N2-butyl-2-(6-methyl-4-oxo-4H-chromen-3-yl)-N1,N1-di(1-naphthyl)ethane-1,1,2-tricarboxamide | 1334482-32-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡喃
• 英文名称: N2-butyl-2-(6-methyl-4-oxo-4H-chromen-3-yl)-N1,N1-di(1-naphthyl)ethane-1,1,2-tricarboxamide
• CAS: 1334482-32-4
• 化学式: C₃₉H₃₅N₃O₅
• 分子量: 625.724
• InChiKey: JOSLXOLEZWIIPW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.3
• 重原子数：
  47.0
• 可旋转键数：
  10.0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  117.51
• 氢给体数：
  3.0
• 氢受体数：
  5.0

反应信息

• 作为产物：
  描述：

  6-甲基-4-氧-4H-1-苯并吡喃-3-甲醛 以 二氯甲烷 为溶剂， 反应 15.0h， 生成 N2-butyl-2-(6-methyl-4-oxo-4H-chromen-3-yl)-N1,N1-di(1-naphthyl)ethane-1,1,2-tricarboxamide
  参考文献：
  名称：

  Pseudo-Five-Component Reaction between 3-Formylchromones, Meldrum’s Acid, Isocyanides and Primary Arylamines: Diversity-Oriented Synthesis of Novel Chromone-Containing Peptidomimetics

  摘要：

  An efficient and practical method has been developed for the diversity-oriented synthesis of chromone-containing tripeptides via pseudo-five-component reaction between 3-formylchromones, Meldrum's acid, isocyanides and primary aromatic amines for the generation of a wide range of structurally interesting and pharmacologically significant compounds at ambient temperature. It is worth mentioning that in the course of this reaction, five new bonds (two C-C bonds, two C-N bonds and one C=O bond) are formed. In the present reaction three amide bonds are newly formed.

  DOI：

  10.1021/co200125a