Reacción #350769

ord-f26a61c9982548f782393bbc19885058

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooling
  2. 2
    workup.STIRRINGThe mixture was stirred at the same temperature for 30 minutes
  3. 3
    OtroAfter the completion of a reaction
  4. 4
    Otrothe solvent was removed by distillation
  5. 5
    OtroThe residue was purified by silica gel column chromatography (eluent: dichloromethane/n-hexane =4/1)
  6. 6
    Otrorecrystallized from diethyl ether

Procedimiento

111 mg of sodium boron hydride was added to a solution of 1.3 g of 2-(3,4-diethoxyphenyl)-4-(3-methoxycarbonyl-4-hydroxy-5-formylmethylphenyl)thiazole in 30 ml of methanol, with stirring under ice-cooling. The mixture was stirred at the same temperature for 30 minutes. After the completion of a reaction, the solvent was removed by distillation. The residue was purified by silica gel column chromatography (eluent: dichloromethane/n-hexane =4/1) and recrystallized from diethyl ether to obtain 570 mg of 2-(3,4-diethoxyphenyl)-4-[3-methoxycarbonyl-4-hydroxy-5-(2-hydroxyethyl)phenyl]-thiazole.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05643932uspto-grants-1997_07