反应详情

To a solution of 2,4,6-trichloropyrimidine-5-carboxylic acid (5.69 g, 25.02 mmol) in DMF (60 mL) was added Et3N (8 mL, 57.4 mmol) and m-toluidine (3.2 mL, 29.5 mmol) at 0° C. The mixture was stirred at RT for 12 h. To the mixture was added 1N HCl. The mixture was extracted with EtOAc. The organic layers were basified with saturated aq NaHCO3 and the aqueous layers were washed with EtOAc. The washed aqueous layer was acidified with 1N HCl and extracted with EtOAc. The combined organic layers were washed with 1N HCl, water, and brine, were dried over anhydrous Na2SO4, and then filtered. The filtrate was concentrated under reduced pressure, triturated with hexane, and filtered to give a first batch of the title compound (4.36 g). The filtrate was concentrated, triturated with hexane, and filtered to give a second batch (0.36 g) of the title compound (total 4.72 g, 63%). 1H NMR (500 MHz, DMSO-d6) δ ppm 2.30 (s, 3H), 7.00-7.02 (m, 1H), 7.25-7.28 (m, 2H), 7.33-7.35 (m, 2H), 10.13 (s, 1H), 1H not detected. [M+H] calc'd for C12H10Cl2N3O2, 298; found, 298.

1. extractionThe mixture was extracted with EtOAc
2. washthe aqueous layers were washed with EtOAc
3. extractionextracted with EtOAc
4. washThe combined organic layers were washed with 1N HCl, water, and brine
5. dry with materialwere dried over anhydrous Na2SO4
6. filtrationfiltered
7. concentrationThe filtrate was concentrated under reduced pressure
8. customtriturated with hexane
9. filtrationfiltered