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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15022Erstellt: 25. Oktober 2026

1,1-Dimethylethyl (trans)-3-hydroxy4-[[(phenylmethyl)amino]methyl]-1-piperidinecarboxylate → trans-1-Boc-4-aminomethyl-3-hydroxypiperidine

https://huagongshe.com/reaction/15022

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1-Dimethylethyl (trans)-3-hydroxy4-[[(phenylmethyl)amino]methyl]-1-piperidinecarboxylateHCID 11738727—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
Produkttrans-1-Boc-4-aminomethyl-3-hydroxypiperidineHCID 1107522972,9%

Reaktionsschritte

A mixture of intermediate (43) (0.028 mol) in methanol (100 ml) was hydrogenated with palladium-on-carbon (10%, 2 g) as a catalyst. After uptake of hydrogen (1 equivalent) the catalyst was filtered off and the filtrate was evaporated, yielding 4.7 g of 1,1-dimethylethyl (3S-trans)-4-(aminomethyl)-3-hydroxy-1-piperidinecarboxylate (intermediate (44); [α]D20=+4.37° (c=24.03 mg/5 ml in CH3OH)).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732464B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-215187a38156403f81f9176d9ddfd99e
Quellennotizuspto-grants-2010_06