1-(2,4,6-trimethylphenyl)-2-phenyl-1H-indole | 844819-41-6

• 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: 1-(2,4,6-trimethylphenyl)-2-phenyl-1H-indole
• 英文别名: 2-phenyl-1-(2,4,6-trimethylphenyl)-1H-indole；1-mesityl-2-phenyl-1H-indole；2-phenyl-1-(2,4,6-trimethylphenyl)indole
• CAS: 844819-41-6
• 化学式: C₂₃H₂₁N
• 分子量: 311.426
• InChiKey: BWJMQIUUKNJRTC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.4
• 重原子数：
  24
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.13
• 拓扑面积：
  4.9
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为产物：
  描述：

  1-氯-2-碘苯 在 palladium diacetate copper(l) iodide 、 potassium tert-butylate 、 caesium carbonate 、 1,3-双(2,6-二异丙基苯基)氯化咪唑鎓 作用下， 以 甲苯 为溶剂， 反应 35.0h， 生成 1-(2,4,6-trimethylphenyl)-2-phenyl-1H-indole
  参考文献：
  名称：

  Three-component indole synthesis using ortho-dihaloarenes

  摘要：

  A three-component synthesis of substituted indoles is accomplished starting from ortho-dihaloarenes through the use of a multicatalytic system consisting of an N-heterocyclic carbene palladium complex and CuI. The corresponding indole derivatives are obtained as single regioisomers in high yields of isolated product. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2005.09.095

文献信息

• Palladium-catalyzed sequential indole synthesis using sterically hindered amines
  作者：Lutz Ackermann、René Sandmann、Marvin Schinkel、Mikhail V. Kondrashov

  DOI：10.1016/j.tet.2009.07.073

  日期：2009.10

  A palladium catalyst derived from a bulky N-heterocyclic carbene ligand enabled a modular synthesis of indoles bearing sterically hindered N-alkyl or N-aryl substituents through a reaction sequence comprising an intermolecular N-arylation and an intramolecular hydroamination.

  衍生自庞大的N-杂环卡宾配体的钯催化剂能够通过包含分子间N-芳基化和分子内加氢胺化的反应序列来模块化合成带有空间位阻N-烷基或N-芳基取代基的吲哚。
• Nickel-catalyzed, base-mediated amination/hydroamination reaction sequence for a modular synthesis of indoles
  作者：Lutz Ackermann、Weifeng Song、René Sandmann

  DOI：10.1016/j.jorganchem.2010.08.047

  日期：2011.1

  A catalytic system consisting of [Ni(cod)2] and ligand dppf enabled an efficient synthesis of differently substituted indoles through a modular reaction sequence, which consists of intermolecular aminations and intramolecular hydroaminations with ortho-alkynylhaloarenes.

  由[Ni（cod）2 ]和配体dppf组成的催化系统能够通过模块化反应序列有效合成不同取代的吲哚，该反应序列由分子间胺化和分子内氢化氨基化与邻炔基卤代芳烃组成。
• General and Efficient Indole Syntheses Based on Catalytic Amination Reactions
  作者：Lutz Ackermann

  DOI：10.1021/ol047649j

  日期：2005.2.1

  Highly flexible and efficient syntheses of the indole backbone are presented starting from o-alkynylhaloarenes. These transformations proceed via a palladium- or a copper-catalyzed amination reaction and a subsequent cyclization reaction in good to excellent yields. Furthermore. a multicatalytic one-pot indole synthesis starting from o-chloroiodobenzene is viable using a single catalyst consisting of an N-heterocyclic carbene palladium complex and Cul.
• Three-component indole synthesis using ortho-dihaloarenes
  作者：Ludwig T. Kaspar、Lutz Ackermann

  DOI：10.1016/j.tet.2005.09.095

  日期：2005.11

  A three-component synthesis of substituted indoles is accomplished starting from ortho-dihaloarenes through the use of a multicatalytic system consisting of an N-heterocyclic carbene palladium complex and CuI. The corresponding indole derivatives are obtained as single regioisomers in high yields of isolated product. (c) 2005 Elsevier Ltd. All rights reserved.