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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251495Generated: November 4, 2026

Methanol → 6-Bromo-2-methoxypyridin-3-amine

https://huagongshe.com/reaction/1251495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
Reactant6-Methoxy-3-pyridinylamineHCID 81121—
ReactantBenzyltrimethylammoniumtribromideHCID 53442637—
SolventWaterHCID 962—
Product6-Bromo-2-methoxypyridin-3-amineHCID 10536137—

Reaction Steps

Part A: To 3.18 grams (25.6 mmol) of commercially available 5-amino-2-methoxypyridine in a solution of methylene chloride (50 ml) and methanol (20 ml) was added benzyltrimethylammonium tribromide (10 g, 25.6 mmol) and the mixture was stirred at room temperature for 24 hours. The solvent was then stripped and the resulting residue was taken up in water and extracted (3×100 mL) with ethyl acetate. The organic extracts were dried with magnesium sulfate, filtered, and concentrated in vacuo. The crude material was chromatographed on silica using 30% ethyl acetate in hexanes as solvent to afford 5-amino-2-bromo-6-methoxypyridine. C6H7N2OBr MS 203 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06342503B1
Source datasetuspto-grants-2002_01
ORD IDord-3a170b9c823f40688c32e8fda4e8639f
Source noteuspto-grants-2002_01