Reacción #65761
ord-267f4a4c64be4094bf7e33962104fd3f
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Temperatura
100°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Extracciónfollowed by extraction with ethyl acetate
- 2LavadoThe organic layer was washed with water
- 3Secadoa saturated aqueous solution of sodium chloride and dried
- 4workup.DISTILLATIONThe solvent was distilled off
- 5OtroThe 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).