Réaction #1528393

ord-97bb07007ba0436e8f83216950f31a10

Équation de réaction

O=[N+]([O-])c1cc(F)c(F)cc1F
2,4,5-trifluoronitrobenzene
Cn1c(C(F)(F)F)cc(=O)[nH]c1=O
3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydro pyrimidine
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cn1c(C(F)(F)F)cc(=O)n(-c2cc(F)c([N+](=O)[O-])cc2F)c1=O
2,5-difluoro-4-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]nitrobenzene
Rendement 43.0%

Conditions de réaction

Température
80°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe reaction solution was cooled to room temperature
  2. 2
    Extractionextracted with ethyl acetate
  3. 3
    LavageThe organic layer was washed with saturated aqueous sodium chloride solution
  4. 4
    Séchagedried over anhydrous magnesium sulfate
  5. 5
    Concentrationconcentrated

Mode opératoire

Into 10 ml of dimethylsulfoxide was dissolved 1.77 g of 2,4,5-trifluoronitrobenzene and 1.94 g of 3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydro pyrimidine. After adding 1.52 g of anhydrous potassium carbonate at room temperature, the mixture was stirred at 80° C. for 1 hour. The reaction solution was cooled to room temperature, and then the solution was poured into ice-water and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica-gel column chromatography to give 1.51 g of 2,5-difluoro-4-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]nitrobenzene.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07655598B2uspto-grants-2010_02