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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024412Generated: November 1, 2026

2,6-Dibromopyridine → 6-Bromo-N-(4-chlorobenzyl)pyridin-2-amine

https://huagongshe.com/reaction/1024412

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DibromopyridineHCID 12274—
Reactant4-ChlorobenzylamineHCID 66036—
SolventDiethyl EtherHCID 3283—
Product6-Bromo-N-(4-chlorobenzyl)pyridin-2-amineHCID 57597938100.8%

Reaction Conditions

Temperature150 °C

Reaction Steps

A microwave vial was charged with 4-chloro benzylamine (700 mg; 5 mmol; 5 equivalents) and 2,6-dibromo pyridine (238 mg, 1 mmol). The reaction mixture was stirred in the microwave at 150° C. for three times ten minutes (200 W maximum). The reaction mixture was diluted with diethyl ether (50 ml), washed with 10% aqueous citric acid, saturated aqueous sodium bicarbonate and brine. The organic was dried over magnesium sulfate and, after filtration, concentrated in vacuo to afford an oil as the title compound (300 mg, 100% yield). LC/MS: 299 [M+H]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722889B2
Source datasetuspto-grants-2014_05
ORD IDord-3eab978e7f6449a891a0972e1304a09c
Source noteuspto-grants-2014_05