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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685458Generated: October 30, 2026

(2R,4R)-1-tert-butyl 2-methyl 4-azidopiperidine-1,2-dicarboxylate → (2R,4R)-1-tert-butyl 2-methyl 4-aminopiperidine-1,2-dicarboxylate

https://huagongshe.com/reaction/1685458

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2R,4R)-1-tert-butyl 2-methyl 4-azidopiperidine-1,2-dicarboxylateHCID 54053444—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(2R,4R)-1-tert-butyl 2-methyl 4-aminopiperidine-1,2-dicarboxylateHCID 5420975598%

Reaction Steps

(2R,4R)-1-tert-butyl 2-methyl 4-azidopiperidine-1,2-dicarboxylate (22.5 g, 79 mmol) was dissolved in methanol (400 mL), Pd/C (10%, 6 g) was added, and the apparatus was flushed three times with N2 and H2. The reaction mixture was hydrogenated at a pressure of 50 psi at room temperature for 20 hours, filtered through Celite and rinsed with methanol and then concentrated under reduced pressure to give the amine as a colorless oil 20 g (96%). GC-MS: 258 (t=2.8 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148401B2
Source datasetuspto-grants-2012_04
ORD IDord-e6368dc771c24e2bba31a857dd21f3bf
Source noteuspto-grants-2012_04