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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12307Generated: October 23, 2026

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

https://huagongshe.com/en/reaction/12307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium ThiosulfateHCID 24477—
Reactant6-Methoxy-3-pyridinylamineHCID 81121—
ReactantSodium AcetateHCID 517045—
SolventAcetic AcidHCID 176—
Product2-Bromo-6-methoxypyridin-3-amineHCID 15209324—

Reaction Steps

A mixture of 1.83 g (14.7 mM) of 5-amino-2-methoxypyridine and 1.21 g (14.7 mM) of sodium acetate in 12 ml of acetic acid is prepared and 0.75 ml (14.7 mM) of bromine is added gently, with stirring and while maintaining at room temperature. The reaction mixture is kept stirring for 30 minutes, at room temperature, and 200 ml of saturated sodium thiosulfate solution are then added. The aqueous phase obtained is extracted twice with ethyl acetate. The combined organic phases are dried over magnesium sulfate and concentrated under reduced pressure. 3 g of the expected compound are obtained in the form of a violet-colored solid (quantitative yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728002B2
Source datasetuspto-grants-2010_06
ORD IDord-27352282c0af4dfbb16addeee00b36b0
Source noteuspto-grants-2010_06