反应详情

2-(8-Chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)-1-cyclopropyl-1-(4-fluorophenyl)ethanol (1 g, 2.51 mmol, 1 equiv) was refluxed with 25% sulfuric acid (7 mL) for 2 h. The reaction mixture was cooled to 5° C. in ice-water bath. KOH (15% aqueous solution) was added dropwise to the reaction mixture until pH 9-10 was achieved. The reaction mixture was extracted with EtOAc (3×10 mL). The combined organic layer was washed with water (10 mL) followed by brine, dried over sodium sulfate and evaporated under vacuum. The crude product was purified by silica gel chromatography (100-200 mesh) using a gradient of MeOH-EtOAc (0-10%) to obtain a mixture of isomers, which were separated by HPLC. 1H NMR (CD3OD, TFA salt) δ (ppm): 7.50 (m, 2H), 7.40 (d, 1H), 7.20 (m, 3H), 7.05 (m, 1H), 6.80 (d, 1H), 4.75 (m, 1H), 4.40 (m, 1H), 3.90 (m, 1H), 3.60 (m, 1H), 3.30 (m, 3H), 3.12 (s, 3H), 2.80 (m, 1H), 2.0 (m, 1H), 1.80 (m, 1H), 1.15 (m, 1H).

1. extractionThe reaction mixture was extracted with EtOAc (3×10 mL)
2. washThe combined organic layer was washed with water (10 mL)
3. dry with materialdried over sodium sulfate
4. customevaporated under vacuum
5. customThe crude product was purified by silica gel chromatography (100-200 mesh)
6. customto obtain
7. additiona mixture of isomers, which
8. customwere separated by HPLC