1,4-bis(4-fluorophenyl)-2-(1H-indol-3-yl)butane-1,4-dione | 1198214-04-8

• 分子结构分类: 有机化合物 - 木脂素、新木脂素和相关化合物
• 英文名称: 1,4-bis(4-fluorophenyl)-2-(1H-indol-3-yl)butane-1,4-dione
• CAS: 1198214-04-8
• 化学式: C₂₄H₁₇F₂NO₂
• 分子量: 389.401
• InChiKey: RNTKFIXQKZGIDS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.9
• 重原子数：
  29
• 可旋转键数：
  6
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  49.9
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  1,4-bis(4-fluorophenyl)-2-(1H-indol-3-yl)butane-1,4-dione 在 劳森试剂 作用下， 以 甲苯 为溶剂， 反应 0.5h， 以80%的产率得到3-(2,5-bis(4-fluorophenyl)thiophen-3-yl)-1H-indole
  参考文献：
  名称：

  Indirect regioselective heteroarylation of indoles through a Friedel–Crafts reaction with (E)-1,4-diaryl-2-buten-1,4-diones

  摘要：

  A two-step synthesis of 3-heteroaryl indoles has been developed. The first step of the sequence involves a Friedel-Crafts alkylation of indoles with 1,4-diaryl-2-buten-1,4-diones to give the corresponding indoles bearing a 1,4-dicarbonyl moiety. The reaction is catalyzed by InCl3 and takes place with good yields. Cyclization of the diones under different Paal-Knorr conditions allows to prepare indoles substituted at the C3 position with 3-furanyl, 3-pyrrolyl- and 3-thienyl moieties. (c) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2009.09.011
• 作为产物：
  描述：

  吲哚 、 (E)-1,4-bis(4-fluorophenyl)but-2-ene-1,4-dione 在 indium(III) chloride 作用下， 以 二氯甲烷 为溶剂， 以90%的产率得到1,4-bis(4-fluorophenyl)-2-(1H-indol-3-yl)butane-1,4-dione
  参考文献：
  名称：

  Indirect regioselective heteroarylation of indoles through a Friedel–Crafts reaction with (E)-1,4-diaryl-2-buten-1,4-diones

  摘要：

  A two-step synthesis of 3-heteroaryl indoles has been developed. The first step of the sequence involves a Friedel-Crafts alkylation of indoles with 1,4-diaryl-2-buten-1,4-diones to give the corresponding indoles bearing a 1,4-dicarbonyl moiety. The reaction is catalyzed by InCl3 and takes place with good yields. Cyclization of the diones under different Paal-Knorr conditions allows to prepare indoles substituted at the C3 position with 3-furanyl, 3-pyrrolyl- and 3-thienyl moieties. (c) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2009.09.011