반응 #1095887
ord-46697b3d13954b728fae4507e6014bad
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후처리
- 1온도The reaction mixture was cooled to near room temperature
- 2추출the mixture was extracted with tert-butyl methyl ether three times
- 3세척The organic layers were washed with a saturated sodium chloride aqueous solution
- 4건조dried over anhydrous magnesium sulfate
- 5농축concentrated
실험 절차
Into 2 ml of acetonitrile were added 0.20 g of 4-(2-butynyloxy)-6-chloro-5-fluoropyrimidine, 0.54 g of potassium carbonate and 0.30 g of 3,3,5,5-tetramethylpiperidine hydrochloride, and the mixture was stirred for 4 hours at 70° C. The reaction mixture was cooled to near room temperature, a saturated ammonium chloride aqueous solution was added therein, and the mixture was extracted with tert-butyl methyl ether three times. The organic layers were washed with a saturated sodium chloride aqueous solution, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.22 g of 4-(2-butynyloxy)-5-fluoro-6-(3,3,5,5-tetramethylpiperidino)pyrimidine (hereinafter, referred to as Compound (39)).