反应详情

Triethylamine (45 mL, 0.32 mmol) was added to a solution of N-(3,5-dimethylphenyl)-2-thioxo-1,2-dihydropyridine-3-carboxamide (28 mg, 0.11 mmol, Reference Compound No. 13-1) and 2-acetylamino-4-(chloromethyl)pyrimidine (18 mg, 0.10 mmol, Reference Compound No. 11-1) in anhydrous N,N-dimethylformamide (1.0 mL) at room temperature, and the mixture was stirred for 16 hours. Ethyl acetate (30 mL) was added thereto, then the whole was washed with saturated aqueous sodium hydrogencarbonate solution (30 mL) and brine (30 mL), and the organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and then the precipitated solid was filtered off with diethyl ether and washed. The solid was dried at 50° C. under reduced pressure to give 21 mg of the target compound as a light orange solid (Yield: 52%).

1. washthe whole was washed with saturated aqueous sodium hydrogencarbonate solution (30 mL) and brine (30 mL)
2. dry with materialthe organic layer was dried over anhydrous magnesium sulfate
3. customThe solvent was evaporated under reduced pressure
4. filtrationthe precipitated solid was filtered off with diethyl ether
5. washwashed
6. customThe solid was dried at 50° C. under reduced pressure