3-(4'-chloro-biphenyl-4-yl)-propylamine | 935692-73-2

• 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: 3-(4'-chloro-biphenyl-4-yl)-propylamine
• 英文别名: 3-[4-(4-Chlorophenyl)phenyl]propan-1-amine
• CAS: 935692-73-2
• 化学式: C₁₅H₁₆ClN
• 分子量: 245.752
• InChiKey: MNBOUZNSLXISGT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  17
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  26
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  3-(4'-chloro-biphenyl-4-yl)-propylamine 、 1-(4-溴苄基)哌啶 在 tris-(dibenzylideneacetone)dipalladium(0) 、 sodium cyanoborohydride 、 溶剂黄146 、 2-(二叔丁基膦)联苯 、 sodium t-butanolate 作用下， 以 四氢呋喃 、 甲苯 、 乙腈 为溶剂， 生成 N-[3-[4-(4-chlorophenyl)phenyl]propyl]-N-methyl-4-(piperidin-1-ylmethyl)aniline
  参考文献：
  名称：

  Design, synthesis and evaluation of MCH receptor 1 antagonists—Part II: Optimization of pyridazines toward reduced phospholipidosis and hERG inhibition

  摘要：

  Despite recent success there remains a high therapeutic need for the development of drugs targeting diseases associated with the metabolic syndrome. As part of our search for safe and effective MCH-R1 antagonists for the treatment of obesity, a series of 3,6-disubstituted pyridazines was evaluated. During optimization several issues of the initial lead structures had to be resolved, such as selectivity over related GPCRs, inhibition of the hERG channel as well as the potential to induce phospholipidosis. Utilizing property-based design, we could demonstrate that all parameters can significantly be improved by consequently increasing the polarity of the compounds. By this strategy, we succeeded in identifying potent and orally available MCH-R1 antagonists with good selectivity over M1 and 5-HT2A and an improved safety profile with respect to hERG inhibition and phospholipidosis. (C) 2015 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2015.05.074
• 作为产物：
  描述：

  3-(4'-chloro-biphenyl-4-yl)-propionamide 在 lithium aluminium tetrahydride 、 sodium hydroxide 、 水 作用下， 以 四氢呋喃 为溶剂， 反应 10.0h， 以42%的产率得到3-(4'-chloro-biphenyl-4-yl)-propylamine
  参考文献：
  名称：

  WO2007/48802

  摘要：

  公开号：

文献信息

• New (hetero)aryl compounds with MCH antagonistic activity and medicaments comprising these compounds
  申请人：Roth Juergen Gerald

  公开号：US20070111981A1

  公开（公告）日：2007-05-17

  The present invention relates to (hetero)aryl compounds of general formula I wherein the groups and radicals A, B, Q, W, X, Y, Z, R 1 , R 2 , R 4a , R 4b , R 5a , R 5b , have the meanings given in claim 1 . Moreover the invention relates to pharmaceutical compositions containing at least one compound according to the invention. By virtue of their MCH-receptor antagonistic activity the pharmaceutical compositions according to the invention are suitable for the treatment of metabolic disorders and/or eating disorders, particularly obesity, bulimia, anorexia, hyperphagia and diabetes.

  本发明涉及一般式I的（杂）芳基化合物，其中A、B、Q、W、X、Y、Z、R1、R2、R4a、R4b、R5a和R5b基团和基团具有权利要求1中给出的含义。此外，本发明涉及至少含有本发明中的一种化合物的制药组合物。由于其MCH受体拮抗活性，根据本发明的制药组合物适用于治疗代谢紊乱和/或进食障碍，尤其是肥胖症、贪食症、厌食症、暴食症和糖尿病。
• (HETERO)ARYL COMPOUNDS WITH MCH ANTAGONISTIC ACTIVITY AND MEDICAMENTS COMPRISING THESE COMPOUNDS
  申请人：BOEHRINGER INGELHEIM INTERNATIONAL GMBH

  公开号：EP1943231A1

  公开（公告）日：2008-07-16
• [EN] (HETERO)ARYL COMPOUNDS WITH MCH ANTAGONISTIC ACTIVITY AND MEDICAMENTS COMPRISING THESE COMPOUNDS<br/>[FR] COMPOSÉS HÉTÉROARYLIQUES DOTÉS D'UNE ACTIVITÉ ANTAGONISTE DE MCH ET MÉDICAMENTS COMPRENANT CES COMPOSÉS
  申请人：BOEHRINGER INGELHEIM INT

  公开号：WO2007048802A1

  公开（公告）日：2007-05-03

  [EN] The present invention relates to (hetero)aryl compounds of general formula (I) wherein the groups and radicals A, B, Q, W, X, Y, Z, R¹, R², R^4a, R^4b, R^5a, R^5b, have the meanings given in claim 1. Moreover the invention relates to pharmaceutical compositions containing at least one compound according to the invention. By virtue of their MCH-receptor antagonistic activity the pharmaceutical compositions according to 10 the invention are suitable for the treatment of metabolic disorders and/or eating disorders, particularly obesity, bulimia, anorexia, hyperphagia and diabetes.
  [FR] La présente invention concerne des composés hétéroaryliques de formule générale (I), les groupements et radicaux A, B, Q, W, X, Y, Z, R¹, R², R^4a, R^4b, R^5a, R^5b ayant les significations données dans la revendication 1. En outre, la présente invention concerne des préparations pharmaceutiques contenant au moins un composé selon l'invention. Grâce à leur activité antagoniste du récepteur MCH, les préparations pharmaceutiques selon l'invention sont adaptées au traitement de troubles métaboliques et/ou de troubles de l'alimentation, en particulier l'obésité, la boulimie, l'anorexie, l'hyperphagie et le diabète.
• WO2007/48802
  申请人：——

  公开号：——

  公开（公告）日：——
• Design, synthesis and evaluation of MCH receptor 1 antagonists—Part II: Optimization of pyridazines toward reduced phospholipidosis and hERG inhibition
  作者：Gerald J. Roth、Armin Heckel、Jörg T. Kley、Thorsten Lehmann、Stephan G. Müller、Thorsten Oost、Klaus Rudolf、Kirsten Arndt、Ralph Budzinski、Martin Lenter、Ralf R.H. Lotz、Marcus Schindler、Leo Thomas、Dirk Stenkamp

  DOI：10.1016/j.bmcl.2015.05.074

  日期：2015.8

  Despite recent success there remains a high therapeutic need for the development of drugs targeting diseases associated with the metabolic syndrome. As part of our search for safe and effective MCH-R1 antagonists for the treatment of obesity, a series of 3,6-disubstituted pyridazines was evaluated. During optimization several issues of the initial lead structures had to be resolved, such as selectivity over related GPCRs, inhibition of the hERG channel as well as the potential to induce phospholipidosis. Utilizing property-based design, we could demonstrate that all parameters can significantly be improved by consequently increasing the polarity of the compounds. By this strategy, we succeeded in identifying potent and orally available MCH-R1 antagonists with good selectivity over M1 and 5-HT2A and an improved safety profile with respect to hERG inhibition and phospholipidosis. (C) 2015 Elsevier Ltd. All rights reserved.