Ethyl 1-(4-cyanophenyl)-6-methylindole-2-carboxylate | 1426681-23-3

• 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
• 英文名称: Ethyl 1-(4-cyanophenyl)-6-methylindole-2-carboxylate
• 英文别名: ethyl 1-(4-cyanophenyl)-6-methylindole-2-carboxylate
• CAS: 1426681-23-3
• 化学式: C₁₉H₁₆N₂O₂
• 分子量: 304.348
• InChiKey: JGEMVHMAFRGCAM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  23
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.16
• 拓扑面积：
  55
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  Ethyl 1-(4-cyanophenyl)-6-methylindole-2-carboxylate 在 lithium aluminium tetrahydride 作用下， 以 四氢呋喃 为溶剂， 以53.1%的产率得到4-[2-(Hydroxymethyl)-6-methylindol-1-yl]benzonitrile
  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-cyanophenyl)-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

文献信息

• Design, synthesis and aromatase inhibitory activities of novel indole-imidazole derivatives
  作者：Rui Wang、Hong-Fan Shi、Jing-Feng Zhao、Yan-Ping He、Hong-Bin Zhang、Jian-Ping Liu

  DOI：10.1016/j.bmcl.2013.01.045

  日期：2013.3

  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.