Reacción #2396544

ord-7a9175df1d2443db8fedf8e73dd579dc

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroAfter reaction for one hour
  2. 2
    Otrotwo layers are separated
  3. 3
    LavadoThe chloroform layer is washed with 100 ml of water
  4. 4
    Secadowith saturated aqueous solution of sodium chloride, and dried over anhydrous sodum sulfate
  5. 5
    workup.DISTILLATIONChloroform is distilled off

Procedimiento

Into a mixture of 10 ml of chloroform and 10 ml of ethanol is dissolved 1.34 g of 2-(4-(4-fluorophenacyl)-piperazinyl)-6-methyl-4-phenyl-thieno[2,3-d]pyrimidine, and then 0.23 g of sodium borohydride is added at room temperature. After reaction for one hour, 60 ml of chloroform and 100 ml of water are added and two layers are separated. The chloroform layer is washed with 100 ml of water and then with saturated aqueous solution of sodium chloride, and dried over anhydrous sodum sulfate. Chloroform is distilled off and 1.27 g of the desired crystal is obtained from methanol. The product has a melting point of 180°-181.5° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04695568uspto-grants-1987_09