trans-8-chloro-3-(2,2,2-trifluoroethyl)-7-[3-chloro-4-(4-hydroxycyclohexylamino)phenyl][1,2,4]triazolo[4,3-a]pyridine | 1255310-80-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 三唑并吡啶类
• 英文名称: trans-8-chloro-3-(2,2,2-trifluoroethyl)-7-[3-chloro-4-(4-hydroxycyclohexylamino)phenyl][1,2,4]triazolo[4,3-a]pyridine
• 英文别名: trans-4-[[2-chloro-4-[8-chloro-3-(2,2,2-trifluoroethyl)-1,2,4-triazolo[4,3-a]-pyridin-7-yl]phenyl]amino]-cyclohexanol
• CAS: 1255310-80-5
• 化学式: C₂₀H₁₉Cl₂F₃N₄O
• 分子量: 459.298
• InChiKey: CKPDPPZRMSOYJQ-JOCQHMNTSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.52
• 重原子数：
  30.0
• 可旋转键数：
  4.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  62.45
• 氢给体数：
  2.0
• 氢受体数：
  5.0

反应信息

• 作为产物：
  描述：

  8-chloro-3-(2,2,2-trifluoroethyl)-7-iodo-1,2,4-triazolo[4,3-a]pyridine 、 (trans)-4-[2-chloro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenylamino]cyclohexanol 在 四(三苯基膦)钯 、 碳酸氢钠 作用下， 以 1,4-二氧六环 、 水 为溶剂， 反应 0.17h， 以39%的产率得到trans-8-chloro-3-(2,2,2-trifluoroethyl)-7-[3-chloro-4-(4-hydroxycyclohexylamino)phenyl][1,2,4]triazolo[4,3-a]pyridine
  参考文献：
  名称：

  Discovery and Kinetic Profiling of 7-Aryl-1,2,4-triazolo[4,3-a]pyridines: Positive Allosteric Modulators of the Metabotropic Glutamate Receptor 2

  摘要：

  We report the synthesis and biological evaluation of a series of 7-aryl-1,2,4-triazolo[4,3-c]pyridines with mGlu(2) positive allosteric modulator (PAM) activity and affinity. Besides traditional in vitro parameters of potency and affinity, kinetic parameters k(on), k(off) and residence time (RT) were determined. The PAMs showed various kinetic profiles; k(on) values ranged over 2 orders of magnitude, whereas RT values were within a 10-fold range. Association rate constant k(on) was linearly correlated to affinity. Evaluation of a short, medium, and long RT compound in a label-free assay indicated a correlation between RT and functional effect. The effects of long RT compound 9 on sleep-wake states indicated long RT was translated into sustained inhibition of rapid eye movement (REM) in vivo. These results show that affinity-only driven selection would have resulted in mGlu(2) PAMs with high values for k(on) but not necessarily optimized RT, which is key to predicting optimal efficacy in vivo.

  DOI：

  10.1021/acs.jmedchem.7b00669

文献信息

• 7-ARYL-1,2,4-TRIAZOLO[4,3-a]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS
  申请人：Cic-Nunez Jose Maria

  公开号：US20120184528A1

  公开（公告）日：2012-07-19

  The present invention relates to novel triazolo[4,3-a]pyridine derivatives of Formula (I) wherein all radicals are as defined in the claims. The compounds according to the invention are positive allosteric modulators of the metabotropic glutamate receptor subtype 2 (“mGluR2”), which are useful for the treatment or prevention of neurological and psychiatric disorders associated with glutamate dysfunction and diseases in which the mGluR 2 subtype of metabotropic receptors is involved. The invention is also directed to pharmaceutical compositions comprising such compounds, to processes to prepare such compounds and compositions, and to the use of such compounds for the prevention or treatment of neurological and psychiatric disorders and diseases in which mGluR 2 is involved.

  本发明涉及式（I）的新型三唑并[4,3-a]吡啶衍生物，其中所有基团如权利要求中所定义。根据本发明的化合物是代谢型谷氨酸受体亚型2（“mGluR2”）的正向变构调节剂，有用于治疗或预防与谷氨酸功能障碍有关的神经和精神障碍以及涉及代谢型受体mGluR2亚型的疾病。本发明还涉及包含这些化合物的制药组合物，制备这些化合物和组合物的过程，以及使用这些化合物预防或治疗涉及mGluR2的神经和精神障碍和疾病。
• 7-ARYL-1,2,4-TRIAZOLO[4,3-A]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS
  申请人：ADDEX PHARMA, S.A.

  公开号：US20140200208A1

  公开（公告）日：2014-07-17

  The present invention relates to novel triazolo[4,3-a]pyridine derivatives of Formula (I) wherein all radicals are as defined in the claims. The compounds according to the invention are positive allosteric modulators of the metabotropic glutamate receptor subtype 2 (“mGluR2”), which are useful for the treatment or prevention of neurological and psychiatric disorders associated with glutamate dysfunction and diseases in which the mGluR2 subtype of metabotropic receptors is involved. The invention is also directed to pharmaceutical compositions comprising such compounds, to processes to prepare such compounds and compositions, and to the use of such compounds for the prevention or treatment of neurological and psychiatric disorders and diseases in which mGluR2 is involved.

  本发明涉及式（I）的新型三唑并[4,3-a]吡啶衍生物，其中所有基团如权利要求中所定义。根据本发明的化合物是代谢型谷氨酸受体亚型2（“mGluR2”）的正向变构调节剂，可用于治疗或预防与谷氨酸功能障碍有关的神经和精神疾病以及涉及代谢型受体mGluR2的疾病。本发明还涉及包含这种化合物的制药组合物，用于制备这种化合物和组合物的过程，以及用于预防或治疗涉及mGluR2的神经和精神疾病和疾病的这种化合物的使用。
• 7-ARYL-1,2,4-TRIAZOLO[4,3-a]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF mGluR2 RECEPTORS
  申请人：Janssen Pharmaceuticals Inc.

  公开号：EP2430021B1

  公开（公告）日：2013-08-28
• US8716480B2
  申请人：——

  公开号：US8716480B2

  公开（公告）日：2014-05-06
• US9085577B2
  申请人：——

  公开号：US9085577B2

  公开（公告）日：2015-07-21