N-((5-bromo-1H-indol-3-yl)methyl)-N,4-dimethylbenzenamine | 1255789-34-4

• 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: N-((5-bromo-1H-indol-3-yl)methyl)-N,4-dimethylbenzenamine
• 英文别名: N-((5-bromo-1H-indol-3-yl)methyl)-N,4-dimethylaniline；N-[(5-bromo-1H-indol-3-yl)methyl]-N,4-dimethylaniline
• CAS: 1255789-34-4
• 化学式: C₁₇H₁₇BrN₂
• 分子量: 329.239
• InChiKey: LXWNYSJKRODFHT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.7
• 重原子数：
  20
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  19
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  5-溴吲哚 、 N,N-二甲基对甲苯胺 在 copper(I) bromide 作用下， 以 癸烷 为溶剂， 反应 3.0h， 以76%的产率得到N-((5-bromo-1H-indol-3-yl)methyl)-N,4-dimethylbenzenamine
  参考文献：
  名称：

  Copper-Catalyzed Cross Dehydrogenative Coupling Reactions of Tertiary Amines with Ketones or Indoles

  摘要：

  A novel cross dehydrogenative coupling (CDC) reaction of N,N-dimethylanilines with methyl ketones by cooperative copper and aminocatalysis has been developed, which leads to the formation of beta-arylamino ketones in 42-73% yields. Moreover, the copper-catalyzed alkylation of free (NH) indoles with N,N-dimethylanilines via CDC reaction is also presented, affording alkylated indoles in 52-78% yields.

  DOI：

  10.1021/ol102252n

文献信息

• Copper-Catalyzed Oxidative Cross-Coupling of <i>N</i>,<i>N</i>-Dimethylanilines with Heteroarenes under Molecular Oxygen
  作者：Lehao Huang、Tianmin Niu、Jun Wu、Yuhong Zhang

  DOI：10.1021/jo1023975

  日期：2011.3.18

  materials, and there has been a growing interest in new synthetic methods for their preparation. In this paper, we report a direct cross-coupling reaction of heteroarenes with N,N-dimethylanilines in the presence of copper catalyst. Oxygen and/or air are successfully used as the oxidant, which is of great importance to the industrialized economies. The reaction is compatible with a wide range of heterocycles

  含氮杂环化合物是药物和功能材料的重要主题，并且对用于其制备的新合成方法的兴趣日益浓厚。在本文中，我们报道了在铜催化剂存在下杂芳烃与N，N-二甲基苯胺的直接交叉偶联反应。氧气和/或空气已成功用作氧化剂，这对工业化经济至关重要。该反应与宽范围的杂环相容，包括吲哚嗪，咪唑，吲哚和苯胺，从而能够在非常温和的反应条件下形成各种烷基化的杂芳烃。
• Copper-Catalyzed Cross Dehydrogenative Coupling Reactions of Tertiary Amines with Ketones or Indoles
  作者：Fei Yang、Jian Li、Jin Xie、Zhi-Zhen Huang

  DOI：10.1021/ol102252n

  日期：2010.11.19

  A novel cross dehydrogenative coupling (CDC) reaction of N,N-dimethylanilines with methyl ketones by cooperative copper and aminocatalysis has been developed, which leads to the formation of beta-arylamino ketones in 42-73% yields. Moreover, the copper-catalyzed alkylation of free (NH) indoles with N,N-dimethylanilines via CDC reaction is also presented, affording alkylated indoles in 52-78% yields.