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
반응식
[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]참가 물질
4
반응물 1
생성물 1
시약·촉매·용매 2
실험 절차
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.
후처리
- filtrationThe mixture was filtered through a pad of celite
- customthe solvent removed
출처 및 근거
- ORD 기록
- ord-74a0c3f58a044d129a8f9e86861c8479
- 출처 데이터셋
- uspto-grants-2001_04
- 특허 번호
- US06211184B1
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