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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851482Generated: November 1, 2026

2-Thiophenesulfonyl chloride → HCID 57901695, compound

https://huagongshe.com/reaction/1851482

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenesulfonyl chlorideHCID 85518—
ReactantHCID 67109617HCID 67109617—
SolventPyridineHCID 1049—
ProductHCID 57901695HCID 5790169547%

Reaction Steps

To a mixed solution of ethyl 7-amino-4-(propylthio)-1H-indole-2-carboxylate (0.90 g) and pyridine (10 mL) was added 2-thiophenesulfonyl chloride (0.72 g) under ice-cooling, and the mixture was stirred at room temperature for 16 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=1:9-1:3), and the obtained crystals were recrystallized from ethyl acetate-hexane to give the title compound (0.64 g, yield 47%) as colorless needle crystals. melting point 150-151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957070B2
Source datasetuspto-grants-2015_02
ORD IDord-252ccb5a1d4d4b79a5444afb600beeb5
Source noteuspto-grants-2015_02