1,1,1-trifluoro-N-[(4-fluoropiperidin-4-yl)methyl]methanesulfonamide | 530116-51-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: 1,1,1-trifluoro-N-[(4-fluoropiperidin-4-yl)methyl]methanesulfonamide
• CAS: 530116-51-9
• 化学式: C₇H₁₂F₄N₂O₂S
• 分子量: 264.244
• InChiKey: ZAYMBWTVBIMRFI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.8
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  66.6
• 氢给体数：
  2
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  1,1,1-trifluoro-N-[(4-fluoropiperidin-4-yl)methyl]methanesulfonamide 、 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 生成 N-((1-(4-chloro-2-(2-fluorophenylsulfonyl)phenylsulfonyl)-4-fluoropiperidin-4-yl)methyl)-1,1,1-trifluoromethanesulfonamide
  参考文献：
  名称：

  Non-aromatic A-ring replacement in the triaryl bis-sulfone CB2 receptor inhibitors

  摘要：

  The triaryl bis-sulfone 1 was modified by converting the aryl A-ring to a piperidine ring. The piperidine ring was further elaborated to a spirocyclopropyl piperidine moiety. The effect on CB2 binding potency, rat calcium channel affinity, and CYP 2C9 inhibition is described. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2009.11.084

文献信息

• Non-aromatic A-ring replacement in the triaryl bis-sulfone CB2 receptor inhibitors
  作者：Eric J. Gilbert、Guowei Zhou、Michael K.C. Wong、Ling Tong、Bandarpalle B. Shankar、Chunli Huang、Joseph Kelly、Brian J. Lavey、Stuart W. McCombie、Lei Chen、Razia Rizvi、Youhao Dong、Youheng Shu、Joseph A. Kozlowski、Neng-Yang Shih、R. William Hipkin、Waldemar Gonsiorek、Asra Malikzay、Charles A. Lunn、Len Favreau、Daniel J. Lundell

  DOI：10.1016/j.bmcl.2009.11.084

  日期：2010.1

  The triaryl bis-sulfone 1 was modified by converting the aryl A-ring to a piperidine ring. The piperidine ring was further elaborated to a spirocyclopropyl piperidine moiety. The effect on CB2 binding potency, rat calcium channel affinity, and CYP 2C9 inhibition is described. (C) 2009 Elsevier Ltd. All rights reserved.