Réaction #3328
ord-d68719fd07424782a508df3f799b02af
Équation de réaction
Réactifs
Réactifs
Conditions de réaction
Traitement
- 1TempératureThe mixture was heated to 70° C.
- 2Températurecooled to room temperature
- 3Autrethe resulting precipitate was removed by filtration
- 4Lavagewashed with water
- 5LavageThis solid was washed with 10% methanol in ethyl acetate
- 6Autreto provide 96 mg of crude product
- 7ConcentrationThe filtrate was concentrated
- 8Autreto provide an additional 77 mg of crude product
- 9AutreAn analytical sample was obtained by purification by flash chromatography
- 10Lavageeluting 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.