1-[3-(4-benzyloxy-phenoxy)-propyl]-piperidine | 398473-99-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 1-[3-(4-benzyloxy-phenoxy)-propyl]-piperidine
• 英文别名: 1-[3-(4-phenylmethoxyphenoxy)propyl]piperidine
• CAS: 398473-99-9
• 化学式: C₂₁H₂₇NO₂
• 分子量: 325.451
• InChiKey: ZHTQDAFKFNIAEJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.6
• 重原子数：
  24
• 可旋转键数：
  8
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.43
• 拓扑面积：
  21.7
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  1-[3-(4-benzyloxy-phenoxy)-propyl]-piperidine 在 palladium on activated charcoal 氢气 作用下， 以 乙醇 为溶剂， 反应 72.0h， 以85%的产率得到4-(3-piperidin-1-yl-propoxy)-phenol
  参考文献：
  名称：

  Synthesis and biological evaluation of diamine-based histamine H3 antagonists with serotonin reuptake inhibitor activity

  摘要：

  The synthesis and structure-activity relationships of a series of novel phenoxyphenyl diamine derivatives with affinity for both the histamine H-3 receptor and the serotonin transporter is described. (C) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.03.034
• 作为产物：
  描述：

  1-哌啶丙醇 、 4-苄氧基苯酚 在 PS-PPh3 、 偶氮二甲酸二苄酯 作用下， 以 二氯甲烷 为溶剂， 反应 20.0h， 以57%的产率得到1-[3-(4-benzyloxy-phenoxy)-propyl]-piperidine
  参考文献：
  名称：

  Synthesis and biological evaluation of diamine-based histamine H3 antagonists with serotonin reuptake inhibitor activity

  摘要：

  The synthesis and structure-activity relationships of a series of novel phenoxyphenyl diamine derivatives with affinity for both the histamine H-3 receptor and the serotonin transporter is described. (C) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.03.034

文献信息

• Phenoxypropylpiperidines and -pyrrolidines and their use as histamine H3-receptor ligands
  申请人：BIOPROJET

  公开号：EP1717234A1

  公开（公告）日：2006-11-02

  The present patent application concerns compounds of formula (I), with R1 and R2 taken together with the nitrogen atom to which they are attached, form a mono or bicyclic saturated nitrogen-containing ring; their preparation and their use as a H3 receptor ligand for treating e.g. CNS disorders like Alzheimer's disease.

  本专利申请涉及公式（I）的化合物，其中R1和R2与它们所连接的氮原子一起形成一个单环或双环饱和氮含环；它们的制备以及它们作为H3受体配体用于治疗例如阿尔茨海默病等中枢神经系统疾病。
• COMBINATION OF MODAFINIL AND AN ANTAGONIST OR INVERSE AGONIST OF THE H3 RECEPTOR
  申请人：Schwartz Jean-Charles

  公开号：US20090312367A1

  公开（公告）日：2009-12-17

  The invention relates to a combination of modafinil and at least one histamine H3 receptor antagonist or inverse agonist, which can be used in particular for the treatment of narcolepsy-cataplexy and more generally for disorders of sleep, wakefulness and vigilance.

  本发明涉及调节药物莫达非尼和至少一种组胺H3受体拮抗剂或反向激动剂的组合，特别适用于治疗嗜睡症-猝倒症，更广泛地适用于睡眠、清醒和警觉障碍的治疗。
• Non-imidazole aryloxyalkylamines
  申请人：——

  公开号：US20020065278A1

  公开（公告）日：2002-05-30

  Substituted aryloxyalkylamines of formula (I), compositions containing them, and methods of making and using them to treat histamine-mediated conditions.

  式(I)的取代的芳氧基烷胺，包含它们的组合物，以及使用它们治疗组胺介导的疾病的方法。
• NON-IMIDAZOLE ARYLOXYALKYLAMINES
  申请人：Apodaca Richard

  公开号：US20100004241A1

  公开（公告）日：2010-01-07

  Substituted aryloxyalkylamines of formula (I), compositions containing them, and methods of making and using them to treat histamine-mediated conditions.

  公式（I）中的取代芳氧基烷胺，包含它们的组合物，以及使用它们治疗组胺介导的疾病的制备和使用方法。
• SUBSTITUTED PHENYL PROPYL AMINES AS HISTAMINE H3 RECEPTOR AND SEROTONIN TRANSPORTER MODULATORS
  申请人：Keith John M.

  公开号：US20080139564A1

  公开（公告）日：2008-06-12

  Certain substituted phenyl propyl amine compounds are histamine H 3 receptor and/or serotonin transporter modulators useful in the treatment of histamine H 3 receptor- and/or serotonin-mediated diseases.

  某些取代苯基丙胺化合物是组胺H3受体和/或血清素转运体调节剂，可用于治疗组胺H3受体和/或血清素介导的疾病。