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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851489Generated: November 1, 2026

2-Thiophenesulfonyl chloride → HCID 57901653, compound

https://huagongshe.com/reaction/1851489

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenesulfonyl chlorideHCID 85518—
Reactantethyl 7-amino-5-methoxy-1H-indole-2-carboxylateHCID 15399415—
SolventPyridineHCID 1049—
ProductHCID 57901653HCID 5790165357%

Reaction Steps

To a mixed solution of ethyl 7-amino-5-methoxy-1H-indole-2-carboxylate (0.40 g) and pyridine (10 mL) was added 2-thiophenesulfonyl chloride (0.38 g) under ice-cooling, and the mixture was stirred at room temperature for 14 hr. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with ethyl acetate, washed with aqueous citric acid solution, aqueous sodium hydrogencarbonate solution and brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (ethyl acetate:hexane=15:85-35:65), and the obtained crystals were recrystallized from ethyl acetate-hexane to give the title compound (370 mg, yield 57%) as colorless needle crystals. melting point 158-159° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957070B2
Source datasetuspto-grants-2015_02
ORD IDord-a12c6b160168497292c4616d56dae2e8
Source noteuspto-grants-2015_02