Reacción #1411

ord-13330458b3c94465aa5dc67623f8b399

Ecuación de reacción

O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
O=C(c1ccccc1)N1CC=CC1
1-benzoyl-2,5-dihydropyrrole
CS(=O)(=O)Cl
methanesulphonyl chloride
N
ammonia
CS[C@@H]1CN(C(=O)c2ccccc2)C[C@H]1N
1-Benzoyl-trans-3-amino-4-methylthio-pyrrolidine

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONare added dropwise at 0° C
  2. 2
    Temperaturathe mixture is heated at 80° C. in an autoclave for 10 hours
  3. 3
    Extracciónthe mixture is extracted with methylene chloride
  4. 4
    Secadothe extract is dried over sodium sulphate
  5. 5
    Concentraciónconcentrated
  6. 6
    OtroThe crude product (50 g) is chromatographed on silica gel (mobile phase initially ethanol:ethyl acetate 1:3

Procedimiento

41.5 g (0.24 mol) of 1-benzoyl-2,5-dihydropyrrole are initially introduced into 240 ml of methylene chloride, and 24.8 g (0.3 mol) of methanesulphonyl chloride are added dropwise at 0° C. The mixture is subsequently stirred at room temperature for 16 hours, the solvent is then stripped off under 8 mbar and the residue is taken up in 240 ml of tetrahydrofuran. After addition of 65 g of 25% strength ammonia solution, the mixture is heated at 80° C. in an autoclave for 10 hours. It is then poured into 5 times the amount of water, the pH is brought to 10-11 with sodium carbonate, the mixture is extracted with methylene chloride and the extract is dried over sodium sulphate and concentrated. The crude product (50 g) is chromatographed on silica gel (mobile phase initially ethanol:ethyl acetate 1:3, then ethanol; Rf value: 0.34 ethanol).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723627uspto-grants-1998_03