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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238899Generated: October 30, 2026

Tetrahydrofuran → 6-chloro-7-[(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acid

https://huagongshe.com/reaction/2238899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
Reactantethyl 6-chloro-7-[(2-thienylsulfonyl)amino]-1H-indole-2-carboxylateHCID 57476027—
SolventMethanolHCID 887—
Product6-chloro-7-[(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acidHCID 5747602695%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of ethyl 6-chloro-7-[(2-thienylsulfonyl)amino]-1H-indole-2-carboxylate (1.00 g), 4N aqueous sodium hydroxide solution (2.3 ml), tetrahydrofuran (5 ml) and methanol (5 ml) was stirred at 50° C. for 2 hr. The reaction mixture was concentrated, and acidified with 10% aqueous citric acid solution, and the resulting crystals were collected by filtration, washed with water, and dried to give the title compound (0.88 g, yield 95%) as colorless crystals. melting point >290° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718798B2
Source datasetuspto-grants-2010_05
ORD IDord-19b41f34407b47329ca6cbd207310a2a
Source noteuspto-grants-2010_05