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3-benzyl-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine | 62717-64-0

中文名称
——
中文别名
——
英文名称
3-benzyl-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine
英文别名
3-benzyl-5-phenyl-1,2,4,5-tetrahydro-3-benzazepine-7,8-diol
3-benzyl-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine化学式
CAS
62717-64-0
化学式
C23H23NO2
mdl
——
分子量
345.441
InChiKey
JPMFSMDSBJSCSH-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

  • 沸点:
    532.4±50.0 °C(Predicted)
  • 密度:
    1.214±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.5
  • 重原子数:
    26
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    43.7
  • 氢给体数:
    2
  • 氢受体数:
    3

SDS

SDS:4260364b8d3a6e5a6f6fb3ef7031ceed
查看

上下游信息

  • 上游原料
    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

  • 7,8-Amino, hydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepines
    申请人:SmithKline Corporation
    公开号:US04284556A1
    公开(公告)日:1981-08-18
    A group of 1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepines whose structures have amino, hydroxy substituents at the 7,8-positions of the benzazepine nucleus is disclosed. Novel intermediates and routes of synthesis used for preparing them are also described. The end products have pharmacodynamic activity.
    一组1-苯基-2,3,4,5-四氢-1H-3-苯并哌啶的结构,在苯并哌啶核的7,8-位置具有氨基、羟基取代基。还披露了用于制备它们的新型中间体和合成路线。最终产物具有药效活性。
  • Pharmaceutical compositions and method of producing anti-Parkinsonism
    申请人:SmithKline Corporation
    公开号:US04052506A1
    公开(公告)日:1977-10-04
    Pharmaceutical compositions and method of producing anti-Parkinsonism activity by administering internally a nontoxic effective quantity of a benzazepine derivative to an animal.
    药物组合物和通过内服对动物施加一种苯并二氮杂环衍生物的无毒有效量来产生抗帕金森症活性的制备方法。
  • Process useful for preparing 7,8-acetamido,
    申请人:SmithKline Beckman Corporation
    公开号:US04382029A1
    公开(公告)日:1983-05-03
    A chemical process is described for preparing 7,8-acetamido, hydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepines which involves reacting a 7,8-quinone derivative of a 1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine with a benzyl or benzhydrylamine followed by hydrolysis of the resulting imine and reaction with acetic anhydride or acetyl chloride.
    描述了一种化学过程,用于制备7,8-乙酰胺基,羟基-1-苯基-2,3,4,5-四氢-1H-3-苯并哌啶,其中涉及将1-苯基-2,3,4,5-四氢-1H-3-苯并哌啶的7,8-醌衍生物与苄基或苯甲基胺反应,随后水解所得亚胺并与乙酸酐或乙酰氯反应。
  • Intermediates for preparing 7,8-amino,
    申请人:SmithKline Corporation
    公开号:US04327023A1
    公开(公告)日:1982-04-27
    A group of new chemical compounds are described which are intermediates for preparing 7,8-amino, hydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepines. The intermediates are distinguished in structure by a benzyloxy substituent at either the 7 or 8-position.
    描述了一组新的化合物,它们是制备7,8-氨基,羟基-1-苯基-2,3,4,5-四氢-1H-3-苯并哌啶的中间体。这些中间体在结构上以7位或8位的苄氧基取代物为特征。
  • 7,8-Amino, hydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepines, process for their preparation and pharmaceutical compositions containing them
    申请人:SMITHKLINE BECKMAN CORPORATION
    公开号:EP0033632A2
    公开(公告)日:1981-08-12
    A group of 1-phenyl-2,3,4,5-tetrahydro-1H-3-benz- azepines having structures with amino, hydroxy substituents at the 7,8-positions of the benzazepine nucleus is disclosed. Also described are pharmacodynamic pharmaceutical compositions containing them and processes for their preparation.
    本研究公开了一组 1-苯基-2,3,4,5-四氢-1H-3-苯并氮杂卓,其结构在苯并氮杂卓核的 7、8 位上具有氨基和羟基取代基。还描述了含有它们的药效学药物组合物及其制备工艺。
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