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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411770Generated: November 2, 2026

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

https://huagongshe.com/reaction/1411770

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-5-nitropyridineHCID 78240—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventAcetonitrileHCID 6342—
Producttert-Butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylateHCID 1621794354.1%

Reaction Steps

A mixture of 2-bromo-5-nitropyridine (5.0 g, 24.6 mmol), tert-butyl piperazine-1-carboxylate (13.8 g, 74.2 mmol), acetonitrile (150 mL) was stirred at reflux for 2.5 h. After the reaction was completed, the solvent was removed under reduced pressure to afford 197a as a yellow solid (4.1 g, 54%). MS-ESI: [M+H]+ 309.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921353B2
Source datasetuspto-grants-2014_12
ORD IDord-96e6abd69573444ab5dee028148835f5
Source noteuspto-grants-2014_12