Reacción #45598

Ecuación de reacción

pyridine

2-(2,2-dimethylpropionylamino)-4-fluoro-5-iodo-3-methoxy-6-methylbenzamide

Trifluoromethanesulfonic acid anhydride

→

compound

N-(2-Cyano-5-fluoro-4-iodo-6-methoxy-3-methylphenyl)-2,2-dimethylpropionamide

Disolventes

ethyl acetate

Condiciones de reacción

Tratamiento posterior

1. 1
   LavadoThe organic layer was washed with 1 N hydrochloric acid (300 ml×5), saturated brine (300 ml×2)
2. 2
   Secadodried over anhydrous magnesium sulfate
3. 3
   Concentraciónconcentrated under reduced pressure
4. 4
   Otrothe residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=5:1)

Procedimiento

4-Dimethylaminopyridine (149 mg, 1.22 mmol) was added to a pyridine (100 ml) suspension of 2-(2,2-dimethylpropionylamino)-4-fluoro-5-iodo-3-methoxy-6-methylbenzamide (I-68) (4.97 g, 1.22 mmol), and cooled at 0° C. Trifluoromethanesulfonic acid anhydride (6.17 ml, 36.5 mmol) was dropwise added to it, followed by stirring at room temperature for 1 hour, then ethyl acetate (400 ml) was put thereinto. The organic layer was washed with 1 N hydrochloric acid (300 ml×5), saturated brine (300 ml×2), then dried over anhydrous magnesium sulfate, concentrated under reduced pressure, the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=5:1) to obtain the entitled compound (4.47 g, 94%) as a pale yellow solid.

Fuente