Réaction #3328

ord-d68719fd07424782a508df3f799b02af

Conditions de réaction

Température
70°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe mixture was heated to 70° C.
  2. 2
    Températurecooled to room temperature
  3. 3
    Autrethe resulting precipitate was removed by filtration
  4. 4
    Lavagewashed with water
  5. 5
    LavageThis solid was washed with 10% methanol in ethyl acetate
  6. 6
    Autreto provide 96 mg of crude product
  7. 7
    ConcentrationThe filtrate was concentrated
  8. 8
    Autreto provide an additional 77 mg of crude product
  9. 9
    AutreAn analytical sample was obtained by purification by flash chromatography
  10. 10
    Lavageeluting with a gradient of ethyl acetate to 10% methanol in ethyl acetate

Mode opératoire

To a suspension of NaH (60% in mineral oil, 32 mg) in 6 mL of dimethylformamide was added 2-amino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-7(8H)-one (200 mg, 0.65 mmol) and the mixture heated to 70° C. In a second flask containing triethyl amine (220 μL, 1.59 mmol) in 4 mL of dimethylformamide was added 4-picolyl chloride hydrochloride (137 mg, 0.84 mmol). This dark red mixture was added to the above solution of the sodium salt of 2-amino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-7(8H)-one. The mixture was heated to 70° C., then cooled to room temperature. The mixture was poured into 20 mL of ice water, and the resulting precipitate was removed by filtration and washed with water. This solid was washed with 10% methanol in ethyl acetate to provide 96 mg of crude product. The filtrate was concentrated to provide an additional 77 mg of crude product. An analytical sample was obtained by purification by flash chromatography, eluting with a gradient of ethyl acetate to 10% methanol in ethyl acetate to provide 2-amino-6-(2,6-dichlorophenyl)-8-pyridin-4-ylmethyl-8H-pyrido[2,3-d]pyrimidin-7-one; mp 268°-270° C. dec.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05733914uspto-grants-1998_03