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1-(1-benzyl-1,2,3,6-tetrahydro-pyridin-4-yl)-5,6-dimethyl-1,3-dihydro-benzoimidazol-2-one | 2147-82-2

中文名称
——
中文别名
——
英文名称
1-(1-benzyl-1,2,3,6-tetrahydro-pyridin-4-yl)-5,6-dimethyl-1,3-dihydro-benzoimidazol-2-one
英文别名
5,6-dimethyl-1-[1-(phenylmethyl)-1,2,3,6-tetrahydro-4-pyridinyl]-1,3-dihydro-2H-benzimidazol-2-one;3-(1-benzyl-3,6-dihydro-2H-pyridin-4-yl)-5,6-dimethyl-1H-benzimidazol-2-one
1-(1-benzyl-1,2,3,6-tetrahydro-pyridin-4-yl)-5,6-dimethyl-1,3-dihydro-benzoimidazol-2-one化学式
CAS
2147-82-2
化学式
C21H23N3O
mdl
——
分子量
333.433
InChiKey
VZSIMBAKXIUZJY-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

  • 熔点:
    180.5-184.5 °C
  • 密度:
    1.210±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.3
  • 重原子数:
    25
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    35.6
  • 氢给体数:
    1
  • 氢受体数:
    2

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Compounds Which Have Activity at M1 Receptor and Their Uses In Medicine
    申请人:Budzik Brian
    公开号:US20080293770A1
    公开(公告)日:2008-11-27
    Compounds of formula (I) and salts are provided: wherein R 5 is selected from halogen, C 1-6 alkyl, C 1-6 alkyl substituted with one or more fluorine atoms, C 1-6 alkoxy, C 1-6 alkoxy substituted with one or more fluorine atoms, and cyano; R 6 is selected from 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 M 1 agonists and are useful for therapy, for example in the treatment of psychotic disorders and cognitive impairment.
    提供化学式(I)的化合物和盐:其中R5选择自卤素、C1-6烷基、C1-6烷基上取代一个或多个氟原子、C1-6烷氧基、C1-6烷氧基上取代一个或多个氟原子和氰基;R6选择自卤素、C1-6烷基、C1-6烷基上取代一个或多个氟原子、C3-6环烷基、C3-6环烷基上取代一个或多个氟原子、C1-6烷氧基、C1-6烷氧基上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,例如治疗精神障碍和认知障碍。
  • BENZIMIDAZOLES WHICH HAVE ACTIVITY AT M1 RECEPTOR AND THEIR USES IN MEDICINE
    申请人:COOPER David Gwyn
    公开号:US20120041027A1
    公开(公告)日:2012-02-16
    Compounds of formula (I) and salts and solvates are provided: wherein Uses of the compounds for therapy, for example in the treatment of psychotic disorders and cognitive impairment, are also disclosed.
    提供公式(I)的化合物、盐和溶剂化合物,其中公式(I)如下: 该化合物可用于治疗精神失常和认知障碍等疾病。
  • Compounds which have activity at M1 receptor and their uses in medicine
    申请人:Glaxo Group Limited
    公开号:US08288412B2
    公开(公告)日:2012-10-16
    Compounds of formula (I) and salts are provided: wherein R5 is selected from halogen, C1-6alkyl, C1-6alkyl substituted with one or more fluorine atoms, C1-6 alkoxy, C1-6 alkoxy substituted with one or more fluorine atoms, and cyano; R6 is selected from 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)的化合物和盐: 其中,R5选自卤素、C1-6烷基、C1-6烷基(其中一个或多个氟原子被取代)、C1-6烷氧基、C1-6烷氧基(其中一个或多个氟原子被取代)和氰基;R6选自卤素、C1-6烷基、C1-6烷基(其中一个或多个氟原子被取代)、C3-6环烷基、C3-6环烷基(其中一个或多个氟原子被取代)、C1-6烷氧基、C1-6烷氧基(其中一个或多个氟原子被取代)和氰基;Q为氢或C1-6烷基。这些化合物是M1激动剂,可用于治疗,例如治疗精神障碍和认知障碍。
  • WO2007/36718
    申请人:——
    公开号:——
    公开(公告)日:——
  • COMPOUNDS WHICH HAVE ACTIVITY AT M1 RECEPTOR AND THEIR USES IN MEDICINE
    申请人:GLAXO GROUP LIMITED
    公开号:EP1960389B1
    公开(公告)日:2012-08-15
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