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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050349Generated: November 2, 2026

2-Dimethylaminopyridine → HCID 20342661, compound

https://huagongshe.com/reaction/2050349

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-DimethylaminopyridineHCID 21885—
Reactant2,4-Imidazolidinedione, 3-(hydroxymethyl)-1-(2-propynyl)-HCID 11789597—
Reactant3-(4-Chlorophenyl)-4-isopropyloxazolidine-2,5-dioneHCID 13229494—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20342661HCID 20342661—

Reaction Steps

To a solution of 3-(4-chlorophenyl)-4-isopropyloxazolidine-2,5-dione (1.32 mmol) and dimethylaminopyridine in 5 ml of dry tetrahydrofuran is added a solution of (2,4-dioxo-1-propargyl-3-imidazolidinyl)methanol (1.26 mmol) in 3 ml of dry tetrahydrofuran. The reaction mixture is stirred for about 20 hours, under dry air, and then diluted with ether followed by washing with saturated aqueous sodium bicarbonate, water and saturated aqueous sodium chloride. After drying over calcium sulfate, solvent is evaporated. The crude product is chromatographed on a rotary chromatograph eluting with 15% ether/hexane to give (2,4-dioxo-1-propargyl-3-imidazolidinyl)methyl 2-(4-chlorophenylamino)-3-methylbutanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04200758
Source datasetuspto-grants-1980_04
ORD IDord-cc6ec4a96f164068a70efbd2438114eb
Source noteuspto-grants-1980_04