Reacción #78383

ord-e66a2bd1a4454751acefae1930059942

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaheated to reflux
  2. 2
    TemperaturaThe mixture was cooled in an ice bath
  3. 3
    Otrothe deposited precipitate was isolated by means of a suction
  4. 4
    Filtraciónfilter
  5. 5
    OtroAfter drying
  6. 6
    Otro2.72 g of crude product were obtained in the form of a yellowish solid

Procedimiento

5.00 g of methyl 2-[1-amino-1-(4-fluorophenyl)-methylene]-4-methyl-3-oxopentanoate (18.7 mmol) were treated with 5 ml of N-N-dimethylacetamide and 15.71 g of a 50% strength aqueous cyanamide solution (187 mmol) and heated to reflux. After 5 h, the solution was poured onto 50 ml of water. The mixture was cooled in an ice bath and the deposited precipitate was isolated by means of a suction filter. After drying, 2.72 g of crude product were obtained in the form of a yellowish solid. After flash chromatography (150 g of silica gel; eluent: hexane/ethyl acetate 3:2), 1.19 g of methyl 2-amino-4-(4-fluorophenyl)-6-isopropylpyrimidine-5-carboxylate were isolated in the form of a colourless solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06710178B2uspto-grants-2004_03