HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 507804Erstellt: 24. Oktober 2026
4-Methylpiperazine-1-carbonyl chloride monohydrochloride → Zopiclone
https://huagongshe.com/de/reaction/507804
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 4-Methylpiperazine-1-carbonyl chloride monohydrochloride | HCID 3016934 | — |
| Edukt | 6-(5-Chloro-2-pyridyl)-6,7-dihydro-7-hydroxy-5H-pyrrolo(3,4-b)pyrazin-5-one | HCID 6451972 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | Zopiclone | HCID 5735 | — |
Reaktionsschritte
In another embodiment, the invention provides a process to recycle the (R)-zopiclone, which remains in solution as waste product. (R)-zopiclone is recovered from the solution by any known conventional methods, for example, by solvent distillation, evaporation, or precipitation by adding a non-polar solvent, etc. This is followed by neutralization with base, extraction using methylene chloride followed by removal of the solvent. The (R)-isomer isolated is subjected to acid hydrolysis using aqueous HCl, obtaining 6-(5-chloropyrid-2-yl)-5-hydroxy-7-oxo-5,6-dihydropyrrolo-[3,4-b]pyrazine. The compound, 6-(5-chloropyrid-2-yl)-5-hydroxy-7-oxo-5,6-dihydropyrrolo-[3,4-b]pyrazine, is reacted with 1-chlorocarbonyl-4-methylpiperazine hydrochloride in a suitable organic solvent in the presence of triethyl amine and N,N-dimethylamino pyridine to obtain zopiclone in high yields. The racemate thus obtained is further resolved to obtain eszopiclone by the above stated method.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07786304B2 |
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| Quelldatensatz | uspto-grants-2010_08 |
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| ORD ID | ord-d2f026dc95fe4e5e926d80d824a76b3f |
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| Quellennotiz | uspto-grants-2010_08 |
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