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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453570Generated: October 30, 2026

2-Thiophenesulfonyl chloride → Methyl 5-methyl-4-[(2-thienylsulfonyl)amino]thiophene-2-carboxylate

https://huagongshe.com/reaction/453570

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenesulfonyl chlorideHCID 85518—
ReactantMethyl 4-amino-5-methylthiophene-2-carboxylateHCID 59640747—
SolventPyridineHCID 1049—
ProductMethyl 5-methyl-4-[(2-thienylsulfonyl)amino]thiophene-2-carboxylateHCID 5941139596.3%

Reaction Steps

To a mixture of methyl 4-amino-5-methylthiophene-2-carboxylate (20 g) and pyridine (100 mL) was added 2-thiophen-sulfonyl chloride (23.5 g) at 0° C., and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated, water was added, 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-[(2-thienylsulfonyl)amino]thiophene-2-carboxylate (35.7 g, yield 96%) as pale-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-f98ef8475d544d2f9dc0ff43e6baba46
Source noteuspto-grants-2013_07