Reacción #41698
ord-f2e8ac05eb444e859d33d2bdfc902757
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Otrothe reaction liquid
- 2OtroPyridine was evaporated away under reduced pressure
- 3workup.ADDITIONthe residue was diluted with ethyl acetate
- 4Lavadowashed with water
- 5Secadodried with anhydrous magnesium sulfate
- 6OtroThe solvent was evaporated away under reduced pressure
- 7Lavadothe 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.