Reacción #3289
ord-0aaab490559345e3a5659881e04302db
Ecuación de reacción
6-(2,6-dichlorophenyl)-2-methanesulfonyl-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one
6-(2,6-Dichlorophenyl)-2-methanesulfonyl-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one
aniline
→
6-(2,6-Dichlorophenyl)-8-methyl-2-phenylamino-8H-pyrido[2,3-d]pyrimidin-7-one
Reactantes
Reactivos
Ninguno
Condiciones de reacción
Temperatura
184°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1OtroMost of the excess aniline was evaporated at reduced pressure
- 2workup.DISSOLUTIONThe remaining gum was dissolved in 1.0 mL of ethyl acetate
- 3OtroFurther purification
- 4Otroto remove dark colors
- 5Lavadoeluting with chloroform
- 6Otro50% hexane-ethyl acetate to obtain pure crystalline product
Procedimiento
A solution of 0.113 g (0.29 mmol) of 6-(2,6-dichlorophenyl)-2-methanesulfonyl-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one of Example 39 in 1.00 g (10.70 mmol) of aniline was maintained at reflux (184° C.) for 3 minutes. Most of the excess aniline was evaporated at reduced pressure. The remaining gum was dissolved in 1.0 mL of ethyl acetate. Crystals developed on inducement; wt 0.088 g. Further purification to remove dark colors was effected by silica gel chromatography, eluting with chloroform and then 50% hexane-ethyl acetate to obtain pure crystalline product; wt 0.046 g; mp 247°-249° C.