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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691836Generated: November 2, 2026

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

https://huagongshe.com/reaction/1691836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantDimethyl SulfateHCID 6497—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 178508959HCID 178508959—
SolventDimethylformamideHCID 6228—
Product3-Bromo-6-methoxypyridin-2-amineHCID 2343587913%

Reaction Steps

To a solution of 6-amino-5-bromo-pyridin-2-ol (1.0 g) in DMF (30 mL) was added at 0° C. 0.5 M potassium bis(trimethylsilyl)amide in toluene (11.7 mL, 5.83 mmol) under Ar atmosphere. After stirring for 10 minutes, dimethyl sulfate (0.64 mL, 5.26 mmol) was added at 0° C. The mixture was allowed to warm to room temperature, and was stirred for an additional two hours. Buffer (pH 7) was added and mixture was extracted with diethyl ether. The combined organic extracts were washed with brine, dried (Na2SO4), filtered and concentrated to dryness. Purification of the residue by flash chromatography (hexane/toluene 45:55) gave pure 3-bromo-6-methoxy-pyridin-2-ylamine (260 mg, 13% overall).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153809B2
Source datasetuspto-grants-2012_04
ORD IDord-ce2cadbc33ae4ac9b518f9027dcd802b
Source noteuspto-grants-2012_04