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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851509Generated: November 4, 2026

2-Thiophenesulfonyl chloride → HCID 136060832, compound

https://huagongshe.com/reaction/1851509

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenesulfonyl chlorideHCID 85518—
ReactantHCID 136060813HCID 136060813—
SolventPyridineHCID 1049—
ProductHCID 136060832HCID 13606083243%

Reaction Steps

To a mixture of 2-(1,2,4-thiadiazol-5-yl)-1H-indole-7-amine (0.35 g) and pyridine (8 ml) was added thiophene-2-sulfonyl chloride (0.34 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 resulting crystals were filtrated, washed with water and dried. The obtained crystals were subjected to silica gel column chromatography, and eluted with ethyl acetate. The eluate was treated with activated carbon and concentrated to give the title compound (0.25 g, yield 43%) as colorless crystals. The crystals were recrystallized from ethyl acetate-hexane. melting point 232-233° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957070B2
Source datasetuspto-grants-2015_02
ORD IDord-7ec6bf648c654ecaa2e075311232e4e1
Source noteuspto-grants-2015_02