Reacción #43407

ord-186390d6ffe74cdbb70148554e5003f6

Condiciones de reacción

Temperatura
100°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónthen extracted with ethyl acetate (3×500 ml)
  2. 2
    SecadoThe combined organic extracts were dried over magnesium sulphate
  3. 3
    Otroevaporated
  4. 4
    OtroThe residue was chromatographed
  5. 5
    Lavadoeluting with 0-40% dichloromethane in petrol affording the product as a white solid (36.35 g, 83%)

Procedimiento

A mixture of 2-chloro-5-fluoro-6-(methyloxy)-3-pyridinecarboxylic acid (32.65 g, 159 mmol) in toluene/triethylamine/tert-butanol (300 ml/26.4 ml/75 ml) was treated with diphenylphosphoryl azide (37.7 ml, 174.8 mmol) and heated to 100° C. for 2 hours. The mixture was treated with saturated aqueous sodium bicarbonate solution (500 ml) then extracted with ethyl acetate (3×500 ml). The combined organic extracts were dried over magnesium sulphate and evaporated. The residue was chromatographed eluting with 0-40% dichloromethane in petrol affording the product as a white solid (36.35 g, 83%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07732460B2uspto-grants-2010_06