Реакция #4776
ord-8bcae92e09434b79989104d97d819e5f
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Условия реакции
Обработка
- 1Температураwas refluxed for 2 hours
- 2ДругоеAfter evaporating the solvent
- 3workup.DISSOLUTIONthe residue was dissolved in a suspension of water (200 ml) and chloroform (200 ml)
- 4ПромывкаThe separated organic layer was washed with saturated aqueous sodium chloride
- 5Сушкаdried over magnesium sulfate
- 6workup.ADDITIONTo this solution was added activated manganese dioxide (120 g)
- 7Температураthe mixture was refluxed for 1 hour
- 8Фильтрацияmanganese dioxide was filtered off
- 9ДругоеThe filtrate was evaporated in vacuo
- 10Промывкаeluting with chloroform
- 11workup.ADDITIONThe fractions containing the object compound
- 12Концентрированиеconcentrated under reduced pressure
- 13ДругоеThe crystals were recrystallized from diethyl ether
Методика
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.