Citric Acid → 4-[2-(t-Butyldimethyl silanyloxy)ethyl]-1-(6-trifluoromethyl benzothiazole-2-yl)piperidine-4-carboxaldehyde
反応式
[C:1]([Si:5]([CH3:31])([CH3:30])[O:6][CH2:7][CH2:8][C:9]1([C:28]#N)[CH2:14][CH2:13][N:12]([C:15]2[S:16][C:17]3[CH:23]=[C:22]([C:24]([F:27])([F:26])[F:25])[CH:21]=[CH:20][C:18]=3[N:19]=2)[CH2:11][CH2:10]1)([CH3:4])([CH3:3])[CH3:2].[H-].C([Al+]CC(C)C)C(C)C.C(O)(=O)CC(CC(O)=O)(C(O)=O)[OH:45]>COCCOC>[C:1]([Si:5]([CH3:30])([CH3:31])[O:6][CH2:7][CH2:8][C:9]1([CH:28]=[O:45])[CH2:14][CH2:13][N:12]([C:15]2[S:16][C:17]3[CH:23]=[C:22]([C:24]([F:26])([F:25])[F:27])[CH:21]=[CH:20][C:18]=3[N:19]=2)[CH2:11][CH2:10]1)([CH3:3])([CH3:2])[CH3:4]参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of 4-[2-(t-butyldimethyl silyloxy)ethyl]-1-(6-trifluoromethyl benzothiazole-2-yl)piperidine-4-carbonitrile (600 mg) in 1,2-dimethoxyethane (12 mL) was added diisobutylaluminum hydride (1.0 M toluene solution, 6.39 mL) at 0° C. The mixture was stirred for 4 hours. To the reaction solution was added aqueous citric acid solution and extracted with ethyl acetate. The organic layer was sequentially washed with aqueous citric acid solution, water and brine, and dried over magnesium sulphate. The solvent was evaporated under reduced pressure and the residue was purified by column chromatograph on silica gel to give the title compound (526 mg). Yield: 87%.
後処理
- extractionextracted with ethyl acetate
- washThe organic layer was sequentially washed with aqueous citric acid solution, water and brine
- dry with materialdried over magnesium sulphate
- customThe solvent was evaporated under reduced pressure
- customthe residue was purified by column chromatograph on silica gel
出典と根拠
- ORDレコード
- ord-2925e47cd1d7440da6bbcccc25ac52ea
- 出典データセット
- uspto-grants-2012_01
- 特許番号
- US08097610B2
反応ノート
読み込み中…