4-amino-N-benzyl-N-phenylbenzamide | 499188-13-5

• 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: 4-amino-N-benzyl-N-phenylbenzamide
• CAS: 499188-13-5
• 化学式: C₂₀H₁₈N₂O
• 分子量: 302.376
• InChiKey: CLJXDOQPZLALOA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  23
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.05
• 拓扑面积：
  46.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  邻碘苯甲酰氯 、 4-amino-N-benzyl-N-phenylbenzamide 在 吡啶 作用下， 以 二氯甲烷 为溶剂， 以100%的产率得到N-benzyl-4-(2-iodobenzamido)-N-phenylbenzamide
  参考文献：
  名称：

  Conformational studies of tertiary oligo-m-benzanilides and oligo-p-benzanilides in solution

  摘要：

  A series of oligo-m- and p-benzanilides were made and their conformations in solution were studied by NMR. In most cases, conformational mixtures were observed as soon as three or more monomers were incorporated into the oligomer. Some crystal structures were obtained, which indicated that helical conformations were adopted in the solid state. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2010.06.037
• 作为产物：
  描述：

  N-benzyl-4-nitro-N-phenylbenzamide 在 tin(II) chloride dihdyrate 作用下， 以 乙酸乙酯 为溶剂， 以91%的产率得到4-amino-N-benzyl-N-phenylbenzamide
  参考文献：
  名称：

  Conformational studies of tertiary oligo-m-benzanilides and oligo-p-benzanilides in solution

  摘要：

  A series of oligo-m- and p-benzanilides were made and their conformations in solution were studied by NMR. In most cases, conformational mixtures were observed as soon as three or more monomers were incorporated into the oligomer. Some crystal structures were obtained, which indicated that helical conformations were adopted in the solid state. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2010.06.037

文献信息

• Transition metal-free N-arylation of secondary amides through iodonium salts as aryne precursors
  作者：Ming Wang、Zhijian Huang

  DOI：10.1039/c6ob01649a

  日期：——

  By using a diaryliodonium salt as a benzyne precursor, a transition metal-free approach for N-arylation of secondary amides is developed. This novel benzyne precursor, which can be prepared easily by a one step process from an aryl iodide, shows different reactivities with previous benzyne precursors in the N-arylation reaction. Mechanistic studies confirm the involvement of benzyne species (generated

  通过使用二芳基碘鎓盐作为苯并炔前体，开发了无过渡金属的仲酰胺N-芳基化方法。可以通过一步法由芳基碘化物容易地制备的这种新型苯并炔前体在N-芳基化反应中显示出与先前的苯并炔前体不同的反应性。机理研究证实，苯并炔物种（由二芳基碘鎓盐原位生成）作为关键中间体参与其中。
• Conformational studies of tertiary oligo-m-benzanilides and oligo-p-benzanilides in solution
  作者：Laurent Chabaud、Jonathan Clayden、Madeleine Helliwell、Abigail Page、James Raftery、Lluís Vallverdú

  DOI：10.1016/j.tet.2010.06.037

  日期：2010.8

  A series of oligo-m- and p-benzanilides were made and their conformations in solution were studied by NMR. In most cases, conformational mixtures were observed as soon as three or more monomers were incorporated into the oligomer. Some crystal structures were obtained, which indicated that helical conformations were adopted in the solid state. (C) 2010 Elsevier Ltd. All rights reserved.