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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851478Generated: November 2, 2026

2-Thiophenesulfonyl chloride → HCID 57476231, compound

https://huagongshe.com/reaction/1851478

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenesulfonyl chlorideHCID 85518—
Reactantethyl 7-amino-5-methyl-1H-indole-2-carboxylateHCID 21218299—
SolventPyridineHCID 1049—
ProductHCID 57476231HCID 5747623191%

Reaction Steps

To a mixed solution of ethyl 7-amino-5-methyl-1H-indole-2-carboxylate (0.60 g) and pyridine (10 mL) was added 2-thiophenesulfonyl chloride (0.66 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=3:7-5:5), and the obtained crystals were recrystallized from ethyl acetate-hexane to give the title compound (910 mg, yield 91%) as colorless needle crystals. melting point 168-169° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957070B2
Source datasetuspto-grants-2015_02
ORD IDord-821e049db7bc426d8af712a7bde9ab6e
Source noteuspto-grants-2015_02