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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851374Generated: November 1, 2026

2-Thiophenesulfonyl chloride → HCID 57901854, compound

https://huagongshe.com/reaction/1851374

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenesulfonyl chlorideHCID 85518—
ReactantHCID 57901783HCID 57901783—
SolventPyridineHCID 1049—
ProductHCID 57901854HCID 5790185496.2%

Reaction Steps

To a mixture of 3-chloro-1-(methoxymethyl)-2-(1,3-thiazol-2-yl)-1H-indole-7-amine (0.25 g) and pyridine (8 mL) was added thiophene-2-sulfonyl chloride (0.19 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 mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The obtained residue was subjected to silica gel column chromatography and the title compound (0.36 g, yield 96%) was obtained as yellow crystals from a fraction eluted with ethyl acetate-hexane (1:2, volume ratio). melting point 128-129° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957070B2
Source datasetuspto-grants-2015_02
ORD IDord-b3a2c31ccfaf4044932d8aa1924337f5
Source noteuspto-grants-2015_02