Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851485Generated: November 1, 2026

2-Thiophenesulfonyl chloride → HCID 57901838, compound

https://huagongshe.com/reaction/1851485

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenesulfonyl chlorideHCID 85518—
ReactantHCID 67109346HCID 67109346—
SolventPyridineHCID 1049—
ProductHCID 57901838HCID 5790183881.1%

Reaction Steps

To a mixed solution of ethyl 7-amino-6-methyl-1H-indole-2-carboxylate (0.50 g) and pyridine (10 mL) was added 2-thiophenesulfonyl chloride (0.54 g) under ice-cooling, and the mixture was stirred at room temperature for 15 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 (677 mg, yield 81%) as colorless needle crystals. melting point 184-185° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957070B2
Source datasetuspto-grants-2015_02
ORD IDord-69ce595bb0a9413ab156e19a0449d7a1
Source noteuspto-grants-2015_02