Reacción #62696

ord-466fb6c4ab7441e8a00eb8577f676e6a

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe acetone is then removed
  2. 2
    Extracciónthe resulting mixture extracted with EtOAc
  3. 3
    ExtracciónThe ethyl acetate extract
  4. 4
    Lavadois washed with water
  5. 5
    Otrodried
  6. 6
    Otroevaporated

Procedimiento

The resulting (-)-1-ethoxymethyl-2,6-dimethyl-3-carbomethoxy-4-(3-nitrophenyl)-5-carboxy-1,4-dihydropyridine is then dissolved in acetone (100 mL), and treated with 1N HCl (20 mL) at room temperature for 1 h. The acetone is then removed, the residue taken up in water (20 mL), and the resulting mixture extracted with EtOAc. The ethyl acetate extract is washed with water, dried, and evaporated to yield (-)-2,6-dimethyl-3-carbomethoxy-4-(3-nitrophenyl)-5-carboxy-1,4-dihydropyridine (12-(-), mp=196°-197° C., αD22 =-19.6°). The (+) isomer is similarly prepared (12-(+), mp=194°-195° C., αD22 =+19.1°).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04761420uspto-grants-1988_08