Reacción #48600
ord-abb1c6f593064b278921ff370239f3b1
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Otrothen evaporated under reduced pressure
- 2OtroThe residue was partitioned between ethyl acetate and brine
- 3Otrothe ethyl acetate layer was separated
- 4Secadodried (MgSO4)
- 5Filtraciónfiltered
- 6Otroevaporated
- 7OtroThe crude material was purified by flash column chromatography
- 8Lavadoeluting with 1:3 ethyl acetate/hexane
- 9workup.ADDITIONthe product containing fractions
- 10Otroevaporated
Procedimiento
A solution of 4-iodo-1H-pyrazole-3-carboxylic acid phenylamide (670 mg; 2.14 mmol) in acetonitrile (10 ml) was treated with potassium carbonate (360 mg; 2.57 mmol)) followed by 4-methoxybenzyl chloride (320 μl; 2.35 mmol). The mixture was stirred at room temperature overnight then evaporated under reduced pressure. The residue was partitioned between ethyl acetate and brine; the ethyl acetate layer was separated, dried (MgSO4), filtered and evaporated. The crude material was purified by flash column chromatography eluting with 1:3 ethyl acetate/hexane and the product containing fractions combined and evaporated to give 660 mg of 4-iodo-1-(4-methoxy-benzyl)-1H-pyrazole-3-carboxylic acid phenylamide.