3,5-bis[(4,6-dichloro-1,3,5-triazin-2-yl)oxy]-N-[(1R)-1-phenylethyl]benzamide | 957473-28-8

• 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: 3,5-bis[(4,6-dichloro-1,3,5-triazin-2-yl)oxy]-N-[(1R)-1-phenylethyl]benzamide
• CAS: 957473-28-8
• 化学式: C₂₁H₁₃Cl₄N₇O₃
• 分子量: 553.191
• InChiKey: KPFZXLRAVILKTI-SNVBAGLBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.8
• 重原子数：
  35
• 可旋转键数：
  7
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.1
• 拓扑面积：
  125
• 氢给体数：
  1
• 氢受体数：
  9

反应信息

• 作为反应物：
  描述：

  3,5-bis[(4,6-dichloro-1,3,5-triazin-2-yl)oxy]-N-[(1R)-1-phenylethyl]benzamide 在 potassium carbonate 、 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 、 丙酮 为溶剂， 反应 58.0h， 生成
  参考文献：
  名称：

  En route to inherently chiral tetraoxacalix[2]arene[2]triazines

  摘要：

  This paper describes our attempts to synthesize inherently chiral heteroatom-bridged calixaromatics. Based on a stepwise fragment-coupling approach using a chiral 3,5-dihydroxybenzamide or benzoate, 2,4-dihydroxyacetophenone, and cyanuric chloride as reactants, chiral tetraoxacalix[2]arene[2]triazine derivatives 16 and 17 were synthesized in good yields. Subsequent macrocyclic condensation with a diamine 6 furnished efficiently the pairs of diastereomers of inherently chiral tetraoxacalix[2]arene[2]triazine azacrowns 18 and 19. (C) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2007.05.129
• 作为产物：
  描述：

  3,5-二羟基苯甲酸 在 sodium hydroxide 、 乙醇 、 硫酸 、 4-甲基苯磺酸吡啶 、 1-羟基苯并三唑 、 N,N-二异丙基乙胺 、 N,N'-二环己基碳二亚胺 作用下， 以 四氢呋喃 、 乙醇 、 二氯甲烷 、 水 为溶剂， 反应 51.0h， 生成 3,5-bis[(4,6-dichloro-1,3,5-triazin-2-yl)oxy]-N-[(1R)-1-phenylethyl]benzamide
  参考文献：
  名称：

  En route to inherently chiral tetraoxacalix[2]arene[2]triazines

  摘要：

  This paper describes our attempts to synthesize inherently chiral heteroatom-bridged calixaromatics. Based on a stepwise fragment-coupling approach using a chiral 3,5-dihydroxybenzamide or benzoate, 2,4-dihydroxyacetophenone, and cyanuric chloride as reactants, chiral tetraoxacalix[2]arene[2]triazine derivatives 16 and 17 were synthesized in good yields. Subsequent macrocyclic condensation with a diamine 6 furnished efficiently the pairs of diastereomers of inherently chiral tetraoxacalix[2]arene[2]triazine azacrowns 18 and 19. (C) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2007.05.129

文献信息

• En route to inherently chiral tetraoxacalix[2]arene[2]triazines
  作者：Bao-Yong Hou、Qi-Yu Zheng、De-Xian Wang、Mei-Xiang Wang

  DOI：10.1016/j.tet.2007.05.129

  日期：2007.10

  This paper describes our attempts to synthesize inherently chiral heteroatom-bridged calixaromatics. Based on a stepwise fragment-coupling approach using a chiral 3,5-dihydroxybenzamide or benzoate, 2,4-dihydroxyacetophenone, and cyanuric chloride as reactants, chiral tetraoxacalix[2]arene[2]triazine derivatives 16 and 17 were synthesized in good yields. Subsequent macrocyclic condensation with a diamine 6 furnished efficiently the pairs of diastereomers of inherently chiral tetraoxacalix[2]arene[2]triazine azacrowns 18 and 19. (C) 2007 Elsevier Ltd. All rights reserved.