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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436585Generated: October 26, 2026

Methyl iodide → Methyl 2-chloro-6-[methyl(methylsulfonyl)amino]isonicotinate

https://huagongshe.com/reaction/1436585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 2-chloro-6-methanesulphonylamino-isonicotinateHCID 86615008—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-chloro-6-[methyl(methylsulfonyl)amino]isonicotinateHCID 8661206472.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Add sodium hydride (257 mg, 6.43 mmol, 60% dispersion in mineral oil) at 0° C. to a solution of 2-chloro-6-methanesulfonylamino-isonicotinic acid methyl ester (1.31 g, 4.95 mmol) in DMF (10 mL). After stirring at 0° C. for 15 min, add iodomethane (0.4 mL, 6.43 mmol). Stir the reaction at 0° C. for 1 h and at room temperature for 2 h. Quench the reaction with ice and extract the reaction mixture with ethyl acetate. Wash the organic layer with saturated aqueous sodium chloride, dry (sodium sulfate), concentrate and purify (silica gel chromatography, eluting with 30:70 ethyl acetate:hexanes) to give the title compound (1.0 g,72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618978B2
Source datasetuspto-grants-2009_11
ORD IDord-9a0f7221b90145a9870c2225921b03e7
Source noteuspto-grants-2009_11