Reacción #1005932

Ecuación de reacción

iodomethane

4-amino-5-fluoro-1-(4-methoxyphenylsulfonyl)pyrimidin-2(1H)-one

potassium carbonate

N,N-dimethylformamide

→

title compound

Rendimiento 12.0%

5-Fluoro-4-imino-1-(4-methoxyphenylsulfonyl)-3-methyl-3,4-dihydropyrimidin-2(1H)-one

Rendimiento 12.0%

Disolventes

EtOAc

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroTo an 8-mL screw capped vial
2. 2
   OtroThe reaction vessel was sealed
3. 3
   TemperaturaThe reaction mixture was cooled to room temperature
4. 4
   Lavadowashed with water (H2O; 3×10 mL)
5. 5
   SecadoThe organic phase was dried over MgSO4
6. 6
   Filtraciónfiltered
7. 7
   Otrothe solvent was evaporated under reduced pressure
8. 8
   OtroPurification by flash chromatography (silica gel (SiO2), EtOAc/Hexanes gradient)

Procedimiento

To an 8-mL screw capped vial were added 4-amino-5-fluoro-1-(4-methoxyphenylsulfonyl)pyrimidin-2(1H)-one (0.293 g, 0.979 mmol), anhydrous potassium carbonate (K2CO3; 0.271 g, 1.96 mmol), and N,N-dimethylformamide (DMF; 4 mL), followed by iodomethane (CH3I; 0.208 g, 1.47 mmol). The reaction vessel was sealed, and the reaction mixture was warmed to 60° C. and stirred for 4 h. The reaction mixture was cooled to room temperature, diluted with EtOAc (20 mL), and washed with water (H2O; 3×10 mL). The organic phase was dried over MgSO4, filtered, and the solvent was evaporated under reduced pressure. Purification by flash chromatography (silica gel (SiO2), EtOAc/Hexanes gradient) afforded the title compound as a pale yellow solid (36 milligrams (mg), 12%): mp 158-162° C.; 1H NMR (400 MHz, DMSO-d6) δ 8.01 (d, J=9.22 Hz, 2H), 7.74 (d, J=5.27 Hz, 1H), 7.04 (d, J=9.23 Hz, 2H), 3.90 (s, 3H), 3.31 (s, 3H); ESIMS m/z 314 ([M+H]+).

Fuente