丁二酸,2-[[4-(1-甲基-4-吡啶-4-基吡唑-3-基)苯氧基]甲基]喹啉 | 1037309-45-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 中文名称: 丁二酸,2-[[4-(1-甲基-4-吡啶-4-基吡唑-3-基)苯氧基]甲基]喹啉
• 英文名称: 2-[4-(1-methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl]quinoline succinate
• 英文别名: 2-[4-[1-methyl-4-(4-pyridyl)-1H-pyrazol-3-yl]phenoxymethyl]quinoline succinate；MP-10 succinate；2-((4-(1-Methyl-4-(pyridin-4-yl)-1H-pyrazol-3-yl)phenoxy)methyl)quinoline succinate；butanedioic acid;2-[[4-(1-methyl-4-pyridin-4-ylpyrazol-3-yl)phenoxy]methyl]quinoline
• CAS: 1037309-45-7
• 化学式: C₄H₆O₄*C₂₅H₂₀N₄O
• 分子量: 510.549
• InChiKey: AVSAEIJRBBJXNR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.21
• 重原子数：
  38
• 可旋转键数：
  8
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  127
• 氢给体数：
  2
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  3-dimethylamino-2-pyridin-4-yl-1-[4-(quinolin-2-ylmethoxy)-phenyl]-propenone 以56的产率得到丁二酸,2-[[4-(1-甲基-4-吡啶-4-基吡唑-3-基)苯氧基]甲基]喹啉
  参考文献：
  名称：

  Heteroaromatic quinoline compounds

  摘要：

  本发明涉及异杂环化合物，其作为有效的磷酸二酯酶（PDE）抑制剂。具体而言，本发明涉及选择性抑制PDE10的化合物。本发明还涉及制备上述化合物的中间体；包含上述化合物的制药组合物；以及在治疗某些中枢神经系统（CNS）或其他疾病的方法中使用上述化合物。

  公开号：

  US07429665B2

文献信息

• [EN] PYRIMIDINE PDE10 INHIBITORS<br/>[FR] INHIBITEURS PYRIMIDINES DE PDE10
  申请人：MERCK SHARP & DOHME

  公开号：WO2014081619A1

  公开（公告）日：2014-05-30

  The present invention is directed to pyrimidine compounds which are useful as therapeutic agents for the treatment of central nervous system disorders associated with phosphodiesterase 10 (PDE10). The present invention also relates to the use of such compounds for treating neurological and psychiatric disorders, such as schizophrenia, psychosis or Huntington's disease, and those associated with striatal hypofunction or basal ganglia dysfunction.

  本发明涉及嘧啶化合物，这些化合物用作治疗与磷酸二酯酶10（PDE10）相关的中枢神经系统障碍的治疗剂。本发明还涉及使用这些化合物来治疗神经和精神障碍，如精神分裂症、精神疾病或亨廷顿病，以及与纹状体功能减退或基底神经节功能障碍相关的疾病。
• [EN] SUBSTITUTED PYRIDONE DERIVATIVES AS PDE10 INHIBITORS<br/>[FR] DÉRIVÉS DE PYRIDONE SUBSTITUÉS UTILISÉS EN TANT QU'INHIBITEURS DE PDE10
  申请人：MERCK SHARP & DOHME

  公开号：WO2014081617A1

  公开（公告）日：2014-05-30

  The present invention is directed to substituted pyridinone compounds which are useful as therapeutic agents for the treatment of central nervous system disorders associated with phosphodiesterase 10 (PDE10). The present invention also relates to the use of such compounds for treating neurological and psychiatric disorders, such as schizophrenia, psychosis or Huntington's disease, and those associated with striatal hypofunction or basal ganglia dysfunction.

  本发明涉及取代吡啶酮化合物，其可用作治疗与磷酸二酯酶10（PDE10）相关的中枢神经系统疾病的治疗剂。本发明还涉及利用这些化合物治疗神经学和精神疾病，如精神分裂症、精神病或亨廷顿病，以及与纹状体功能不足或基底神经节功能障碍相关的疾病。
• [EN] ALKOXY TETRAHYDRO-PYRIDOPYRIMIDINE PDE10 INHIBITORS<br/>[FR] INHIBITEURS DE PDE10 À L'ALCOXY TÉTRAHYDRO-PYRIDOPYRIMIDINE
  申请人：MERCK SHARP & DOHME

  公开号：WO2010138430A1

  公开（公告）日：2010-12-02

  The present invention is directed to alkoxy tetrahydro-pyridopyrimidine compounds which are useful as therapeutic agents for the treatment of central nervous system disorders associated with phosphodiesterase 10 (PDE10). The present invention also relates to the use of such compounds for treating neurological and psychiatric disorders, such as schizophrenia, psychosis or Huntington's disease, and those associated with striatal hypofunction or basal ganglia dysfunction.

  本发明涉及一种作为治疗与磷酸二酯酶10（PDE10）相关的中枢神经系统疾病的治疗剂的烷氧基四氢吡啶嘧啶化合物。本发明还涉及利用这类化合物治疗神经学和精神疾病，如精神分裂症、精神病或亨廷顿病，以及与纹状体功能不足或基底神经节功能障碍相关的疾病。
• [EN] SUBSTITUTED PYRIDIZINONE DERIVATIVES AS PDE10 INHIBITORS<br/>[FR] DÉRIVÉS DE PYRIDIZINONE SUBSTITUÉS UTILISÉS EN TANT QU'INHIBITEURS DE LA PDE10
  申请人：MERCK SHARP & DOHME

  公开号：WO2014139150A1

  公开（公告）日：2014-09-18

  The present invention is directed to substituted pyridizinone compounds of formula (I) which are useful as therapeutic agents for the treatment of central nervous system disorders associated with phosphodiesterase 10 (PDE10). The present invention also relates to the use of such compounds for treating neurological and psychiatric disorders, such as schizophrenia, psychosis or Huntington's disease, and those associated with striatal hypofunction or basal ganglia dysfunction.

  本发明涉及一种具有式（I）的取代吡啶酮化合物，其可用作治疗与磷酸二酯酶10（PDE10）相关的中枢神经系统疾病的治疗剂。本发明还涉及利用这种化合物治疗神经学和精神疾病，如精神分裂症、精神病或亨廷顿病，以及与纹状体功能不足或基底节功能障碍相关的疾病。
• [EN] 1,3-SUBSTITUTED AZETIDINE PDE10 INHIBITORS<br/>[FR] INHIBITEURS AZÉTIDINES SUBSTITUÉS EN 1,3 DE PDE10
  申请人：MERCK SHARP & DOHME

  公开号：WO2013052395A1

  公开（公告）日：2013-04-11

  The present invention is directed to substituted azetidinecompounds which are useful as therapeutic agents for the treatment of central nervous system disorders associated with phosphodiesterase 10 (PDE10). The present invention also relates to the use of such compounds for treating neurological and psychiatric disorders, such as schizophrenia, psychosis or Huntington's disease, and those associated with striatal hypofunction or basal ganglia dysfunction.

  本发明涉及用作治疗与磷酸二酯酶10（PDE10）相关的中枢神经系统疾病的治疗药物的取代氮杂环丙烷化合物。本发明还涉及利用这类化合物治疗神经和精神障碍，如精神分裂症、精神病或亨廷顿病，以及与纹状体功能不足或基底神经节功能障碍相关的疾病。