Reacción #1534
ord-9db8bda42ddd42569da026335543c4dd
Ecuación de reacción
N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-3-(1-acetoxy-2-fluoroethyl)-2-thiophenesulfonamide
N-[(4,6-dimethoxypyrimidin-2-yl)-aminocarbonyl]-3-(1-acetoxy-2-fluoroethyl)-2-thiophenesulfonamide
HCl
→
pure title compound
Rendimiento 92.0%
N-[(4,6-dimethoxypyrimidin-2-yl)-aminocarbonyl]-3-(1-hydroxy-2-fluoroethyl)-2-thiophenesulfonamide
Rendimiento 92.0%
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Extracciónextracted with methylene chloride
- 2ConcentraciónThe extract was concentrated
Procedimiento
650 mg (0.0015 mole) of N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-3-(1-acetoxy-2-fluoroethyl)-2-thiophenesulfonamide synthesized in Example 4 was dissolved in 5 ml of aqueous sodium hydroxide solution and then stirred at normal temperature for one hour. The reaction mixture was adjusted to pH4 by adding 5% aqueous HCl solution and then extracted with methylene chloride. The extract was concentrated to obtain 540 mg (Yield: 92%) of the pure title compound.