Potassium Carbonate → Eszopiclone

HRID 501886Notes

Reaction equation

HRID 501886 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]1

Participants

4

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

  1. temperatureThe slurry was maintained for 1.5 hours at this temperature
  2. customThe product was isolated by filtration
  3. washwashed twice with 1.4 ml of water
  4. 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

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