Reacción #326770

ord-af02630388c54004994bcd5295e4de7c

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe reaction mixture was quenched with water (5 mL)
  2. 2
    Extracciónextracted with EtOAc (3×)
  3. 3
    OtroThe extract was dried
  4. 4
    Filtraciónfiltered
  5. 5
    Concentraciónconcentrated
  6. 6
    OtroThe residue was purified

Procedimiento

To a solution of 1,1-dimethylethyl 4-[4-(3-amino-2-fluorophenyl)-5-(2-chloro-4-pyrimidinyl)-1,3-thiazol-2-yl]-4-methyl-1-piperidinecarboxylate (280 mg, 0.556 mmol) in pyridine (3 mL) was added 3-furansulfonyl chloride (139 mg, 0.833 mmol), and the reaction mixture was stirred for 3 h. The reaction mixture was quenched with water (5 mL) and extracted with EtOAc (3×). The extract was dried, filtered and concentrated. The residue was purified using column chromatography (40 to 100% EtOAc/hexane) to the title compound (310 mg). MS (ESI): 634.1 [M+1]+.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08642759B2uspto-grants-2014_02