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3-methyl-5-phenyl-2,3,4,5-tetrahydro-benzo[d]azepin-7-amine | 98626-71-2

中文名称
——
中文别名
——
英文名称
3-methyl-5-phenyl-2,3,4,5-tetrahydro-benzo[d]azepin-7-amine
英文别名
(5R)-3-methyl-5-phenyl-1,2,4,5-tetrahydro-3-benzazepin-7-amine
3-methyl-5-phenyl-2,3,4,5-tetrahydro-benzo[d]azepin-7-amine化学式
CAS
98626-71-2
化学式
C17H20N2
mdl
——
分子量
252.359
InChiKey
JNDPGFKINLFTLJ-QGZVFWFLSA-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):
    3
  • 重原子数:
    19
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    29.3
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2-((2,5-二氯嘧啶-4-基)氨基)-N-甲基苯甲酰胺3-methyl-5-phenyl-2,3,4,5-tetrahydro-benzo[d]azepin-7-amineD(+)-10-樟脑磺酸 作用下, 以 异丙醇 为溶剂, 反应 1.0h, 生成 2-((5-chloro-2-((3-methyl-5-phenyl-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-yl)amino)pyrimidin-4-yl)amino)-N-methylbenzamide
    参考文献:
    名称:
    Novel 2,4-Diarylaminopyrimidine Analogues (DAAPalogues) Showing Potent c-Met/ALK Multikinase Inhibitory Activities
    摘要:
    By repurposing a typical dopamine D-1/D-5 receptor agonist motif, C1-substituted-N3-benzazepine or benzazecine, into the classical RTK inhibitor 2,4-diaminopyrimidine skeleton, a series of new 2,4-diarylaminopyrimidine analogues (DAAPalogues) were developed. Compounds 7 and 8a were identified possessing high potency against both c-Met and ALK kinases. Compound 8a displayed appreciable antitumor efficacy at the dose of 1 mg/kg in the ALK-driven BF3/EML4-ALK xenograft mice model.
    DOI:
    10.1021/ml400373j
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文献信息

  • Benzazepine derivatives, pharmaceutical compositions containing them and processes for the preparation of such compounds and compositions
    申请人:SCHERING CORPORATION
    公开号:EP0135767A1
    公开(公告)日:1985-04-03
    Substituted 8-amino-1-phenyl-2,3,4,5-tetrahydro-1H-3- benzazepines useful in the treatment of mental disorders such as schizophrenia and depression, and having activities of prolonged duration, are disclosed. Methods for preparing these compounds and methods for their use are also described.
    本发明公开了可用于治疗精神障碍(如精神分裂症和抑郁症)且活性持续时间长的取代型 8-氨基-1-苯基-2,3,4,5-四氢-1H-3-苯并氮杂卓。还描述了制备这些化合物的方法及其使用方法。
  • BENZAZEPINE DERIVATIVES, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AND PROCESSES FOR THE PREPARATION OF SUCH COMPOUNDS AND COMPOSITIONS
    申请人:SCHERING CORPORATION
    公开号:EP0153400A1
    公开(公告)日:1985-09-04
  • [EN] BENZAZEPINE DERIVATIVES, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AND PROCESSES FOR THE PREPARATION OF SUCH COMPOUNDS AND COMPOSITIONS
    申请人:SCHERING CORP.
    公开号:WO1985000808A1
    公开(公告)日:1985-02-28
    (EN) Substituted 8-amino-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepines useful in the treatment of mental disorders such as schizophrenia and depression, and having activities of prolonged duration. Methods for preparing these compounds and methods for their use are also described.(FR) 8-amino-1-phényl-2,3,4,5-tétrahydro-1H-3-benzazépines substituées utiles pour le traitement d'aliénations mentales comme la schizophrénie et la dépression, et dont la durée d'activité est prolongée. Procédé de préparation de ces composés et procédés d'utilisation de ces derniers.
  • Novel 2,4-Diarylaminopyrimidine Analogues (DAAPalogues) Showing Potent c-Met/ALK Multikinase Inhibitory Activities
    作者:Zhiqing Liu、Jing Ai、Xia Peng、Zilan Song、Kui Wu、Jing Zhang、Qizheng Yao、Yi Chen、Yinchun Ji、Yanhong Yang、Meiyu Geng、Ao Zhang
    DOI:10.1021/ml400373j
    日期:2014.4.10
    By repurposing a typical dopamine D-1/D-5 receptor agonist motif, C1-substituted-N3-benzazepine or benzazecine, into the classical RTK inhibitor 2,4-diaminopyrimidine skeleton, a series of new 2,4-diarylaminopyrimidine analogues (DAAPalogues) were developed. Compounds 7 and 8a were identified possessing high potency against both c-Met and ALK kinases. Compound 8a displayed appreciable antitumor efficacy at the dose of 1 mg/kg in the ALK-driven BF3/EML4-ALK xenograft mice model.
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