Reacción #4493

ord-c8eb97027f2c4870835f040d585e95f1

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas hydrogenated at 40° C. and at atmospheric pressure
  2. 2
    workup.WAIThydrogenation was continued for 4 hours
  3. 3
    FiltraciónThe catalyst was filtered off
  4. 4
    Concentraciónthe filtrate was concentrated

Procedimiento

A stirred mixture of 5-{4-[2-(5-methyl-2-phenyl-4-oxazolyl)-2-oxoethoxy]benzylidene}-2,4-thiazolidinedione (1.0 g), Pd-black (3 g) and dioxane (100 ml) was hydrogenated at 40° C. and at atmospheric pressure. After 4 hours, another Pd-black (3 g) was added and hydrogenation was continued for 4 hours. The catalyst was filtered off and the filtrate was concentrated to yield 5-{4-[2-(5-methyl-2-phenyl-4-oxazolyl)-2-oxoethoxy]benzyl}-2,4-thiazolidinedione (the same compound as that obtained in Example 48) as crystals (0.95 g, 94.1%). Recrystallization from ethyl acetate-hexane gave colorless needles, m.p. 168°-169° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04725610uspto-grants-1988_02