反应详情

3-(2-pyridin-4-ylethyl)-1H-indole (667 mg, 3 mmol, synthesis cf. WO2008009415, indole unit Ind-14) together with 4-butyl-4-(pyrrolidin-1-yl)cyclohexanone (671 mg, 3 mmol, synthesis cf. WO2008009415, ketone unit Ket-14) was dissolved in abs. dichloromethane (45 ml) and mixed with trifluoromethane sulphonic acid (0.613 ml, 6.9 mmol). The batch was stirred for 64 h at RT, and a brown oil separated out. For work up the reaction solution was mixed with 1N NaOH (30 ml) and methanol (10 ml). The mixture was stirred a further 60 min. After separation of the phases the aqueous phase was extracted with dichloromethane (3×10 ml). The combined organic extracts were dried over Na2SO4 and then concentrated to low volume. The raw product obtained (1.35 g) was purified by column chromatography [silica gel 60 (90 g); ethyl acetate/methanol (1:1 (2400 ml)].

1. customa brown oil separated out
2. additionFor work up the reaction solution was mixed with 1N NaOH (30 ml) and methanol (10 ml)
3. stirringThe mixture was stirred a further 60 min
4. customAfter separation of the phases the aqueous phase
5. extractionwas extracted with dichloromethane (3×10 ml)
6. dry with materialThe combined organic extracts were dried over Na2SO4
7. concentrationconcentrated to low volume