1-Methyl-1,4,5,6-tetrahydro-5-methoxycarbonylpyrimidine | 146422-22-2

• 分子结构分类: 有机化合物 - 有机杂环化合物
• 英文名称: 1-Methyl-1,4,5,6-tetrahydro-5-methoxycarbonylpyrimidine
• 英文别名: 1-Methyl-5-methoxycarbonyl-1,4,5,6-tetrahydropyrimidine；methyl 1-methyl-5,6-dihydro-4H-pyrimidine-5-carboxylate
• CAS: 146422-22-2
• 化学式: C₇H₁₂N₂O₂
• 分子量: 156.184
• InChiKey: ZENLXWQBIREBMO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.7
• 重原子数：
  11
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.71
• 拓扑面积：
  41.9
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  1-Methyl-1,4,5,6-tetrahydro-5-methoxycarbonylpyrimidine 、 N-hydroxyacetamidine 以 四氢呋喃 、 乙醇 、 mineral oil 为溶剂， 生成 1-Methyl-1,4,5,6-Tetrahydro-5-(3-methyl-1,2,4-oxadiazol-5-yl)pyrimidine
  参考文献：
  名称：

  Muscarinic agonists

  摘要：

  揭示了替代的1,4,5,6-四氢嘧啶组合物、替代的1,2,3,6-四氢嘧啶组合物和替代的3,4,5,6-四氢吡啶组合物。它们可用于刺激肌氨酸受体，例如治疗认知障碍的症状，特别是与乙酰胆碱合成减少和胆碱能细胞退化相关的记忆障碍。

  公开号：

  US05175166A1
• 作为产物：
  描述：

  1-Methyl-3-triphenylmethyl-5-methoxycarbonyl-1,4,5,6-tetrahydropyrimidinium iodide 在 乙醚 、 氯仿 、 hexane chloroform 、 crystals 作用下， 以 三氟乙酸 为溶剂， 反应 18.0h， 生成 1-Methyl-1,4,5,6-tetrahydro-5-methoxycarbonylpyrimidine
  参考文献：
  名称：

  Muscarinic agonists

  摘要：

  本文介绍了1,4,5,6-四氢嘧啶组合物、1,2,3,6-四氢嘧啶组合物和3,4,5,6-四氢吡啶组合物。它们可用于刺激毒蕈碱受体，包括治疗与乙酰胆碱合成减少和胆碱能细胞退化相关的认知障碍症状，特别是受损的记忆。

  公开号：

  US05175166A1

文献信息

• [EN] COMPOUNDS AND COMPOSITIONS FOR COGNITION-ENHANCEMENT, METHODS OF MAKING, AND METHODS OF TREATING<br/>[FR] COMPOSÉS ET COMPOSITIONS POUR AMÉLIORER LA FONCTION COGNITIVE, PROCÉDÉS DE FABRICATION ET MÉTHODES DE TRAITEMENT
  申请人：MITHRIDION INC

  公开号：WO2010102218A1

  公开（公告）日：2010-09-10

  Muscarinic agonists, which are useful for stimulating muscarinic receptors and treating cognitive disorders, are provided. Methods of synthesizing such agonists also are provided. Also provided are compositions for enhancing cognitive function in subjects such as humans, the compositions comprising a muscarinic agonist or a pharmaceutically suitable form thereof. Also provided are methods of treating animals such as humans by administering such compositions.

  提供了用于刺激肌气受体并治疗认知障碍的肌气受体激动剂。还提供了合成这类激动剂的方法。还提供了用于增强人类等受试者认知功能的组合物，该组合物包括肌气受体激动剂或其药用适宜形式。还提供了通过给予这类组合物来治疗动物如人类的方法。
• COMPOUNDS AND COMPOSITIONS FOR COGNITION-ENHANCEMENT, METHODS OF MAKING, AND METHODS OF TREATING
  申请人：Twose Trevor M.

  公开号：US20120046273A1

  公开（公告）日：2012-02-23

  Muscarinic agonists, which are useful for stimulating muscarinic receptors and treating cognitive disorders, are provided. Methods of synthesizing such agonists also are provided. Also provided are compositions for enhancing cognitive function in subjects such as humans, the compositions comprising a muscarinic agonist or a pharmaceutically suitable form thereof. Also provided are methods of treating animals such as humans by administering such compositions.

  提供了用于刺激毒蕈碱受体和治疗认知障碍的毒蕈碱激动剂。还提供了合成这种激动剂的方法。还提供了用于增强人类等受试者认知功能的组合物，其中组合物包括毒蕈碱激动剂或其药学上适宜的形式。还提供了通过给予这样的组合物治疗人类等动物的方法。
• Cognition Enhancing Compounds and Compositions, Methods of Making, and Methods of Treating
  申请人：Mithridion, Inc.

  公开号：US20130274299A1

  公开（公告）日：2013-10-17

  The invention relates generally to muscarinic agonists, which are useful for stimulating muscarine receptors, and treating cognitive disorders. Included among the muscarinic agonists disclosed herein are oxadiazole derivatives, compositions, and preparations thereof. Methods of synthesizing oxadiazole compounds also are provided. This disclosure also relates in part to compositions for enhancing cognitive function in subjects such as humans, the compositions comprising a muscarinic agonist or a pharmaceutically suitable form thereof. This disclosure relates in part to methods of treating animals such as humans by administering such compositions.

  本发明涉及肌肉碱受体激动剂，其可用于刺激肌肉碱受体和治疗认知障碍。本文所披露的肌肉碱受体激动剂包括噁唑烷衍生物、组合物及其制备。还提供了合成噁唑烷化合物的方法。本公开还涉及用于增强人类等受试者认知功能的组合物，该组合物包括肌肉碱受体激动剂或其药学适宜形式。本公开还涉及通过给予该类组合物治疗动物，如人类的方法。
• Compounds and Compositions for Cognition-Enhancement, Methods of Making, and Methods of Treating
  申请人：NeuroSolis, Inc.

  公开号：US20150099765A1

  公开（公告）日：2015-04-09

  Disclosed are muscarinic agonist compounds including oxadiazole derivatives, compositions and preparations thereof. Also disclosed are methods of synthesizing such oxadiazole compounds. Further disclosed are methods for treating a subject with said muscarinic agonists or a pharmaceutically suitable form thereof to enhance cognitive function.

  本发明涉及包括噁唑烷衍生物在内的毒蕈碱受体激动剂化合物，以及其组合物和制备方法。本发明还涉及合成这种噁唑烷化合物的方法。本发明还涉及使用所述毒蕈碱受体激动剂或其药学适宜形式来增强认知功能的方法。
• MUSCARINIC AGONISTS
  申请人：THE UNIVERSITY OF TOLEDO

  公开号：EP0630244A1

  公开（公告）日：1994-12-28