Reacción #3300

ord-68d8ae5623a045faa4752c54188d8074

Ecuación de reacción

CCn1c(=O)c(-c2c(Cl)cccc2Cl)cc2cnc(S(C)(=O)=O)nc21
6-(2,6-dichlorophenyl)-8-ethyl-2-methanesulfonyl-8H-pyrido[2,3-d]pyrimidin-7-one
CCn1c(=O)c(-c2c(Cl)cccc2Cl)cc2cnc(S(C)(=O)=O)nc21
6-(2,6-Dichlorophenyl)-8-ethyl-2-methanesulfonyl-8H-pyrido[2,3-d]pyrimidin-7-one
COc1ccc(N)cc1
4-methoxyaniline
CCn1c(=O)c(-c2c(Cl)cccc2Cl)cc2cnc(Nc3ccc(OC)cc3)nc21
6-(2,6-Dichlorophenyl)-8-ethyl-2-(4-methoxyphenylamino)-8H-pyrido[2,3-d]pyrimidin-7-one

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaat reflux for 10 minutes
  2. 2
    OtroCrystals separated on inducement
  3. 3
    workup.ADDITIONAn additional 3 drops of water were added
  4. 4
    Otroto precipitate additional tacky solid
  5. 5
    OtroAfter decantation, the solid was triturated with 0.5 mL of ethyl acetate and 0.5 mL of petroleum ether
  6. 6
    FiltraciónThe solids were filtered
  7. 7
    Lavadowashed with 50% ethyl acetate/petroleum ether
  8. 8
    Otrodried
  9. 9
    OtroPurification
  10. 10
    Filtraciónby filtering an ethyl acetate solution through a layer of silica gel
  11. 11
    OtroConcentration 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.

Fuente

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