Реакция #7872

ord-640654338223404497e09faf1387ac75

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    КонцентрированиеThe mixture was concentrated in vacuo
  2. 2
    Другоеthe residue partitioned between EtOAc and H2O
  3. 3
    Другоеthe layers separated
  4. 4
    Экстракцияextracted with EtOAc
  5. 5
    ПромывкаThe combined organic layers were washed with saturated NaHCO3 and brine
  6. 6
    Сушкаdried over MgSO4
  7. 7
    Фильтрацияfiltered
  8. 8
    Концентрированиеconcentrated 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).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07087601B2uspto-grants-2006_08