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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851431Generated: November 2, 2026

2-Thiophenesulfonyl chloride → HCID 25213949, compound

https://huagongshe.com/reaction/1851431

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenesulfonyl chlorideHCID 85518—
ReactantHCID 57901811HCID 57901811—
SolventPyridineHCID 1049—
ProductHCID 25213949HCID 2521394984.1%

Reaction Steps

To a mixture of 2-(pyridin-2-yl)-1H-indole-7-amine (0.35 g) and pyridine (6 mL) was added thiophene-2-sulfonyl chloride (0.38 g) at 0° C., and the mixture was stirred at room temperature for 2 hr. 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 residue was subjected to silica gel column chromatography and the title compound (0.50 g, yield 82%) was obtained as pale-yellow crystals from a fraction eluted with ethyl acetate-hexane (1:3, volume ratio). The crystals were recrystallized from ethyl acetate-hexane. melting point 161-162° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957070B2
Source datasetuspto-grants-2015_02
ORD IDord-fd1508b96a604f59accf2d3de35c2422
Source noteuspto-grants-2015_02