Reacción #41698

ord-f2e8ac05eb444e859d33d2bdfc902757

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe reaction liquid
  2. 2
    OtroPyridine was evaporated away under reduced pressure
  3. 3
    workup.ADDITIONthe residue was diluted with ethyl acetate
  4. 4
    Lavadowashed with water
  5. 5
    Secadodried with anhydrous magnesium sulfate
  6. 6
    OtroThe solvent was evaporated away under reduced pressure
  7. 7
    Lavadothe resulting solid was washed with a mixed solvent of ethyl acetate and hexane

Procedimiento

2.56 g of pyrazine-2-carboxylic acid and 4.66 g of 1-ethyl-3-(3′-dimethylaminopropyl)-carbodiimide hydrochloride were added to a pyridine (20 ml) solution of 3.7 g of 4-amino-2-fluoro-N-methoxy-N-methylbenzamide, and the reaction liquid was stirred at room temperature for 1 hour. Pyridine was evaporated away under reduced pressure, and the residue was diluted with ethyl acetate, washed with water, and dried with anhydrous magnesium sulfate. The solvent was evaporated away under reduced pressure, and the resulting solid was washed with a mixed solvent of ethyl acetate and hexane to obtain the entitled compound as a pale yellow solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07728025B2uspto-grants-2010_06