Triethylamine → 1-(5-Bromo-4-chloro-2-fluoro-benzenesulfonyl)-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline
反応式
[Br:1][C:2]1[C:3]([Cl:13])=[CH:4][C:5]([F:12])=[C:6]([S:8](Cl)(=[O:10])=[O:9])[CH:7]=1.[CH3:14][C:15]1([CH3:25])[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[NH:18][CH2:17][CH2:16]1.C(N(CC)CC)C.S(Cl)(Cl)(=O)=O>C(Cl)Cl>[Br:1][C:2]1[C:3]([Cl:13])=[CH:4][C:5]([F:12])=[C:6]([S:8]([N:18]2[C:19]3[C:24](=[CH:23][CH:22]=[CH:21][CH:20]=3)[C:15]([CH3:25])([CH3:14])[CH2:16][CH2:17]2)(=[O:10])=[O:9])[CH:7]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
To 5-bromo-4-chloro-2-fluorobenzenesulfonyl chloride (3.15 g, 10.8 mmol) in dry DCM (40 mL), was added 4,4-dimethyl-1,2,3,4-tetrahydro-quinoline (1.50 g, 9.3 mmol) and triethylamine (2.15 mL, 15.5 mmol). The mixture was stirred at ambient temperature for 16 hrs. Additional sulfonyl chloride (0.93 g, 3.2 mmole) was added and the mixture was stirred an additional 72 hrs. The mixture was washed with 1N hydrochloric acid solution, saturated sodium bicarbonate solution and brine. The organic layer was dried over MgSO4 and the filtrate evaporated. The residue was purified by silica gel chromatography [eluent: 5% ethyl acetate in hexane] to give 1-(5-bromo-4-chloro-2-fluoro-benzenesulfonyl)-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline as a yellow solid (3.6 g). tR=2.82 min (method 1).
後処理
- stirringthe mixture was stirred an additional 72 hrs
- washThe mixture was washed with 1N hydrochloric acid solution, saturated sodium bicarbonate solution and brine
- dry with materialThe organic layer was dried over MgSO4
- customthe filtrate evaporated
- customThe residue was purified by silica gel chromatography [eluent: 5% ethyl acetate in hexane]
出典と根拠
- ORDレコード
- ord-8b6819cd73404dbdb71e1a7718c9a3d2
- 出典データセット
- uspto-grants-2013_08
- 特許番号
- US08507536B2
反応ノート
読み込み中…