Ethyl 1-(4-methoxyphenyl)-6-methylindole-2-carboxylate | 1426681-19-7

• 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: Ethyl 1-(4-methoxyphenyl)-6-methylindole-2-carboxylate
• 英文别名: ethyl 1-(4-methoxyphenyl)-6-methylindole-2-carboxylate
• CAS: 1426681-19-7
• 化学式: C₁₉H₁₉NO₃
• 分子量: 309.365
• InChiKey: ZYDOGOZBRKDERC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.5
• 重原子数：
  23
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  40.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  Ethyl 1-(4-methoxyphenyl)-6-methylindole-2-carboxylate 在 lithium aluminium tetrahydride 作用下， 以 四氢呋喃 为溶剂， 以87.2%的产率得到[1-(4-Methoxyphenyl)-6-methylindol-2-yl]methanol
  参考文献：
  名称：

  Design, synthesis and aromatase inhibitory activities of novel indole-imidazole derivatives

  摘要：

  A series of novel indole-imidazole derivatives have been prepared and evaluated in vitro on the aromatase inhibitory activities. The results suggested that proton or a small electron-withdrawing group at para-position of the phenyl ring would enhance the inhibitory activities and any bulky group should be avoided in order to keep a relative small volume for this kind of molecules. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2013.01.045
• 作为产物：
  描述：

  Ethyl α-azido-4-methylcinnamate 在 dirhodium tetraacetate 、 potassium phosphate 、 copper(l) iodide 、 N,N'-二甲基乙二胺 作用下， 以 甲苯 为溶剂， 反应 24.0h， 生成 Ethyl 1-(4-methoxyphenyl)-6-methylindole-2-carboxylate
  参考文献：
  名称：

  Design, synthesis and aromatase inhibitory activities of novel indole-imidazole derivatives

  摘要：

  A series of novel indole-imidazole derivatives have been prepared and evaluated in vitro on the aromatase inhibitory activities. The results suggested that proton or a small electron-withdrawing group at para-position of the phenyl ring would enhance the inhibitory activities and any bulky group should be avoided in order to keep a relative small volume for this kind of molecules. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2013.01.045