Reacción #362829

ord-4abb63068c0a4f0a818134184308a10e

Disolventes

Condiciones de reacción

Temperatura
65°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawhich is maintained under nitrogen
  2. 2
    Temperaturacooled down
  3. 3
    Extracciónextracted with 100 ml of dichloromethane and 100 ml of distilled water
  4. 4
    OtroThe aqueous phase is separated off
  5. 5
    Lavadowashed with 3 times 100 ml of dichloromethane
  6. 6
    Lavadowashed with 100 ml of water
  7. 7
    Otrowith 100 ml of a saturated solution of NaCl, separated off
  8. 8
    Secadodried over magnesium sulphate
  9. 9
    Filtraciónthe phases are filtered
  10. 10
    Otroevaporated to dryness under reduced pressure (50 kPa) in order

Procedimiento

4,6 g of diethyl 4-aminobenzylacetamidomalonate in 104 ml of acetic acid are placed in a three-necked flask which is maintained under nitrogen. 7.02 g of sodium acetate are added, followed by 1.87 ml of 2,5-dimethoxytetrahydrofuran. The mixture is heated at 65° C. for 1 h 15 min, then cooled down and extracted with 100 ml of dichloromethane and 100 ml of distilled water. The aqueous phase is separated off after settling and then washed with 3 times 100 ml of dichloromethane. The organic phases are combined, washed with 100 ml of water and then with 100 ml of a saturated solution of NaCl, separated off after settling and then dried over magnesium sulphate; the phases are filtered and then evaporated to dryness under reduced pressure (50 kPa) in order to yield 6.2 g of a solid which is purified by flash chromatography (eluent CH2Cl2/acetone 75/25 by volume). This results in 3.57 g of diethyl 4-(1-pyrrolyl)benzylacetamidomalonate in the form of a beige solid which melts at 110° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06352839B1uspto-grants-2002_03