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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366824Generated: November 2, 2026

Methyl iodide → 5-Bromo-N-methylpyridin-2-amine

https://huagongshe.com/reaction/2366824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant2-Amino-5-bromopyridineHCID 70622—
SolventDimethylformamideHCID 6228—
Product5-Bromo-N-methylpyridin-2-amineHCID 1564566323.6%

Reaction Steps

NaH (47.3 mg, 1.971 mmol) and 5-bromo-2-pyridinamine (310 mg, 1.792 mmol, available from Aldrich) were added to N,N-Dimethylformamide (DMF) (7 mL) and stirred in an ice bath for 30 mins. The reaction mixture was then allowed to warm to room temperature and methyl iodide (0.123 mL, 1.971 mmol) was added and the reaction mixture stirred for 24 hr. The reaction mixture was partitioned between DCM (20 mL) and water (20 mL) and the organic layer washed with more water (20 mL) before being dried through an hydrophobic frit and concentrated. The residue was dissolved in DCM and purified by SP4 on a 25+S silica cartridge using a gradient of 10%-40% EtOAc in cyclohexane. Appropriate fractions were collected and concentrated to yield the desired product as a white solid (79.1 mg). LCMS (Method C): Rt 0.39, MH+=187

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697725B2
Source datasetuspto-grants-2014_04
ORD IDord-62d4a30bb12f449587ab7aa55963bc3d
Source noteuspto-grants-2014_04