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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736851Generated: October 26, 2026

Benzenesulfonamide → HCID 15104381, compound

https://huagongshe.com/reaction/1736851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonamideHCID 7370—
ReactantThionyl ChlorideHCID 24386—
Reactant2-[4-(2-Butylbenzimidazol-1-yl)methylphenyl]benzoic acidHCID 4110026—
SolventDichloromethaneHCID 6344—
SolventSodium chloride ethyl acetateHCID 86643102—
ProductHCID 15104381HCID 15104381—

Reaction Conditions

Temperature140 °C

Reaction Steps

960 mg (2.5 mmol) of 4'-[(2-n-butyl-benzimidazol-1-yl)-methyl]biphenyl-2-carboxylic acid are dissolved in 25 ml of methylene chloride, treated with 2 ml of thionyl chloride and heated under reflux for one hour. The solvent is then distilled off and evaporated 2 times after adding methylene chloride. 390 mg (2.5 mmol) of benzenesulphonamide are added to the residue and the mixture is heated for one hour at 140° C. After cooling, the oil obtained is taken up in ethyl acetate/sodium chloride solution and extracted 3 times using ethyl acetate. The combined ethyl acetate phases are dried over sodium sulphate, evaporated and the crude product obtained is purified over a silica gel column using methylene chloride/ethanol as eluting agent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541229
Source datasetuspto-grants-1996_07
ORD IDord-105e333f5c414dd6a974571542bd329c
Source noteuspto-grants-1996_07