Реакция #7872
ord-640654338223404497e09faf1387ac75
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1КонцентрированиеThe mixture was concentrated in vacuo
- 2Другоеthe residue partitioned between EtOAc and H2O
- 3Другоеthe layers separated
- 4Экстракцияextracted with EtOAc
- 5ПромывкаThe combined organic layers were washed with saturated NaHCO3 and brine
- 6Сушкаdried over MgSO4
- 7Фильтрацияfiltered
- 8Концентрированиеconcentrated in vacuo
Методика
To a stirred solution of 3-aminopyridine (9.41 g, 100 mmol) and triethylamine (16.7 mL, 120 mmol) in CH2Cl2 (300 mL) at 0° C. was added trimethylacetyl chloride (14.8 mL, 120 mmol) dropwise over 15 min. The reaction was warmed to rt and stirred overnight. The mixture was concentrated in vacuo, the residue partitioned between EtOAc and H2O, and the layers separated. The aqueous layer was made basic with saturated NaHCO3 and extracted with EtOAc. The combined organic layers were washed with saturated NaHCO3 and brine, dried over MgSO4, filtered, and concentrated in vacuo to give N-(pyridin-3-yl)-2,2-dimethylpropanamide as a tan solid. 1H NMR (CDCl3, 300 MHz) δ 8.57 (d, 1H), 8.33 (dd, 1H), 8.17 (ddd, 1H), 7.69 (br s, 1H), 7.27 (dd, 1H), 1.33 (s, 9H).