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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496662Generated: November 2, 2026

tert-Butyl (3R)-3-{[(benzyloxy)carbonyl]amino}piperidine-1-carboxylate → tert-butyl (3R)-3-aminopiperidine-1-carboxylate

https://huagongshe.com/reaction/496662

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (3R)-3-{[(benzyloxy)carbonyl]amino}piperidine-1-carboxylateHCID 51656152—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-butyl (3R)-3-aminopiperidine-1-carboxylateHCID 150197499%

Reaction Steps

To a slurry of Pd—C (10%, 170 mg) in MeOH (2 ml) was added a solution of the 3(R)-Benzyloxycarbonylamino-piperidine-1-carboxylic acid tert-butyl ester (1.0 g) in MeOH (60 ml). The mixture was stirred under H2 (1 atm) for 8 hr. After being filtered through Celite, the filtrate was evaporated to give a light yellow oil (572 mg, 99%). 1H-NMR (300 MHz, CDCl3) δ 4.00-3.78 (m, 2H), 3.80 (m, 2H), 3.60 (m, 1H), 1.90 (m, 1H), 1.70 (m, 1H), 1.60-1.40 (m, 12H), 1.30 (m, 1H) ppm; IR (film) 3485, 3361, 3292, 2975, 22931, 2862, 1692, 1608, 1548, 1479, 1427, 1367, 1266, −1242, 1162 cm−1; LRMS (calculated for C10H20N2O2) 200. found 200.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06946477B2
Source datasetuspto-grants-2005_09
ORD IDord-09d41855664f415a896078dd872b7d21
Source noteuspto-grants-2005_09