Reacción #1534

ord-9db8bda42ddd42569da026335543c4dd

Ecuación de reacción

COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2sccc2C(CF)OC(C)=O)n1
N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-3-(1-acetoxy-2-fluoroethyl)-2-thiophenesulfonamide
COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2sccc2C(CF)OC(C)=O)n1
N-[(4,6-dimethoxypyrimidin-2-yl)-aminocarbonyl]-3-(1-acetoxy-2-fluoroethyl)-2-thiophenesulfonamide
Cl
HCl
COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2sccc2C(O)CF)n1
pure title compound
Rendimiento 92.0%
COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2sccc2C(O)CF)n1
N-[(4,6-dimethoxypyrimidin-2-yl)-aminocarbonyl]-3-(1-hydroxy-2-fluoroethyl)-2-thiophenesulfonamide
Rendimiento 92.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextracted with methylene chloride
  2. 2
    ConcentraciónThe 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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05726127uspto-grants-1998_03