1-[2-(ethylamino)phenyl]propan-1-one | 1399859-11-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1-[2-(ethylamino)phenyl]propan-1-one
• CAS: 1399859-11-0
• 化学式: C₁₁H₁₅NO
• 分子量: 177.246
• InChiKey: FZHJVECKLWOFJT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  13
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  29.1
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  吗啉 、 1-[2-(ethylamino)phenyl]propan-1-one 在 bis(1,5-cyclooctadiene)nickel (0) 、 potassium phosphate 、 三甲基膦 作用下， 以 N,N-二甲基甲酰胺 、 氯苯 为溶剂， 反应 48.0h， 以73%的产率得到1-ethylquinolin-4(1H)-one
  参考文献：
  名称：

  Synthesis of 4-Quinolones through Nickel-Catalyzed Intramolecular Amination on the β-Carbon of o-(N-Alkylamino)propiophenones

  摘要：

  o-(N-Alkylamino)propiophenones are converted into 4-quinolones in the presence of chlorobenzene, potassium phosphate, morpholine, and nickel(0) catalyst. The reaction proceeds through the nickel-catalyzed formation of beta-enaminones from o-(N-alkylamino)propiophenones and morpholine, followed by the intramolecular transamination.

  DOI：

  10.1055/s-0031-1291146
• 作为产物：
  描述：

  N-乙基苯胺 、 丙腈 在 三氯化硼 、 aluminum (III) chloride 作用下， 以 苯 为溶剂， 以19%的产率得到1-[2-(ethylamino)phenyl]propan-1-one
  参考文献：
  名称：

  Synthesis of 4-Quinolones through Nickel-Catalyzed Intramolecular Amination on the β-Carbon of o-(N-Alkylamino)propiophenones

  摘要：

  o-(N-Alkylamino)propiophenones are converted into 4-quinolones in the presence of chlorobenzene, potassium phosphate, morpholine, and nickel(0) catalyst. The reaction proceeds through the nickel-catalyzed formation of beta-enaminones from o-(N-alkylamino)propiophenones and morpholine, followed by the intramolecular transamination.

  DOI：

  10.1055/s-0031-1291146

文献信息

• 11-Beta HSD1 inhibitors
  申请人：Xiang Shaoyun Jason

  公开号：US20060025445A1

  公开（公告）日：2006-02-02

  This invention relates to inhibiting 11-beta HSD1.

  这项发明涉及抑制11-beta HSD1。
• Inhibitors of Ion Channels
  申请人：Marron Brian Edward

  公开号：US20130072471A1

  公开（公告）日：2013-03-21

  Compounds, compositions and methods are provided which are useful in the treatment of diseases through the inhibition of sodium ion flux through voltage-gated sodium channels. More particularly, the invention provides substituted aryl sulfonamides, compositions comprising these compounds, as well as methods of using these compounds or compositions in the treatment of central or peripheral nervous system disorders, particularly pain and chronic pain by blocking sodium channels associated with the onset or recurrence of the indicated conditions. The compounds, compositions and methods of the present invention are of particular use for treating neuropathic or inflammatory pain by the inhibition of ion flux through a voltage-gated sodium channel.

  本发明提供了在通过抑制电压门控钠通道中的钠离子流来治疗疾病方面有用的化合物、组合物和方法。更具体地，本发明提供了取代芳基磺酰胺、包含这些化合物的组合物，以及使用这些化合物或组合物治疗中枢或外周神经系统疾病，特别是疼痛和慢性疼痛的方法，通过阻断与所示条件的发生或复发相关的钠通道来实现。本发明的化合物、组合物和方法特别适用于通过抑制电压门控钠通道中的离子流来治疗神经病性或炎症性疼痛。
• INHIBITORS OF ION CHANNELS
  申请人：Marron Brian Edward

  公开号：US20090143358A1

  公开（公告）日：2009-06-04

  Compounds, compositions and methods are provided which are useful in the treatment of diseases through the inhibition of sodium ion flux through voltage-gated sodium channels. More particularly, the invention provides substituted aryl sulfonamides, compositions comprising these compounds, as well as methods of using these compounds or compositions in the treatment of central or peripheral nervous system disorders, particularly pain and chronic pain by blocking sodium channels associated with the onset or recurrence of the indicated conditions. The compounds, compositions and methods of the present invention are of particular use for treating neuropathic or inflammatory pain by the inhibition of ion flux through a voltage-gated sodium channel.

  本发明提供了化合物、组合物和方法，通过抑制电压门控钠通道中的钠离子流来治疗疾病。更具体地，本发明提供了取代芳基磺酰胺、包含这些化合物的组合物，以及使用这些化合物或组合物治疗中枢或外周神经系统疾病，特别是疼痛和慢性疼痛的方法，通过阻止与所示疾病的发生或复发有关的钠通道。本发明的化合物、组合物和方法特别适用于通过抑制电压门控钠通道中的离子流来治疗神经病理性或炎症性疼痛。
• US8357711B2
  申请人：——

  公开号：US8357711B2

  公开（公告）日：2013-01-22
• US8741934B2
  申请人：——

  公开号：US8741934B2

  公开（公告）日：2014-06-03