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7-(4-hydroxy-6-methyl-2-oxo-2H-1-pyran-3-yl)-1H,3H-pyrido[2,3-d]pyrimidine-2,4-dione | 1401620-86-7

中文名称
——
中文别名
——
英文名称
7-(4-hydroxy-6-methyl-2-oxo-2H-1-pyran-3-yl)-1H,3H-pyrido[2,3-d]pyrimidine-2,4-dione
英文别名
4-hydroxy-7-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)pyrido[2,3-d]pyrimidin-2(1H)-one;7-(4-hydroxy-6-methyl-2-oxopyran-3-yl)-1H-pyrido[2,3-d]pyrimidine-2,4-dione
7-(4-hydroxy-6-methyl-2-oxo-2H-1-pyran-3-yl)-1H,3H-pyrido[2,3-d]pyrimidine-2,4-dione化学式
CAS
1401620-86-7
化学式
C13H9N3O5
mdl
——
分子量
287.232
InChiKey
DXEAQYNQZAJLQF-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):
    0
  • 重原子数:
    21
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    118
  • 氢给体数:
    3
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    去氢乙酸 在 ammonium acetate 作用下, 以 neat (no solvent) 为溶剂, 反应 0.5h, 生成 7-(4-hydroxy-6-methyl-2-oxo-2H-1-pyran-3-yl)-1H,3H-pyrido[2,3-d]pyrimidine-2,4-dione
    参考文献:
    名称:
    Silica supported sodium hydrogen sulfate (NaHSO4–SiO2): A novel, green catalyst for synthesis of pyrazole and pyranyl pyridine derivatives under solvent-free condition via heterocyclic β-enaminones
    摘要:
    NaHSO4-SiO2 is used as an efficient, mild and reusable catalyst for the synthesis of novel heterocyclic pyrazole (5a-h) and pyranyl pyridine (7a-h) derivatives via heterocyclic beta-enaminones (3a-d) under thermal solvent-free conditions. The remarkable features of this green, new methodology are high conversions, cleaner reaction profile, simple experimental and work-up procedures. Structures of the newly synthesized compounds have been elucidated on the basis of elemental analysis and spectral data (IR, H-1 NMR, C-13 NMR and mass spectrometry). The catalyst is characterized for the first time by using scanning electron microscopy-energy dispersive X-ray (SEM-EDX) and powder XRD. The catalyst can be reused several times without significant loss of its catalytic activity. (c) 2012 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.molcata.2012.07.024
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文献信息

  • Highly efficient solvent-free synthesis of novel pyranyl pyridine derivatives via β-enaminones using ZnO nanoparticles
    作者:Zeba N. Siddiqui、Nayeem Ahmed、Farheen Farooq、Kulsum Khan
    DOI:10.1016/j.tetlet.2013.04.072
    日期:2013.7
    Highly efficient ZnO nanoparticle catalyzed one-pot solvent-free synthesis of novel pyridine derivatives by three-component reaction of β-enaminones, different active methylene compounds, and ammonium acetate via Michael addition, cyclodehydration, and elimination sequence is reported. The catalyst was recyclable up to six catalytic cycles without a significant loss in the catalytic activity. This
    据报道,高效的ZnO纳米颗粒通过迈克尔-加成反应,β-烯胺酮,不同活性亚甲基化合物和乙酸铵的三组分反应,一环脱水和消除顺序,可以一锅无溶剂地合成新型吡啶衍生物。该催化剂可循环使用多达六个催化循环,而催化活性没有明显损失。该新方案具有环境友好,产率高,无溶剂,催化剂载量低,反应时间短和操作程序方便的优点。通过XRD,SEM和TEM分析对ZnO纳米颗粒进行了表征。
  • Silica supported sodium hydrogen sulfate (NaHSO4–SiO2): A novel, green catalyst for synthesis of pyrazole and pyranyl pyridine derivatives under solvent-free condition via heterocyclic β-enaminones
    作者:Zeba N. Siddiqui、Farheen Farooq
    DOI:10.1016/j.molcata.2012.07.024
    日期:2012.11
    NaHSO4-SiO2 is used as an efficient, mild and reusable catalyst for the synthesis of novel heterocyclic pyrazole (5a-h) and pyranyl pyridine (7a-h) derivatives via heterocyclic beta-enaminones (3a-d) under thermal solvent-free conditions. The remarkable features of this green, new methodology are high conversions, cleaner reaction profile, simple experimental and work-up procedures. Structures of the newly synthesized compounds have been elucidated on the basis of elemental analysis and spectral data (IR, H-1 NMR, C-13 NMR and mass spectrometry). The catalyst is characterized for the first time by using scanning electron microscopy-energy dispersive X-ray (SEM-EDX) and powder XRD. The catalyst can be reused several times without significant loss of its catalytic activity. (c) 2012 Elsevier B.V. All rights reserved.
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