Reacción #65761

ord-267f4a4c64be4094bf7e33962104fd3f

Condiciones de reacción

Temperatura
100°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónfollowed by extraction with ethyl acetate
  2. 2
    LavadoThe organic layer was washed with water
  3. 3
    Secadoa saturated aqueous solution of sodium chloride and dried
  4. 4
    workup.DISTILLATIONThe solvent was distilled off
  5. 5
    OtroThe residue was purified by silica gel column chromatography (eluent:ethyl acetate/hexane 1:1)

Procedimiento

To 300 mg of 3,4-diethoxycarbonyl-6-(4-methoxyphenyl)-5-nitro-2(1H)pyridone were added 0.5 ml of phosphorus oxychloride and two drops of DMF. The mixture was heated at 100° C. for 1 hour. After ice water was added, the mixture was neutralized with sodium hydrogencarbonate, followed by extraction with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of sodium chloride and dried. The solvent was distilled off. The residue was purified by silica gel column chromatography (eluent:ethyl acetate/hexane 1:1).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05420275uspto-grants-1995_05