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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519335Generated: October 29, 2026

(S)-tert-Butyl 3-Ethyl-4-(6-nitropyridin-3-yl)piperazine-1-carboxylate → (S)-tert-Butyl 4-(6-Aminopyridin-3-yl)-3-ethylpiperazine-1-carboxylate

https://huagongshe.com/reaction/519335

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-tert-Butyl 3-Ethyl-4-(6-nitropyridin-3-yl)piperazine-1-carboxylateHCID 86683738—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(S)-tert-Butyl 4-(6-Aminopyridin-3-yl)-3-ethylpiperazine-1-carboxylateHCID 8668373989.1%

Reaction Steps

A 100-mL single-neck round-bottomed flask was purged with nitrogen and charged with 114a (0.7 g, 2.08 mmol), 10% palladium on carbon (50% wet, 208 mg), and methanol (40 mL). The mixture was evacuated, charged with hydrogen gas, and stirred at room temperature for 6 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 114b (568 mg, 89%). MS: [M+H]+ 306

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115152B2
Source datasetuspto-grants-2015_08
ORD IDord-a26dab6cce6c4ca6ae140d1b0ed18231
Source noteuspto-grants-2015_08