到2,2,4-trimethyl-3-phenyl-1,2,3,4-tetrahydrocyclopenta[b]indole
  参考文献：
  名称：

  Incorporation of an indole-containing diarylbutylamine pharmacophore into furo[2,3-a]carbazole ring systems

  摘要：

  Due to concurrent oxidation of the indole moiety in the starting carbazole alkenol, an epoxidation route aiming at incorporation of a conformationally constrained diarylbutylamine failed to give the desired furo[2,3-a]carbazole ring system. Instead, an indole epoxide intermediate was generated, which underwent rearrangement involving participation of a vicinal OH group. The required furo[2,3-a]2 carbazole could, however, be accessed via a Hg2+-induced cyclisation of a carbazole alkynol. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2004.12.049