Reacción #3277

ord-bfb87e53646f4c08bf6331ebf2a578a0

Ecuación de reacción

O=C(OO)c1cccc(Cl)c1
m-chloroperbenzoic acid
CSc1ncc2cc(-c3c(Cl)cccc3Cl)c(=O)n(C)c2n1
6-(2,6-dichlorophenyl)-8-methyl-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-one
CSc1ncc2cc(-c3c(Cl)cccc3Cl)c(=O)n(C)c2n1
6-(2,6-Dichlorophenyl)-8-methyl-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-one
CS(C)=O
dimethylsulfoxide
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

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.WAITAfter 15 minutes
  2. 2
    Lavadothe chloroform solution was washed with 30 mL of saturated sodium bicarbonate
  3. 3
    SecadoThe separated organic layer was dried over sodium sulfate
  4. 4
    Filtraciónfiltered
  5. 5
    Concentraciónconcentrated to ca. 5 mL volume
  6. 6
    OtroCrystals separated
  7. 7
    workup.ADDITIONAdded ca. 5 mL of petroleum ether
  8. 8
    Filtraciónfiltered

Procedimiento

A quantity of 0.346 g (1.00 mmol) of 50% to 60% m-chloroperbenzoic acid (assuming 50% peracid was present) was added at 25° C. to a stirred solution of 0.165 g (0.47 mmol) of 6-(2,6-dichlorophenyl)-8-methyl-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-one of Example 37 in 15 mL of chloroform, and the solution was stirred overnight. A quantity of 0.25 g (3.20 mmol) of dimethylsulfoxide was added to reduce any excess peracid. After 15 minutes, the chloroform solution was washed with 30 mL of saturated sodium bicarbonate and then with water. The separated organic layer was dried over sodium sulfate, filtered, and concentrated to ca. 5 mL volume. Crystals separated. Added ca. 5 mL of petroleum ether and filtered; wt 0.165 g (92%); mp >290° C.

Fuente

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