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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 2-chloro-6-methanesulphonylamino-isonicotinate | HCID 86615008 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-chloro-6-[methyl(methylsulfonyl)amino]isonicotinate | HCID 86612064 | 72.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07618978B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-9a0f7221b90145a9870c2225921b03e7 |
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| Source note | uspto-grants-2009_11 |
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