反应详情

A solution of (1-benzhydryl-azetidin-3-yl)-acetaldehyde (0.30 g, 1.2 mmol), 5-fluoroindole (0.8 g, 6.0 mmol) and sodium hydroxide (0.6 g, 1.6 mmol) in methanol (20 mL) was refluxed for 6 hours. The reaction was quenched with water and extracted with methylene chloride (3×100 mL). The organic layer was washed with water (3×80 mL), dried over anhydrous sodium sulfate, filtered and concentrated in vacuum. The crude oil was column chromatographed on silica gel (30-40% ethyl acetate/hexane). The product-containing fractions were concentrated under vacuum to give 0.27 g (56%) of the title compound as a light yellow oil. 1H NMR (500 MHz, DMSO-D6): δ 2.62 (t, J=6.4 Hz, 1H), 2.90-2.95 (m, 2H), 3.02 (t, J=6.1 Hz, 1H), 3.09 (s, 3H), 3.26-3.31 (m, 1H), 4.40 (br, 1H), 4.58 (d, J=8.8 Hz, 1H), 6.89 (m, 1H), 7.13-7.18 (m, 2H), 7.22-7.27 (m, 4H), 7.31-7.39 (m, 7H) 11.10 (br, 1H).

1. customThe reaction was quenched with water
2. extractionextracted with methylene chloride (3×100 mL)
3. washThe organic layer was washed with water (3×80 mL)
4. dry with materialdried over anhydrous sodium sulfate
5. filtrationfiltered
6. concentrationconcentrated in vacuum
7. customchromatographed on silica gel (30-40% ethyl acetate/hexane)
8. concentrationThe product-containing fractions were concentrated under vacuum