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6-[(4-fluorophenyl)oxy]-3-pyridinecarbonyl chloride | 862089-10-9

中文名称
——
中文别名
——
英文名称
6-[(4-fluorophenyl)oxy]-3-pyridinecarbonyl chloride
英文别名
6-(4-fluorophenoxy)pyridine-3-carbonyl chloride
6-[(4-fluorophenyl)oxy]-3-pyridinecarbonyl chloride化学式
CAS
862089-10-9
化学式
C12H7ClFNO2
mdl
——
分子量
251.644
InChiKey
VTTXCTMIAUVERP-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    351.5±37.0 °C(predicted)
  • 密度:
    1.368±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.3
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    39.2
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

文献信息

  • NOVEL BENZOFURAN DERIVATIVE, MEDICINAL COMPOSITION CONTAINING THE SAME, AND USES OF THESE
    申请人:Nakamura Tetsuya
    公开号:US20090239860A1
    公开(公告)日:2009-09-24
    The present invention provides compounds represented by general formula (I): or pharmaceutical acceptable salts thereof, wherein R 1 is hydrogen or lower alkyl; R 2 is lower alkyl, halo-lower alkyl, cycloalkyl, heterocycloalkyl, aryl, aralkyl, arylalkenyl, aryloxy-lower alkyl, heteroaryl, heteroaryl-lower alkyl, etc; R 3 , R 4 , R 5 and R 6 are each hydrogen, halogen, cyano, lower alkyl, halo-lower alkyl, lower alkoxy, hydroxy, aryl, etc; provided that at least one of R 3 , R 4 , R 5 and R 6 is other than hydrogen. Compound (I) of the present invention shows a potent adenosine A 2A receptor antagonistic activity, and are useful for treating or preventing a disease mediated by adenosine A 2A receptors such as motor function disorders, depression, anxiety disorders, cognitive function disorders, cerebral ischemia disorders, restless legs syndrome and the like.
    本发明提供了通式(I)所表示的化合物或其药物可接受的盐,其中R1是氢或低碳基;R2是低碳基,卤代低碳基,环烷基,杂环烷基,芳基,芳基烷基,芳基烯基,芳氧基-低碳基,杂芳基,杂芳基-低碳基等;R3、R4、R5和R6均为氢、卤素、氰基、低碳基、卤代低碳基、低碳氧基、羟基、芳基等;其中至少有一个R3、R4、R5和R6不是氢。本发明的化合物(I)表现出强大的腺苷A2A受体拮抗活性,并且可用于治疗或预防由腺苷A2A受体介导的疾病,例如运动功能障碍、抑郁症、焦虑症、认知功能障碍、脑缺血性疾病、不宁腿综合征等。
  • Compounds
    申请人:Mitchell Jason Darren
    公开号:US20080027065A1
    公开(公告)日:2008-01-31
    The invention relates to compounds of formula (I) processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of conditions or disorders which are mediated via the GPR38 receptor.
    本发明涉及式(I)化合物,其制备方法,含有它们的制药组合物以及它们在治疗通过GPR38受体介导的疾病或疾病中的应用。
  • Gpr38 Receptor Agonists
    申请人:Glaxo Group Limited
    公开号:US07700599B2
    公开(公告)日:2010-04-20
    The invention relates to compounds of formula (I) processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of conditions or disorders which are mediated via the GPR38 receptor.
    本发明涉及化合物(I)的配方、其制备过程、含有它们的药物组合物以及它们在治疗通过GPR38受体介导的疾病或疾病中的应用。
  • COMPOUNDS
    申请人:MITCHELL Darren Jason
    公开号:US20090192160A1
    公开(公告)日:2009-07-30
    The invention relates to compounds of formula (I) processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of conditions or disorders which are mediated via the GPR38 receptor.
    本发明涉及公式(I)化合物,其制备方法,包含它们的药物组合物以及它们在治疗通过GPR38受体介导的疾病或疾病的用途。
  • PIPERAZINYL DERIVATIVES USEFUL IN THE TREATMENT OF GPR38 RECEPTOR MEDIATED DISEASES
    申请人:Glaxo Group Limited
    公开号:EP2041093A1
    公开(公告)日:2009-04-01
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