(8-methyl-8-aza-bicyclo[3.2.1]oct-3-yl)-(2-nitro-phenyl)-amine | 1023699-51-5

• 分子结构分类: 有机化合物 - 生物碱及其衍生物 - 托烷生物碱
• 英文名称: (8-methyl-8-aza-bicyclo[3.2.1]oct-3-yl)-(2-nitro-phenyl)-amine
• 英文别名: (endo)-8-methyl-N-(2-nitrophenyl)-8-azabicyclo[3.2.1]octan-3-amine
• CAS: 1023699-51-5
• 化学式: C₁₄H₁₉N₃O₂
• 分子量: 261.324
• InChiKey: IACRRVAMRCOGIQ-ZSBIGDGJSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.63
• 重原子数：
  19.0
• 可旋转键数：
  3.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.57
• 拓扑面积：
  58.41
• 氢给体数：
  1.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  (8-methyl-8-aza-bicyclo[3.2.1]oct-3-yl)-(2-nitro-phenyl)-amine 在 1-氯乙基氯甲酸酯 、 甲醇 作用下， 以 氯仿 为溶剂， 反应 7.5h， 以81%的产率得到(endo)-N-(2-nitrophenyl)-8-azabicyclo[3.2.1]octan-3-amine hydrochloride
  参考文献：
  名称：

  [EN] SUBSTITUTED-QUINOXALINE-TYPE-PIPERIDINE COMPOUNDS AND THE USES THEREOF
  [FR] COMPOSÉS DE PIPÉRIDINE DE TYPE QUINOXALINE SUBSTITUÉE ET LEURS UTILISATIONS

  摘要：

  公开号：

  WO2009027820A3
• 作为产物：
  描述：

  1-氟-2-硝基苯 、 (1S,5R)-8-Methyl-8-azabicyclo[3.2.1]octan-3-amine 在 potassium carbonate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 24.0h， 生成 (8-methyl-8-aza-bicyclo[3.2.1]oct-3-yl)-(2-nitro-phenyl)-amine
  参考文献：
  名称：

  Parallel synthesis of a series of potentially brain penetrant aminoalkyl benzoimidazoles

  摘要：

  Alpha7 agonists were identified via GOLD (CCDC) docking in the putative agonist binding site of an alpha7 homology model and a series of aminoalkyl benzoimidazoles was synthesised to obtain potentially brain penetrant drugs. The array was prepared starting from the reaction of ortho-fluoronitrobenzenes with a selection of diamines, followed by reduction of the nitro group to obtain a series of monoalkylated phenylene diamines. N,N'-Carbonyidiimidazole (CDI) mediated acylation, followed by a parallel automated work-up procedure, afforded the monoacylated phenylenediamines which were cyclised under acidic conditions. Parallel work-up and purification afforded the array products in good yields and purities with a robust parallel methodology which will be useful for other libraries. Screening for alpha7 activity revealed compounds with agonist activity for the receptor. (C) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2007.11.068

文献信息

• Substituted-Quinoxaline-Type Piperidine Compounds and the Uses Thereof
  申请人：FUCHINO Kouki

  公开号：US20100216726A1

  公开（公告）日：2010-08-26

  The invention relates to Substituted-Quinoxaline-Type Piperidine Compounds, compositions comprising an effective amount of a Substituted-Quinoxaline-Type Piperidine Compound and methods to treat or prevent a condition, such as pain, comprising administering to an animal in need thereof an effective amount of a Substituted-Quinoxaline-Type Piperidine Compound.

  本发明涉及取代喹喔啉型哌啶化合物、包含有效量取代喹喔啉型哌啶化合物的组合物以及治疗或预防某种疾病（如疼痛）的方法，包括向需要治疗的动物施用有效量取代喹喔啉型哌啶化合物。
• SUBSTITUTED-QUINOXALINE-TYPE PIPERIDINE COMPOUNDS AND THE USES THEREOF
  申请人：Purdue Pharma L.P.

  公开号：US20150141643A1

  公开（公告）日：2015-05-21

  The invention relates to Substituted-Quinoxaline-Type Piperidine Compounds, compositions comprising an effective amount of a Substituted-Quinoxaline-Type Piperidine Compound and methods to treat or prevent a condition, such as pain, comprising administering to an animal in need thereof an effective amount of a Substituted-Quinoxaline-Type Piperidine Compound.

  该发明涉及取代喹喔啉型哌啶化合物，包括一种有效量的取代喹喔啉型哌啶化合物的组合物以及治疗或预防疾病的方法，例如疼痛，通过向需要治疗的动物施用一种有效量的取代喹喔啉型哌啶化合物。
• Substituted-quinoxaline-type-piperidine compounds and the uses thereof
  申请人：Purdue Pharma LP

  公开号：EP2433935A1

  公开（公告）日：2012-03-28

  The invention relates to Substituted-Quinoxaline-Type Piperidine Compounds of Formula (I) and Formula (II), compositions comprising an effective amount of a Substituted-Quinoxaline-Type Piperidine Compound and methods to treat or prevent a condition, such as pain, comprising administering to an animal in need thereof an effective amount of a Substituted-Quinoxaline-Type Piperidine Compound.

  本发明涉及式（I）和式（II）的取代喹喔啉型哌啶化合物、包含有效量的取代喹喔啉型哌啶化合物的组合物，以及治疗或预防疼痛等疾病的方法，包括向有需要的动物施用有效量的取代喹喔啉型哌啶化合物。
• PIPERIDINE INTERMEDIATES
  申请人：Purdue Pharma L.P.

  公开号：EP3564240A1

  公开（公告）日：2019-11-06

  The invention relates to intermediates A3 and A4 for making Substituted-Quinoxaline-Type Piperidine Compounds.

  本发明涉及用于制造取代喹喔啉型哌啶化合物的中间体 A3 和 A4。
• SUBSTITUTED-QUINOXALINE-TYPE-PIPERIDINE COMPOUNDS AND THE USES THEREOF
  申请人：Purdue Pharma LP

  公开号：EP2086958B1

  公开（公告）日：2015-01-14