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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860051Generated: November 1, 2026

2,6-Dibromopyridine → 6-Bromo-(4-methoxybenzylamino)pyridine

https://huagongshe.com/reaction/860051

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DibromopyridineHCID 12274—
Reactant4-MethoxybenzylamineHCID 75452—
ReactantDiisopropylethylamineHCID 81531—
Solvent1,4-DioxaneHCID 31275—
Product6-Bromo-(4-methoxybenzylamino)pyridineHCID 2343550991.3%

Reaction Steps

A solution of 2,6-dibromopyridine 6-1 (37.3 g, 157 mmol), 4-methoxybenzylamine (21.6 g, 157 mmol), and diisopropylethylamine (22.4 g, 173 mmol) in 1,4-dioxane (150 mL) was heated at reflux for 24 h. The reaction mixture was cooled, concentrated in vacuo, and the residue was partitioned between EtOAc (100 mL) and saturated aqueous NaHCO3 (125 mL). The organic layer was washed with water (100 mL) followed by brine (100 mL) and dried (Na2SO4). The organic layer was filtered, concentrated in vacuo, and purified by flash chromatography (silica, 10% to 40% EtOAc/hexanes) affording 42 g of amine 6-2 as a white solid in 91% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153862B2
Source datasetuspto-grants-2006_12
ORD IDord-2c3ec9912dbe4a03ac48fae93f428979
Source noteuspto-grants-2006_12