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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(Methoxymethylcarbamoyl)piperidine-1-carboxylic acid tert-butyl esterHCID 44203202—
EduktHCID 86601787HCID 86601787—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-Boc-(2,3-dimethoxyphenyl)-4-piperidinylmethanoneHCID 46780868—

Reaktionsbedingungen

Temperatur-17 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713627B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-c8f698ddb7974c3886831d2a88cae10f
Quellennotizuspto-grants-2004_03