1-(2'-fluoro-11'-oxo-11'H-spiro[cyclopentane-1,10'-dibenzo[b,f]thiepin]-3-yl)-4-piperidinecarboxylic acid | 1111639-64-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并硫平类
• 英文名称: 1-(2'-fluoro-11'-oxo-11'H-spiro[cyclopentane-1,10'-dibenzo[b,f]thiepin]-3-yl)-4-piperidinecarboxylic acid
• 英文别名: 1-(2'-fluoro-11'-oxo-11'H-spiro[cyclopentane-1,10'-dibenzo[b,f]thiepin]-3-yl)piperidine-4-carboxylic acid；2'-Fluoro-11'-oxo-11'H-spiro[cyclopentane-1,10'-dibenzo[b,f]thiepin]-3-yl-4-piperidinecarboxylic acid；1-(3-fluoro-5-oxospiro[benzo[b][1]benzothiepine-6,3'-cyclopentane]-1'-yl)piperidine-4-carboxylic acid
• CAS: 1111639-64-5
• 化学式: C₂₄H₂₄FNO₃S
• 分子量: 425.524
• InChiKey: GSUXFSXZSCBDQK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  30
• 可旋转键数：
  2
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.42
• 拓扑面积：
  82.9
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  ethyl 1-(2'-fluoro-11'-oxo-11'H-spiro[cyclopentane-1,10'-dibenzo[b,f]thiepin]-3-yl)-4-piperidinecarboxylate 在 水 、 cHex 作用下， 以 盐酸 、 水 为溶剂， 反应 3.0h， 以to afford the title compound as an off-white solid (8 mg)的产率得到1-(2'-fluoro-11'-oxo-11'H-spiro[cyclopentane-1,10'-dibenzo[b,f]thiepin]-3-yl)-4-piperidinecarboxylic acid
  参考文献：
  名称：

  Novel compounds

  摘要：

  本发明涉及式(I)的新颖螺环戊烷衍生物或其药学上可接受的盐，用于治疗中枢神经系统(CNS)的疾病和病状，特别是睡眠障碍。

  公开号：

  US20100190764A1

文献信息

• [EN] SPIRO CYCLOPENTANE COMPOUNDS USEFUL AS ANTAGONISTS OF THE H1-RECEPTOR<br/>[FR] NOUVEAUX COMPOSÉS
  申请人：GLAXO GROUP LTD

  公开号：WO2009016084A1

  公开（公告）日：2009-02-05

  This invention relates to novel spiro cyclopentane derivatives of formula (I) or a pharmaceutically acceptable salt thereof, for treating diseases and conditions of the central nervous system (CNS), in particular sleep disorders.

  该发明涉及公式（I）的新颖螺环戊烷衍生物或其药用盐，用于治疗中枢神经系统（CNS）的疾病和病症，特别是睡眠障碍。
• Novel compounds
  申请人：Castiglioni Emiliano

  公开号：US20100190764A1

  公开（公告）日：2010-07-29

  This invention relates to novel Spiro cyclopentane derivatives of formula (I) or a pharmaceutically acceptable salt thereof, for treating diseases and conditions of the central nervous system (CNS), in particular sleep disorders.

  本发明涉及式(I)的新颖螺环戊烷衍生物或其药学上可接受的盐，用于治疗中枢神经系统(CNS)的疾病和病状，特别是睡眠障碍。
• Novel Spirotetracyclic Zwitterionic Dual H₁/5-HT_2A Receptor Antagonists for the Treatment of Sleep Disorders
  作者：Massimo Gianotti、Maurizio Botta、Stephen Brough、Renzo Carletti、Emiliano Castiglioni、Corrado Corti、Michele Dal-Cin、Sonia Delle Fratte、Denana Korajac、Marija Lovric、Giancarlo Merlo、Milan Mesic、Francesca Pavone、Laura Piccoli、Slavko Rast、Maja Roscic、Anna Sava、Mario Smehil、Luigi Stasi、Andrea Togninelli、Mark J. Wigglesworth

  DOI：10.1021/jm100856p

  日期：2010.11.11

  Histamine H-1 and serotonin 5-HT2A receptors mediate two different mechanisms involved in sleep regulation: H-1 antagonists are sleep inducers, while 5-HT2A antagonists are sleep maintainers. Starting from 9'a, a novel spirotetracyclic compound endowed with good H-1/5-HT2A potency but poor selectivity, very high Cli, and a poor P450 profile, a specific optimization strategy was set up. In particular, we investigated the possibility of introducing appropriate amino acid moieties to optimize the developability profile of the series. Following this zwitterionic approach, we were able to identify several advanced leads (51, 65, and 73) with potent dual H-1/5-HT2A activity and appropriate developability profiles. These compounds exhibited efficacy as hypnotic agents in a rat telemetric sleep model with minimal effective doses in the range 3-10 mg/kg po.