4-Benzyloxy-1-pyridin-2-yl-isoquinoline-3-carboxylic acid butyl ester → 4-Hydroxy-1-pyridin-2-yl-isoquinoline-3-carboxylic acid butyl ester
Reaction equation
[CH2:1]([O:5][C:6]([C:8]1[N:9]=[C:10]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][N:27]=2)[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].C1C=CC(C([C@@H]2OC[C@H](NCC3C=CC(F)=CC=3)C(O)C2)C2C=CC=CC=2)=CC=1>>[CH2:1]([O:5][C:6]([C:8]1[N:9]=[C:10]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][N:27]=2)[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]Participants
3
Procedure
Synthesized from 4-Benzyloxy-1-pyridin-2-yl-isoquinoline-3-carboxylic acid butyl ester in analogy to example D-153 b); MS-(−)-ion M−1=321.4.
Sources & evidence
- ORD record
- ord-8627020df7524d03a22dcc95f7ccdcb4
- Source dataset
- uspto-grants-2011_01
- Patent number
- US07863292B2
Reaction notes
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