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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164789Generated: October 25, 2026

4-Chlorobenzenesulfonyl chloride → 2-(4-chlorobenzenesulphonamido)-N-(3-imidazol-1-ylpropyl)benzamide

https://huagongshe.com/reaction/2164789

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzenesulfonyl chlorideHCID 7398—
ReactantSodium BicarbonateHCID 516892—
Reactant2-amino-N-(3-imidazol-1-ylpropyl)benzamideHCID 2798335—
SolventWaterHCID 962—
Product2-(4-chlorobenzenesulphonamido)-N-(3-imidazol-1-ylpropyl)benzamideHCID 279833645.4%

Reaction Steps

4-Chlorobenzenesulphonyl chloride (1.56 g) was added in portions over 2 minutes to a solution of 2-amino-N-(3-imidazol-1-ylpropyl)benzamide (1.8 g) in water (50 ml) at 80° C. on a steam bath. The mixture was stirred at 80°-90° C. for 3 hours, cooled to room temperature and brought to pH 7 with saturated aqueous sodium bicarbonate solution. The crude product which had precipitated was extracted into dichloromethane (2×100 ml); the resulting solution was dried over magnesium sulphate and evaporated to give a solid. The solid was recrystallised from ethanol to give 2-(4-chlorobenzenesulphonamido)-N-(3-imidazol-1-ylpropyl)benzamide (1.4 g), in the form of a white solid, m.p. 174°-176° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04507315
Source datasetuspto-grants-1985_03
ORD IDord-6238ef570f9e42dd95371431c4a2d662
Source noteuspto-grants-1985_03