N,N-dimethyl-N-{2-[3-(thien-2-ylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-1-yl]ethyl}amine | 763924-99-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯并吡啶类
• 英文名称: N,N-dimethyl-N-{2-[3-(thien-2-ylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-1-yl]ethyl}amine
• 英文别名: N,N-dimethyl-2-(3-thiophen-2-ylsulfonylpyrrolo[2,3-b]pyridin-1-yl)ethanamine
• CAS: 763924-99-8
• 化学式: C₁₅H₁₇N₃O₂S₂
• 分子量: 335.451
• InChiKey: UMIQCSRFYTVZEC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  22
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  91.8
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  N,N-dimethyl-N-{2-[3-(thien-2-ylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-1-yl]ethyl}amine 在 盐酸 作用下， 以 乙醇 、 水 为溶剂， 生成
  参考文献：
  名称：

  Novel 1-aminoethyl-3-arylsulfonyl-1H-pyrrolo[2,3-b]pyridines are potent 5-HT6 agonists

  摘要：

  A series of 1-aminoethyl-3-arylsulfonyl-1H-pyrrolo[2,3-b]pyridines 10a-z was prepared as novel 5-HT6 ligands. The best compounds were high affinity, full agonists at 5-HT6 receptors. Several agonists demonstrated good selectivity over other serotonergic and dopaminergic receptors. Acute administration of selective agonist 10e significantly increased extracellular GABA concentrations in rat frontal cortex. This compound also reduced adjunctive drinking behavior in the rat schedule-induced polydipsia assay, possibly predictive of efficacy in obsessive compulsive disorder and other anxiety related disorders. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2009.05.055
• 作为产物：
  描述：

  3-(thien-2-ylsulfonyl)-1H-pyrrolo[2,3-b]pyridine 、 二甲氨基氯乙烷盐酸 在 sodium hydride 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 N,N-dimethyl-N-{2-[3-(thien-2-ylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-1-yl]ethyl}amine
  参考文献：
  名称：

  Novel 1-aminoethyl-3-arylsulfonyl-1H-pyrrolo[2,3-b]pyridines are potent 5-HT6 agonists

  摘要：

  A series of 1-aminoethyl-3-arylsulfonyl-1H-pyrrolo[2,3-b]pyridines 10a-z was prepared as novel 5-HT6 ligands. The best compounds were high affinity, full agonists at 5-HT6 receptors. Several agonists demonstrated good selectivity over other serotonergic and dopaminergic receptors. Acute administration of selective agonist 10e significantly increased extracellular GABA concentrations in rat frontal cortex. This compound also reduced adjunctive drinking behavior in the rat schedule-induced polydipsia assay, possibly predictive of efficacy in obsessive compulsive disorder and other anxiety related disorders. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2009.05.055

文献信息

• Novel 1-aminoethyl-3-arylsulfonyl-1H-pyrrolo[2,3-b]pyridines are potent 5-HT6 agonists
  作者：Ronald C. Bernotas、Steven Lenicek、Schuyler Antane、Derek C. Cole、Boyd L. Harrison、Albert J. Robichaud、Guo Ming Zhang、Deborah Smith、Brian Platt、Qian Lin、Ping Li、Joseph Coupet、Sharon Rosenzweig-Lipson、Chad E. Beyer、Lee E. Schechter

  DOI：10.1016/j.bmc.2009.05.055

  日期：2009.7

  A series of 1-aminoethyl-3-arylsulfonyl-1H-pyrrolo[2,3-b]pyridines 10a-z was prepared as novel 5-HT6 ligands. The best compounds were high affinity, full agonists at 5-HT6 receptors. Several agonists demonstrated good selectivity over other serotonergic and dopaminergic receptors. Acute administration of selective agonist 10e significantly increased extracellular GABA concentrations in rat frontal cortex. This compound also reduced adjunctive drinking behavior in the rat schedule-induced polydipsia assay, possibly predictive of efficacy in obsessive compulsive disorder and other anxiety related disorders. (C) 2009 Elsevier Ltd. All rights reserved.