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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593191Generated: 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/593191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(6-nitropyridin-3-yl)piperazine-1-carboxylateHCID 11243758—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylateHCID 1173752597%

Reaction Steps

A 500-mL round-bottomed flask was purged with nitrogen and charged with 339a (3.1 g, 10 mmol), 10% palladium on carbon (50% wet, 1.0 g), and ethanol (100 mL). It was evacuated, charged with hydrogen gas via a balloon, and stirred at room temperature for 16 h. The hydrogen was then evacuated and nitrogen was charged into the flask. The catalyst was removed by filtration through a pad of CELITE® and the filtrate was concentrated under reduced pressure to afford 339b (2.7 g, 97%). MS-ESI: [M+H]+ 279

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238655B2
Source datasetuspto-grants-2016_01
ORD IDord-288c70467c9345ef8a7a1bc35e31a262
Source noteuspto-grants-2016_01