Réaction #1095908
ord-06070ca4325c40d0b0e2298465a0c6df
Équation de réaction
Réactifs
Conditions de réaction
Traitement
- 1workup.STIRRINGstirred for 4 hours
- 2Extractionthe mixture was extracted with tert-butyl methyl ether three times
- 3LavageThe organic layers were washed with water
- 4Séchagedried over anhydrous magnesium sulfate
- 5Concentrationconcentrated
Mode opératoire
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.