反应详情

To a solution of 4-isopropyl-N-[6-(1-propionyl-azetidin-3-yl)-pyridin-3-yl]-benzenesulfonamide (150 mg, 0.38 mmol) in THF (15 ml) was added dropwise 1M BH3. THF (3.8 ml) and the mixture was stirred at room temperature for 12 h. It was then quenched by careful addition of 1N aqueous HCl (10 ml) and the resulting solution was heated at reflux for 4 h. The solution was next cooled to room temperature, adjusted to pH˜8 with 2 N NaOH solution and diluted with CH2Cl2. Separation of the layers, drying (Na2SO4) of the organic phase, filtration and evaporation in vacuo provided the crude material, which was purified by flash column chromatography (CH2Cl2:methanol, 95:5) to give the title compound (95 mg, 66%) as a light yellow oil.

1. customIt was then quenched by careful addition of 1N aqueous HCl (10 ml)
2. temperaturethe resulting solution was heated
3. temperatureat reflux for 4 h
4. additiondiluted with CH2Cl2
5. customSeparation of the layers
6. customdrying
7. filtration(Na2SO4) of the organic phase, filtration and evaporation in vacuo
8. customprovided the crude material, which
9. customwas purified by flash column chromatography (CH2Cl2:methanol, 95:5)