HCID 68973677, compound → HCID 11956452, compound
Reaction equation
C[O:2][C:3](=[O:44])[C@@H:4]([NH:14][C:15]([C:17]1[N:18]=[C:19]([CH2:38][CH:39]2[CH2:43][CH2:42][CH2:41][CH2:40]2)[C:20]2[C:25]([CH:26]=1)=[CH:24][CH:23]=[C:22]([O:27][C:28]1[CH:33]=[CH:32][C:31]([C:34]([CH3:37])([CH3:36])[CH3:35])=[CH:30][CH:29]=1)[CH:21]=2)=[O:16])[CH2:5][C:6]1[S:7][C:8]([C:11]([CH3:13])=[CH2:12])=[CH:9][CH:10]=1>[Pd]>[C:34]([C:31]1[CH:30]=[CH:29][C:28]([O:27][C:22]2[CH:21]=[C:20]3[C:25]([CH:26]=[C:17]([C:15]([NH:14][C@@H:4]([CH2:5][C:6]4[S:7][C:8]([CH:11]([CH3:12])[CH3:13])=[CH:9][CH:10]=4)[C:3]([OH:44])=[O:2])=[O:16])[N:18]=[C:19]3[CH2:38][CH:39]3[CH2:40][CH2:41][CH2:42][CH2:43]3)=[CH:24][CH:23]=2)=[CH:33][CH:32]=1)([CH3:36])([CH3:35])[CH3:37]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared by the treatment of 2(S)-{[7-(4-tert-Butyl-phenoxy)-1-cyclopentylmethyl-isoquinoline-3-carbonyl]-amino}-3-(5-isopropenylthiophen-2-yl)-propionic acid methyl ester (prepared in Example 29) with Pd/C and H2 gas (1 atm) by the general procedure N to afford 2(S)-{[7-(4-tert-Butyl-phenoxy)-1-cyclopentylmethyl-1-isoquinoline-3-carbonyl]-amino}-3-(5-isopropylthiophen-2-yl)-propionic acid methyl ester. This ester was hydrolyzed by the general procedure C to afford the title compound.
Sources & evidence
- ORD record
- ord-1e1cf81d5b424759a43e11c93cba19ab
- Source dataset
- uspto-grants-2007_04
- Patent number
- US07208601B2
Reaction notes
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