반응 #42823
ord-2ad59e5f749d454e82d839a242595785
반응 방정식
반응물
시약
반응 조건
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 3 ml of acetonitrile were added 0.30 g of 4-(2-butynyloxy)-6-chloropyrimidine, 0.68 g of potassium carbonate and 0.33 g of 3,4-dimethylpyrrolidine hydrochloride (cis and trans diastereomer mixture), 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 0.42 g of 4-(2-butynyloxy)-6-(3,4-dimethylpyrrolidin-1-yl) pyrimidine (hereinafter, referred to as Compound (37)).