Reaktion #4776
ord-8bcae92e09434b79989104d97d819e5f
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturwas refluxed for 2 hours
- 2SonstigeAfter evaporating the solvent
- 3workup.DISSOLUTIONthe residue was dissolved in a suspension of water (200 ml) and chloroform (200 ml)
- 4WaschenThe separated organic layer was washed with saturated aqueous sodium chloride
- 5Trocknendried over magnesium sulfate
- 6workup.ADDITIONTo this solution was added activated manganese dioxide (120 g)
- 7Temperaturthe mixture was refluxed for 1 hour
- 8Filtrationmanganese dioxide was filtered off
- 9SonstigeThe filtrate was evaporated in vacuo
- 10Wascheneluting with chloroform
- 11workup.ADDITIONThe fractions containing the object compound
- 12Einengenconcentrated under reduced pressure
- 13SonstigeThe crystals were recrystallized from diethyl ether
Vorschrift
A mixture of 2-(4-methylpiperazin-1-ylcarbonyl)-1-(3-nitrophenyl)-1-buten-3-one (20 g), benzamidine hydrochloride (9.9 g) and triethylamine (11.4 ml) in n-butanol (200 ml) was refluxed for 2 hours. After evaporating the solvent, the residue was dissolved in a suspension of water (200 ml) and chloroform (200 ml). The separated organic layer was washed with saturated aqueous sodium chloride and dried over magnesium sulfate. To this solution was added activated manganese dioxide (120 g) and the mixture was refluxed for 1 hour with stirring vigorously. After cooling to a room temperature, manganese dioxide was filtered off. The filtrate was evaporated in vacuo, and the residue was subjected to column chromatography on alumina (200 g) eluting with chloroform. The fractions containing the object compound were combined and concentrated under reduced pressure. The crystals were recrystallized from diethyl ether to give 6-methyl-5-(4-methylpiperazin-1-ylcarbonyl)-4-(3-nitrophenyl)-2-phenylpyrimidine.