Ammonium Chloride → 7-(4'-Fluoro[1,1'-biphenyl]-3-yl)-6,7-dihydro-5h-pyrrolo[1,2-c]imidazol-7-ol
反応式
C([Li])CCC.Br[C:7]1[CH:8]=[C:9]([C:13]2[CH:18]=[CH:17][C:16]([F:19])=[CH:15][CH:14]=2)[CH:10]=[CH:11][CH:12]=1.[CH:20]1[N:24]=[CH:23][N:22]2[CH2:25][CH2:26][C:27](=[O:28])[C:21]=12.[Cl-].[NH4+]>CCCCCC.C1COCC1>[F:19][C:16]1[CH:17]=[CH:18][C:13]([C:9]2[CH:10]=[CH:11][CH:12]=[C:7]([C:27]3([OH:28])[C:21]4[N:22]([CH:23]=[N:24][CH:20]=4)[CH2:25][CH2:26]3)[CH:8]=2)=[CH:14][CH:15]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- -78 °C
実験手順
A solution (1.6 M; 1.98 ml) of n-butyl lithium in hexane was gently added dropwise to a solution of 3-bromo-4′-fluoro-1,1′-biphenyl (753 mg) in THF (10 ml) at −78° C., and the mixture was stirred at −78° C. for 30 min. A solution of 5,6-dihydro-7Hpyrrolo[1,2-c]imidazol-7-one (244 mg) in THF (10 ml) solution was gently added dropwise and the mixture was stirred at −78° C. for 1 h. A saturated aqueous ammonium chloride solution was added to the reaction mixture and the mixture was extracted with ethyl acetate, washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (eluent, ethyl acetate→ethyl acetate:methanol=5:1) and recrystallized from acetone-hexane to give the title compound (265 mg) as colorless needle crystals.
後処理
- stirringthe mixture was stirred at −78° C. for 1 h
- extractionthe mixture was extracted with ethyl acetate
- washwashed with saturated brine
- dry with materialdried over anhydrous magnesium sulfate
- customThe solvent was evaporated under reduced pressure
- customthe residue was purified by silica gel column chromatography (eluent, ethyl acetate→ethyl acetate:methanol=5:1)
- customrecrystallized from acetone-hexane
出典と根拠
- ORDレコード
- ord-6d5d550a3d10474193688d5d4178dcce
- 出典データセット
- uspto-grants-2006_11
- 特許番号
- US07141598B2
反応ノート
読み込み中…