[2-(2-Chloro-4-trifluoromethoxy-phenyl)-3-nitro-pyridin-4-yl]-((S)-1-methyl-butyl)-amine | 514206-42-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: [2-(2-Chloro-4-trifluoromethoxy-phenyl)-3-nitro-pyridin-4-yl]-((S)-1-methyl-butyl)-amine
• CAS: 514206-42-9
• 化学式: C₁₇H₁₇ClF₃N₃O₃
• 分子量: 403.788
• InChiKey: SAVALHNRTJMQIJ-JTQLQIEISA-N

反应信息

• 作为反应物：
  描述：

  [2-(2-Chloro-4-trifluoromethoxy-phenyl)-3-nitro-pyridin-4-yl]-((S)-1-methyl-butyl)-amine 在 ammonium hydroxide 、 sodium sulfate 作用下， 以 1,4-二氧六环 、 水 为溶剂， 生成 2-(2-Chloro-4-trifluoromethoxy-phenyl)-N⁴-((S)-1-methyl-butyl)-pyridine-3,4-diamine
  参考文献：
  名称：

  Imidazo[4,5-b]pyridines as corticotropin releasing factor receptor ligands

  摘要：

  A series of high affinity CRF receptor ligands with an imidazo[4,5-b]pyridine core is described. Individual analogues were synthesized and tested in a rat CRF receptor binding assay. The best compounds were further tested in the dog N-in-1 pharmaco-kinetic model to assess plasma levels at 1 mg/kg (po) and in the rat situational anxiety model to assess anxiolytic efficacy at 3 mg/kg (po). The structure-activity relationships for good receptor binding affinity are described herein. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(02)00833-8
• 作为产物：
  描述：

  (2-Chloro-3-nitro-pyridin-4-yl)-((S)-1-methyl-butyl)-amine 、 2-氯-4-三氟甲氧基苯硼酸 在 bis-triphenylphosphine-palladium(II) chloride 、 barium dihydroxide 作用下， 以 乙二醇二甲醚 、 水 为溶剂， 生成 [2-(2-Chloro-4-trifluoromethoxy-phenyl)-3-nitro-pyridin-4-yl]-((S)-1-methyl-butyl)-amine
  参考文献：
  名称：

  Imidazo[4,5-b]pyridines as corticotropin releasing factor receptor ligands

  摘要：

  A series of high affinity CRF receptor ligands with an imidazo[4,5-b]pyridine core is described. Individual analogues were synthesized and tested in a rat CRF receptor binding assay. The best compounds were further tested in the dog N-in-1 pharmaco-kinetic model to assess plasma levels at 1 mg/kg (po) and in the rat situational anxiety model to assess anxiolytic efficacy at 3 mg/kg (po). The structure-activity relationships for good receptor binding affinity are described herein. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(02)00833-8