HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Dimethylaminopyridine → HCID 20342661, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 2,4-Imidazolidinedione, 3-(hydroxymethyl)-1-(2-propynyl)- | HCID 11789597 | — |
| Reactant | 3-(4-Chlorophenyl)-4-isopropyloxazolidine-2,5-dione | HCID 13229494 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20342661 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04200758 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-cc6ec4a96f164068a70efbd2438114eb |
| Source note | uspto-grants-1980_04 |