HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 73503Erstellt: 23. Oktober 2026
3-Methylpyridine → (2S,5R)-6-benzyloxy-7-oxo-1,6-diaza-bicyclo[3.2.1]octane-2-carboxylic acid benzyl ester
https://huagongshe.com/de/reaction/73503
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-Methylpyridine | HCID 7970 | — |
| Edukt | Triphosgene | HCID 94429 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Benzyl (2S,5R)-5-((benzyloxy)amino)piperidine-2-carboxylate oxalate | HCID 70673933 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (2S,5R)-6-benzyloxy-7-oxo-1,6-diaza-bicyclo[3.2.1]octane-2-carboxylic acid benzyl ester | HCID 57389438 | — |
Reaktionsschritte
3-picoline (45 ml, 464, 4 eq) was added to a slurry of benzyl (2S,5R)-5-[(benzyloxy)amino]piperidine-2-carboxylate ethanedioate (50 g, 116 mmol, 1 eq) in dichloromethane (1000 ml) at 0° C., followed by a solution of triphosgene (31.0 g, 104.4 mmol, 0.9 eq) in dichloromethane (200 ml). The mixture was stirred at 0° C. until the reaction was deemed to be complete. The reaction was quenched with a solution of sodium bicarbonate (24.4 g, 290 mmol, 2.5 eq) in water (300 ml), and the layers were separated. The aqueous layer was extracted with dichloromethane (100 ml) and the combined organic layers were washed with water. The organic layer was concentrated in vacuo to give (2S,5R)-6-benzyloxy-7-oxo-1,6-diaza-bicyclo[3.2.1]octane-2-carboxylic acid benzyl ester as a solution in dichloromethane.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08829191B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-338dc3c7bae043a6b4044df29382baec |
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| Quellennotiz | uspto-grants-2014_09 |
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