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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851875Generated: October 30, 2026

Triethylamine → N-[2-(Aminosulphonyl)4-methoxyphenyl]-4-chlorobutanamide

https://huagongshe.com/reaction/851875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Chlorobutyryl chlorideHCID 78370—
Reactant2-Amino-5-methoxybenzenesulfonamideHCID 11252665—
SolventTetrahydrofuranHCID 8028—
ProductN-[2-(Aminosulphonyl)4-methoxyphenyl]-4-chlorobutanamideHCID 15908218—

Reaction Steps

144 mmol of triethylamine and then, dropwise, a solution containing 135 mmol of 4-chlorobutanoic acid chloride in 30 ml of tetrahydrofuran (THF), are added to a solution containing 96.4 mmol of 2-amino-5-methoxybenzenesulphonamide in 200 ml of THF. After stirring overnight at ambient temperature, the THF is evaporated off and the residue is taken up in water. Following extraction with ethyl acetate, the organic phase is washed and dried. After evaporation, the expected product is obtained in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253161B2
Source datasetuspto-grants-2007_08
ORD IDord-dfdf212ed3e34cef8c7f22471cfe2e7b
Source noteuspto-grants-2007_08