Hydrochloric Acid → HCID 69737865、化合物

反応式

[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][N:10]2[C:15](=O)[CH2:14][C:13]([CH3:18])([CH3:17])[CH:12]([C:19]#[N:20])[C:11]2=O)=[CH:4][CH:3]=1.B.O1CCCC1.Cl>>[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][N:10]2[CH2:15][CH2:14][C:13]([CH3:18])([CH3:17])[CH:12]([CH2:19][NH2:20])[CH2:11]2)=[CH:4][CH:3]=1

参加物

反応物 4

HCID 313Hydrochloric Acid

HCID 6331Borane

HCID 8028Tetrahydrofuran

HCID 22350238HCID 22350238、化合物

生成物 1

HCID 69737865HCID 69737865、化合物収率 33%

実験手順

1-[2-(4-Fluorophenyl)-ethyl]-4,4-dimethyl-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 18 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 10% methanol in dichloromethane, to provide an oil (300 mg, 33%). 1H NMR (300 MHz, CDCl3) δ7.15 (m, 2H), 6.96 (t, J=9 Hz, 2H), 3.66 (m, 1H), 3.11 (m, 2H), 2.97 (m, 1H), 2.9-2.7 (m, 3H), 2.60 (m, 2H), 2.39 (m, 1H), 2.24 (m, 1H), 2.00 (m, 1H), 1.7-1.3 (3H), 1.00 (s, 3H), 0.80 (s, 3H).