Reaktion #3300
ord-68d8ae5623a045faa4752c54188d8074
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturat reflux for 10 minutes
- 2SonstigeCrystals separated on inducement
- 3workup.ADDITIONAn additional 3 drops of water were added
- 4Sonstigeto precipitate additional tacky solid
- 5SonstigeAfter decantation, the solid was triturated with 0.5 mL of ethyl acetate and 0.5 mL of petroleum ether
- 6FiltrationThe solids were filtered
- 7Waschenwashed with 50% ethyl acetate/petroleum ether
- 8Sonstigedried
- 9SonstigePurification
- 10Filtrationby filtering an ethyl acetate solution through a layer of silica gel
- 11SonstigeConcentration of the filtrate to 1 mL volume yielded pure crystalline product
Vorschrift
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.