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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485489Generated: October 30, 2026

2-Chloro-5-nitropyridine → 1-Ethyl-4-(5-nitropyridin-2-yl)piperazine

https://huagongshe.com/reaction/1485489

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-nitropyridineHCID 78308—
Reactant1-EthylpiperazineHCID 79196—
ReactantDiisopropylethylamineHCID 81531—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product1-Ethyl-4-(5-nitropyridin-2-yl)piperazineHCID 284898088%

Reaction Conditions

Temperature70 °C

Reaction Steps

2-Chloro-5-nitropyridine (800 mg, 5.05 mmol) was dissolved in dioxane (20 mL) and then 1-ethylpiperazine (1.7 g, 15.15 mmol) and N,N-diisopropylethylamine (927 mL, 5.05 mmol) were added. The reaction mixture solution was stirred at 70° C. for a day. The reaction solution was cooled to room temperature, diluted with ethyl acetate, and then washed with brine. The organic layer was concentrated by drying with magnesium sulfate. The target compound (1.05 g, 87% yield) was used in the following reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422307B2
Source datasetuspto-grants-2016_08
ORD IDord-9d618501bbbb48b1ac2129bfe2c05047
Source noteuspto-grants-2016_08