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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042210Generated: November 1, 2026

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

https://huagongshe.com/reaction/2042210

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 numberUS08586580B2
Source datasetuspto-grants-2013_11
ORD IDord-27c945d55a6245ecad8134a2572a5ecb
Source noteuspto-grants-2013_11