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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504673Generated: November 3, 2026

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

https://huagongshe.com/reaction/504673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
Reactantethyl 6-chloro-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxylateHCID 57476030—
SolventMethanolHCID 887—
Product6-chloro-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acidHCID 57476031100.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of ethyl 6-chloro-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxylate (0.74 g), 4N aqueous sodium hydroxide solution (1.2 ml), tetrahydrofuran (6 ml) and methanol (4 ml) was stirred at 60° 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 (0.69 g, quantitative) as colorless crystals. melting point 286-288° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07777047B2
Source datasetuspto-grants-2010_08
ORD IDord-5b7ba7d094594b3e9905beaa7a89cec7
Source noteuspto-grants-2010_08