反应详情

1,8-Diazabicyclo[5.4.0]undec-7-ene (4.22 mmol, 0.631 mL, 0.643 g) was added to a cooled (ice/slurry) solution of (4-amino-3-chlorophenyl)(4-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperazin-1-yl)methanone (3.25 mmol, 1.61 g) and tert-butyldimethylchlorosilane (4.22 mmol, 0.636 g) in dichloromethane (20 mL) under nitrogen. The resulting solution was stirred for 15 minutes prior to the removal of the external cooling bath. The reaction was allowed to warm to room temperature and stirred for 16 hours. The reaction mixture was diluted with dichloromethane (100 ml) and washed with 0.5M hydrochloric acid (100 ml), 0.5M sodium hydroxide (100 ml) and brine (100 ml). The organic phase was dried on magnesium sulfate, filtered and concentrated under vacuum to give a crude oil. This oil was purified by SCX chromatography to afford the title compound (1.616 g).

1. customto the removal of the external cooling bath
2. stirringstirred for 16 hours
3. additionThe reaction mixture was diluted with dichloromethane (100 ml)
4. washwashed with 0.5M hydrochloric acid (100 ml), 0.5M sodium hydroxide (100 ml) and brine (100 ml)
5. customThe organic phase was dried on magnesium sulfate
6. filtrationfiltered
7. concentrationconcentrated under vacuum
8. customto give a crude oil
9. customThis oil was purified by SCX chromatography