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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851449Generated: October 30, 2026

Tetrahydrofuran → 7-{[(5-Chloro-2-thienyl)sulfonyl]amino}-1H-indole-2-carboxylic acid

https://huagongshe.com/reaction/1851449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 7-{[(5-chloro-2-thienyl)sulfonyl]amino}-1H-indole-2-carboxylateHCID 57901736—
SolventEthanolHCID 702—
Product7-{[(5-Chloro-2-thienyl)sulfonyl]amino}-1H-indole-2-carboxylic acidHCID 5790182896.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of ethyl 7-{[(5-chloro-2-thienyl)sulfonyl]amino}-1H-indole-2-carboxylate (1.03 g), 8N aqueous sodium hydroxide solution (1.3 mL), tetrahydrofuran (5 mL) and ethanol (15 mL) was stirred at 60° C. for 2 hr. The reaction mixture was concentrated, and water was added to the residue. The mixture was acidified with 10% aqueous citric acid solution, and the resulting crystals were filtrated, washed with water, and dried to give the title compound (0.92 g, yield 90%) as colorless crystals. melting point>277° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957070B2
Source datasetuspto-grants-2015_02
ORD IDord-962c90df62b2416a9bb034b994beadb2
Source noteuspto-grants-2015_02