反応式
[C:1]([O:5][C:6]([NH:8][C@@H:9]1[C:29](=[O:30])[N:11]2[C:12]([C:22]([O:24][C:25]([CH3:28])([CH3:27])[CH3:26])=[O:23])=[C:13]([C:16]([O:18]CC=C)=[O:17])[CH2:14][CH2:15][C@H:10]12)=[O:7])([CH3:4])([CH3:3])[CH3:2].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[SnH](CCCC)(CCCC)CCCC.Cl>CC#N.CCOCC.O.C(Cl)(Cl)Cl>[C:1]([O:5][C:6]([NH:8][C@@H:9]1[C:29](=[O:30])[N:11]2[C:12]([C:22]([O:24][C:25]([CH3:28])([CH3:27])[CH3:26])=[O:23])=[C:13]([C:16]([OH:18])=[O:17])[CH2:14][CH2:15][C@H:10]12)=[O:7])([CH3:4])([CH3:2])[CH3:3]参加物
反応条件
- 温度
- 0 °C
実験手順
To 700 mg (1.657 mMol) of 4-t-butyl 7β-t-butyloxycarbonylamino-3-allyloxycarbonyl-1-carba-3-cephem-4-carboxylate, dissolved in 12 ml of (1:1) CH3CN/(CH3CH2)2O, was added 174 mg (0.663 mMol) of triphenylphosphine and 20.34 mg (0.0829 mMol) of ##STR153## The reaction mixture was stirred for approximately 20 minutes and then cooled to 0° C. and treated with 0.464 ml (1.724 l) of (CH3CH2CH2CH2)3SnH. The reaction mixture was then allowed to cool and stirring was continued for 50 minutes. The crude reaction mixture was then treated with 1N HCl. This mixture was then poured into 100 ml of CHCl3 and 25 ml of H2O. The organic layer was separated, dried over anhydrous MgSO4, filtered, and concentrated, under reduced pressure to provide an oily solid. The crude product was recrystallized from CH2Cl2 /hexane to yield 570 mg (90%) of the title compound.
後処理
- temperatureto cool
- stirringstirring
- waitwas continued for 50 minutes
- customThe crude reaction mixture
- customThe organic layer was separated
- dry with materialdried over anhydrous MgSO4
- filtrationfiltered
- concentrationconcentrated, under reduced pressure
- customto provide an oily solid
- customThe crude product was recrystallized from CH2Cl2 /hexane
出典と根拠
- ORDレコード
- ord-8c4ecdf71a2946e985d12e9cb2ad5e2c
- 出典データセット
- uspto-grants-1990_01
- 特許番号
- US04892942
関連ノート
読み込み中…