2-(1-甲基-2-苯基吲哚-3-基)-乙胺 | 101574-20-3

• 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
• 中文名称: 2-(1-甲基-2-苯基吲哚-3-基)-乙胺
• 英文名称: 2-(1-methyl-2-phenyl-indol-3-yl)-ethylamine
• 英文别名: 2-(1-Methyl-2-phenyl-indol-3-yl)-aethylamin；2-(1-Methyl-2-phenylindol-3-yl)ethanamine
• CAS: 101574-20-3
• 化学式: C₁₇H₁₈N₂
• 分子量: 250.343
• InChiKey: KYEUJXLZHNAKKF-UHFFFAOYSA-N

物化性质

• 沸点：
  457.4±33.0 °C(Predicted)
• 密度：
  1.10±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  19
• 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：
  31
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  2-(1-甲基-2-苯基吲哚-3-基)-乙胺 、 环丁基甲酰氯 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 3.0h， 以82%的产率得到N-<2-(N-methyl-2-phenylindol-3-yl)ethyl>cylobutanecarboxamide
  参考文献：
  名称：

  Mapping the Melatonin Receptor. 3. Design and Synthesis of Melatonin Agonists and Antagonists Derived from 2-Phenyltryptamines

  摘要：

  Three series of 2-phenyltryptamides were prepared as melatonin analogues to investigate the nature of the binding site of the melatonin receptor in chicken brain and in Xenopus laevis melanophore cells. The 5-methoxy-2-phenyltryptamides (6a-j) have high binding affinities for the chicken brain receptor, in some cases (6a-d) greater than that for melatonin, confirming and extending the work of Spadoni et al., and act as agonists in the Xenopus melanophore assay. Analogues lacking the 5-methoxyl group (2a-n) had a considerably lower affinity for the chicken brain receptor. In the Xenopus melanophore assay the compounds acylated on nitrogen by an alkyl group (2a-d) were agonists whereas the compounds acylated on nitrogen by an alicyclic group (2a-d) were antagonists. Introducing a methyl group at N-1 (7) led to an increase in binding affinity in the chicken brain assay, whereas introducing an ethyl group (13) led to a decrease in binding affinity. A methyl substituent at the beta-position of the 3-amidoethane side chain (8, 11) also led to an increase in the binding affinity. The only analogue acylated on nitrogen with an alkyl group (acetyl) which showed antagonist activity was 9, which has a beta-methoxymethyl side chain. In the absence of the 5-methoxyl group the methoxymethyl function may cause the molecule to bind in a different configuration so that it is no longer able to activate the receptor. All of these observations are in agreement with a model of melatonin at the receptor site in which the 3-amidoethane side chain is in a conformation close to the 5-methoxyl group.

  DOI：

  10.1021/jm00007a010
• 作为产物：
  描述：

  1-甲基-2-苯基吲哚 在 lithium aluminium tetrahydride 、 乙二醇二甲醚 、 正丁胺 、 三氯氧磷 作用下， 生成 2-(1-甲基-2-苯基吲哚-3-基)-乙胺
  参考文献：
  名称：

  Ames et al., Journal of the Chemical Society, 1959, p. 3388,3396

  摘要：

  DOI：

文献信息

• Mapping the Melatonin Receptor. 3. Design and Synthesis of Melatonin Agonists and Antagonists Derived from 2-Phenyltryptamines
  作者：Peter J. Garratt、Rob Jones、Derek A. Tocher、David Sugden

  DOI：10.1021/jm00007a010

  日期：1995.3

  Three series of 2-phenyltryptamides were prepared as melatonin analogues to investigate the nature of the binding site of the melatonin receptor in chicken brain and in Xenopus laevis melanophore cells. The 5-methoxy-2-phenyltryptamides (6a-j) have high binding affinities for the chicken brain receptor, in some cases (6a-d) greater than that for melatonin, confirming and extending the work of Spadoni et al., and act as agonists in the Xenopus melanophore assay. Analogues lacking the 5-methoxyl group (2a-n) had a considerably lower affinity for the chicken brain receptor. In the Xenopus melanophore assay the compounds acylated on nitrogen by an alkyl group (2a-d) were agonists whereas the compounds acylated on nitrogen by an alicyclic group (2a-d) were antagonists. Introducing a methyl group at N-1 (7) led to an increase in binding affinity in the chicken brain assay, whereas introducing an ethyl group (13) led to a decrease in binding affinity. A methyl substituent at the beta-position of the 3-amidoethane side chain (8, 11) also led to an increase in the binding affinity. The only analogue acylated on nitrogen with an alkyl group (acetyl) which showed antagonist activity was 9, which has a beta-methoxymethyl side chain. In the absence of the 5-methoxyl group the methoxymethyl function may cause the molecule to bind in a different configuration so that it is no longer able to activate the receptor. All of these observations are in agreement with a model of melatonin at the receptor site in which the 3-amidoethane side chain is in a conformation close to the 5-methoxyl group.
• Ames et al., Journal of the Chemical Society, 1959, p. 3388,3396
  作者：Ames et al.

  DOI：——

  日期：——