6-[2-cyclobutyl-4-(2-dimethylamino-ethoxy)-phenyl]-pyridin-2-yl-amine | 211494-50-7

• 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: 6-[2-cyclobutyl-4-(2-dimethylamino-ethoxy)-phenyl]-pyridin-2-yl-amine
• 英文别名: 6-[2-cyclobutyl-4-(2-dimethylamino-ethoxy)-phenyl]-pyridin-2-ylamine；6-[2-CYCLOBUTYL4-(2-DIMETHYLAMINO-ETHOXY)-PHENYL]-PYRIDIN-2-YLAMINE；6-[2-cyclobutyl-4-[2-(dimethylamino)ethoxy]phenyl]pyridin-2-amine
• CAS: 211494-50-7
• 化学式: C₁₉H₂₅N₃O
• 分子量: 311.427
• InChiKey: UCHJMWBPLULYLR-UHFFFAOYSA-N

物化性质

• 沸点：
  481.139±45.00 °C(Press: 760.00 Torr)(predicted)
• 密度：
  1.125±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  23
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.42
• 拓扑面积：
  51.4
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  4-(6-amino-pyridin-2-yl)-3-cyclobutyl-phenol 、 2-氯-N,N-二甲基乙胺 生成 6-[2-cyclobutyl-4-(2-dimethylamino-ethoxy)-phenyl]-pyridin-2-yl-amine
  参考文献：
  名称：

  2-amino-6-(2-substituted-4-phenoxy)-substituted-pyridines

  摘要：

  本发明涉及公式1的化合物，其中G、R1和R2如规范中所定义，以及含有它们的制药组合物，以及它们在治疗和预防中枢神经系统和其他疾病方面的用途。

  公开号：

  US20030162765A1

文献信息

• 2-AMINO-6-(2-SUBSTITUTED-4-PHENOXY)-SUBSTITUTED-PYRIDINES
  申请人：——

  公开号：US20010007873A1

  公开（公告）日：2001-07-12

  This present invention relates to compounds of the formula 1 wherein G, R 1 and R 2 are defined as in the specification, to pharmaceutical compositions containing them and to their use in the treatment and prevention of central nervous system and other disorders.

  这项发明涉及公式1中定义的化合物，其中G、R1和R2如规范中所定义，以及含有它们的药物组合物，以及它们在治疗和预防中枢神经系统和其他疾病中的用途。
• New pharmaceutical combinations for NOS inhibitors
  申请人：Pfizer Inc

  公开号：US20040229911A1

  公开（公告）日：2004-11-18

  The present invention relates to new pharmaceutical uses for compounds that exhibit activity as nitric oxide synthase (NOS) inhibitors. Specifically, it relates to the use of NOS inhibitors, particularly selective neuronal NOS (nNOS) inhibitors, alone or in combination with another active agent, in particular, either an SSRI or an NK-1 receptor antagonist, for the treatment of disorders or conditions the treatment which can be effected or facilitated by altering circadian rhythms. Examples of such disorders and conditions are blindness, obesity, seasonal affective disorder, bipolar disorder; jet lag, circadian sleep rhythms disorder, sleep deprivation, parasomnias, REM sleep disorders, hypersomnia, sleep-wake cycle disorders, narcolepsy and sleep disorders associated with shift work or irregular work schedules; nocturnal enuresis, and restless-legs syndrome.

  本发明涉及表现为一氧化氮合酶（NOS）抑制剂活性的化合物的新药物用途。具体地，涉及使用NOS抑制剂，特别是选择性神经元NOS（nNOS）抑制剂，单独或与另一种活性剂联合使用，特别是SSRI或NK-1受体拮抗剂，用于治疗可以通过改变昼夜节律来达到或促进治疗的疾病或病况。这些疾病和病况的例子包括失明、肥胖症、季节性情感障碍、双相情感障碍、时差反应、昼夜节律睡眠障碍、睡眠剥夺、睡眠障碍、REM睡眠障碍、嗜睡症、睡眠-觉醒周期障碍、嗜睡症和与轮班工作或不规则工作时间表相关的睡眠障碍、夜尿症和不宁腿综合症。
• [EN] NEW PHARMACEUTICAL COMBINATIONS FOR NOS INHIBITORS<br/>[FR] NOUVELLES COMBINAISONS PHARMACEUTIQUES POUR LES INHIBITEURS DE NOS
  申请人：PFIZER PROD INC

  公开号：WO2000071107A2

  公开（公告）日：2000-11-30

  The present invention relates to new pharmaceutical uses for compounds that exhibit activity as nitric oxide synthase (NOS) inhibitors. Specifically, it relates to the use of NOS inhibitors, particularly selective neuronal NOS (nNOS) inhibitors, alone or in combination with another active agent, in particular, either an SSRI or an NK-1 receptor antagonist, for the treatment of disorders or conditions the treatment which can be effected or facilitated by altering circadian rhythms. Examples of such disorders and conditions are blindness, obesity, seasonal affective disorder, bipolar disorder, jet lag, circadian sleep rhythms disorder, sleep deprivation, parasomnias, REM sleep disorders, hypersomnia, sleep-wake cycle disorders, narcolepsy and sleep disorders associated with shift work or irregular work schedules; nocturnal enuresis, and restless-legs syndrome.

  本发明涉及表现为一氧化氮合酶（NOS）抑制剂的化合物的新药物用途。具体而言，涉及使用NOS抑制剂，特别是选择性神经元NOS（nNOS）抑制剂，单独或与另一活性剂，特别是SSRI或NK-1受体拮抗剂结合使用，治疗可以通过改变昼夜节律来实现或促进的疾病或状况。这些疾病和状况的例子包括失明，肥胖症，季节性情感障碍，双相情感障碍，时差反应，昼夜节律睡眠障碍，睡眠剥夺，睡眠障碍，REM睡眠障碍，嗜睡症，睡眠-清醒周期障碍，嗜睡症和与轮班或不规则工作时间表相关的睡眠障碍；夜尿症和不安腿综合症。
• Pharmaceutical combinations for the treatment of neurodegenerative diseases
  申请人：Pfizer, Inc.

  公开号：US20030045449A1

  公开（公告）日：2003-03-06

  This invention relates to methods of treating neurodegenerative diseases, comprising administering to a patient in need of such treatment an N-NOS inhibitor in combination with either: (a) NMDA receptor antagonist; (b) a sodium channel antagonist; (c) an acetylcholine esterase inhibitor; (d) a dopamine agonist; (e) a potassium channel opener; (f) an AMPA/kainate receptor antagonist; (g) a calcium channel antagonist; (h) a GABA-A receptor modulator (e.g., a GABA-A receptor agonist); (i) TPA (j) matrix-metalloprotease inhibitor or (k) L-Dopa. The pharmaceutical compounds are also disclosed.

  本发明涉及治疗神经退行性疾病的方法，包括向需要此类治疗的患者施用 N-NOS 抑制剂与以下任一种药物的组合：(a) NMDA 受体拮抗剂；(b) 钠通道拮抗剂；(c) 乙酰胆碱酯酶抑制剂；(d) 多巴胺激动剂；(e) 钾通道开启剂；(f) AMPA/kainate 受体拮抗剂；(g) 钙通道拮抗剂；(h) GABA-A 受体调节剂（例如g.,(i) TPA (j) 基质金属蛋白酶抑制剂或 (k) 左旋多巴。还公开了药物化合物。
• NEW PHARMACEUTICAL COMBINATIONS FOR NOS INHIBITORS
  申请人：Pfizer Products Inc.

  公开号：EP1178784A1

  公开（公告）日：2002-02-13