HuagongsheHuagongshe Chemistry Print Report · For research reference only
Zopiclone → Eszopiclone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Zopiclone | HCID 5735 | — |
| Reactant | HCID 10284017 | HCID 10284017 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Eszopiclone | HCID 969472 | — |
Reaction Steps
Accordingly, racemic zopiclone is preferably reacted with a resolving agent (+)-O,O′-dibenzoyl tartaric acid in methylene dichloride at room temperature to obtain the diastereomeric salt (Scheme IV) which is crystallized from acetonitrile followed by conversion into eszopiclone by treating with an inorganic base, such as NaOH. Eszopiclone thus obtained has a purity above 99%. Eszopiclone is recrystallized from ethyl acetate to obtain the product with purity of 99.9%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07786304B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-2cbdcbc8be4a42369650ca5dc097ab87 |
| Source note | uspto-grants-2010_08 |