N-[2-(4,5-dimethoxy-2-phenylacetylphenyl)ethyl]formamide | 894419-48-8

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 二苯乙烯类
• 英文名称: N-[2-(4,5-dimethoxy-2-phenylacetylphenyl)ethyl]formamide
• 英文别名: N-[2-[4,5-dimethoxy-2-(2-phenylacetyl)phenyl]ethyl]formamide
• CAS: 894419-48-8
• 化学式: C₁₉H₂₁NO₄
• 分子量: 327.38
• InChiKey: MQFHFSXPAWLDOY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  24
• 可旋转键数：
  8
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.26
• 拓扑面积：
  64.6
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  N-[2-(4,5-dimethoxy-2-phenylacetylphenyl)ethyl]formamide 在 polyphophoric acid 、 对甲苯磺酸 作用下， 以 1,2-二氯乙烷 为溶剂， 反应 0.5h， 生成 1-benzyl-6,7-dimethoxy-3,4-dihydro-isoquinoline
  参考文献：
  名称：

  A Synthesis of N-Formylenamides of Isoquinoline

  摘要：

  N-Formylenamides of isoquinoline (6) were obtained from N-[2-(2-acyl-4,5 -dimethoxyphenyl)ethyl] formamides (5) by cyclization in the presence of catalytic amount of p-toluensulfonic acid. The starting keto formamides (5) were obtained by acylation of a N-[2-(3,4-dimethoxyphenyl)ethyl] formam ides (1) with carboxylic acids or their anhydrides in polyphosphoric acid (PPA).

  DOI：

  10.3987/com-05-10645
• 作为产物：
  描述：

  N-(3,4-二甲氧基苯乙基)甲酰胺 、 苯甲酸酐 在 PPA 作用下， 以 二氯甲烷 为溶剂， 反应 2.0h， 以60%的产率得到N-[2-(4,5-dimethoxy-2-phenylacetylphenyl)ethyl]formamide
  参考文献：
  名称：

  A Synthesis of N-Formylenamides of Isoquinoline

  摘要：

  N-Formylenamides of isoquinoline (6) were obtained from N-[2-(2-acyl-4,5 -dimethoxyphenyl)ethyl] formamides (5) by cyclization in the presence of catalytic amount of p-toluensulfonic acid. The starting keto formamides (5) were obtained by acylation of a N-[2-(3,4-dimethoxyphenyl)ethyl] formam ides (1) with carboxylic acids or their anhydrides in polyphosphoric acid (PPA).

  DOI：

  10.3987/com-05-10645

文献信息

• A Synthesis of N-Formylenamides of Isoquinoline
  作者：Iliyan Ivanov、Stoyanka Nikolova、Stela Statkova-Abeghe、Plamen Angelov

  DOI：10.3987/com-05-10645

  日期：——

  N-Formylenamides of isoquinoline (6) were obtained from N-[2-(2-acyl-4,5 -dimethoxyphenyl)ethyl] formamides (5) by cyclization in the presence of catalytic amount of p-toluensulfonic acid. The starting keto formamides (5) were obtained by acylation of a N-[2-(3,4-dimethoxyphenyl)ethyl] formam ides (1) with carboxylic acids or their anhydrides in polyphosphoric acid (PPA).