Reacción #929003

ord-e6c828d862e4476782f31f0d022f92cb

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Lavadothe organic phase washed sequentially with water, and brine
  2. 2
    Secadodried over anhydrous magnesium sulfate
  3. 3
    Filtraciónfiltered
  4. 4
    Concentraciónconcentrated under vacuum

Procedimiento

7-[(4′-Trifluoromethyl-biphenyl-2-carbonyl)-amino]-quinoline-3-carboxylic acid (50 mg, 0.11 mmol) was combined with diethylamine hydrochloride (15 mg, 0.14 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (26 mg, 0.14 mmol), 1-hydroxybenzotriazole (17 mg, 0.13 mmol), and triethylamine (0.064 ml, 0.46 mmol) in 1 ml of dichloromethane. After stirring overnight at ambient temperature, the reaction mixture was diluted with 30 ml of ethyl acetate, and the organic phase washed sequentially with water, and brine, and then dried over anhydrous magnesium sulfate, filtered and concentrated under vacuum to afford 46 mg of the title compound as a yellow solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06369075B1uspto-grants-2002_04