反应详情

A mixture of 2-{[(3,5-dichloropyridin-4-yl)methyl]sulfanyl}-6-methylpyrimidin-4-amine (500 mg, 1.7 mmol) in acetic anhydride (10 mL) was stirred at reflux overnight. After cooling to room temperature, the mixture was neutralized slowly with a saturated solution of NaHCO3 (aq.) until pH 7-8 was reached. The mixture was extracted with ethyl acetate (2×25 mL) The organic extracts were combined, dried over MgSO4, filtered, evaporated, and dried in vacuo. The crude product was purified by flash chromatography (0-3% MeOH/CH2Cl2), affording the title compound (136 mg, 23% yield); 1H NMR (400 MHz, DMSO-d6): δ 2.11 (s, 3H), 2.51 (s, 3H), 4.70 (s, 2H), 7.70 (s, 1H), 8.67 (s, 2H), 10.87 (s (br), 1H); M+287.

1. temperatureat reflux overnight
2. extractionThe mixture was extracted with ethyl acetate (2×25 mL) The organic extracts
3. dry with materialdried over MgSO4
4. filtrationfiltered
5. customevaporated
6. customdried in vacuo
7. customThe crude product was purified by flash chromatography (0-3% MeOH/CH2Cl2)