N-methyl-N-((1-methyl-1H-indol-3-yl)(p-tolyl)methyl)benzenamine | 1173282-82-0

• 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
• 英文名称: N-methyl-N-((1-methyl-1H-indol-3-yl)(p-tolyl)methyl)benzenamine
• 英文别名: methyl-[(1-methyl-1H-indol-3-yl)-p-tolyl-methyl]-phenyl-amine；N-methyl-N-[(1-methylindol-3-yl)-(4-methylphenyl)methyl]aniline
• CAS: 1173282-82-0
• 化学式: C₂₄H₂₄N₂
• 分子量: 340.468
• InChiKey: VBNLLIFEKNSRFU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.7
• 重原子数：
  26
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  8.2
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  (4-甲基苯基)甲醇 在 Iron(III) nitrate nonahydrate 、 2,2,6,6-四甲基哌啶氧化物 、 potassium hydroxide 作用下， 以 甲苯 为溶剂， 生成 N-methyl-N-((1-methyl-1H-indol-3-yl)(p-tolyl)methyl)benzenamine
  参考文献：
  名称：

  Iron mediated one pot three component synthesis of 3-substituted indoles via aerobic iminium ion formation

  摘要：

  An efficient and economical method was developed for the synthesis of 3 substituted indoles by a highly efficient one-pot three component coupling reaction of substituted or unsubstituted benzyl alcohol, N-methyl aniline or pyrrolidine, and indoles or substituted indoles. (C) 2015 Published by Elsevier Ltd.

  DOI：

  10.1016/j.tetlet.2015.12.047

文献信息

• Micelle promoted multicomponent synthesis of 3-amino alkylated indoles via a Mannich-type reaction in water
  作者：Atul Kumar、Maneesh Kumar Gupta、Mukesh Kumar、Deepti Saxena

  DOI：10.1039/c2ra22428c

  日期：——

  An efficient micelle promoted one-pot synthesis of 3-amino alkylated indoles has been developed via a three-component Mannich-type reaction from secondary amines, aldehydes and indoles in water under mild reaction conditions. In this Mannich-type reaction, micelles stabilize iminium ions, which undergo a nucleophilic addition of the indole to give 3-amino alkylated indoles in very good yields.

  在温和的反应条件下，通过仲胺、醛和吲哚在水中的三组分曼尼希式反应，开发出了一种高效的胶束促进的单锅合成 3-氨基烷基化吲哚的方法。在这种曼尼希式反应中，胶束稳定了铵离子，铵离子与吲哚发生亲核加成反应，从而以非常高的产率得到 3-氨基烷基化吲哚。
• One-pot three-component coupling reaction: solvent-free synthesis of novel 3-substituted indoles catalyzed by PMA–SiO2
  作者：P. Srihari、Vinay K. Singh、Dinesh C. Bhunia、J.S. Yadav

  DOI：10.1016/j.tetlet.2009.02.176

  日期：2009.7

  Solvent-free PMA–SiO2-catalyzed synthesis of 3-substituted indole derivatives by a one-pot three-component coupling reaction between aldehyde, N-methyl aniline and indole is described.

  描述了无溶剂的PMA-SiO 2催化醛，N-甲基苯胺和吲哚之间的一锅三组分偶联反应，合成了3-取代的吲哚衍生物。
• 3-Substitued indoles: One-pot synthesis and evaluation of anticancer and Src kinase inhibitory activities
  作者：V. Kameshwara Rao、Bhupender S. Chhikara、Amir Nasrolahi Shirazi、Rakesh Tiwari、Keykavous Parang、Anil Kumar

  DOI：10.1016/j.bmcl.2011.05.010

  日期：2011.6

  An efficient and economical method was developed for the synthesis of 3-substituted indoles by one-pot three-component coupling reaction of a substituted or unsubstituted benzaldehyde, N-methylaniline, and indole or N-methylindole using Yb(OTf)(3)-SiO2 as a catalyst. All the synthesized compounds were evaluated for inhibition of cell proliferation of human colon carcinoma (HT-29), human ovarian adenocarcinoma (SK-OV-3), and c-Src kinase activity. The 4-methylphenyl (4o and 4p) and 4-methoxyphenyl (4q) indole derivatives inhibited the cell proliferation of SK-OV-3 and HT-29 cells by 70-77% at a concentration of 50 mu M. The unsubstituted phenyl (4d) and 3-nitrophenyl (4l) derivatives showed the inhibition of c-Src kinase with IC50 values of 50.6 and 58.3 mu M, respectively. (C) 2011 Elsevier Ltd. All rights reserved.