3-chloro-N-(4-chlorophenyl)-5-(5,6,7,8-tetrahydroimidazo[1,5-a]pyridin-3-yl)pyridin-2-amine

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 咪唑并吡啶类
• 英文名称: 3-chloro-N-(4-chlorophenyl)-5-(5,6,7,8-tetrahydroimidazo[1,5-a]pyridin-3-yl)pyridin-2-amine
• 英文别名: (4-chloro-phenyl)-[3-chloro-5-(5,6,7,8-tetrahydro-imidazo[1,5-a]pyridin-3-yl)-pyridin-2-yl]-amine
• 化学式: C₁₈H₁₆Cl₂N₄
• 分子量: 359.258
• InChiKey: VWPKCLDSEUHBJO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.5
• 重原子数：
  24
• 可旋转键数：
  3
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  42.7
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  5-溴-2,3-二氯吡啶 在 四(三苯基膦)钯 、 正丁基锂 、 sodium hydride 、 sodium carbonate 作用下， 以 四氢呋喃 、 甲醇 、 水 、 苯 为溶剂， 反应 18.17h， 生成 3-chloro-N-(4-chlorophenyl)-5-(5,6,7,8-tetrahydroimidazo[1,5-a]pyridin-3-yl)pyridin-2-amine
  参考文献：
  名称：

  Benzimidazoles as Potent and Orally Active mGlu5 Receptor Antagonists with an Improved PK Profile

  摘要：

  A focused chemical optimization effort of a compound 1 based on metabolite elucidation is described, resulting in 15i, a highly potent and selective mGlu5 receptor antagonist with an improved pharmacokinetic profile compared to 1. Characterization of 15i in vivo in the fear potentiated startle (FPS) paradigm revealed a robust reduction of conditioned fear behavior. This effect nicely correlates with the rat brain pharmacokinetics.

  DOI：

  10.1021/ml100215b

文献信息

• NOVEL BI-ARYL AMINES
  申请人：Glatthar Ralf

  公开号：US20090286827A1

  公开（公告）日：2009-11-19

  The present invention relates to novel bi-aryl amines of formula (I) and to pharmaceutically acceptable prodrugs, salts, solvates, hydrates, and N-oxides thereof and to pharmaceutical compositions comprising them, methods of their use, and methods of their preparation.

  本发明涉及公式（I）的新型双芳基胺，以及其药学上可接受的前药、盐、溶剂合物、水合物和N-氧化物，以及包含它们的制药组合物、使用方法和制备方法。
• [EN] NOVEL BI-ARYL AMINES<br/>[FR] NOUVELLES BI-ARYLE AMINES
  申请人：NOVARTIS AG

  公开号：WO2007113276A1

  公开（公告）日：2007-10-11

  [EN] The present invention relates to novel bi-aryl amines of formula (I) and to pharmaceutically acceptable prodrugs, salts, solvates, hydrates, and N-oxides thereof and to pharmaceutical compositions comprising them, methods of their use, and methods of their preparation.
  [FR] La présente invention concerne de nouvelles bi-aryle amines de formule (I) et leurs promédicaments, sels, solvates, hydrates et N-oxydes pharmaceutiquement acceptables, ainsi que des compositions pharmaceutiques les comprenant, leurs procédés d'utilisation et de préparation.
• Benzimidazoles as Potent and Orally Active mGlu5 Receptor Antagonists with an Improved PK Profile
  作者：David Carcache、Ivo Vranesic、Joachim Blanz、Sandrine Desrayaud、Markus Fendt、Ralf Glatthar

  DOI：10.1021/ml100215b

  日期：2011.1.13

  A focused chemical optimization effort of a compound 1 based on metabolite elucidation is described, resulting in 15i, a highly potent and selective mGlu5 receptor antagonist with an improved pharmacokinetic profile compared to 1. Characterization of 15i in vivo in the fear potentiated startle (FPS) paradigm revealed a robust reduction of conditioned fear behavior. This effect nicely correlates with the rat brain pharmacokinetics.