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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400761Generated: November 1, 2026

Piperazine → HCID 64369269, compound

https://huagongshe.com/reaction/2400761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,6-Dichloro-3-nitropyridineHCID 85239—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
ProductHCID 64369269HCID 6436926979.3%

Reaction Steps

piperazine (1.38 g) was added to a stirred solution of 2,6-dichloro-3-nitropyridine (3.0 g, prepared according to J. Heterocyclic Chem. 1994, 31, 73) and diisopropylethylamine (3.0 ml) in dichloromethane (100 ml) at 0° C. under N2. The resulting solution was stirred at room temperature for 2 hours then poured into saturated aqueous sodium bicarbonate, extracted with dichloromethane, dried over sodium sulfate and concentrated in vacuo. The residue was subjected to silica gel chromatography (ethyl acetate:methanol 8:2) to afford 1-(6-Chloro-3-nitro-pyridin-2-yl)-piperazine (2.99 g) as a red solid. M.p. 50-53° C.; MS (ES+) 243/245 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796274B2
Source datasetuspto-grants-2014_08
ORD IDord-5d0b96cf0dab4d64b10478f3e7f8400b
Source noteuspto-grants-2014_08