6-氧代-3-氮杂双环[3.2.1]辛烷-3-甲酸乙酯 | 850991-53-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 中文名称: 6-氧代-3-氮杂双环[3.2.1]辛烷-3-甲酸乙酯
• 中文别名: (1R,5R)-6-氧代-3-氮杂双环[3.2.1]辛烷-3-羧酸乙酯
• 英文名称: ethyl 6-oxo-3-azabicyclo[3.2.1 ]octane-3-carboxylate
• 英文别名: Ethyl 6-oxo-3-azabicyclo[3.2.1]octane-3-carboxylate
• CAS: 850991-53-6
• 化学式: C₁₀H₁₅NO₃
• 分子量: 197.234
• InChiKey: YMCVBSNHYFZDOU-UHFFFAOYSA-N

物化性质

• 沸点：
  311.3±25.0 °C(Predicted)
• 密度：
  1.198

计算性质

• 辛醇/水分配系数(LogP)：
  0.4
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.8
• 拓扑面积：
  46.6
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  6-氧代-3-氮杂双环[3.2.1]辛烷-3-甲酸乙酯 在 氯化铵 作用下， 以 乙醚 、 正己烷 、 四氢呋喃 、 水 为溶剂， 反应 0.5h， 以84%的产率得到ethyl 6-hydroxy-6-(5-phenoxy-3-pyridinyl)-3-azabicyclo[3.2.1]octane-3-carboxylate
  参考文献：
  名称：

  [EN] AZABICYCYCLIC COMPOUNDS FOR RELIEVING PAIN AND TREATING CENTRAL NERVOUS SYSTEM DISORDERS
  [FR] COMPOSITIONS PHARMACEUTIQUES ET METHODES DESTINEES AU SOULAGEMENT DE LA DOULEUR ET AU TRAITEMENT DE TROUBLES DU SYSTEME NERVEUX CENTRAL

  摘要：

  公开号：

  WO2005037832A3
• 作为产物：
  描述：

  ethyl 6-oxo-3-azabicyclo[3.2.1]octane-3-carboxylate ethylene ketal 在 硫酸 作用下， 以 水 为溶剂， 反应 1.0h， 以64%的产率得到6-氧代-3-氮杂双环[3.2.1]辛烷-3-甲酸乙酯
  参考文献：
  名称：

  [EN] AZABICYCYCLIC COMPOUNDS FOR RELIEVING PAIN AND TREATING CENTRAL NERVOUS SYSTEM DISORDERS
  [FR] COMPOSITIONS PHARMACEUTIQUES ET METHODES DESTINEES AU SOULAGEMENT DE LA DOULEUR ET AU TRAITEMENT DE TROUBLES DU SYSTEME NERVEUX CENTRAL

  摘要：

  公开号：

  WO2005037832A3

文献信息

• [EN] MUSCARINIC RECEPTOR AGONISTS<br/>[FR] AGONISTES DU RÉCEPTEUR MUSCARINIQUE
  申请人：HEPTARES THERAPEUTICS LTD

  公开号：WO2015140559A1

  公开（公告）日：2015-09-24

  This invention relates to compounds that are agonists of the muscarinic M1 receptor and which are useful in the treatment of muscarinic M1 receptor mediated diseases. Also provided are pharmaceutical compositions containing the compounds and the therapeutic uses of the compounds. Compounds provided are of formula where m, p, q, W, Z, Y, X1, X2, R1, R2 R3 and R4 are as defined herein.

  这项发明涉及激动母胞素M1受体的化合物，这些化合物在治疗母胞素M1受体介导的疾病中很有用。还提供了含有这些化合物的药物组合物以及这些化合物的治疗用途。所提供的化合物的化学式如下，其中m、p、q、W、Z、Y、X1、X2、R1、R2、R3和R4的定义如本文所述。
• PHARMACEUTICAL COMPOSITIONS AND METHODS FOR RELIEVING PAIN AND TREATING CENTRAL NERVOUS SYSTEM DISORDERS
  申请人：Breining R. Scott

  公开号：US20050282823A1

  公开（公告）日：2005-12-22

  Patients susceptible to or suffering from disorders, such as central nervous system disorders, which are characterized by an alteration in normal neurotransmitter release, such as dopamine release (e.g., Parkinsonism, Parkinson's Disease, Tourette's Syndrome, attention deficient disorder, or schizophrenia), are treated by administering a compound of Formulas 1 or 2, as described herein. The compounds of Formulas 1 and 2 are also useful for treating pain, and treating drug addiction, nicotine addiction, and/or obesity. The compounds can exist as individual stereoisomers, racemic mixtures, diastereomers and the like.

  对于易感受或患有疾病的患者，例如中枢神经系统疾病，其特征为正常神经递质释放的改变，例如多巴胺释放（例如帕金森症，帕金森氏病，抽动症，注意力缺陷障碍或精神分裂症），可以通过给予本文所述的1或2式化合物来治疗。 1和2式化合物也可用于治疗疼痛，药物成瘾，尼古丁成瘾和/或肥胖症。这些化合物可以存在于单个立体异构体，混合物，对映异构体等形式。
• Pharmaceutical Compositions and Methods for Relieving Pain and Treating Central Nervous System Disorders
  申请人：Breining Scott R.

  公开号：US20080242693A1

  公开（公告）日：2008-10-02

  Patients susceptible to or suffering from disorders, such as central nervous system disorders, which are characterized by an alteration in normal neurotransmitter release, such as dopamine release (e.g., Parkinsonism, Parkinson's Disease, Tourette's Syndrome, attention deficient disorder, or schizophrenia), are treated by administering a compound of Formulas 1 or 2, as described herein. The compounds of Formulas 1 and 2 are also useful for treating pain, and treating drug addiction, nicotine addiction, and/or obesity. The compounds can exist as individual stereoisomers, racemic mixtures, diastereomers and the like.

  患有或易感染神经系统紊乱（例如帕金森氏症、多动症、注意力缺陷障碍、精神分裂症等）的患者，其特征为神经递质释放（例如多巴胺释放）的异常改变，可通过给予本文所述的1或2式化合物治疗。1和2式化合物也可用于治疗疼痛、药物成瘾、尼古丁成瘾和/或肥胖症。这些化合物可以存在为单一立体异构体、混合物、对映异构体等形式。
• Pharmaceutical compositions and methods for relieving pain and treating central nervous system disorders
  申请人：Targacept, Inc.

  公开号：US07402592B2

  公开（公告）日：2008-07-22

  Patients susceptible to or suffering from disorders, such as central nervous system disorders, which are characterized by an alteration in normal neurotransmitter release, such as dopamine release (e.g., Parkinsonism, Parkinson's Disease, Tourette's Syndrome, attention deficient disorder, or schizophrenia), are treated by administering a compound of Formulas 1 or 2, as described herein. The compounds of Formulas 1 and 2 are also useful for treating pain, and treating drug addiction, nicotine addiction, and/or obesity. The compounds can exist as individual stereoisomers, racemic mixtures, diastereomers and the like.

  易感受或患有诸如中枢神经系统失调的疾病的患者，这些疾病的特征是神经递质的正常释放发生改变，例如多巴胺释放（例如帕金森症，帕金森氏病，抽动症，注意力缺陷障碍或精神分裂症），通过给予本文中所描述的1或2号配方的化合物进行治疗。 公式1和2的化合物还可用于治疗疼痛，药物成瘾，尼古丁成瘾和/或肥胖症。 这些化合物可以存在于单个立体异构体，混合物，对映异构体等形式。
• Muscarinic receptor agonists
  申请人：Heptares Therapeutics Limited

  公开号：US10030035B2

  公开（公告）日：2018-07-24

  This invention relates to compounds that are agonists of the muscarinic M1 receptor and which are useful in the treatment of muscarinic M1 receptor mediated diseases. Also provided are pharmaceutical compositions containing the compounds and the therapeutic uses of the compounds. Compounds provided are of formula where m, p, q, W, Z, Y, X1, X2, R1, R2 R3 and R4 are as defined herein.

  本发明涉及的化合物是毒蕈碱 M1 受体的激动剂，可用于治疗毒蕈碱 M1 受体介导的疾病。本发明还提供了含有这些化合物的药物组合物以及这些化合物的治疗用途。所提供的化合物为式 其中m、p、q、W、Z、Y、X1、X2、R1、R2 R3和R4如本文所定义。