Reacción #452033
ord-78f83968b276484e84174936b7abbb93
Ecuación de reacción
trimethylaluminum
2-(1-methyl-1H-pyrazol-4-yl)benzenesulfonamide
methyl (4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamate
→
title compound
Rendimiento 17.6%
N-[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-(1-methyl-1H-pyrazol-4-yl)benzenesulfonamide
Rendimiento 17.6%
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1OtroAfter work up and evaporation of the methylene chloride solvent
- 2Otrothe residue was triturated with ethyl acetate
Procedimiento
By the procedure of Example 14, 2 g of 2-(1-methyl-1H-pyrazol-4-yl)benzenesulfonamide, prepared in Example 19, was reacted in 100 ml of methylene chloride with 0.7 g of trimethylaluminum (5 ml of 2M toluene solution) followed by 1.7 g of methyl (4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamate. After work up and evaporation of the methylene chloride solvent, the residue was triturated with ethyl acetate to yield 0.6 g of the title compound; m.p. 221°-224° C. The IR spectrum showed a carbonyl absorption at 1700 cm-1 indicative for a sulfonylurea.