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6-(4-methoxyphenyl)-5,7,8-trimethyl-2-phenyl-2H-1,4-benzoxazin-3(4H)-one | 1277193-29-9

中文名称
——
中文别名
——
英文名称
6-(4-methoxyphenyl)-5,7,8-trimethyl-2-phenyl-2H-1,4-benzoxazin-3(4H)-one
英文别名
Na2CO3;6-(4-methoxyphenyl)-5,7,8-trimethyl-2-phenyl-4H-1,4-benzoxazin-3-one
6-(4-methoxyphenyl)-5,7,8-trimethyl-2-phenyl-2H-1,4-benzoxazin-3(4H)-one化学式
CAS
1277193-29-9
化学式
C24H23NO3
mdl
——
分子量
373.452
InChiKey
ZKIJOYLIRZQFOX-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):
    5.3
  • 重原子数:
    28
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    47.6
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    2-phenyl-6-bromo-5,7,8-trimethyl-1,4-benzoxazinone 、 4-甲氧基苯硼酸四(三苯基膦)钯 、 sodium carbonate 作用下, 以 乙二醇二甲醚 为溶剂, 反应 0.08h, 以91%的产率得到6-(4-methoxyphenyl)-5,7,8-trimethyl-2-phenyl-2H-1,4-benzoxazin-3(4H)-one
    参考文献:
    名称:
    Divergent synthesis of 2,6-diaryl-substituted 5,7,8-trimethyl-1,4-benzoxazines via microwave-promoted palladium-catalyzed Suzuki–Miyaura cross coupling and biological evaluation
    摘要:
    An efficient palladium-catalyzed Suzuki-Miyaura cross-coupling protocol effected in a mixture of DME/water (2:1) enables the reaction of sterically hindered and electron rich 6-chloro or 6-bromo-1,4-benzoxazines(ones) with a variety of aryl, vinyl or alkylboronic acids. Coupling is effected with catalyst loading of 5 mol % using sealed-vessel microwave processing. The resulting compounds exhibit potent activity against Toxoplasma gondii tachyzoite proliferation. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2012.10.009
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文献信息

  • Divergent synthesis of 2,6-diaryl-substituted 5,7,8-trimethyl-1,4-benzoxazines via microwave-promoted palladium-catalyzed Suzuki–Miyaura cross coupling and biological evaluation
    作者:Eftychia N. Koini、Nicolaos Avlonitis、Erica S. Martins-Duarte、Wanderley de Souza、Rossiane C. Vommaro、Theodora Calogeropoulou
    DOI:10.1016/j.tet.2012.10.009
    日期:2012.12
    An efficient palladium-catalyzed Suzuki-Miyaura cross-coupling protocol effected in a mixture of DME/water (2:1) enables the reaction of sterically hindered and electron rich 6-chloro or 6-bromo-1,4-benzoxazines(ones) with a variety of aryl, vinyl or alkylboronic acids. Coupling is effected with catalyst loading of 5 mol % using sealed-vessel microwave processing. The resulting compounds exhibit potent activity against Toxoplasma gondii tachyzoite proliferation. (C) 2012 Elsevier Ltd. All rights reserved.
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