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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387161Generated: October 30, 2026

2-Chloro-5-nitropyridine → HCID 178526686, compound

https://huagongshe.com/reaction/1387161

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-nitropyridineHCID 78308—
ReactantHCID 178510931HCID 178510931—
SolventIsopropanolHCID 3776—
ProductHCID 178526686HCID 178526686—

Reaction Steps

A solution of 0.158 g (0.97 mmol) of 3-(1H-imidazol-4-yl)propylamine and of 0.154 g (0.97 mmol) of 2-chloro-5-nitropyridine in 10 ml of 2-propanol is brought to reflux for 21 h while stirring and evaporated under reduced pressure. The resulting residue is chromatographed on a column of silica gel, using a chloroform/methanol (1/1) mixture, to give the title compound in the form of a yellow oil. The latter is treated with oxalic acid in heated absolute ethanol to provide the oxalate salt which, after crystallization from 2-propanol, melts at 181°-182° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037303E1
Source datasetuspto-grants-2001_07
ORD IDord-1567fcc0c50f468ca0f8614faae9c2ed
Source noteuspto-grants-2001_07