HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453571Generated: October 29, 2026
Water → Methyl 5-methyl-4-[methyl(2-thienylsulfonyl)amino]thiophene-2-carboxylate
https://huagongshe.com/reaction/453571
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 5-methyl-4-[(2-thienylsulfonyl)amino]thiophene-2-carboxylate | HCID 59411395 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 5-methyl-4-[methyl(2-thienylsulfonyl)amino]thiophene-2-carboxylate | HCID 59411375 | 99% |
Reaction Steps
To a solution of methyl 5-methyl-4-[(2-thienylsulfonyl)amino]thiophene-2-carboxylate (35.7 g) in N,N-dimethylformamide (200 mL) was slowly added sodium hydride (60%, oily, 5.2 g) at 0° C., and the mixture was stirred at room temperature for 30 min. Methyl iodide (8.0 mL) was added to the reaction mixture, and the mixture was stirred at room temperature for 1 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography to give methyl 5-methyl-4-[methyl(2-thienylsulfonyl)amino]thiophene-2-carboxylate (37.5 g, yield 99%) as yellow crystals from a fraction eluted with ethyl acetate-hexane (1:3, volume ratio).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492405B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-3ae1d7e9e193439aab83b9c2c206b2b7 |
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| Source note | uspto-grants-2013_07 |
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