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
Conditions
- Temperature
- 17.5 °C
Procedure
2 g of pure Perindopril free acid and (L)-Arginine (0.9 g) are dissolved in 10 ml of water at 25 to 30° C. To this clear solution indicated solvents at the indicated volumes was added at 25 to 30° C. and stirred for 30 minutes. The resulting solution was cooled to 15 to 20° C. and an indicated anti solvent at the indicated volumes are added slowly. The resulting reaction mass was stirred for 1 hour at 15 to 20° C. The solid was filtered and washed with 5 ml of indicated solvents. The wet solid was dried at 50 to 55° C. under vacuum for 12 hours. The results are shown in following table 4
Workup
- additionwas added at 25 to 30° C.
- additionare added slowly
- customThe resulting reaction mass
- stirringwas stirred for 1 hour at 15 to 20° C
- filtrationThe solid was filtered
- washwashed with 5 ml of indicated solvents
- customThe wet solid was dried at 50 to 55° C. under vacuum for 12 hours
Sources & evidence
- ORD record
- ord-d798a498237a491baff30cca26e3a430
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08686161B2
Reaction notes
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