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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592831Generated: October 31, 2026

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

https://huagongshe.com/reaction/592831

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 numberUS09238655B2
Source datasetuspto-grants-2016_01
ORD IDord-1cebb3fbf5974fcbabb0b4475f371154
Source noteuspto-grants-2016_01