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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591756Generated: October 25, 2026

Ethylenediamine → 2,3-Dichloro-N-[2-(3-{2-[4-(4,5-dihydro-1H-imidazol-2-yl) phenyl]ethyl}-2-oxoimidazolidin-1-yl)ethyl]-N-methylbenzenesulphonamide hydrochloride

https://huagongshe.com/reaction/1591756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantSulfurHCID 5362487—
Reactant2,3-dichloro-N-(2-{3-[2-(4-cyanophenyl)ethyl]-2-oxoimidazolidin-1-yl}ethyl)-N-methylbenzenesulphonamideHCID 69424668—
SolventWaterHCID 962—
Product2,3-Dichloro-N-[2-(3-{2-[4-(4,5-dihydro-1H-imidazol-2-yl) phenyl]ethyl}-2-oxoimidazolidin-1-yl)ethyl]-N-methylbenzenesulphonamide hydrochlorideHCID 69422960—

Reaction Steps

A solution of 137 mg (0.29 mmol) of 2,3-dichloro-N-(2-{3-[2-(4-cyanophenyl)ethyl]-2-oxoimidazolidin-1-yl}ethyl)-N-methylbenzenesulphonamide, 2 ml of ethylenediamine and 4.6 mg (0.14 mmol) of sulphur was stirred at 100° C. for two hours. Water was then added, and the mixture was extracted with ethyl acetate. The organic extracts were washed with saturated sodium chloride solution, dried over sodium sulphate and concentrated. The crude product obtained in this manner was purified by column chromatography on silica gel (mobile phase: dichloromethane/methanol/NH3 13:1:0.1 to 8:1:0.1). Using etheral hydrochloric acid, the product was then converted into the hydrochloride and freeze-dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291642B2
Source datasetuspto-grants-2007_11
ORD IDord-40b7d3b4905546ae83aed4274c92ce92
Source noteuspto-grants-2007_11