HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → 2,2-Dimethyl-5-oxo-3-(4-hydroxy-2-oxo-1-pyrrolidineacetyl)-1-imidazolidineacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Pyrrolidineacetic acid, 4-hydroxy-2-oxo-, (+-)- | HCID 11126541 | — |
| Reactant | 2,2-Dimethyl-5-oxo-1-imidazolidineacetamide | HCID 20155466 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,2-Dimethyl-5-oxo-3-(4-hydroxy-2-oxo-1-pyrrolidineacetyl)-1-imidazolidineacetamide | HCID 20163736 | — |
Reaction Steps
To a stirred solution of 4-hydroxy-2-oxo-1-pyrrolidine acetic acid (3.18 g) and 2,2-dimethyl-5-oxo-1-imidazolidineacetamide (3.5 g) in 100 ml of dimethylformamide at room temperature, 4.12 g of DCC were added at once. After 5 hours the solvent was evaporated under vacuum and the residue was suspended in 50 ml of stirred water. After 10 minutes the solid was filtered off and the water evaporated under reduced pressure. The residue was triturated with isopropanol and collected, affording the title product as a white powder m.p. 248°-250° C. (decomp).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04703054 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-b5c5db79365543d2a04389841ef4802c |
| Source note | uspto-grants-1987_10 |