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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442912Generated: November 1, 2026

tert-Butyl 4-(((benzyloxy)carbonyl)amino)-4-carbamoylpiperidine-1-carboxylate → tert-Butyl 4-amino-4-carbamoylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1442912

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(((benzyloxy)carbonyl)amino)-4-carbamoylpiperidine-1-carboxylateHCID 10714606—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-Butyl 4-amino-4-carbamoylpiperidine-1-carboxylateHCID 10562199104.6%

Reaction Steps

10% Palladium on carbon (200 mg) was added to a solution of tert-Butyl 4-(aminocarbonyl)-4-{[(benzyloxy)carbonyl]amino}piperidine-1-carboxylate (430 mg, 1.14 mmol) in EtOH (20 mL). The reaction vessel was evacuated and back-filled with nitrogen (3×), then back-filled with hydrogen (1 atm). After 24 h, the mixture was filtered though celite and concentrated to give the title compound (0.29 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659264B2
Source datasetuspto-grants-2010_02
ORD IDord-a319e4dc21d743e1825a43e2486e4261
Source noteuspto-grants-2010_02