1,3-bis[(1'-methyl-1,3-dihydro-1'H-[3,3']biindolyl-2-on)-1-yl]propane | 1356031-27-0

• 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: 1,3-bis[(1'-methyl-1,3-dihydro-1'H-[3,3']biindolyl-2-on)-1-yl]propane
• 英文别名: 3-(1-methylindol-3-yl)-1-[3-[3-(1-methylindol-3-yl)-2-oxo-3H-indol-1-yl]propyl]-3H-indol-2-one
• CAS: 1356031-27-0
• 化学式: C₃₇H₃₂N₄O₂
• 分子量: 564.687
• InChiKey: KYGHBGWDYOFPSK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.6
• 重原子数：
  43
• 可旋转键数：
  6
• 环数：
  8.0
• sp3杂化的碳原子比例：
  0.19
• 拓扑面积：
  50.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  3-diazo-indolin-2-one 在 dirhodium tetraacetate 、 potassium carbonate 作用下， 以 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 0.33h， 生成 1,3-bis[(1'-methyl-1,3-dihydro-1'H-[3,3']biindolyl-2-on)-1-yl]propane
  参考文献：
  名称：

  Rhodium(II) catalyzed intermolecular double C-alkylation: a method for the synthesis of tetraindoles and indolophanes

  摘要：

  Double C-alkylation of cyclic diazoamides or bis-diazoamides with indoles or bis-indoles has been achieved to synthesize tetraindole derivatives using rhodium(II) acetate as a catalyst under mild reaction conditions with complete regioselectivity. The intermolecular double C-alkylation reaction strategy was successfully applied to synthesize indolophanes in moderate yield with excellent regiocontrol. The structure and stereochemistry of macrocycles were unequivocally confirmed with the help of single-crystal X-ray structure analyses. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2011.11.073

文献信息

• Rhodium(II) catalyzed intermolecular double C-alkylation: a method for the synthesis of tetraindoles and indolophanes
  作者：Sengodagounder Muthusamy、Thangaraju Karikalan、Chidambaram Gunanathan、Eringathodi Suresh

  DOI：10.1016/j.tet.2011.11.073

  日期：2012.2

  Double C-alkylation of cyclic diazoamides or bis-diazoamides with indoles or bis-indoles has been achieved to synthesize tetraindole derivatives using rhodium(II) acetate as a catalyst under mild reaction conditions with complete regioselectivity. The intermolecular double C-alkylation reaction strategy was successfully applied to synthesize indolophanes in moderate yield with excellent regiocontrol. The structure and stereochemistry of macrocycles were unequivocally confirmed with the help of single-crystal X-ray structure analyses. (C) 2011 Elsevier Ltd. All rights reserved.