4-Benzyloxy-1-isobutyl-isoquinoline-3-carboxylic acid butyl ester → 4-Hydroxy-1-isobutyl-isoquinoline-3-carboxylic acid butyl ester
반응식
[CH2:1]([O:5][C:6]([C:8]1[N:9]=[C:10]([CH2:26][CH:27]([CH3:29])[CH3:28])[C:11]2[C:16]([C:17]=1[O:18]CC1C=CC=CC=1)=[CH:15][CH:14]=[CH:13][CH:12]=2)=[O:7])[CH2:2][CH2:3][CH3:4]>[Pd].CCOC(C)=O>[CH2:1]([O:5][C:6]([C:8]1[N:9]=[C:10]([CH2:26][CH:27]([CH3:28])[CH3:29])[C:11]2[C:16]([C:17]=1[OH:18])=[CH:15][CH:14]=[CH:13][CH:12]=2)=[O:7])[CH2:2][CH2:3][CH3:4]참가 물질
4
실험 절차
A mixture of 4-Benzyloxy-1-isobutyl-isoquinoline-3-carboxylic acid butyl ester (125 mg, 0.32 mmol), Pd/C (50 mg, Aldrich, 10 wt % Pd) and EtOAc (15 ml) were stirred at ambient pressure and temperature under an H2 atmosphere for 24 h. The mixture was then filtered through a pad of celite. Concentration of the filtrate in vacuo yielded the title compound as a yellowish oil (87 mg); MS-(+)-ion M+1=302.2.
후처리
- filtrationThe mixture was then filtered through a pad of celite
출처 및 근거
- ORD 기록
- ord-6028ff85defe4c899cb1f779d6ae3ee5
- 출처 데이터셋
- uspto-grants-2011_01
- 특허 번호
- US07863292B2
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