反应详情

A solution of N-Boc-azetidin-3-ol (500 mg, 2.89 mmol) in THF (10 mL) was cooled to 0° C. t-BuOK (1M in THF, 11.6 mL) was added dropwise and the reaction mixture was stirred at room temperature for 0.25 h then cooled to 0° C. A solution of 4-bromomethylpyridine hydrobromide (2.19 g, 8.67 mmol) in dichloromethane (5 mL) stirred with DIPEA (4 mL, 24 mmol) for 0.5 h was then added. The reaction mixture was stirred at room temperature for 24 h. The reaction mixture was diluted with H2O and extracted twice with EtOAc. The organics were separated from the aqueous layer and combined, dried over Na2SO4 and concentrated to dryness. The crude mixture was purified by column chromatography (eluent: Pentane/EtOAc, 1/1 to 7/3) to give the title product (313 mg, 41%) as a yellow oil.

1. additionwas added dropwise
2. temperaturethen cooled to 0° C
3. additionwas then added
4. stirringThe reaction mixture was stirred at room temperature for 24 h
5. extractionextracted twice with EtOAc
6. customThe organics were separated from the aqueous layer
7. dry with materialdried over Na2SO4
8. concentrationconcentrated to dryness
9. customThe crude mixture was purified by column chromatography (eluent: Pentane/EtOAc, 1/1 to 7/3)