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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919000Generated: November 3, 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/1919000

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 bottle was purged with nitrogen and charged with tert-butyl 4-(6-nitropyridin-3-yl)piperazine-1-carboxylate (3.1 g, 10 mmol), 10% palladium on carbon (50% wet, 1 g) and ethanol (100 mL). The bottle was evacuated, charged with hydrogen gas, and stirred for 16 h at room temperature. The hydrogen was then evacuated and nitrogen charged into the bottle. The catalyst was removed by filtration through a pad of Celite and the filtrate concentrated under reduced pressure to afford tert-butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate (2.7 g, 97%). MS: [M+H]+ 279

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618107B2
Source datasetuspto-grants-2013_12
ORD IDord-5430f715f3894e7b8e0b2f6a497f576d
Source noteuspto-grants-2013_12