Reacción #3289

ord-0aaab490559345e3a5659881e04302db

Ecuación de reacción

Cn1c(=O)c(-c2c(Cl)cccc2Cl)cc2cnc(S(C)(=O)=O)nc21
6-(2,6-dichlorophenyl)-2-methanesulfonyl-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one
Cn1c(=O)c(-c2c(Cl)cccc2Cl)cc2cnc(S(C)(=O)=O)nc21
6-(2,6-Dichlorophenyl)-2-methanesulfonyl-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one
Nc1ccccc1
aniline
Cn1c(=O)c(-c2c(Cl)cccc2Cl)cc2cnc(Nc3ccccc3)nc21
6-(2,6-Dichlorophenyl)-8-methyl-2-phenylamino-8H-pyrido[2,3-d]pyrimidin-7-one

Condiciones de reacción

Temperatura
184°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroMost of the excess aniline was evaporated at reduced pressure
  2. 2
    workup.DISSOLUTIONThe remaining gum was dissolved in 1.0 mL of ethyl acetate
  3. 3
    OtroFurther purification
  4. 4
    Otroto remove dark colors
  5. 5
    Lavadoeluting with chloroform
  6. 6
    Otro50% 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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05733914uspto-grants-1998_03