naphthalen-2-yl 1-methyl-1H-indole-3-carboxylate | 1392408-62-6

• 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: naphthalen-2-yl 1-methyl-1H-indole-3-carboxylate
• 英文别名: 2-naphthyl 1-methylindole-3-carboxylate；Naphthalen-2-yl 1-methylindole-3-carboxylate；naphthalen-2-yl 1-methylindole-3-carboxylate
• CAS: 1392408-62-6
• 化学式: C₂₀H₁₅NO₂
• 分子量: 301.345
• InChiKey: OZCWUHHKUNFYBU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.7
• 重原子数：
  23
• 可旋转键数：
  3
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.05
• 拓扑面积：
  31.2
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  1-甲基吲哚 、 2-萘基甲酸酯 在 碘 、 palladium diacetate 、 potassium carbonate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 12.0h， 以78%的产率得到naphthalen-2-yl 1-methyl-1H-indole-3-carboxylate
  参考文献：
  名称：

  Pd-Catalyzed C–H Carbonylation of (Hetero)arenes with Formates and Intramolecular Dehydrogenative Coupling: A Shortcut to Indolo[3,2-c]coumarins

  摘要：

  An efficient protocol for the synthesis of (hetero)aryl carboxylic esters has been achieved by Pd-catalyzed CH carbonylation of (hetero)arenes with aryl formates. A relatively wide range of functional groups can be tolerated in this transformation, and the corresponding esters are obtained in good yields. On this basis, an intramolecular oxidative CH/CH coupling has been developed to prepare indolo[3,2-c]coumarins.

  DOI：

  10.1021/ol502749b

文献信息

• A General Method for Palladium-Catalyzed Direct Carbonylation of Indole with Alcohol and Phenol
  作者：Rui Lang、Lijun Shi、Dengfeng Li、Chungu Xia、Fuwei Li

  DOI：10.1021/ol3017726

  日期：2012.8.17

  A novel strategy involving a first oxidative iodination and subsequent Pd-0-catalyzed carbonylation to yield indole-3-carboxylate has been developed. It showed perfect generality to indole, alcohol, and phenol. The current methodology could also be conveniently applied to the synthesis of biologically active tropisetron from simple indole and tropine.
• Pd-Catalyzed C–H Carbonylation of (Hetero)arenes with Formates and Intramolecular Dehydrogenative Coupling: A Shortcut to Indolo[3,2-<i>c</i>]coumarins
  作者：Jie Wu、Jingbo Lan、Siyuan Guo、Jingsong You

  DOI：10.1021/ol502749b

  日期：2014.11.21

  An efficient protocol for the synthesis of (hetero)aryl carboxylic esters has been achieved by Pd-catalyzed CH carbonylation of (hetero)arenes with aryl formates. A relatively wide range of functional groups can be tolerated in this transformation, and the corresponding esters are obtained in good yields. On this basis, an intramolecular oxidative CH/CH coupling has been developed to prepare indolo[3,2-c]coumarins.