Perindopril → HCID 178448324, compound
Reaction equation
[CH3:1][CH2:2][CH2:3][C@H:4]([NH:10][C@H:11]([C:13]([N:15]1[C@H:23]([C:24]([OH:26])=[O:25])[CH2:22][C@H:21]2[C@@H:16]1[CH2:17][CH2:18][CH2:19][CH2:20]2)=[O:14])[CH3:12])[C:5]([O:7][CH2:8][CH3:9])=[O:6].[NH2:27][C@H:28]([C:36]([OH:38])=[O:37])[CH2:29][CH2:30][CH2:31][NH:32][C:33](=[NH:35])[NH2:34]>O>[CH3:1][CH2:2][CH2:3][C@H:4]([NH:10][C@H:11]([C:13]([N:15]1[C@H:23]([C:24]([OH:26])=[O:25])[CH2:22][C@H:21]2[C@@H:16]1[CH2:17][CH2:18][CH2:19][CH2:20]2)=[O:14])[CH3:12])[C:5]([O:7][CH2:8][CH3:9])=[O:6].[NH2:27][C@H:28]([C:36]([OH:38])=[O:37])[CH2:29][CH2:30][CH2:31][NH:32][C:33](=[NH:34])[NH2:35]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
5 g of Perindopril free acid was dissolved in appropriate solvents (10 ml) at room temperature and solution of (L)-Arginine (2.3 g) in water (6 ml) was added to it and stirred for 2 hours. The results obtained are represented in Table 5
Workup
- customThe results obtained
Sources & evidence
- ORD record
- ord-b6a153f50ec043a28b4e43985fb04b7f
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08686161B2
Reaction notes
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