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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591748Generated: October 29, 2026

Triethylamine → 3-(4-Cyanophenyl)-N-{3-[(2,3-dichlorobenzenesulphonyl)methyl-amino]propyl}propionamide

https://huagongshe.com/reaction/1591748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant2-(4-Cyanophenyl)propanoic acidHCID 22569863—
ReactantN-(3-aminopropyl)-2,3-dichloro-N-methylbenzenesulphonamideHCID 69423487—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Cyanophenyl)-N-{3-[(2,3-dichlorobenzenesulphonyl)methyl-amino]propyl}propionamideHCID 69421741—

Reaction Steps

A solution of 1.47 g (8.41 mmol) of 4-cyanophenylpropionic acid, 3.1 g (9.65 mmol) of TBTU and 5.0 ml of triethylamine in 150 ml of tetrahydrofuran was stirred at room temperature for 30 minutes, 2.5 g (8.41 mmol) of N-(3-aminopropyl)-2,3-dichloro-N-methylbenzenesulphonamide were than added and the mixture was stirred overnight. The mixture was evaporated to dryness, potassium carbonate solution (10%) was added to the residue and the mixture was extracted with ethyl acetate. The organic phase was washed with water and saturated sodium chloride solution, drive over sodium sulphate and concentrated. The crude product obtained in this manner was purified by column chromatography (mobile phase: dichloromethane/methanol 150:1 to 100:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291642B2
Source datasetuspto-grants-2007_11
ORD IDord-3ef57e68456c4b97a671b3306a2a44c1
Source noteuspto-grants-2007_11