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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848362Generated: October 31, 2026

Methyl iodide → 3-Bromo-6-methoxypyridin-2-amine

https://huagongshe.com/reaction/1848362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178508959HCID 178508959—
SolventDimethylformamideHCID 6228—
Product3-Bromo-6-methoxypyridin-2-amineHCID 2343587912.1%

Reaction Steps

Under an argon atmosphere 6-amino-5-bromo-pyridin-2-ol (23 g, 122 mmol) was dissolved in DMF (300 mL). K2CO3 (50.6 g, 366 mmol) was added followed by the addition of methyl iodide (11.4 mL, 183 mmol). The mixture was stirred for 4 h while keeping the temperature at 20-25° C. The suspension was poured onto H2O (1 L) and the aqueous phase was extracted with EtOAc (×2). The combined organic phases washed with H2O (0.5 L) and brine (200 mL), dried over Na2SO4, filtered and concentrated in vacuo. The crude product was purified by flash chromatography, eluent toluene:heptane 2:1->100:0 followed by toluene:EtOAc 95:5 to afford 3-bromo-6-methoxy-pyridin-2-ylamine as a solid (3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952162B2
Source datasetuspto-grants-2015_02
ORD IDord-c770a1b1092a44f2bb4fce3b0585347d
Source noteuspto-grants-2015_02