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ethyl 4-ethoxy-2-hydroxy-6-(methylthio)pyrimidin-5-carboxylate | 1234464-47-1

中文名称
——
中文别名
——
英文名称
ethyl 4-ethoxy-2-hydroxy-6-(methylthio)pyrimidin-5-carboxylate
英文别名
ethyl 6-ethoxy-4-methylsulfanyl-2-oxo-1H-pyrimidine-5-carboxylate
ethyl 4-ethoxy-2-hydroxy-6-(methylthio)pyrimidin-5-carboxylate化学式
CAS
1234464-47-1
化学式
C10H14N2O4S
mdl
——
分子量
258.298
InChiKey
SFJDYMDHXKAKCB-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):
    1.2
  • 重原子数:
    17
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    102
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    2-双甲基磺酰-亚甲基丙二酸二乙酯硫脲乙醇 为溶剂, 反应 3.0h, 以85%的产率得到ethyl 4-ethoxy-2-hydroxy-6-(methylthio)pyrimidin-5-carboxylate
    参考文献:
    名称:
    Synthesis of new polysubstituted (pyrazoles, pyrimidines and quinolines) five and six-membered heterocycles: reaction of α,α-dioxoketene dithioacetals with nucleophiles
    摘要:
    A novel synthesis of polysubstituted pyrazoles 3a-d, pyrimidines 4a-f and quinolines 5a-c via the reaction of alpha,alpha-oxoketene dithioacetals 2a-c with hydrazine hydrate, malonohydrazide, urea, thiourea and aniline is reported and the synthetic potential of the method is demonstrated. The structure of the new compounds was established upon their elemental analysis, IR, H-1 NMR and C-13 NMR. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2010.04.003
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文献信息

  • Synthesis of new polysubstituted (pyrazoles, pyrimidines and quinolines) five and six-membered heterocycles: reaction of α,α-dioxoketene dithioacetals with nucleophiles
    作者:M.A. Ebraheem、K.M. Lokanatha Rai、N.U. Kudva.N、A.S. Bahjat
    DOI:10.1016/j.tetlet.2010.04.003
    日期:2010.7
    A novel synthesis of polysubstituted pyrazoles 3a-d, pyrimidines 4a-f and quinolines 5a-c via the reaction of alpha,alpha-oxoketene dithioacetals 2a-c with hydrazine hydrate, malonohydrazide, urea, thiourea and aniline is reported and the synthetic potential of the method is demonstrated. The structure of the new compounds was established upon their elemental analysis, IR, H-1 NMR and C-13 NMR. (C) 2010 Elsevier Ltd. All rights reserved.
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