1-[4-(1,4-dioxa-spiro[4.5]dec-7-en-8-yl)-phenyl]-pyrrolidine | 1252615-73-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯烷类
• 英文名称: 1-[4-(1,4-dioxa-spiro[4.5]dec-7-en-8-yl)-phenyl]-pyrrolidine
• 英文别名: 1-[4-(1,4-Dioxaspiro[4.5]dec-7-en-8-yl)phenyl]pyrrolidine
• CAS: 1252615-73-8
• 化学式: C₁₈H₂₃NO₂
• 分子量: 285.386
• InChiKey: AWCXDOABCGBYGG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  21
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.56
• 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-[4-(1,4-dioxa-spiro[4.5]dec-7-en-8-yl)-phenyl]-pyrrolidine 在 palladium 10% on activated carbon 、 氢气 作用下， 以 甲醇 为溶剂， 20.0 ℃ 、344.75 kPa 条件下， 反应 2.0h， 生成 1-[4-(1,4-dioxa-spiro[4.5]dec-8-yl)-phenyl]-pyrrolidine
  参考文献：
  名称：

  Overcoming hERG activity in the discovery of a series of 4-azetidinyl-1-aryl-cyclohexanes as CCR2 antagonists

  摘要：

  A series of 4-azetidinyl-1-aryl-cyclohexanes as potent CCR2 antagonists with high selectivity over activity for the hERG potassium channel is discovered through divergent SARs of CCR2 and hERG. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.06.080
• 作为产物：
  描述：

  N-对溴苯吡咯烷 、 1,4-二氧杂-螺[4,5]癸-7-烯-8-硼酸频哪醇酯 在 四(三苯基膦)钯 、 sodium carbonate 作用下， 以 1,4-二氧六环 、 水 为溶剂， 反应 24.0h， 生成 1-[4-(1,4-dioxa-spiro[4.5]dec-7-en-8-yl)-phenyl]-pyrrolidine
  参考文献：
  名称：

  Overcoming hERG activity in the discovery of a series of 4-azetidinyl-1-aryl-cyclohexanes as CCR2 antagonists

  摘要：

  A series of 4-azetidinyl-1-aryl-cyclohexanes as potent CCR2 antagonists with high selectivity over activity for the hERG potassium channel is discovered through divergent SARs of CCR2 and hERG. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.06.080

文献信息

• 4-AZETIDINYL-1-PHENYL-CYCLOHEXANE ANTAGONISTS OF CCR2
  申请人：Zhang Xuqing

  公开号：US20100267689A1

  公开（公告）日：2010-10-21

  The present invention comprises compounds of Formula (I): wherein: X, R 1 , R 2 , R 3 , and R 4 are as defined in the specification. The invention also comprises a method of preventing, treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is type II diabetes, obesity and asthma. The invention also comprises a method of inhibiting CCR2 activity in a mammal by administration of a therapeutically effective amount of at least one compound of Formula (I).

  本发明涵盖了以下式（I）的化合物： 其中：X，R1，R2，R3和R4如规范中所定义。该发明还涵盖了一种预防、治疗或改善综合征、疾病或疾病的方法，其中所述综合征、疾病或疾病是II型糖尿病、肥胖和哮喘。该发明还涵盖了通过给哺乳动物施用至少一种式（I）化合物的治疗有效量来抑制CCR2活性的方法。
• US8513229B2
  申请人：——

  公开号：US8513229B2

  公开（公告）日：2013-08-20
• [EN] 4-AZETIDINYL-1-PHENYL-CYCLOHEXANE ANTAGONISTS OF CCR2<br/>[FR] ANTAGONISTES DE CCR2 A BASE DE 4-AZETIDINYL-1-PHENYL-CYCLOHEXANE
  申请人：JANSSEN PHARMACEUTICA NV

  公开号：WO2010121046A1

  公开（公告）日：2010-10-21

  The present invention comprises compounds of Formula (I) wherein: X, R1, R2, R3, and R4 are as defined in the specification. The invention also comprises a method of preventing, treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is type II diabetes, obesity and asthma. The invention also comprises a method of inhibiting CCR2 activity in a mammal by administration of a therapeutically effective amount of at least one compound of Formula (I).
• Overcoming hERG activity in the discovery of a series of 4-azetidinyl-1-aryl-cyclohexanes as CCR2 antagonists
  作者：Xuqing Zhang、Heather Hufnagel、Thomas Markotan、James Lanter、Chaozhong Cai、Cuifen Hou、Monica Singer、Evan Opas、Sandra McKenney、Carl Crysler、Dana Johnson、Zhihua Sui

  DOI：10.1016/j.bmcl.2011.06.080

  日期：2011.9

  A series of 4-azetidinyl-1-aryl-cyclohexanes as potent CCR2 antagonists with high selectivity over activity for the hERG potassium channel is discovered through divergent SARs of CCR2 and hERG. (C) 2011 Elsevier Ltd. All rights reserved.