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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 5-methyl-4-[(2-thienylsulfonyl)amino]thiophene-2-carboxylateHCID 59411395—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-methyl-4-[methyl(2-thienylsulfonyl)amino]thiophene-2-carboxylateHCID 5941137599%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492405B2
Source datasetuspto-grants-2013_07
ORD IDord-3ae1d7e9e193439aab83b9c2c206b2b7
Source noteuspto-grants-2013_07