Reacción #40421

ord-78423b0ee2724e0eb24f94e6674e11e0

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónAfter concentration
  2. 2
    workup.DISSOLUTIONthe residue was dissolved in dichloromethane (5 ml)
  3. 3
    FiltraciónThe precipitate was filtered
  4. 4
    Lavadowashed with a little amount of dichloromethane

Procedimiento

A solution of 2-fluoro-4-cyanobenzoic acid (1 g, 6.06 mmol) in thionyl chloride (5 ml) was refluxed for 2 hr. After concentration, the residue was dissolved in dichloromethane (5 ml). And a solution of the compound of (2-amino-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamide (1.2 g, 4.25 mmol) in dichloromethane (10 ml) and pyridine (1.47 ml, 18.18 mmol) were added. The mixture was stirred at r.t. overnight. The precipitate was filtered and washed with a little amount of dichloromethane to give N-{4-chloro-2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}(2-fluoro-4-cyanophenyl)carboxamide (2.03 g, 78%). MS found for C20H11Cl2FN4O2 M+=429, (M+2)+=431.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07727982B2uspto-grants-2010_06