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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 43936Erstellt: 23. Oktober 2026

Water → HCID 68406269, Verbindung

https://huagongshe.com/de/reaction/43936

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium hydrideHCID 24758—
Edukt1-IodopropaneHCID 33643—
EduktBenzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylateHCID 21981786—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 68406269HCID 6840626926,7%

Reaktionsschritte

A solution of benzyl 4-[(tert-butoxycarbonyl)amino]piperidine-1-carboxylate obtained in Example (241a) (1.00 g, 2.99 mmol) in THF (5 mL) was added to a suspension of sodium hydride (55%) (261 mg, 5.98 mmol) in THF (25 mL) at 0° C. Subsequently, propyl iodide (1.46 mL, 15.0 mmol) was added at 0° C., and the mixture was stirred at room temperature for 22 hours. Thereafter, sodium hydride (55%) (130 mg, 2.99 mmol) and propyl iodide (0.58 mL, 5.98 mmol) were added, and the mixture was heated under reflux for 22 hours. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. Thereafter, the combined organic layers were washed with brine and dried over anhydrous magnesium sulfate. Following filtration, the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=5/1) to obtain 301 mg of the title compound as a pale yellow oily substance (27%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536197B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-62988030973a43508cfc013c231c063f
Quellennotizuspto-grants-2013_09