Water → 1-[4-(3-Hydroxypropylamino)phenyl]-2-dimethylamino-2-benzyl-propan-1-one
反応式
F[C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:21])[C:9]([N:18]([CH3:20])[CH3:19])([CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH3:10])=[CH:4][CH:3]=1.[NH2:22][CH2:23][CH2:24][CH2:25][OH:26].C(=O)([O-])[O-].[K+].[K+].O>CC(N(C)C)=O>[OH:26][CH2:25][CH2:24][CH2:23][NH:22][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:21])[C:9]([N:18]([CH3:20])[CH3:19])([CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH3:10])=[CH:4][CH:3]=1参加物
実験手順
10.0 g (0.035 mol) of 1-(4-fluorophenyl)-2-dimethylamino-2-benzyl-propan-1-one and 18.4 g (0.25 mol) of 3-amino-1-propanol are dissolved in 20 ml of dry dimethylacetamide, and the solution is heated up to 150° C. together with 9.7 g (0.07 mol) of potassium carbonate, and stirred overnight (about 12 hours). After the solution is cooled down, it is poured into 300 ml of water and extracted with toluene. The organic phase is washed with water and saturated sodium chloride solution, and dried over MgSO4. After distilling off the toluene, the residue is purified by means of column chromatography on silica gel with ethyl acetate-hexane (1:1) as an eluent, and an oily product is obtained. The structure is confirmed by the 1H-NMR spectrum (CDCl3): δ [ppm]:1.14 (s, 3H), 1.50 (br, 1H), 1.93 (m, 2H), 2.33 (s, 6H), 2.96 (d, 1H), 3.37 (m, 2H), 3.42 (d, 1H), 3.85 (m, 2H), 4.45 (br, 1H), 6.56 (d, 2H), 6.89-6.91 (m, 2H), 7.10-7.12 (m, 3H), 8.45 (d, 2H).
後処理
- temperatureAfter the solution is cooled down
- extractionextracted with toluene
- washThe organic phase is washed with water and saturated sodium chloride solution
- dry with materialdried over MgSO4
- distillationAfter distilling off the toluene
- customthe residue is purified by means of column chromatography on silica gel with ethyl acetate-hexane (1:1) as an eluent
- customan oily product is obtained
出典と根拠
- ORDレコード
- ord-e4270b9bfd6d4d28876be1e60ddaef99
- 出典データセット
- uspto-grants-2000_02
- 特許番号
- US06022906
反応ノート
読み込み中…