4-((3-acetamidophenyl)(1-benzylpiperidin-4-yl)amino)-N,N-diethylbenzamide | 1198602-09-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: 4-((3-acetamidophenyl)(1-benzylpiperidin-4-yl)amino)-N,N-diethylbenzamide
• 英文别名: 4-(3-acetamido-N-(1-benzylpiperidin-4-yl)anilino)-N,N-diethylbenzamide
• CAS: 1198602-09-3
• 化学式: C₃₁H₃₈N₄O₂
• 分子量: 498.668
• InChiKey: XTJAWYNXRXRTMU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.1
• 重原子数：
  37
• 可旋转键数：
  9
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.35
• 拓扑面积：
  55.9
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  4-((3-aminophenyl)(1-benzylpiperidin-4-yl)amino)-N,N-diethylbenzamide 、 乙酰氯 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 以66%的产率得到4-((3-acetamidophenyl)(1-benzylpiperidin-4-yl)amino)-N,N-diethylbenzamide
  参考文献：
  名称：

  Delta agonist hydroxy bioisosteres: The discovery of 3-((1-benzylpiperidin-4-yl){4-[(diethylamino)carbonyl]phenyl}amino)benzamide with improved delta agonist activity and in vitro metabolic stability

  摘要：

  We have investigated phenol replacements in a series of diaryl amino piperidine delta opioid agonists. From this study we have demonstrated that the hydroxy functional group can be replaced with a primary amide group, giving enhanced activity at the delta receptor, increased selectivity versus mu and kappa as well as improved in vitro metabolic stability. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2009.09.068

文献信息

• Delta agonist hydroxy bioisosteres: The discovery of 3-((1-benzylpiperidin-4-yl){4-[(diethylamino)carbonyl]phenyl}amino)benzamide with improved delta agonist activity and in vitro metabolic stability
  作者：Andrew M. Griffin、William Brown、Christopher Walpole、Martin Coupal、Lynda Adam、Mylene Gosselin、Dominic Salois、Pierre-Emmanuel Morin、Marie Roumi

  DOI：10.1016/j.bmcl.2009.09.068

  日期：2009.11

  We have investigated phenol replacements in a series of diaryl amino piperidine delta opioid agonists. From this study we have demonstrated that the hydroxy functional group can be replaced with a primary amide group, giving enhanced activity at the delta receptor, increased selectivity versus mu and kappa as well as improved in vitro metabolic stability. (C) 2009 Elsevier Ltd. All rights reserved.