2-[3-bromo-5-[2,6-dibromo-4-[2-[2-(3,4-dimethoxyphenyl)ethylamino]-2-oxoethyl]phenoxy]-4-methoxyphenyl]-N-[2-(3,4-dimethoxyphenyl)ethyl]acetamide | 1246431-49-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2-[3-bromo-5-[2,6-dibromo-4-[2-[2-(3,4-dimethoxyphenyl)ethylamino]-2-oxoethyl]phenoxy]-4-methoxyphenyl]-N-[2-(3,4-dimethoxyphenyl)ethyl]acetamide
• CAS: 1246431-49-1
• 化学式: C₃₇H₃₉Br₃N₂O₈
• 分子量: 879.437
• InChiKey: DCWCCYNSAAWEID-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.7
• 重原子数：
  50
• 可旋转键数：
  17
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  114
• 氢给体数：
  2
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  2-[3-bromo-5-[2,6-dibromo-4-[2-[2-(3,4-dimethoxyphenyl)ethylamino]-2-oxoethyl]phenoxy]-4-methoxyphenyl]-N-[2-(3,4-dimethoxyphenyl)ethyl]acetamide 在 三氯氧磷 、 sodium tetrahydroborate 作用下， 以 甲苯 为溶剂， 以100%的产率得到1-[[3-Bromo-5-[2,6-dibromo-4-[(6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl]phenoxy]-4-methoxyphenyl]methyl]-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline
  参考文献：
  名称：

  Electrochemical construction of the diaryl ethers: a synthetic approach to o-methylthalibrine

  摘要：

  Electrochemical dimerization of halogenated p-hydroxyphenylacetic acid derivatives followed by Zn reduction provided the corresponding diaryl ethers. Manipulation of the reduction step using several procedures increased its efficiency, which enabled the construction of o-methylthalibrine, an isoquinoline-class alkaloid. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2010.07.037
• 作为产物：
  描述：

  2-[3-Bromo-5-[2,6-dibromo-4-(carboxymethyl)phenoxy]-4-methoxyphenyl]acetic acid 、 3,4-二甲氧基苯乙胺 在 (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate 、 三乙胺 作用下， 以100%的产率得到2-[3-bromo-5-[2,6-dibromo-4-[2-[2-(3,4-dimethoxyphenyl)ethylamino]-2-oxoethyl]phenoxy]-4-methoxyphenyl]-N-[2-(3,4-dimethoxyphenyl)ethyl]acetamide
  参考文献：
  名称：

  Electrochemical construction of the diaryl ethers: a synthetic approach to o-methylthalibrine

  摘要：

  Electrochemical dimerization of halogenated p-hydroxyphenylacetic acid derivatives followed by Zn reduction provided the corresponding diaryl ethers. Manipulation of the reduction step using several procedures increased its efficiency, which enabled the construction of o-methylthalibrine, an isoquinoline-class alkaloid. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2010.07.037

文献信息

• Electrochemical construction of the diaryl ethers: a synthetic approach to o-methylthalibrine
  作者：Yu Naito、Takamasa Tanabe、Yuki Kawabata、Yuichi Ishikawa、Shigeru Nishiyama

  DOI：10.1016/j.tetlet.2010.07.037

  日期：2010.9

  Electrochemical dimerization of halogenated p-hydroxyphenylacetic acid derivatives followed by Zn reduction provided the corresponding diaryl ethers. Manipulation of the reduction step using several procedures increased its efficiency, which enabled the construction of o-methylthalibrine, an isoquinoline-class alkaloid. (C) 2010 Elsevier Ltd. All rights reserved.