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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268252Generated: October 25, 2026

1-Methylpiperazine → 1-Methyl-4-(5-nitropyridin-2-yl)piperazine

https://huagongshe.com/reaction/268252

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant2-Chloro-5-nitropyridineHCID 78308—
SolventEthanolHCID 702—
Product1-Methyl-4-(5-nitropyridin-2-yl)piperazineHCID 2764066—

Reaction Conditions

Temperature5 °C

Reaction Steps

A 500 ml. 3-neck, r.b. flask fitted with y-tube and condenser and thermometer, stirrer and addition funnel was charged with a mixture of 2-chloro-5-nitropyridine (15.8 g. 0.1 mole) in ethanol (300 ml.). To this was added N-methylpiperazine (20 g. 0.2 mole) dropwise while stirring. After the addition (ca. 5 min.), the mixture was heated at reflux for 3 hr. while stirring continued. The solution was chilled to 5°C and the crystals were collected by filtration and dried at 60°C to yield 12 g. yellow crystals, m.p. 94°-96°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03947434
Source datasetuspto-grants-1976_03
ORD IDord-7fc1113a06b84f7ba20783a28fe98238
Source noteuspto-grants-1976_03