Réaction #81611

ord-01837250ab324f05a14ab0fe8ca15583

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurewas heated
  2. 2
    Températureunder reflux for 1 hour
  3. 3
    Autreevaporated
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in a small volume of water
  5. 5
    ExtractionThe resulting mixture was extracted several times with ether
  6. 6
    Séchagethe combined extracts were dried (MgSO4)
  7. 7
    Autreevaporated

Mode opératoire

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%.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05618941uspto-grants-1997_04