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6-(2,4-dimethoxyphenyl)-4-phenyl-1H-pyrimidin-2-one | 912960-78-2

中文名称
——
中文别名
——
英文名称
6-(2,4-dimethoxyphenyl)-4-phenyl-1H-pyrimidin-2-one
英文别名
——
6-(2,4-dimethoxyphenyl)-4-phenyl-1H-pyrimidin-2-one化学式
CAS
912960-78-2
化学式
C18H16N2O3
mdl
——
分子量
308.337
InChiKey
OYQYXXCCMDGHMZ-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):
    2.8
  • 重原子数:
    23
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    59.9
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    苯乙酮2,4-二甲氧基苯甲醛尿素 作用下, 反应 0.13h, 以91%的产率得到6-(2,4-dimethoxyphenyl)-4-phenyl-1H-pyrimidin-2-one
    参考文献:
    名称:
    Iodine-Catalyzed Versatile Synthesis of 4,6-Diarylpyrimidin-2(1H)-ones (DAPMs) via One-Pot, Multicomponent Reaction
    摘要:
    [image omitted] An efficient, solvent-free, one-pot, three-component cyclocondensation reaction between aldehyde, ketone, and urea to give 4,6-diarylpyrimidin-2(1H)-ones (DAPMs) using iodine as catalyst is described. This new protocol provides a simple and environmentally benign route along with the associated advantages of good to excellent yield of the products (90-96%) and short reaction times (5-15min) at 80 degrees C.
    DOI:
    10.1080/00397911.2010.493263
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文献信息

  • TCT (2,4,6-Trichloro-1,3,5-triazine) Promoted Single-Step Syntheis of 4,6-Diarylpyrimidin-2(1H)-ones under Microwave Irradiation
    作者:Ahmad Reza Khosropour、Ahmad R. Khosropour、Iraj Mohammadpoor-Baltork、Mohammad M. Khodaei、Mahbubeh Jokar
    DOI:10.3987/com-05-10613
    日期:——
  • Iodine-Catalyzed Versatile Synthesis of 4,6-Diarylpyrimidin-2(1<i>H</i>)-ones (DAPMs) via One-Pot, Multicomponent Reaction
    作者:M. B. Madhusudana Reddy、M. A. Pasha
    DOI:10.1080/00397911.2010.493263
    日期:2011.7.1
    [image omitted] An efficient, solvent-free, one-pot, three-component cyclocondensation reaction between aldehyde, ketone, and urea to give 4,6-diarylpyrimidin-2(1H)-ones (DAPMs) using iodine as catalyst is described. This new protocol provides a simple and environmentally benign route along with the associated advantages of good to excellent yield of the products (90-96%) and short reaction times (5-15min) at 80 degrees C.
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