4-Benzoyl-2(S)-trifluoroacetamidobutyric acid → 5-Phenyl-2(S)-trifluoroacetamidopentanoic acid
反応式
[C:1]([CH2:9][CH2:10][C@H:11]([NH:15][C:16](=[O:21])[C:17]([F:20])([F:19])[F:18])[C:12]([OH:14])=[O:13])(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>[OH-].[OH-].[Pd+2].CCOC(C)=O.C(O)C>[C:2]1([CH2:1][CH2:9][CH2:10][C@H:11]([NH:15][C:16](=[O:21])[C:17]([F:19])([F:20])[F:18])[C:12]([OH:14])=[O:13])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
5
実験手順
Reduce the product of Step 1 (9.7 g) with Pearlman's catalyst (3.5 g) in EtOAc (75 ml) and ethanol (25 ml) at 50 psi H2 for 3 hours. Filter, concentrate and wash the resultant residue with 3:1 hexane:diethyl ether to give the title compound (7.8 g).
後処理
- customfor 3 hours
- filtrationFilter
- concentrationconcentrate
- washwash the resultant residue with 3:1 hexane
出典と根拠
- ORDレコード
- ord-83712812cadf47c69e940dbef19fc374
- 出典データセット
- uspto-grants-1990_05
- 特許番号
- US04929641
反応ノート
読み込み中…