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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265154Generated: October 30, 2026

2-Amino-4-methylpyridine → 2-Amino-5-bromo-4-methylpyridine

https://huagongshe.com/reaction/2265154

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-methylpyridineHCID 1533—
ReactantSodium SulfiteHCID 24437—
ReactantPyridinium hydrobromideHCID 21226041—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-5-bromo-4-methylpyridineHCID 81769553.5%

Reaction Steps

In a nitrogen atmosphere, 1.08 g of 2-amino-4-methylpyridine was dissolved in 75 mL of tetrahydrofuran, and tetrahydrofuran (75 mL) solution of 3.20 g of pyridinium hydrobromide perbromide was dropwise added thereto at room temperature, over 1.5 hours. After the addition, this was stirred at room temperature for 40 minutes, and 100 mL of aqueous saturated sodium sulfite solution was added to the reaction mixture. This was extracted with ethyl acetate, and the ethyl acetate layer was dried with magnesium sulfate. The solvent was evaporated off under reduced pressure, and the residue was separated and purified through silica gel column chromatography (hexane/ethyl acetate=4/1 to ethyl acetate) to obtain 1.00 g of the entitled compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855294B2
Source datasetuspto-grants-2010_12
ORD IDord-1f01f493708f42c2b5f93d1f57d3ee6c
Source noteuspto-grants-2010_12