HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 51271Erstellt: 25. Oktober 2026
4-(Methoxymethylcarbamoyl)piperidine-1-carboxylic acid tert-butyl ester → N-Boc-(2,3-dimethoxyphenyl)-4-piperidinylmethanone
https://huagongshe.com/reaction/51271
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-(Methoxymethylcarbamoyl)piperidine-1-carboxylic acid tert-butyl ester | HCID 44203202 | — |
| Edukt | HCID 86601787 | HCID 86601787 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | N-Boc-(2,3-dimethoxyphenyl)-4-piperidinylmethanone | HCID 46780868 | — |
Reaktionsschritte
Into a 500-mL jacketed-bottom-drain resin pot fitted with a five-joint head equipped with a mechanical stirrer, a thermocouple, a reflux condenser topped with a nitrogen bubbler, a septum, and a stopper was placed 28.9 g (0.092 mol) of 4-[(methoxymethylamino)carbonyl]-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester (15) (28.9 g, 0.092 mol, 87% pure) and 80 g of tetrahydrofuran. The solution was cooled to −17° C. and the cold lithiated veratrole/tetrahydrofuran slurry was added via cannula while maintaining the internal reaction temperature below −10° C. (15 minutes addition). The reaction mixture was then warmed to 10° C. and stirred for 3 hours. The solution may be used directly in Scheme L, step a, Example 109.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06713627B2 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-c8f698ddb7974c3886831d2a88cae10f |
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| Quellennotiz | uspto-grants-2004_03 |
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