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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 407925Erstellt: 24. Oktober 2026

tert-Butyl 4-oxopiperidine-1-carboxylate → (S)-2-(benzyloxycarbonylamino)-5-(1-(tert-butoxycarbonyl)piperidin-4-ylamino)pentanoic acid

https://huagongshe.com/de/reaction/407925

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
EduktSodium cyanoborohydrideHCID 5003444—
EduktN-alpha-Benzyloxycarbonyl-L-ornithineHCID 7010490—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(S)-2-(benzyloxycarbonylamino)-5-(1-(tert-butoxycarbonyl)piperidin-4-ylamino)pentanoic acidHCID 58787298—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

(S)-5-amino-2-(benzyloxycarbonylamino)pentanoic acid (50 g, 188 mmol) was dissolved in THF (800 mL) and water (100 mL). Tert-butyl 4-oxopiperidine-1-carboxylate (37 g, 188 mmol) was added and the reaction was stirred for 1 hour. The reaction was cooled to 0° C. and sodium cyanoborohydride (12 g, 188 mmol) was added and the reaction stirred at ambient temperature overnight. The reaction was concentrated to provide (S)-2-(benzyloxycarbonylamino)-5-(1-(tert-butoxycarbonyl)piperidin-4-ylamino)pentanoic acid, which was used directly in the next step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754226B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-2574fbdf2f8f41c9bbe86b41ad067089
Quellennotizuspto-grants-2014_06