1-(丁-1-烯-4-基)-2-碘吲哚 | 189124-99-0

• 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
• 中文名称: 1-(丁-1-烯-4-基)-2-碘吲哚
• 英文名称: 1-(but-1-en-4-yl)-2-iodoindole
• 英文别名: 1-But-3-enyl-2-iodoindole；1-but-3-enyl-2-iodoindole
• CAS: 189124-99-0
• 化学式: C₁₂H₁₂IN
• 分子量: 297.138
• InChiKey: BOYPUNFYIMWPLY-UHFFFAOYSA-N

物化性质

• 沸点：
  359.8±25.0 °C(Predicted)
• 密度：
  1.51±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  14
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.17
• 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：

  1-(丁-1-烯-4-基)-2-碘吲哚 在 Pd(PPh₃)(OAc)2 、 四乙基氯化铵 、 potassium carbonate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 6.0h， 以35%的产率得到2,3-dihydro-1-(methylene)pyrrolo<1,2-a>indole
  参考文献：
  名称：

  1—Azatriene cyclisation as a route to annelated pyrido[4,3- b ]indoles

  摘要：

  Derivatives of indole-3-carbaldehyde oxime have been prepared that bear a carbon-carbon double bond at C-2 and a five- or six-membered ring linking the alpha-carbon artom of the vinyl group and the indole nitrogen atom. Compound 9, with a five-membered ring linking the two atoms, failed to undergo a cyclisation reaction on heating. However the oximes 16 and 22, with a six-memberd ring linking the two atoms. cyclised in boiling toluene. The cyclisation led to the formation of the pyrido-indoles 17 and 18, respectively. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0040-4020(97)00117-8
• 作为产物：
  描述：

  4-溴-1-丁烯 、 2-碘-1H-吲哚 在 sodium hydride 作用下， 生成 1-(丁-1-烯-4-基)-2-碘吲哚
  参考文献：
  名称：

  1—Azatriene cyclisation as a route to annelated pyrido[4,3- b ]indoles

  摘要：

  Derivatives of indole-3-carbaldehyde oxime have been prepared that bear a carbon-carbon double bond at C-2 and a five- or six-membered ring linking the alpha-carbon artom of the vinyl group and the indole nitrogen atom. Compound 9, with a five-membered ring linking the two atoms, failed to undergo a cyclisation reaction on heating. However the oximes 16 and 22, with a six-memberd ring linking the two atoms. cyclised in boiling toluene. The cyclisation led to the formation of the pyrido-indoles 17 and 18, respectively. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0040-4020(97)00117-8

文献信息

• 1—Azatriene cyclisation as a route to annelated pyrido[4,3- b ]indoles
  作者：Thomas L. Gilchrist、Paul D. Kemmitt、Andrew L. Germain

  DOI：10.1016/s0040-4020(97)00117-8

  日期：1997.3

  Derivatives of indole-3-carbaldehyde oxime have been prepared that bear a carbon-carbon double bond at C-2 and a five- or six-membered ring linking the alpha-carbon artom of the vinyl group and the indole nitrogen atom. Compound 9, with a five-membered ring linking the two atoms, failed to undergo a cyclisation reaction on heating. However the oximes 16 and 22, with a six-memberd ring linking the two atoms. cyclised in boiling toluene. The cyclisation led to the formation of the pyrido-indoles 17 and 18, respectively. (C) 1997 Elsevier Science Ltd.