Hydrochloric Acid → trans-1-[2-(4-Fluorophenyl)-ethyl]-4-ethylpiperidin-3-ylmethylamine

1-[2-(4-Fluorophenyl)ethyl]-4-ethyl-2,6-dioxopiperidine-3-carbonitrile (1.0 g, 3.47 mmol) was treated with 1.0 M borane in tetrahydrofuran (69.4 mL, 69.4 mmol) and stirred at room temperature for 65 hours. The solution was cooled on an ice bath and treated very slowly with 2.0 N hydrochloric acid. The mixture was concentrated under vacuum to remove the tetrahydrofuran, and the aqueous residue was heated at reflux for 60 minutes. The mixture was cooled to room temperature and treated with 50% aqueous sodium hydroxide to adjust the pH to about 11. The mixture was extracted with ethyl acetate, and the organic extracts were dried over sodium sulfate and concentrated. The residue was purified by flash chromatography, eluting with 5% methanol in dichloromethane containing 0.5% aqueous ammonia, to provide an oil (340 mg, 37%). 1H NMR (300 MHz, CDCl3) δ7.16 (m, 2H), 6.97 (t, J=9 Hz, 2H), 3.13 (m, 1H), 3.00 (m, 1H), 2.92 (dd, J=13, 3 Hz, 1H), 2.83 (m, 2H), 2.58 (m, 2H), 1.99 (td, J=12, 3 Hz, 1H), 1.9-1.0 (m, 8H), 0.90 (t, J=7 Hz, 3H). Mass spec (ES+) m/z 265.4 (M+H+, 100%).

1. temperatureThe solution was cooled on an ice bath
2. concentrationThe mixture was concentrated under vacuum
3. customto remove the tetrahydrofuran
4. temperaturethe aqueous residue was heated
5. temperatureat reflux for 60 minutes
6. temperatureThe mixture was cooled to room temperature
7. additiontreated with 50% aqueous sodium hydroxide
8. extractionThe mixture was extracted with ethyl acetate
9. dry with materialthe organic extracts were dried over sodium sulfate
10. concentrationconcentrated
11. customThe residue was purified by flash chromatography
12. washeluting with 5% methanol in dichloromethane containing 0.5% aqueous ammonia

ORD 기록

ord-f6eceaf89f614f7ea2fc15111b89a6ef

출처 데이터셋

uspto-grants-2005_07

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US06919356B2