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methyl (R)-(+)-8-hydroxy-3-oxo-2-(2,2,2-trifluoroethyl)-2,3,4,5-tetrahydro-2-benzazepine-4-acetate | 205677-03-8

中文名称
——
中文别名
——
英文名称
methyl (R)-(+)-8-hydroxy-3-oxo-2-(2,2,2-trifluoroethyl)-2,3,4,5-tetrahydro-2-benzazepine-4-acetate
英文别名
methyl 2-[(4R)-8-hydroxy-3-oxo-2-(2,2,2-trifluoroethyl)-4,5-dihydro-1H-2-benzazepin-4-yl]acetate
methyl (R)-(+)-8-hydroxy-3-oxo-2-(2,2,2-trifluoroethyl)-2,3,4,5-tetrahydro-2-benzazepine-4-acetate化学式
CAS
205677-03-8
化学式
C15H16F3NO4
mdl
——
分子量
331.292
InChiKey
NLQPTCGXBABSPV-SNVBAGLBSA-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:
    456.358±45.00 °C(Press: 760.00 Torr)(predicted)
  • 密度:
    1.317±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.8
  • 重原子数:
    23
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    66.8
  • 氢给体数:
    1
  • 氢受体数:
    7

反应信息

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文献信息

  • [EN] PROCESS<br/>[FR] PROCÉDÉ
    申请人:SMITHKLINE BEECHAM CORP
    公开号:WO2009111679A2
    公开(公告)日:2009-09-11
    The present invention generally relates to a novel process for preparing vitronectin receptor antagonist compounds having a benzodiazepinyl core structure. This invention relates to the preparation of pharmaceutically active compounds which inhibit the vitronectin receptor and are useful for treatment of inflammation, cancer and cardiovascular disorders, such as atherosclerosis and restenosis, and diseases wherein bone resorption is a factor, such as osteoporosis. In particular, the present invention relates to a novel process for preparing (±)-3-oxo-8-[3-(pyridin-2-ylamino)propyl]oxy}- 2-(2,2,2-trifluoroethyl)-2,3,4,5-tetrahydro-1H-2-benzazepine-4-acetic acid, (R)-3-oxo-8- [3-(pyridin-2-ylamino) propyl]oxy}-2-(2,2,2-trifluoroethyl)-2,3,4,5-tetrahydro-1H-2- benzazepine-4-acetic acid and (S)-3-oxo-8-[3-(pyridin-2-ylamino)propyl]oxy}-2-(2,2,2- trifluoroethyl)-2,3,4,5-tetrahydro-1H-2-benzazepine-4-acetic acid or a pharmaceutically acceptable salt thereof.
  • Vitronectin receptor antagonists
    申请人:SmithKline Beecham Corporation
    公开号:US20030125317A1
    公开(公告)日:2003-07-03
    Compounds having a benzodiazepinyl core structure are disclosed which are vitronectin receptor antagonists useful in the treatment of osteoporosis, angiogenesis, tumor growth and metastasis, atherosclerosis, restenosis and inflammation.
    本文披露了具有苯二氮卓环核结构的化合物,这些化合物是维腾蛋白受体拮抗剂,可用于治疗骨质疏松症、血管生成、肿瘤生长和转移、动脉粥样硬化、再狭窄和炎症。
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