Реакция #42846
ord-cfcbc0ba66804e69949d8072ec909492
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1workup.STIRRINGstirred for 4 hours
- 2Экстракцияthe mixture was extracted with tert-butyl methyl ether three times
- 3ПромывкаThe organic layers were washed with water
- 4Сушкаdried over anhydrous magnesium sulfate
- 5Концентрированиеconcentrated
Методика
0.07 g of sodium hydride (60% oil suspension) was suspended in 3 ml of tetrahydrofuran. 1 ml of tetrahydrofuran solution of 0.14 g of 2-ethylpiperidine was added dropwise at room temperature therein slowly, and the mixture was stirred for 10 minutes. Into the mixture was added dropwise 1 ml of tetrahydrofuran solution of 0.2 g of 4,6-dichloro-5-fluoropyrimidine at room temperature, and stirred for 4 hours. The reaction mixture was poured into a saturated ammonium chloride aqueous solution, and the mixture was extracted with tert-butyl methyl ether three times. The organic layers were washed with water, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.22 g of 4-chloro-6-(2-ethylpiperidino)-5-fluoropyrimidine.