Potassium Carbonate → Eszopiclone
Reaction equation
C(=O)([O-])[O-].[K+].[K+].[CH3:7][N:8]1[CH2:13][CH2:12][N:11]([C:14]([O:16][C@@H:17]2[N:26]([C:27]3[CH:28]=[CH:29][C:30]([Cl:33])=[CH:31][N:32]=3)[C:24](=[O:25])[C:19]3[N:20]=[CH:21][CH:22]=[N:23][C:18]2=3)=[O:15])[CH2:10][CH2:9]1.C(N[C@@H](C([O-])=O)CC([O-])=O)(=O)C>O>[CH3:7][N:8]1[CH2:13][CH2:12][N:11]([C:14]([O:16][C@@H:17]2[N:26]([C:27]3[CH:28]=[CH:29][C:30]([Cl:33])=[CH:31][N:32]=3)[C:24](=[O:25])[C:19]3[N:20]=[CH:21][CH:22]=[N:23][C:18]2=3)=[O:15])[CH2:10][CH2:9]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2.7 ml of a 40% aqueous solution of potassium carbonate were added to a solution of 2 g of (S)-zopiclone N-acetyl-D-aspartate in 18 ml of water in about 30 minutes at room temperature. The slurry was maintained for 1.5 hours at this temperature. The product was isolated by filtration and washed twice with 1.4 ml of water. The product was dried under vacuum at room temperature obtaining 1.29 g of eszopiclone (94%) as a white solid.
Workup
- temperatureThe slurry was maintained for 1.5 hours at this temperature
- customThe product was isolated by filtration
- washwashed twice with 1.4 ml of water
- customThe product was dried under vacuum at room temperature
Sources & evidence
- ORD record
- ord-edc6701b81a04b92a23442fcf90b3028
- Source dataset
- uspto-grants-2010_08
- Patent number
- US07772396B2
Reaction notes
Loading…