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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169405Generated: October 26, 2026

Benzyl 2-[4-(tert-butoxycarbonylamino)piperidin-1-yl]ethylcarbamate → 1,1-Dimethylethyl N-[1-(2-aminoethyl)-4-piperidinyl]carbamate

https://huagongshe.com/reaction/1169405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 2-[4-(tert-butoxycarbonylamino)piperidin-1-yl]ethylcarbamateHCID 22989976—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1,1-Dimethylethyl N-[1-(2-aminoethyl)-4-piperidinyl]carbamateHCID 23562647124.1%

Reaction Steps

A mixture of benzyl 2-[4-(tert-butoxycarbonylamino)piperidin-1-yl]ethylcarbamate (3.0 g), Pd-C (0.3 g), and ethanol (100 ml) was stirred vigorously for 3 days under a hydrogen atmosphere. Pd-C was removed by filtration, and the filtrate was concentrated under reduced pressure to obtain tert-butyl 1-(2-aminoethyl)-4-piperidinylcarbamate (2.4 g) as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06627651B1
Source datasetuspto-grants-2003_09
ORD IDord-29e43d51fbee459a8113259ad8adbd7c
Source noteuspto-grants-2003_09