反应 #302870

ord-a7fb018e00bd445d9c7fe8eb47e50dcb

反应方程式

O=C=Nc1ccccc1
phenylisocyanate
COC(=O)c1cccnc1N
2-aminonicotinic acid methyl ester
O=c1[nH]c2ncccc2c(=O)n1-c1ccccc1
3-phenyl-1H-pyrido[2,3-d]pyrimidine-2,4-dione
收率 61.2%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The mixture was refluxed for 16 hours
  2. 2
    其他The pyridine is was removed under reduced pressure
  3. 3
    workup.ADDITIONthe residue was treated with 280 ml ethanol
  4. 4
    温度The mixture is refluxed for 10 minutes
  5. 5
    温度Upon cooling down 3-phenyl-1H-pyrido[2,3-d]pyrimidine-2,4-dione
  6. 6
    其他crystallized from the medium
  7. 7
    其他was recrystallized from methoxypropanol

实验过程

17.22 g (144.6 mmol, 15.7 ml) phenylisocyanate was added to a suspenssion of 7.00 g (46.0 mmol) 2-aminonicotinic acid methyl ester in dry pyridine. The mixture was refluxed for 16 hours. The pyridine is was removed under reduced pressure and the residue was treated with 280 ml ethanol. The mixture is refluxed for 10 minutes. Upon cooling down 3-phenyl-1H-pyrido[2,3-d]pyrimidine-2,4-dione crystallized from the medium and was recrystallized from methoxypropanol. 6.73 g (61%) 3-phenyl-1H-pyrido[2,3-d]pyrimidine-2,4-dione was isolated (m.p. 304° C.).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08192918B2uspto-grants-2012_06