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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851376Generated: October 31, 2026

2-Thiophenesulfonyl chloride → Ethyl 2-{1-(methoxymethyl)-7-[(2-thienylsulfonyl)amino]-1H-indol-2-yl}-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/1851376

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenesulfonyl chlorideHCID 85518—
ReactantEthyl 2-[7-amino-1-(methoxymethyl)-1H-indol-2-yl]-1,3-thiazole-5-carboxylateHCID 57901657—
SolventPyridineHCID 1049—
ProductEthyl 2-{1-(methoxymethyl)-7-[(2-thienylsulfonyl)amino]-1H-indol-2-yl}-1,3-thiazole-5-carboxylateHCID 5790170070%

Reaction Steps

To a mixture of ethyl 2-[7-amino-1-(methoxymethyl)-1H-indol-2-yl]-1,3-thiazole-5-carboxylate (2.18 g) and pyridine (25 mL) was added thiophene-2-sulfonyl chloride (1.50 g) at 0° C., and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated, 10% aqueous citric acid solution was added, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The obtained residue was subjected to silica gel column chromatography and the title compound (2.19 g, yield 70%) was obtained as yellow crystals from a fraction eluted with ethyl acetate-hexane (1:3, volume ratio). melting point 133-134° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957070B2
Source datasetuspto-grants-2015_02
ORD IDord-0ee45517b648483ea7772f4857e647fb
Source noteuspto-grants-2015_02