Reacción #55414

ord-17aafc8a8d6d4384bb37bf8ee908d9a0

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaTo a stirred, cooled (-20°) solution of 10.2 g
  2. 2
    workup.ADDITIONAfter addition the reaction mixture
  3. 3
    Temperaturais warmed to 25°
  4. 4
    Extracciónextracted with ether
  5. 5
    TemperaturaThe remaining aqueous phase is cooled
  6. 6
    workup.ADDITIONof ethyl acetate is added
  7. 7
    OtroThe layers are separated
  8. 8
    Extracciónthe aqueous phase is extracted twice more with ethyl acetate
  9. 9
    SecadoThe combined extracts are dried (MgSO4)
  10. 10
    Otroevaporated to dryness

Procedimiento

To a stirred, cooled (-20°) solution of 10.2 g. (0.026 mol.) of 7-amino-3-[1-(2-carbamoylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid in 220 ml. of 3% sodium bicarbonate and 220 ml. of acetone is dropwise added a solution of 3.66 g. (0.029 mol.) of methylmercaptoacetyl chloride in 52 ml. of acetone, during which time the pH of the reaction mixture is maintained at 8.0 by addition of 10% sodium hydroxide. After addition the reaction mixture is stirred an additional 20 minutes at -15°, then is warmed to 25° and extracted with ether. The remaining aqueous phase is cooled, 250 ml. of ethyl acetate is added and the slurry is acidified with 3N hydrochloric acid. The layers are separated and the aqueous phase is extracted twice more with ethyl acetate. The combined extracts are dried (MgSO4) and evaporated to dryness to yield the title compound.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04220644uspto-grants-1980_09