Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276913Generated: October 29, 2026

Triethylamine → N-benzenesulfonyl-3-(biphenyl-4-ylmethylamino)-4-butyrylaminobenzamide

https://huagongshe.com/reaction/1276913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantButyryl chlorideHCID 8855—
ReactantN-benzenesulfonyl-4-amino-3-(biphenyl-4-ylmethylamino)benzamideHCID 53635937—
SolventDimethylformamideHCID 6228—
ProductN-benzenesulfonyl-3-(biphenyl-4-ylmethylamino)-4-butyrylaminobenzamideHCID 1868082672.3%

Reaction Steps

Triethylamine (0.060 g) and 0.084 g of butyryl chloride were added to a solution of 0.300 g of N-benzenesulfonyl-4-amino-3-(biphenyl-4-ylmethylamino)benzamide in 2 ml of N,N-dimethylformamide, and the mixture was stirred at room temperature for 1.5 hours. The reaction solution was directly purified through silica-gel column chromatography to obtain 0.250 g of N-benzenesulfonyl-3-(biphenyl-4-ylmethylamino)-4-butyrylaminobenzamide. To this compound were added 5 ml of methanol and 0.50 g of 35% hydrochloric acid, and the mixture was stirred at 60° C. for 3 hours. Then, 20% potassium hydrogencarbonate was added thereto to stop the reaction, and the reaction solution was extracted with ethyl acetate and with water. The organic layer was concentrated, and the product was dissolved in a small amount of chloroform. Ether was added thereto for crystallization. The crystals precipitated were separated through filtration, and were dried to give 0.157 g of 6-benzenesulfonylcarbamoyl-1-(biphenyl-4-ylmethyl)-2-n-propylbenzimidazole potassium salt (232).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166219
Source datasetuspto-grants-2000_12
ORD IDord-082d8c9d0ff44dad9419d1d7a284205d
Source noteuspto-grants-2000_12