Reacción #501984

ord-1e14a20fc96f429da5d5f423068cbdf8

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe suspension is refluxed for 2 hours
  2. 2
    Temperaturawith heating
  3. 3
    TemperaturaAfter cooling
  4. 4
    Otrocrystalline precipitates
  5. 5
    Filtraciónare collected by filtration
  6. 6
    Lavadothe crystals are washed with ethyl acetate
  7. 7
    OtroThe crystals are recrystallized from a mixture of 500 ml of methanol and 50 ml of water
  8. 8
    Otrodried at 70° C. under reduced pressure

Procedimiento

49 g of (Z)-2-(2-tritylaminothiazol-4-yl)-2-[(2-pyrrolidon-3-yl)oxyimino]acetic acid are suspended in a solution of one liter of methanol containing 40 ml of water, and the suspension is refluxed for 2 hours with heating. After cooling, crystalline precipitates are collected by filtration, and the crystals are washed with ethyl acetate. The crystals are recrystallized from a mixture of 500 ml of methanol and 50 ml of water, and dried at 70° C. under reduced pressure. 15.7 g of (Z)-2-(2-aminothiazol-4-yl)-2-[(2-pyrrolidon-3-yl)oxyimino]acetic acid are obtained as colorless prisms. The physico-chemical properties of this product are identical with those of the product obtained in Example 2-(4).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04794186uspto-grants-1988_12