Reacción #43407
ord-186390d6ffe74cdbb70148554e5003f6
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Condiciones de reacción
Temperatura
100°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Extracciónthen extracted with ethyl acetate (3×500 ml)
- 2SecadoThe combined organic extracts were dried over magnesium sulphate
- 3Otroevaporated
- 4OtroThe residue was chromatographed
- 5Lavadoeluting 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%).