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3-Methyl-7-(trifluoromethoxy)quinoxaline-2-carbaldehyde | 1214254-19-9

中文名称
——
中文别名
——
英文名称
3-Methyl-7-(trifluoromethoxy)quinoxaline-2-carbaldehyde
英文别名
——
3-Methyl-7-(trifluoromethoxy)quinoxaline-2-carbaldehyde化学式
CAS
1214254-19-9
化学式
C11H7F3N2O2
mdl
——
分子量
256.184
InChiKey
JOGFJFFSIQLTGV-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):
    2.6
  • 重原子数:
    18
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    52.1
  • 氢给体数:
    0
  • 氢受体数:
    7

文献信息

  • [EN] TRI-SUBSTITUTED PYRIMIDINE COMPOUNDS AND THEIR USE AS PDE10 INHIBITORS<br/>[FR] PYRIMIDINES TRI-SUBSTITUÉES ET LEUR UTILISATION COMME INHIBITEURS DE PDE10
    申请人:MITSUBISHI TANABE PHARMA CORP
    公开号:WO2010027097A1
    公开(公告)日:2010-03-11
    The present invention provides a tri-substituted pyrimidine compound having an excellent PDE10 inhibitory activity. The present invention relates to a tri-substituted pyrimidine compound represented by the following formula [I0] or a pharmaceutically acceptable salt thereof, a method for preparing the same, and use of said compound for PDE10 inhibitor, and a pharmaceutical composition comprising said compounds as an active ingredient: wherein: either one of X1 and X2 is N, and the other of X1 and X2 is CH; A is *-CH=CH-, *-C(Alk)=CH-, *-CH2-CH2- or *-O-CH2- (* is a bond with R1); Alk is a lower alkyl group; Ring B is an optionally substituted nitrogen-containing aliphatic heterocyclic group; R1 is an optionally substituted quinoxalinyl or an optionally substituted quinolyl; Y0 is mono- or di- substituted amino group, or a pharmaceutically acceptable salt thereof.
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