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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957522Generated: November 2, 2026

4-(Aminomethyl)piperidine → 4-(2,3,5,6-Tetrachloropyridin-4-ylaminomethyl)pyridine

https://huagongshe.com/reaction/1957522

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Aminomethyl)piperidineHCID 23527—
Reactant2,3,5,6-Tetrachloro-4-nitropyridineHCID 15229167—
Solvent1,4-DioxaneHCID 31275—
Product4-(2,3,5,6-Tetrachloropyridin-4-ylaminomethyl)pyridineHCID 1906808824.3%

Reaction Steps

1 g 4-nitro-2,3,5,6-tetrachloropyridine, 0.65 g 4-aminomethylpiperidine and 20 ml absolute dioxane were stirred for 1 hour at room temperature. Subsequently the dioxane was removed by distillation, the residue was admixed with water, separated from undissolved material and the aqueous phase was extracted several times with dichloromethane. After drying and evaporating the solvent, the residue can be crystallized from a small amount of diethyl ether. 0.3 g 4-(2,3,5,6-tetrachloropyridin-4-ylaminomethyl)pyridine is obtained as colourless crystals. TLC (mobile solvent: toluene/dioxane/water 90:20:0.2), Rf=0.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05786371
Source datasetuspto-grants-1998_07
ORD IDord-84fabf165bc542ec84c65cb7c38a9b47
Source noteuspto-grants-1998_07