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4,6-bis(4-fluorophenyl)-8,15-dihydro-1H-quinolino[8′,1′:2,3,4][1,4]-oxazocino[6,7-b]quinoxalin-1-one | 1190620-43-9

中文名称
——
中文别名
——
英文名称
4,6-bis(4-fluorophenyl)-8,15-dihydro-1H-quinolino[8′,1′:2,3,4][1,4]-oxazocino[6,7-b]quinoxalin-1-one
英文别名
4,6-Bis(4-fluorophenyl)-8,15-dihydro-1h-quinolino[8',1':2,3,4][1,4]oxazocino[6,7-b]quinoxalin-1-one;16,18-bis(4-fluorophenyl)-14-oxa-1,4,11-triazapentacyclo[13.7.1.03,12.05,10.019,23]tricosa-3,5,7,9,11,15,17,19(23),20-nonaen-22-one
4,6-bis(4-fluorophenyl)-8,15-dihydro-1H-quinolino[8′,1′:2,3,4][1,4]-oxazocino[6,7-b]quinoxalin-1-one化学式
CAS
1190620-43-9
化学式
C31H19F2N3O2
mdl
——
分子量
503.508
InChiKey
ALNMXTJCNWXWME-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):
    5.4
  • 重原子数:
    38
  • 可旋转键数:
    2
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    55.3
  • 氢给体数:
    0
  • 氢受体数:
    6

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

  • 作为产物:
    描述:
    5,7-dibromoquinolonoquinoxalino-oxazocine4-氟苯硼酸三苯基膦钯 作用下, 以 为溶剂, 反应 12.0h, 以90%的产率得到4,6-bis(4-fluorophenyl)-8,15-dihydro-1H-quinolino[8′,1′:2,3,4][1,4]-oxazocino[6,7-b]quinoxalin-1-one
    参考文献:
    名称:
    Synthesis of biaryl pentacyclic quinolonoquinoxalino-oxazocines in aqueous medium using Amberlite IRA 402(OH)
    摘要:
    Amberlite IRA 402(OH) effectively mediates biarylation via Suzuki-Miyaura cross-coupling reaction on complex systems such as dihalo quinolonoquinoxalino-oxazocines. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2009.07.072
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文献信息

  • Combined palladium/eosin Y-catalysed direct synthesis of anticancer biarylquinolinooxazocino-quinoxaline-1-ones under visible light in one-pot sequence: a revisited proof of concept
    作者:Nilmadhab Roy、Priyankar Paira
    DOI:10.1007/s00706-020-02641-2
    日期:2020.7
    A novel, efficient, and green catalytic system under visible light irradiation has been introduced for the synthesis of anticancer biarylquinolooxazocino-quinoxaline-1-ones in one-pot sequence. The developed synthetic approach will be successfully utilized for the synthesis of various bioactive biarylquinolone in near future. Also, the cytotoxicity profile of these scaffolds has unveiled their superb cytoselectivity in HeLa and MCF-7 cell line compared to cisplatin. Graphic abstract
  • Synthesis of biaryl pentacyclic quinolonoquinoxalino-oxazocines in aqueous medium using Amberlite IRA 402(OH)
    作者:Priyankar Paira、Rupankar Paira、Abhijit Hazra、Krishnendu B. Sahu、Subhendu Naskar、Pritam Saha、Shyamal Mondal、Arindam Maity、Sukdeb Banerjee、Nirup B. Mondal
    DOI:10.1016/j.tetlet.2009.07.072
    日期:2009.9
    Amberlite IRA 402(OH) effectively mediates biarylation via Suzuki-Miyaura cross-coupling reaction on complex systems such as dihalo quinolonoquinoxalino-oxazocines. (C) 2009 Elsevier Ltd. All rights reserved.
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