Water → tert-butyl (3R*,4S*)-4-{[(4-chlorophenyl)carbonyl]amino}-3-(3,4-dichlorophenyl)piperidine-1-carboxylate
反応式
C1(C)C=CC(S(O)(=O)=O)=CC=1.[NH2:12][C@H:13]1[CH2:18][CH2:17][N:16]([C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])[CH2:15][C@H:14]1[C:26]1[CH:31]=[CH:30][C:29]([Cl:32])=[C:28]([Cl:33])[CH:27]=1.C(N(CC)CC)C.[Cl:41][C:42]1[CH:50]=[CH:49][C:45]([C:46](Cl)=[O:47])=[CH:44][CH:43]=1.O>C(#N)C>[Cl:41][C:42]1[CH:50]=[CH:49][C:45]([C:46]([NH:12][C@H:13]2[CH2:18][CH2:17][N:16]([C:19]([O:21][C:22]([CH3:25])([CH3:23])[CH3:24])=[O:20])[CH2:15][C@H:14]2[C:26]2[CH:31]=[CH:30][C:29]([Cl:32])=[C:28]([Cl:33])[CH:27]=2)=[O:47])=[CH:44][CH:43]=1参加物
6
実験手順
To a solution of the compound (0.55 g) obtained in step 4 and triethylamine (439 μL) in acetonitrile (5 mL) was added 4-chlorobenzoyl chloride (177 μL) at 0° C., and the mixture was stirred at room temperature for 14 hr. The reaction mixture was poured into water, and the resultant product was extracted with ethyl acetate. The organic layer was washed with aqueous sodium hydrogen carbonate solution and brine and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient; 25→50% ethyl acetate/hexane) to give the title compound (0.51 g, 99%) as a white powder.
後処理
- extractionthe resultant product was extracted with ethyl acetate
- washThe organic layer was washed with aqueous sodium hydrogen carbonate solution and brine
- customdried
- customthe solvent was evaporated under reduced pressure
- customThe obtained residue was purified by silica gel column chromatography (solvent gradient; 25→50% ethyl acetate/hexane)
出典と根拠
- ORDレコード
- ord-556895c8a521482582d13d85e50efa70
- 出典データセット
- uspto-grants-2013_06
- 特許番号
- US08470816B2
反応ノート
読み込み中…