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4-(3-methoxyphenyl)-1,6-dimethyl-5-(N-phenylcarboxamido)-2-oxo-1,2,3,4-tetrahydropyrimidine | 1255416-25-1

中文名称
——
中文别名
——
英文名称
4-(3-methoxyphenyl)-1,6-dimethyl-5-(N-phenylcarboxamido)-2-oxo-1,2,3,4-tetrahydropyrimidine
英文别名
3,4-dimethyl-6-(3-methoxyphenyl)-N-phenyl-2-oxo-1,2,3,6-tetrahydropyrimidine-5-carboxamide;6-(3-methoxyphenyl)-3,4-dimethyl-2-oxo-N-phenyl-1,6-dihydropyrimidine-5-carboxamide
4-(3-methoxyphenyl)-1,6-dimethyl-5-(N-phenylcarboxamido)-2-oxo-1,2,3,4-tetrahydropyrimidine化学式
CAS
1255416-25-1
化学式
C20H21N3O3
mdl
——
分子量
351.405
InChiKey
XFMQQNVKBQFLRY-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):
    2.1
  • 重原子数:
    26
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    70.7
  • 氢给体数:
    2
  • 氢受体数:
    3

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    4-(3-methoxyphenyl)-1,6-dimethyl-5-(N-phenylcarboxamido)-2-oxo-1,2,3,4-tetrahydropyrimidine[双(三氟乙酰氧基)碘]苯 、 sodium carbonate 作用下, 以 二氯甲烷 为溶剂, 以18%的产率得到4-(3-methoxyphenyl)-1-methyl-4,7-dihydro-1H,3H-furo[3,4-d]pyrimidine-2,5-dione
    参考文献:
    名称:
    An Intramolecular PIFA-Mediated Metal-Free Allylic Oxycarbonylation Reaction and Its Application to the Preparation of Furopyrimidinones
    摘要:
    The preparation of a series of furo[3,4-d]pyrimidinones by an unprecedented PIFA-mediated intramolecular allylic oxycarbonylation reaction developed on 5-carbamoyl-substituted Biginelli adducts is presented The construction of the fused lactone by a metal-free C-H activation process, without the need of an additional functionalization step, is featured in the present work
    DOI:
    10.1021/jo101797s
  • 作为产物:
    描述:
    N-乙酰乙酰苯胺3-甲氧基苯甲醛N-甲基脲氯乙酸 作用下, 以97%的产率得到4-(3-methoxyphenyl)-1,6-dimethyl-5-(N-phenylcarboxamido)-2-oxo-1,2,3,4-tetrahydropyrimidine
    参考文献:
    名称:
    An Intramolecular PIFA-Mediated Metal-Free Allylic Oxycarbonylation Reaction and Its Application to the Preparation of Furopyrimidinones
    摘要:
    The preparation of a series of furo[3,4-d]pyrimidinones by an unprecedented PIFA-mediated intramolecular allylic oxycarbonylation reaction developed on 5-carbamoyl-substituted Biginelli adducts is presented The construction of the fused lactone by a metal-free C-H activation process, without the need of an additional functionalization step, is featured in the present work
    DOI:
    10.1021/jo101797s
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文献信息

  • Synthesis and antimicrobial activity of 6-aryl-3,4-dimethyl-N-phenyl-2-oxo-1,2,3,6-tetrahydropyrimidine-5-carboxamides
    作者:T. M. Zamaraeva、T. F. Odegova、A. Yu. Fedotov、M. V. Tomilov、V. L. Gein、P. A. Slepukhin
    DOI:10.1134/s1070363214100168
    日期:2014.10
    Three-component reaction of acetoacetanilide, aromatic aldehydes, and N-methylurea afforded 6-aryl-3,4-dimethyl-N-phenyl-2-oxo-1,2,3,6-tetrahydropyrimidine-5-carboxamides. IR, H-1 NMR spectroscopy, mass spectrometry, and X-ray diffraction analysis data confirmed the structure of the compounds obtained. Antimicrobial activity of these compounds was investigated.
  • An Intramolecular PIFA-Mediated Metal-Free Allylic Oxycarbonylation Reaction and Its Application to the Preparation of Furopyrimidinones
    作者:Irantzu Couto、Imanol Tellitu、Esther Domínguez
    DOI:10.1021/jo101797s
    日期:2010.11.19
    The preparation of a series of furo[3,4-d]pyrimidinones by an unprecedented PIFA-mediated intramolecular allylic oxycarbonylation reaction developed on 5-carbamoyl-substituted Biginelli adducts is presented The construction of the fused lactone by a metal-free C-H activation process, without the need of an additional functionalization step, is featured in the present work
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