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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411771Generated: November 3, 2026

tert-Butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylate → tert-Butyl 4-(5-aminopyridin-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1411771

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylateHCID 16217943—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-Butyl 4-(5-aminopyridin-2-yl)piperazine-1-carboxylateHCID 1799930491.2%

Reaction Steps

A 250-mL round-bottomed flask was purged with nitrogen and charged with 197a (4.0 g, 13.0 mmol), 10% palladium on carbon (10% wet, 500 mg), and methanol (130 mL). The flask was evacuated, charged with hydrogen gas, and stirred at room temperature for 15 h. Hydrogen was then evacuated and nitrogen was charged to the flask. The catalyst was removed by filtration through a pad of CELITE® and the filtrate was concentrated under reduced pressure to afford 197b (3.3 g, 91%). MS-ESI: [M+H]+ 279

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921353B2
Source datasetuspto-grants-2014_12
ORD IDord-92e2f1ada4ce42d9b025f9bba63024fe
Source noteuspto-grants-2014_12