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10-methoxy-7-(4-methylphenyl)-7,12-dihydrobenzo[b]indeno[1,2-e][1,4]diazepine-5,6-dione | 1189165-31-8

中文名称
——
中文别名
——
英文名称
10-methoxy-7-(4-methylphenyl)-7,12-dihydrobenzo[b]indeno[1,2-e][1,4]diazepine-5,6-dione
英文别名
7-methoxy-10-(4-methylphenyl)-5H-indeno[2,1-c][1,5]benzodiazepine-11,12-dione
10-methoxy-7-(4-methylphenyl)-7,12-dihydrobenzo[b]indeno[1,2-e][1,4]diazepine-5,6-dione化学式
CAS
1189165-31-8
化学式
C24H18N2O3
mdl
——
分子量
382.419
InChiKey
AOGCICBIFSYSOC-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):
    4.4
  • 重原子数:
    29
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    58.6
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    3-[(4-methylphenyl)amino]-N-(4-methylphenyl)-1-oxo-1H-indene-2-carboxamide 在 [双(三氟乙酰氧基)碘]苯 作用下, 以 二氯甲烷 为溶剂, 以35%的产率得到10-methoxy-7-(4-methylphenyl)-7,12-dihydrobenzo[b]indeno[1,2-e][1,4]diazepine-5,6-dione
    参考文献:
    名称:
    A Convenient Approach to Fused Indeno-1,4-diazepinones through Hypervalent Iodine Chemistry
    摘要:
    Indenocarboxamides, resulting from the sequential addition of two arylamine equivalents to indanedione ketene dimer, are oxidized by [bis(trifluoroacetoxy)iodobenzene] to fused indeno-1,4-diazepinones in yields depending on the substituents on both aromatic rings. A plausible reaction pathway explaining the formation of the title compounds, as well as the formation of the two other minor products of the reaction, through a common intermediate, is suggested.
    DOI:
    10.1021/jo9013063
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文献信息

  • A Convenient Approach to Fused Indeno-1,4-diazepinones through Hypervalent Iodine Chemistry
    作者:Elizabeth Malamidou-Xenikaki、Spyros Spyroudis、Maria Tsanakopoulou、Dimitra Hadjipavlou-Litina
    DOI:10.1021/jo9013063
    日期:2009.10.2
    Indenocarboxamides, resulting from the sequential addition of two arylamine equivalents to indanedione ketene dimer, are oxidized by [bis(trifluoroacetoxy)iodobenzene] to fused indeno-1,4-diazepinones in yields depending on the substituents on both aromatic rings. A plausible reaction pathway explaining the formation of the title compounds, as well as the formation of the two other minor products of the reaction, through a common intermediate, is suggested.
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