1-benzyl-3-(4-bromo-3-fluorophenoxy)piperidine-3-carboxylic acid | 1601476-26-9

• 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: 1-benzyl-3-(4-bromo-3-fluorophenoxy)piperidine-3-carboxylic acid
• CAS: 1601476-26-9
• 化学式: C₁₉H₁₉BrFNO₃
• 分子量: 408.267
• InChiKey: NUILJRNZUNFKFH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.09
• 重原子数：
  25.0
• 可旋转键数：
  5.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.32
• 拓扑面积：
  49.77
• 氢给体数：
  1.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  1-benzyl-3-(4-bromo-3-fluorophenoxy)piperidine-3-carboxylic acid 在 5%-palladium/activated carbon 、 氢气 、 1-羟基苯并三唑 、 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 为溶剂， 生成
  参考文献：
  名称：

  Substituted piperidines as HDM2 inhibitors

  摘要：

  Novel small molecule HDM2 inhibitor, substituted piperidine, was identified. Initial SAR study indicated potential for several position optimizations. Additional potency enhancement was achieved by introducing a sidechain off the aromatic ring. DMPK study of one of the active compounds has shown a moderate oral PK and reasonable bioavailability. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2014.01.026
• 作为产物：
  描述：

  1-苄基-3-哌啶酮 、 氯仿 、 4-溴-3-氟苯酚 在 sodium hydroxide 作用下， 生成 1-benzyl-3-(4-bromo-3-fluorophenoxy)piperidine-3-carboxylic acid
  参考文献：
  名称：

  Substituted piperidines as HDM2 inhibitors

  摘要：

  Novel small molecule HDM2 inhibitor, substituted piperidine, was identified. Initial SAR study indicated potential for several position optimizations. Additional potency enhancement was achieved by introducing a sidechain off the aromatic ring. DMPK study of one of the active compounds has shown a moderate oral PK and reasonable bioavailability. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2014.01.026