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N-(8-Chloro-4,4-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl)-4-methoxy-3-trifluoromethylbenzamide | 259147-15-4

中文名称
——
中文别名
——
英文名称
N-(8-Chloro-4,4-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl)-4-methoxy-3-trifluoromethylbenzamide
英文别名
N-(8-chloro-4,4-dimethyl-2,3-dihydro-1H-isoquinolin-7-yl)-4-methoxy-3-(trifluoromethyl)benzamide
N-(8-Chloro-4,4-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl)-4-methoxy-3-trifluoromethylbenzamide化学式
CAS
259147-15-4
化学式
C20H20ClF3N2O2
mdl
——
分子量
412.839
InChiKey
HMLCSIQMWPGBCC-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):
    4.5
  • 重原子数:
    28
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    50.4
  • 氢给体数:
    2
  • 氢受体数:
    6

文献信息

  • SUBSTITUTED ISOQUINOLINE DERIVATIVES AND THEIR USE AS ANTICONVULSANTS
    申请人:SMITHKLINE BEECHAM PLC
    公开号:EP1104404A1
    公开(公告)日:2001-06-06
  • US6492378B1
    申请人:——
    公开号:US6492378B1
    公开(公告)日:2002-12-10
  • [EN] SUBSTITUTED ISOQUINOLINE DERIVATIVES AND THEIR USE AS ANTICONVULSIVANTS<br/>[FR] DERIVES D'ISOQUINOLINE SUBSTITUES ET LEUR UTILISATION COMME ANTIEPILEPTIQUES
    申请人:SMITHKLINE BEECHAM PLC
    公开号:WO2000009486A1
    公开(公告)日:2000-02-24
    Compound of formula (I) or salts thereof or solvates thereof: wherein: R1 is hydrogen, C¿1-6?alkyl (optionally substituted by hydroxy or C1-4alkoxy), C1-6alkenyl, C1-6alkynyl, C1-6alkylCO-, formyl, CF3CO-or C1-6alkylSO2-: R?2¿ is hydrogen or up to three substituents selected from halogen, NO¿2?, CN, N3, CF3O-, CF3S-, CF3CO-, CF3SO2, trifluoromethyldiazirinyl, C1-6alkyl, C1-6alkenyl, C1-6alkynyl, C1-6perfluoroalkyl, C3-6cycloalkyl, C3-6cycloalkyl-C1-4alkyl-, C1-6alkylO-, C1-6alkylCO-, C3-6cycloalkylO-, C3-6cycloalkylCO-, C3-6cycloalkyl-C1-4alkylO-, C3-6cycloalkyl-C1-4alkylCO-, phenyl, phenoxy, benzyloxy, benzoyl, phenyl-C1-4alkyl-, C1-6alkylS-, C1-6alkylSO2-, (C1-4alkyl)2NSO2-, (C1-4alkyl)NHSO2-, (C1-4)2NCO-, (C1-4alkyl)NHCO- and CONH2; or -NR?5R6¿ where R5 is hydrogen or C¿1-4?alkyl, and R?6¿ is hydrogen, C¿1-4?alkyl, formyl, -CO2C1-4alkyl or -COC1-4alkyl; or two R?2¿ groups together form a carbocyclic ring that is saturated or unsaturated and unsubstituted or substituted by -OH or =O; the two R groups, the two R3 groups and the two R4 groups are each independently hydrogen, C¿1-6?alkyl, C1-6alkenyl, benzyl, or phenyl, or the two R groups and/or the two R?3¿ groups and/or the two R4 groups together form a C¿3-6?spiroalkyl group, provided that at least one R, R?3 or R4¿ group is other than hydrogen; and X is selected from the group consisting of hydrogen, halogen, cyano, CF¿3?, alkyl and alkoxy; provided that when X is hydrogen, the two R groups are not both hydrogen are indicated to be useful in the treatment and prophylaxis of epilepsy, migraine, and other disorders.
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