ethyl-benzyl-(3-phenyl-propyl)-amine

• 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: ethyl-benzyl-(3-phenyl-propyl)-amine
• 英文别名: Aethyl-benzyl-(3-phenyl-propyl)-amin；N-benzyl-N-ethyl-3-phenylpropan-1-amine
• 化学式: C₁₈H₂₃N
• 分子量: 253.387
• InChiKey: XKYOEDVINPKWRH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.4
• 重原子数：
  19
• 可旋转键数：
  7
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  3.2
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  1-氯-3-苯基丙烷 在 氢氧化钾 作用下， 生成 ethyl-benzyl-(3-phenyl-propyl)-amine
  参考文献：
  名称：

  Kuelz et al., Chemische Berichte, 1939, vol. 72, p. 2161,2166

  摘要：

  DOI：

文献信息

• Synthesis of Amines by Reductive Amination of Aldehydes and Ketones using Co₃O₄/NGr@C Catalyst
  作者：Sabine Pisiewicz、Tobias Stemmler、Annette-Enrica Surkus、Kathrin Junge、Matthias Beller

  DOI：10.1002/cctc.201402527

  日期：2015.1

  environmentally benign hydrogenations. Here, we have developed a straightforward reductive amination methodology using molecular hydrogen in the presence of a Co3O4/NGr@C catalyst system. Various carbonyl compounds were transformed with secondary amines to the corresponding tertiary amines with good to excellent yields and selectivity. The Co3O4/NGr@C catalyst is recycled up to five times without significant

  异质非贵金属基催化剂可实现经济高效且对环境无害的氢化反应。在这里，我们已经开发出了一种简单的还原胺化方法，该方法是在Co 3 O 4 / NGr @ C催化剂体系存在下使用分子氢。用仲胺将各种羰基化合物以良好或优异的收率和选择性转化为相应的叔胺。Co 3 O 4 / NGr @ C催化剂可循环使用五次，而不会明显降低活性。
• 3-SUBSTITUTED-6-ARYL PYRIDINES
  申请人：Hutchinson Alan J.

  公开号：US20110281837A1

  公开（公告）日：2011-11-17

  3-substituted-6-aryl pyridines of Formula I are provided: wherein R 1 , R 2 , R 3 , R 8 , R 9 , A and Ar are defined herein. Such compounds are ligands of C5a receptors. Preferred compounds of Formula I bind to C5a receptors with high affinity and exhibit neutral antagonist or inverse agonist activity at C5a receptors. The present invention also relates to pharmaceutical compositions comprising such compounds, and to the use of such compounds in treating a variety of inflammatory, cardiovascular, and immune system disorders. In addition, the present invention provides labeled 3-substituted-6-aryl pyridines, which are useful as probes for the localization of C5a receptors.

  本发明提供了式I的3-取代-6-芳基吡啶化合物：其中R1、R2、R3、R8、R9、A和Ar的定义在此处。这些化合物是C5a受体的配体。式I的优选化合物具有高亲和力结合到C5a受体，并在C5a受体上表现出中性拮抗剂或反向激动剂活性。本发明还涉及包含这些化合物的制药组合物，以及将这些化合物用于治疗各种炎症、心血管和免疫系统疾病的用途。此外，本发明提供了标记的3-取代-6-芳基吡啶，可用作C5a受体定位的探针。
• 3-Substituted-6-Aryl Pyridines
  申请人：Hutchison Alan J.

  公开号：US20090176980A1

  公开（公告）日：2009-07-09

  3-substituted-6-aryl pyridines of Formula I are provided: wherein R 1 , R 2 , R 3 , R 8 , R 9 , A and Ar are defined herein. Such compounds are ligands of C5a receptors. Preferred compounds of Formula I bind to C5a receptors with high affinity and exhibit neutral antagonist or inverse agonist activity at C5a receptors. The present invention also relates to pharmaceutical compositions comprising such compounds, and to the use of such compounds in treating a variety of inflammatory, cardiovascular, and immune system disorders. In addition, the present invention provides labeled 3-substituted-6-aryl pyridines, which are useful as probes for the localization of C5a receptors.

  本发明提供了式I中的3-取代-6-芳基吡啶化合物： 其中R1、R2、R3、R8、R9、A和Ar在此定义。这些化合物是C5a受体的配体。式I的优选化合物具有高亲和力结合C5a受体，并在C5a受体上表现出中性拮抗剂或反向激动剂活性。本发明还涉及包含这些化合物的药物组合物，以及在治疗各种炎症，心血管和免疫系统疾病中使用这些化合物的用途。此外，本发明提供了标记的3-取代-6-芳基吡啶，可用作C5a受体的定位探针。
• US7342115B2
  申请人：——

  公开号：US7342115B2

  公开（公告）日：2008-03-11
• US7863454B2
  申请人：——

  公开号：US7863454B2

  公开（公告）日：2011-01-04