Réaction #95076

ord-3857bd8cf78a4782ba6b7bc50758fb4c

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe mixture was heated
  2. 2
    Températureunder reflux for 10 minutes
  3. 3
    TempératureThe mixture was again heated
  4. 4
    Températureunder reflux for 10 minutes
  5. 5
    TempératureThe mixture was heated
  6. 6
    Températureunder reflux for 15 minutes
  7. 7
    AutreThe solvent was removed by evaporation in vacuo
  8. 8
    workup.DISSOLUTIONthe residue was dissolved in 75 ml
  9. 9
    LavageThe ethyl acetate solution was washed successively with water, 1 N sodium hydroxide, water and saturated sodium chloride solution
  10. 10
    SéchageThe ethyl acetate solution was then dried
  11. 11
    Autrethe ethyl acetate was removed by evaporation in vacuo
  12. 12
    AutreThe residue (960 mg.) was recrystallized from isopropyl ether giving 570 mg

Mode opératoire

To a stirred solution of 829 mg. of N-decyl-3-(3-[4-carboxy-2-oxo-pyrrolidino]phenyl)propenamide in 25 ml. of tetrahydrofuran was added 357 mg. of carbonyldiimidazole. The mixture was heated under reflux for 10 minutes, and then 258 mg. of 2-(N,N-diethylamino)ethanol was added. The mixture was again heated under reflux for 10 minutes, and then an additional 258 mg. of 2-(N,N-diethylamino)ethanol was added. The mixture was heated under reflux for 15 minutes and then it was cooled to room temperature. The solvent was removed by evaporation in vacuo, and the residue was dissolved in 75 ml. of ethyl acetate. The ethyl acetate solution was washed successively with water, 1 N sodium hydroxide, water and saturated sodium chloride solution. The ethyl acetate solution was then dried using sodium sulfate, and the ethyl acetate was removed by evaporation in vacuo. The residue (960 mg.) was recrystallized from isopropyl ether giving 570 mg. of the title compound, m.p. 78°-80° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04343813uspto-grants-1982_08