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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948307Generated: October 31, 2026

HCID 86643339, compound → ethyl (3S,4R)-4-amino-3-methoxypiperidine-1-carboxylate

https://huagongshe.com/reaction/1948307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86643339HCID 86643339—
CatalystPalladiumcarbonHCID 14818447—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
Productethyl (3S,4R)-4-amino-3-methoxypiperidine-1-carboxylateHCID 11160773117%

Reaction Steps

ethyl (3S,4R)-4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidine-1-carboxylate (Intermediate 24; 3.98 g) was dissolved in MeOH (100 ml) and 1N HCl (50 ml). 10% Pd-charcoal (600 mg) was added, degassed and hydrogenolysed under an atmosphere of H2 gas at room temperature for 3 h. The catalyst was filtered through a bed of celite, concentrated in vacuo and lyophilized giving the title compound (2.8 g). MS (ES) MH+: 202 for C9H18N2O3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399489B2
Source datasetuspto-grants-2013_03
ORD IDord-569bb0d5fadf496496e558aff8d27dc9
Source noteuspto-grants-2013_03