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| 1609558-93-1

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1609558-93-1
化学式
C13H14N2O4
mdl
——
分子量
262.265
InChiKey
VJOATBKUEDNRDP-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

物化性质

  • 沸点:
    405.4±45.0 °C(Predicted)
  • 密度:
    1.22±0.1 g/cm3(Predicted)

反应信息

  • 作为反应物:
    描述:
    lithium chloride 作用下, 以 四氢呋喃二甲基亚砜 为溶剂, 生成 2-Cyano-3-pyridylacetat
    参考文献:
    名称:
    A Versatile Annulation Route to Primary-Amino-Substituted Naphthyridine Esters
    摘要:
    A straightforward four-step synthesis of primary-amino-substituted naphthyridine esters from commercially available cyanopyridines was described. The route makes use of a condensation reaction between pyridinyl acetates with N,N-dimethylformamide dimethylacetal (DMF-DMA) to form ortho-cyano vinylogous carbamates. These intermediates can undergo facile cyclization with ammonium acetate in acetic acid to generate the corresponding naphthyridine esters in good synthetic yields. The synthesis of primary-amino-substituted 7-azaquinoxaline was also described.
    DOI:
    10.1055/s-0033-1340111
  • 作为产物:
    描述:
    丙二酸二乙酯 、 alkaline earth salt of/the/ methylsulfuric acid 在 sodium hydride 作用下, 以 四氢呋喃 为溶剂, 反应 4.17h, 生成
    参考文献:
    名称:
    A Versatile Annulation Route to Primary-Amino-Substituted Naphthyridine Esters
    摘要:
    A straightforward four-step synthesis of primary-amino-substituted naphthyridine esters from commercially available cyanopyridines was described. The route makes use of a condensation reaction between pyridinyl acetates with N,N-dimethylformamide dimethylacetal (DMF-DMA) to form ortho-cyano vinylogous carbamates. These intermediates can undergo facile cyclization with ammonium acetate in acetic acid to generate the corresponding naphthyridine esters in good synthetic yields. The synthesis of primary-amino-substituted 7-azaquinoxaline was also described.
    DOI:
    10.1055/s-0033-1340111
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