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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483048Generated: October 29, 2026

Tert-butyl 4-(6-nitropyridin-3-yl)piperazine-1-carboxylate → tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1483048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(6-nitropyridin-3-yl)piperazine-1-carboxylateHCID 11243758—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylateHCID 1173752594%

Reaction Steps

A mixture of 4-(6-nitro-pyridin-3-yl)-piperazine-1-carboxylic acid tert-butyl ester (3.40 g, 11.0 mmol) and 10% Pd—C (400 mg, 0.376 mmol) in ethanol (100 ml) and ethyl acetate (100 ml) is agitated under 1 atmosphere pressure of hydrogen overnight. The mixture is filtered and concentrated to give of 4-(6-amino-pyridin-3-yl)-piperazine-1-carboxylic acid tert-butyl ester (2.87 g, 94% yield). MS (ESI) m/z 278 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09416136B2
Source datasetuspto-grants-2016_08
ORD IDord-cee7c178c81f40f59dc3d292bb5ab316
Source noteuspto-grants-2016_08