Reacción #10879

ord-66c9ae911dbb4a32a0ac6929b789a6cc

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONAfter the addition
  2. 2
    Otrothe cooling bath was removed
  3. 3
    workup.ADDITIONThe mixture was poured into ice-water (1 L)
  4. 4
    workup.STIRRINGstirred for 30 minutes
  5. 5
    Extracciónextracted with diethyl ether
  6. 6
    SecadoThe combined extracts were dried over Na2SO4
  7. 7
    Otroevaporated in vacuo

Procedimiento

A solution of 4-(4-aminophenyl)-1-piperazinecarboxylic acid, 1,1-dimethylethyl ester (15 g, 54.1 mmol) (from Step B above) in N,N-dimethylformamide (120 mL) was added dropwise to a cooled (−15° C.) solution of 1,1′-thiocarbonyldiimidazole (9.66 g, 54.2 mmol) (Aldrich) in N,N-dimethylformamide (40 mL). After the addition was complete, the cooling bath was removed and the solution was stirred for 1 h. The mixture was poured into ice-water (1 L), stirred for 30 minutes, and extracted with diethyl ether. The combined extracts were dried over Na2SO4, and evaporated in vacuo to provide 4-(4-isothio-cyanatophenyl)-1-piperazinecarboxylic acid, 1,1-dimethylethyl ester (18 g, 94%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07094896B2uspto-grants-2006_08