1,1-dimethylethyl 4-{[({2-bromo-4-[(trifluoromethyl)oxy]phenyl}amino)carbonyl]amino}-1-piperidinecarboxylate | 932700-84-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 1,1-dimethylethyl 4-{[({2-bromo-4-[(trifluoromethyl)oxy]phenyl}amino)carbonyl]amino}-1-piperidinecarboxylate
• 英文别名: tert-butyl 4-[[2-bromo-4-(trifluoromethoxy)phenyl]carbamoylamino]piperidine-1-carboxylate
• CAS: 932700-84-0
• 化学式: C₁₈H₂₃BrF₃N₃O₄
• 分子量: 482.298
• InChiKey: BUYVNNLRVGPYOV-UHFFFAOYSA-N

物化性质

• 沸点：
  469.6±45.0 °C(Predicted)
• 密度：
  1.48±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  29
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.56
• 拓扑面积：
  79.9
• 氢给体数：
  2
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  1,1-dimethylethyl 4-{[({2-bromo-4-[(trifluoromethyl)oxy]phenyl}amino)carbonyl]amino}-1-piperidinecarboxylate 在 1,1'-双(二苯基膦)二茂铁 、 tris-(dibenzylideneacetone)dipalladium(0) sodium t-butanolate 作用下， 以 1,4-二氧六环 为溶剂， 生成 1,1-dimethylethyl 4-{2-oxo-6-[(trifluoromethyl)oxy]-2,3-dihydro-1H-benzimidazol-1-yl}-1-piperidinecarboxylate
  参考文献：
  名称：

  WO2007/36711

  摘要：

  公开号：
• 作为产物：
  描述：

  1-Boc-4-氨基哌啶 、 2-溴-4-三氟甲氧基苯胺 以 1,4-二氧六环 、 二氯甲烷 为溶剂， 生成 1,1-dimethylethyl 4-{[({2-bromo-4-[(trifluoromethyl)oxy]phenyl}amino)carbonyl]amino}-1-piperidinecarboxylate
  参考文献：
  名称：

  WO2007/107565

  摘要：

  公开号：

文献信息

• Benzimidazolones Which Have Activity at M1 Receptor
  申请人：Budzik Brian

  公开号：US20080306112A1

  公开（公告）日：2008-12-11

  Compounds of formula (I) and salts are provided: wherein R 6 is selected from hydrogen, halogen, C 1-6 alkyl, C 1-6 alkyl substituted with one or more fluorine atoms, C 3-6 cycloalkyl, C 3-6 cycloalkyl substituted with one or more fluorine atoms, C 1-6 alkoxy, C 1-6 alkoxy substituted with one or more fluorine atoms, and cyano, and Q is hydrogen or C 1-6 alkyl. The compounds are M1 agonists and are useful for therapy, for example in the treatment of psychotic disorders and cognitive impairment.

  提供了化学式（I）和盐的化合物：其中R6选择自氢，卤素，C1-6烷基，C1-6烷基取代一个或多个氟原子，C3-6环烷基，C3-6环烷基取代一个或多个氟原子，C1-6烷氧基，C1-6烷氧基取代一个或多个氟原子和氰基，Q为氢或C1-6烷基。这些化合物是M1受体激动剂，可用于治疗精神障碍和认知障碍等疾病。
• BENZIMIDAZOLES WHICH HAVE ACTIVITY AT M1 RECEPTOR AND THEIR USES IN MEDICINE
  申请人：COOPER David Gwyn

  公开号：US20120041028A1

  公开（公告）日：2012-02-16

  Compounds of formula (I), salts and solvates are provided: Uses of the compounds for therapy, for example in the treatment of psychotic disorders and cognitive impairment, are also disclosed.

  提供了化学式（I）的化合物、盐和溶剂化物：还揭示了这些化合物在治疗精神障碍和认知障碍等方面的用途。
• Benzimidazolones which have activity at M1 receptor
  申请人：Glaxo Group Limited

  公开号：US08288413B2

  公开（公告）日：2012-10-16

  Compounds of formula (I) and salts are provided: wherein R6 is selected from hydrogen, halogen, C1-6alkyl, C1-6alkyl substituted with one or more fluorine atoms, C3-6cycloalkyl, C3-6cycloalkyl substituted with one or more fluorine atoms, C1-6 alkoxy, C1-6 alkoxy substituted with one or more fluorine atoms, and cyano, and Q is hydrogen or C1-6alkyl. The compounds are M1 agonists and are useful for therapy, for example in the treatment of psychotic disorders and cognitive impairment.

  提供了式（I）化合物和盐： 其中R6从氢，卤素，C1-6烷基，C1-6烷基取代一个或多个氟原子，C3-6环烷基，C3-6环烷基取代一个或多个氟原子，C1-6烷氧基，C1-6烷氧基取代一个或多个氟原子和氰基中选择，Q为氢或C1-6烷基。这些化合物是M1激动剂，并且在治疗精神障碍和认知障碍等方面非常有用。
• Compounds which have activity at M1 receptor and their uses in medicine
  申请人：COOPER David Gwyn

  公开号：US20120316202A1

  公开（公告）日：2012-12-13

  Compounds of the general formula And their use in the treatment of psychotic disorders and cognitive impairment are disclosed.

  本发明公开了一般式化合物及其在治疗精神障碍和认知障碍中的应用。
• BENZIMIDAZOLONES WHICH HAVE ACTIVITY AT M1 RECEPTOR
  申请人：GLAXO GROUP LIMITED

  公开号：EP1937670A1

  公开（公告）日：2008-07-02