6-acetyl-7-methyl-3,6-dihydro-1H-furo[3,4-e]indol-1-one | 1573112-24-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 异香豆素
• 英文名称: 6-acetyl-7-methyl-3,6-dihydro-1H-furo[3,4-e]indol-1-one
• 英文别名: 6-acetyl-7-methyl-3H-furo[3,4-e]indol-1-one
• CAS: 1573112-24-9
• 化学式: C₁₃H₁₁NO₃
• 分子量: 229.235
• InChiKey: ODZOSXIZZJVCNR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  17
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  48.3
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  N-(3-氧代-1H-2-苯并呋喃-5-基)乙酰胺 、 烯丙基甲基碳酸酯 在 silver hexafluoroantimonate 、 dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer 、 copper diacetate 、 silver carbonate 作用下， 以 1,4-二氧六环 为溶剂， 反应 24.0h， 以71%的产率得到6-acetyl-7-methyl-3,6-dihydro-1H-furo[3,4-e]indol-1-one
  参考文献：
  名称：

  Synthesis of indoles through Rh(III)-catalyzed C–H cross-coupling with allyl carbonates

  摘要：

  A practical Rh-catalyzed reaction was developed to achieve 2-alkyl-substituted indole synthesis. The reaction can tolerate a variety of synthetically important functional groups. The indole products can also be transformed into other important skeletons. Two bioactive compounds, that is indomethacin and pravadoline were prepared using the new method. (C) 2014 Published by Elsevier Ltd.

  DOI：

  10.1016/j.tetlet.2013.11.065

文献信息

• Synthesis of indoles through Rh(III)-catalyzed C–H cross-coupling with allyl carbonates
  作者：Tian-Jun Gong、Wan-Min Cheng、Wei Su、Bin Xiao、Yao Fu

  DOI：10.1016/j.tetlet.2013.11.065

  日期：2014.3

  A practical Rh-catalyzed reaction was developed to achieve 2-alkyl-substituted indole synthesis. The reaction can tolerate a variety of synthetically important functional groups. The indole products can also be transformed into other important skeletons. Two bioactive compounds, that is indomethacin and pravadoline were prepared using the new method. (C) 2014 Published by Elsevier Ltd.