Reacción #4873

ord-c1ad53f92a1a465b9cea596d9c8433a5

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGthe mixture is stirred at room temperature for 5 hours
  2. 2
    Otrocrystalline precipitates
  3. 3
    Filtraciónare collected by filtration
  4. 4
    workup.DISSOLUTIONThe crystals are dissolved in ethyl acetate
  5. 5
    Lavadothe solution is washed with water
  6. 6
    Otrodried
  7. 7
    ConcentraciónThe solution is concentrated under reduced pressure
  8. 8
    Otroto remove solvent
  9. 9
    OtroThen, the residue is crystallized with isopropyl ether
  10. 10
    Filtracióncollected by filtration

Procedimiento

2.7 g of ethyl (Z)-2-(2-tritylaminothiazol-4-yl)-2-hydroxyiminoacetate are dissolved in 12 ml of dimethylsulfoxide, and 1.0 g of anhydrous potassium carbonate is added thereto under nitrogen gas atmosphere. The mixture is stirred at room temperature for 10 minutes. 1.2 g of 1-methyl-3-bromo-2-pyrrolidone are added to the mixture, and the mixture is stirred at room temperature for 5 hours. The reaction mixture is poured into 100 ml of water, and crystalline precipitates are collected by filtration. The crystals are dissolved in ethyl acetate, and the solution is washed with water and then dried. The solution is concentrated under reduced pressure to remove solvent. Then, the residue is crystallized with isopropyl ether and collected by filtration. 2.1 g of ethyl (Z)-2-(2-tritylaminothiazol-4-yl)-2-[(1-methyl-2-pyrrolidon-3-yl)oxyimino]acetate are obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04727071uspto-grants-1988_02