反应详情

温度

0 °C

A solution of 1-allyl-3-[3-cyclopentyl-2-(3,4-dichloro-phenyl)-propionyl]-urea (prepared in Example 12B-e, 132 mg, 0.36 mmol) in tetrahydrofuran (10 mL) cooled to 0° C. was treated with a 1M solution of borane-tetrahydrofuran (0.7 mL, 0.72 mmol). The reaction mixture was allowed to slowly warm from 0° C. to 25° C. over 1 h. At this time, the solution was re-cooled to 0° C. and ethanol (2 mL) followed by a mixture of a saturated aqueous sodium bicarbonate solution (6 mL) and 30% hydrogen peroxide (2 mL) was added slowly. This mixture was allowed to slowly warm to 25° C. while stirring for 1 h. At this time, the reaction was re-cooled to 0° C. and slowly quenched with a saturated aqueous sodium sulfite solution (20 mL). This solution was extracted with ethyl acetate (3×20 mL). The organics were washed with a saturated aqueous sodium chloride solution (1×15 mL), dried over sodium sulfate, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 80/20 hexanes/ethyl acetate) effected the separation of two spots, the second of the two product spots to elute off the column afforded 1-[3-cyclopentyl-2-(3,4-dichloro-phenyl)-propionyl]-3-(3-hydroxy-propyl)-urea (73 mg, 53%) as a white hygroscopic solid: EI-HRMS m/e calcd for C18H24Cl2N2O3 (M+) 386.1164, found 386.1172.

1. temperatureto slowly warm from 0° C. to 25° C. over 1 h
2. additionwas added slowly
3. temperatureto slowly warm to 25° C.
4. temperatureAt this time, the reaction was re-cooled to 0° C.
5. customslowly quenched with a saturated aqueous sodium sulfite solution (20 mL)
6. extractionThis solution was extracted with ethyl acetate (3×20 mL)
7. washThe organics were washed with a saturated aqueous sodium chloride solution (1×15 mL)
8. dry with materialdried over sodium sulfate
9. concentrationconcentrated in vacuo
10. customthe separation of two spots
11. washthe second of the two product spots to elute off the column