Reacción #3295

ord-2385e0240fd44243a34f8caa93efa84f

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
COc1ccc(N)cc1
4-methoxyaniline
COc1ccc(Nc2ncc3cc(-c4c(Cl)cccc4Cl)c(=O)n(C)c3n2)cc1
6-(2,6-Dichlorophenyl)-2-(4-methoxyphenylamino)-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one

Condiciones de reacción

Temperatura
180°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawas heated
  2. 2
    TemperaturaThe resulting solution was heated for 10 minutes
  3. 3
    OtroMuch of the excess aniline was evaporated at reduced pressure
  4. 4
    workup.DISSOLUTIONThe remainder was dissolved in 2 mL of ethyl acetate
  5. 5
    OtroThe crystals that separated from the dark solution
  6. 6
    Filtraciónwere filtered
  7. 7
    Lavadowashed with 2 mL of ethyl acetate, wt 0.102 g

Procedimiento

A mixture 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 and 0.50 g (4.10 mmol) of 4-methoxyaniline was heated, with stirring, in a 180° C. oil bath. The resulting solution was heated for 10 minutes. Much of the excess aniline was evaporated at reduced pressure. The remainder was dissolved in 2 mL of ethyl acetate. The crystals that separated from the dark solution were filtered and washed with 2 mL of ethyl acetate, wt 0.102 g.

Fuente

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