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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1597309Erstellt: 25. Oktober 2026

1-(1-Benzyloxycarbonyl-4-piperidinylmethyl)-4-(t-butoxycarbonylamino)piperidine → 4-(t-Butoxycarbonylamino)-1-(4-piperidinylmethyl)piperidine

https://huagongshe.com/reaction/1597309

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(1-Benzyloxycarbonyl-4-piperidinylmethyl)-4-(t-butoxycarbonylamino)piperidineHCID 12986153—
KatalysatorPalladiumHCID 23938—
LösungsmittelEthanolHCID 702—
Produkt4-(t-Butoxycarbonylamino)-1-(4-piperidinylmethyl)piperidineHCID 12986154107%

Reaktionsschritte

To a solution of 1-(1-benzyloxycarbonyl-4-piperidinylmethyl)-4-(t-butoxycarbonylamino)piperidine (5.6 g) in ethanol (100 ml) is added 5% palladium-on-carbon (0.6 g), and the mixture is hydrogenated at 30° C. under atmospheric pressure. After a theoretical amount of hydrogen is consumed, the catalyst is removed by filtration, and the ethanol in the filtrate is evaporated under reduced pressure to give crude 4-(t-butoxycarbonylamino)-1-(4-piperidinylmethyl)piperidine (4.13 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06294555B1
Quelldatensatzuspto-grants-2001_09
ORD IDord-87d64ad26c6447028e728b7a35ab379e
Quellennotizuspto-grants-2001_09