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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894093Generated: October 25, 2026

Ammonia → N-(4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfonyl)-N'-butyl-urea

https://huagongshe.com/reaction/894093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium SulfiteHCID 24437—
ReactantChlorosulfonic acidHCID 24638—
ReactantN-Butyl-N'-hydroxyureaHCID 79761—
Reactant4-[2-(1-Oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfinic acidHCID 21162398—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductN-(4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfonyl)-N'-butyl-ureaHCID 21162325—

Reaction Steps

3.4 g of 4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfinic acid (crude product, prepared by reduction of the sulfochloride with sodium sulfite) and 1.4 g of N-hydroxy-N'-butyl-urea are suspended in 40 ml of dioxane and a solution of 1 ml of thionyl chloride in 10 ml of dioxane is added dropwise while stirring. The mixture is then heated for 2 hours to 60° C., whereby a limpid solution is formed. The solution is poured into water, the precipitated substance is treated with dilute ammonia, filtered, acidified and the reaction product is recrystallized from dilute acetone. The N-(4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfonyl)-N'-butyl-urea obtained melts at 188°-190° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04282239
Source datasetuspto-grants-1981_08
ORD IDord-2a951a18b4854d6ea0a8d51dfe41047f
Source noteuspto-grants-1981_08