Реакция #48424

Уравнение реакции

Sodium hydride

tert-butyl (3R,6S)-6-(2,3-difluorophenyl)-2-oxoazepan-3-ylcarbamate

2-bromomethylpyridine

→

title compound

Выход 99.6%

tert-Butyl (3R,6S)-6-(2,3-difluorophenyl)-2-oxo-1-(pyridin-2-ylmethyl)azepan-3-ylcarbamate

Выход 99.6%

Растворители

N,N-dimethylformamide

Условия реакции

Обработка

1. 1
   workup.WAITAfter 1 h
2. 2
   Другоеthe reaction was quenched with water
3. 3
   Экстракцияthe mixture was extracted with ethyl acetate
4. 4
   ПромывкаThe organic layer was washed with water (2×), saturated brine
5. 5
   Сушкаdried over magnesium sulfate
6. 6
   Фильтрацияfiltered
7. 7
   Концентрированиеconcentrated

Методика

Sodium hydride (60% dispersion in mineral oil; 30 mg, 1.175 mmol) was added to a solution of tert-butyl (3R,6S)-6-(2,3-difluorophenyl)-2-oxoazepan-3-ylcarbamate (160 mg, 0.470 mmol) in N,N-dimethylformamide (6 mL) at 0° C. After 30 min, 2-bromomethylpyridine (0.125 mg, 0.494 mmol) was added. After 1 h, the reaction was quenched with water and the mixture was extracted with ethyl acetate. The organic layer was washed with water (2×), saturated brine, dried over magnesium sulfate, filtered and concentrated to give the title compound (202 mg). MS 432.2 (M+1).

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