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8-[1-[2-(2-methylquinolin-5-yl)oxyethyl]piperidin-4-yl]oxy-4H-1,4-benzoxazin-3-one;hydrochloride

中文名称
——
中文别名
——
英文名称
8-[1-[2-(2-methylquinolin-5-yl)oxyethyl]piperidin-4-yl]oxy-4H-1,4-benzoxazin-3-one;hydrochloride
英文别名
——
8-[1-[2-(2-methylquinolin-5-yl)oxyethyl]piperidin-4-yl]oxy-4H-1,4-benzoxazin-3-one;hydrochloride化学式
CAS
——
化学式
C25H28ClN3O4
mdl
——
分子量
470.0
InChiKey
POKORALITOKUPR-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

计算性质

  • 辛醇/水分配系数(LogP):
    4.22
  • 重原子数:
    33
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    72.9
  • 氢给体数:
    2
  • 氢受体数:
    6

文献信息

  • Heterocyclymethylpiperidines and -piperazines possessing affinity at 5ht-1 type receptors
    申请人:Ward E. Simon
    公开号:US20050153974A1
    公开(公告)日:2005-07-14
    Compounds of formula (I) and pharmaceutically acceptable salts thereof are disclosed: wherein: A is optionally substituted phenyl, naphthyl, indolyl, quinolinyl, quinazolinyl, indazolyl, isoquinolinyl or benzofuranyl; X is carbon, Y is CH and is a double bond; or X is CH, Y is CH 2 or oxygen and is a single bond; or X is nitrogen, Y is CH 2 and is a single bond; R1 is halogen, cyano, or C 1-6 alkoxy; a is 0, 1, 2 or 3; b is 0 or 1; R2 is hydrogen, C 1-6 alkyl, C 1-6 alkanoyl, fluoroC 1-6 alkanoyl, C 1-6 alkylsulfonyl, fluoroC 1-6 alkylsulfonyl, carbamoyl, C 1-6 alkylcarbamoyl or arylC 1-6 alkyl; and R3, together with the nitrogen atom to which it is attached, forms an optionally substituted 5 to 7 membered heterocyclic group fused to the benzene ring. Methods of preparing the compounds and uses of the compounds in therapy, in particular for a CNS disorder such as depression or anxiety, are also disclosed.
    公开了化学式(I)的化合物及其药用可接受的盐:其中:A是可选取代的苯基、萘基、吲哚基、喹啉基、喹唑啉基、吲唑基、异喹啉基或苯并呋喃基;X是碳,Y是CH且是双键;或X是CH,Y是CH2或氧且是单键;或X是氮,Y是CH2且是单键;R1是卤素、氰基或C1-6烷氧基;a为0、1、2或3;b为0或1;R2是氢、C1-6烷基、C1-6酰基、氟代C1-6酰基、C1-6烷基磺酰基、氟代C1-6烷基磺酰基、氨基甲酰基、C1-6烷基氨基甲酰基或芳基C1-6烷基;R3与其连接的氮原子一起形成一个可选取代的5到7元杂环基固定在苯环上。还公开了制备该化合物的方法以及该化合物在治疗中的用途,特别是用于中枢神经系统紊乱如抑郁症或焦虑症。
  • HETEROCYCLYLMETHYLPIPERIDINES AND -PIPERAZINES POSSESSING AFFINITY AT 5HT-1 TYPE RECEPTORS
    申请人:GLAXO GROUP LIMITED
    公开号:EP1480974A1
    公开(公告)日:2004-12-01
  • US7214674B2
    申请人:——
    公开号:US7214674B2
    公开(公告)日:2007-05-08
  • [EN] HETEROCYCLYMETHYLPIPERIDINES AND -PIPERAZINES POSSESSING AFFINITY AT 5HT-1 TYPE RECEPTORS<br/>[FR] HETEROCYCLYL-METHYLPIPERIDINES ET HETEROCYCLYL-METHYLPIPERAZINES POSSEDANT UNE AFFINITE AVEC DES RECEPTEURS DU TYPE 5HT-1
    申请人:GLAXO GROUP LTD
    公开号:WO2003068771A1
    公开(公告)日:2003-08-21
    Compounds of formula (I) and pharmaceutically acceptable salts thereof are disclosed, wherein: A is optionally substituted phenyl, naphthyl, indolyl, quinolinyl, quinazolinyl, indazolyl, isoquinolinyl or benzofuranyl; X is carbon, Y is CH and === is a double bond; or X is CH, Y is CH2 or oxygen and === is a single bond; or X is nitrogen, Y is CH2 And === is a single bond; R1is halogen, cyano, or C1-6 alkoxy; a is 0, 1, 2 or 3; b is 0 or 1; R2 is hydrogen, C1-6 alkyl, C1-6 alkanoyl, fluoroC1-6 alkanoyl, C1-6 alkylsulfonyl, fluoroC1-6 alkylsulfonyl, carbamoyl, C1-6 alkylcarbamoyl or arylC1-6 alkyl; and R3, together with the nitrogen atom to which it is attached, forms an optionally substituted 5 to 7 membered heterocyclic group fused to the benzene ring. Methods of preparing the compounds and uses of the compounds in therapy, in particular for a CNS disorder such as depression or anxiety, are also disclosed.
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