N2 (benzyloxycarbonyl)-N1-tert.butyl-4(R)-hydroxy-L-prolinamide → N1-tert.butyl-4(R)-hydroxy-L-prolinamide
反応式
N#N.C(OC([C@@:13]1([C:23]([NH2:25])=[O:24])[CH2:17][C@@H:16]([OH:18])[CH2:15][N:14]1[C:19]([CH3:22])([CH3:21])[CH3:20])=O)C1C=CC=CC=1>C(O)C.[Pd]>[C:19]([N:14]1[CH2:15][C@H:16]([OH:18])[CH2:17][C@H:13]1[C:23]([NH2:25])=[O:24])([CH3:22])([CH3:20])[CH3:21]参加物
4
実験手順
0.224 g of N2 -(benzyloxycarbonyl)-N1 -tert.butyl-4(R)-hydroxy-L-prolinamide was dissolved in 20 ml of ethanol and hydrogenated over 50 mg of 10% palladium-on-carbon at room temperature and under atmospheric pressure for 2 hours. The catalyst was filtered off and the filtrate was evaporated to give 0.13 g of N1 -tert.butyl-4(R)-hydroxy-L-prolinamide which was used in the next step without further purification.
後処理
- filtrationThe catalyst was filtered off
- customthe filtrate was evaporated
出典と根拠
- ORDレコード
- ord-1acbadc411604fe7b52d89e70743009c
- 出典データセット
- uspto-grants-1997_04
- 特許番号
- US05620987
反応ノート
読み込み中…