1,1,1-trifluoro-N-(2-piperidin-3-ylethyl)methanesulfonamide | 1343050-76-9

• 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-(2-piperidin-3-ylethyl)methanesulfonamide
• CAS: 1343050-76-9
• 化学式: C₈H₁₅F₃N₂O₂S
• 分子量: 260.281
• InChiKey: DIPHBWHXALVQCU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  16
• 可旋转键数：
  4
• 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：
  7

反应信息

• 作为反应物：
  描述：

  1-(2-氟苯基)磺酰基吲哚-2-磺酰氯 、 1,1,1-trifluoro-N-(2-piperidin-3-ylethyl)methanesulfonamide 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 生成 1,1,1-trifluoro-N-(2-(1-(1-(2-fluorophenylsulfonyl)-1H-indol-2-ylsulfonyl)piperidin-3-yl)ethyl)methanesulfonamide
  参考文献：
  名称：

  Expansion of SAR studies on triaryl bis sulfone cannabinoid CB2 receptor ligands

  摘要：

  We report further expansion of the structure activity relationship (SAR) on the triaryl bis sulfone class of compounds (I), which are potent CB2 receptor ligands with excellent selectivity over the CB1 receptor. This study was extended to B ring changes, followed by simultaneous optimization of the A-, B-, and C-rings. Compound 42 has excellent CB2 potency, selectivity and rat exposure. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.08.126

文献信息

• Expansion of SAR studies on triaryl bis sulfone cannabinoid CB2 receptor ligands
  作者：Ling Tong、B.B. Shankar、Lei Chen、Razia Rizvi、Joseph Kelly、Eric Gilbert、Chunli Huang、De-Yi Yang、Joseph A. Kozlowski、N.-Y. Shih、W. Gonsiorek、R. William Hipkin、Asra Malikzay、Charles A. Lunn、Daniel J. Lundell

  DOI：10.1016/j.bmcl.2010.08.126

  日期：2010.11

  We report further expansion of the structure activity relationship (SAR) on the triaryl bis sulfone class of compounds (I), which are potent CB2 receptor ligands with excellent selectivity over the CB1 receptor. This study was extended to B ring changes, followed by simultaneous optimization of the A-, B-, and C-rings. Compound 42 has excellent CB2 potency, selectivity and rat exposure. (C) 2010 Elsevier Ltd. All rights reserved.