3-(2-{6-methyl-2-oxo-3-(benzyloxycarbonylamino)-2H-pyridin-1-yl}-acetylamino)-3(S)-pyridin-3-yl-propionic acid ethyl ester → 3-(2-{6-methyl-2-oxo-3-amino-2H-pyridin-1-yl}-acetylamino)-3(S)-pyridin-3-yl-propionic acid ethyl ester
反応式
[CH2:1]([O:3][C:4](=[O:36])[CH2:5][C@H:6]([NH:13][C:14](=[O:35])[CH2:15][N:16]1[C:21]([CH3:22])=[CH:20][CH:19]=[C:18]([NH:23]C(OCC2C=CC=CC=2)=O)[C:17]1=[O:34])[C:7]1[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=1)[CH3:2]>CCO.[Pd]>[CH2:1]([O:3][C:4](=[O:36])[CH2:5][C@H:6]([NH:13][C:14](=[O:35])[CH2:15][N:16]1[C:21]([CH3:22])=[CH:20][CH:19]=[C:18]([NH2:23])[C:17]1=[O:34])[C:7]1[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=1)[CH3:2]参加物
4
反応物 1
生成物 1
試薬・触媒・溶媒 2
実験手順
To a degassed solution of the pyridone 16-5 (243 mg; 0.49 mmol) in EtOH (20 mL) was added 10% Pd on carbon (25 mg) and this was then stirred under an atmosphere of hydrogen gas (balloon) for 3 hours. The mixture was filtered through a pad of celite and the solvent removed to give the title compound (16-6) as a viscous oil which was used as such in the next step.
後処理
- filtrationThe mixture was filtered through a pad of celite
- customthe solvent removed
出典と根拠
- ORDレコード
- ord-74a0c3f58a044d129a8f9e86861c8479
- 出典データセット
- uspto-grants-2001_04
- 特許番号
- US06211184B1
反応ノート
読み込み中…