Reacción #3300
ord-68d8ae5623a045faa4752c54188d8074
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Temperaturaat reflux for 10 minutes
- 2OtroCrystals separated on inducement
- 3workup.ADDITIONAn additional 3 drops of water were added
- 4Otroto precipitate additional tacky solid
- 5OtroAfter decantation, the solid was triturated with 0.5 mL of ethyl acetate and 0.5 mL of petroleum ether
- 6FiltraciónThe solids were filtered
- 7Lavadowashed with 50% ethyl acetate/petroleum ether
- 8Otrodried
- 9OtroPurification
- 10Filtraciónby filtering an ethyl acetate solution through a layer of silica gel
- 11OtroConcentration of the filtrate to 1 mL volume yielded pure crystalline product
Procedimiento
A solution of 0.100 g (0.25 mmol) of 6-(2,6-dichlorophenyl)-8-ethyl-2-methanesulfonyl-8H-pyrido[2,3-d]pyrimidin-7-one of Example 68 and 0.061 g (0.50 mmol) of 4-methoxyaniline in 0.5 mL of dimethylformamide was heated at reflux for 10 minutes. Three drops of water were added. Crystals separated on inducement. An additional 3 drops of water were added to precipitate additional tacky solid. After decantation, the solid was triturated with 0.5 mL of ethyl acetate and 0.5 mL of petroleum ether. The solids were filtered and washed with 50% ethyl acetate/petroleum ether and dried; wt 0.080 g. Purification was effected by filtering an ethyl acetate solution through a layer of silica gel. Concentration of the filtrate to 1 mL volume yielded pure crystalline product; wt 0.033 g; mp 213°-215° C.