反应详情

To a solution of 4,6-dimethyl-2-aminopyridine (7, 12.2 g, 100 mmol) in toluene (100 mL) was added acetonylacetone (12.3 mL, 105 mmol) and p-TsOH (190 mg, 1.0 mmol). The reaction mixture was heated in a Dean-Stark apparatus under reflux for 6 h. After cooling to room temperature, the mixture was concentrated with a rotary evaporator, and the resulting brown oil was purified by flash column chromatography (EtOAc/hexanes, 1:19-1:9) to give 8 (18.2 g, 91 mmol, 91%) as a pale yellow solid: 1H NMR (500 MHz, CDCl3) δ 2.13 (s, 6H), 2.40 (s, 3H), 2.56 (s, 3H), 5.88 (s, 2H), 6.85 (s, 1H), 7.00 (s, 1H); 13C NMR (125 MHz, CDCl3) δ 13.4, 21.2, 24.4, 106.8, 119.9, 123.1, 128.6, 149.6, 151.7, 158.4; LCQ-MS (M+H+) calcd for C13H17N2 201. found 201; LC-TOF-MS (M+H+) calcd for C13H17N2 201.13917. found 201.13881.

1. temperatureThe reaction mixture was heated in a Dean-Stark apparatus
2. temperatureunder reflux for 6 h
3. concentrationthe mixture was concentrated with a rotary evaporator
4. customthe resulting brown oil was purified by flash column chromatography (EtOAc/hexanes, 1:19-1:9)