Reacción #81611

ord-01837250ab324f05a14ab0fe8ca15583

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawas heated
  2. 2
    Temperaturaunder reflux for 1 hour
  3. 3
    Otroevaporated
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in a small volume of water
  5. 5
    ExtracciónThe resulting mixture was extracted several times with ether
  6. 6
    Secadothe combined extracts were dried (MgSO4)
  7. 7
    Otroevaporated

Procedimiento

A mixture of ethyl 3-[2-[(4-chlorophenyl)sulphonylamino]ethyl]-5-[(4-fluorophenyl)methyl]benzenepropanoate (500 mg), 2N sodium hydroxide solution (1.5 ml) and methanol (5 ml) was heated under reflux for 1 hour and then evaporated. The residue was dissolved in a small volume of water, and the solution was made acidic with 2N hydrochloric acid. The resulting mixture was extracted several times with ether and the combined extracts were dried (MgSO4) and evaporated to give the title compound,(390 mg), m.p. 85°-87° C. Found: C,60.78A H,5.06; N,2.87. C24H33ClFNO4S requires C,60.56; H,4.87; N,2.94%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05618941uspto-grants-1997_04