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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894095Generated: October 25, 2026

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

https://huagongshe.com/reaction/894095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButylureaHCID 11595—
ReactantSodium hydrideHCID 24758—
Reactant4-[2-(1-Oxo-isoindoline-2-carboxamido)-ethyl]-benzene sulfochlorideHCID 21162349—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfonyl)-N'-butyl-ureaHCID 21162325—

Reaction Steps

4.8 g of butyl urea are dissolved in 100 ml of tetrahydrofurane and, while stirring, 1.5 g of 80% sodium hydride (in oil) are added. The mixture is heated for 3 hours to 60° C. whereupon 7.6 g of 4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzene-sulfochloride in 100 ml of tetrahydrofurane are added while cooling. The temperature is slowly raised to 60°-70° C. and stirring is continued at that temperature for 3 hours. The solvent is removed under reduced pressure, water is added to the residue, the mixture is filtered and the filtrate is acidified with dilute hydrochloric acid. After recrystallization from dilute acetone, the N-(4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]benzenesulfonyl)-N'-butyl-urea melts at 189°-190° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04282239
Source datasetuspto-grants-1981_08
ORD IDord-eeaef196eedc4b268efebd985dfcd232
Source noteuspto-grants-1981_08