N-(2-(2-formyl-1-methyl-1H-indol-3-yl)ethyl)acetamide | 475987-05-4

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: N-(2-(2-formyl-1-methyl-1H-indol-3-yl)ethyl)acetamide
• 英文别名: N-[2-(2-formyl-1-methylindol-3-yl)ethyl]acetamide
• CAS: 475987-05-4
• 化学式: C₁₄H₁₆N₂O₂
• 分子量: 244.293
• InChiKey: GTKYVWXHNGRQQD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  18
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  51.1
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  N-((4-氧代)-1-戊基)乙酰胺 在 草酰氯 、 对甲苯磺酸 、 二甲基亚砜 作用下， 以 二氯甲烷 、 乙腈 为溶剂， 反应 20.5h， 生成 N-(2-(2-formyl-1-methyl-1H-indol-3-yl)ethyl)acetamide
  参考文献：
  名称：

  A one-pot three-component reaction for the preparation of highly functionalized tryptamines

  摘要：

  We have developed a general one-pot method to provide highly functionalized tryptamine derivatives, via a Fischer indole type pathway. In this article, we demonstrate optimal conditions for a one-pot indole synthesis, allowing for the synthesis of a broad scope of 2-methyl tryptamine derivatives and a precursor for the synthesis of the core structure of some akuammiline alkaloids. Additionally, further modification of the indole products is described. Published by Elsevier Ltd.

  DOI：

  10.1016/j.tet.2011.11.032

文献信息

• Oxidation of Tetrahydro-β-carbolines by Persulfate
  作者：Haijun Chen、Fu Ye、Jing Luo、Yu Gao

  DOI：10.1021/acs.orglett.9b02772

  日期：2019.9.20

  The development of persulfate-mediated oxidation of tetrahydro-β-carbolines is reported. This mild reaction facilitates the formation of a variety of 2-formyl N-substituted tryptamines and the related derivatives as key intermediates in moderate to excellent yields. The method is applicable to direct last-stage oxidation of two interesting pharmaceuticals, Cialis and evodiamine.

  据报道过硫酸盐介导的四氢-β-咔啉氧化反应的发展。这种温和的反应有助于以中等至优异的产率形成各种2-甲酰基N-取代的色胺和相关衍生物作为关键中间体。该方法适用于两种有趣的药物Cialis和evodiamine的直接最后阶段氧化。
• A one-pot three-component reaction for the preparation of highly functionalized tryptamines
  作者：Se Jeong Yeo、Yongxiang Liu、Xiang Wang

  DOI：10.1016/j.tet.2011.11.032

  日期：2012.1

  We have developed a general one-pot method to provide highly functionalized tryptamine derivatives, via a Fischer indole type pathway. In this article, we demonstrate optimal conditions for a one-pot indole synthesis, allowing for the synthesis of a broad scope of 2-methyl tryptamine derivatives and a precursor for the synthesis of the core structure of some akuammiline alkaloids. Additionally, further modification of the indole products is described. Published by Elsevier Ltd.