HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-ethoxy-4-oxo-4,5-dihydrofuran-3-carboxylate → Ethyl 4-oxo-2-{[4-(2,2,2-trifluoroethyl)piperazinyl]amino}-4,5-dihydrofuran-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-ethoxy-4-oxo-4,5-dihydrofuran-3-carboxylate | HCID 13791062 | — |
| Reactant | 4-(2,2,2-Trifluoroethyl)piperazin-1-amine | HCID 80035743 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 4-oxo-2-{[4-(2,2,2-trifluoroethyl)piperazinyl]amino}-4,5-dihydrofuran-3-carboxylate | HCID 86708414 | — |
Reaction Steps
To a solution of 4-(2,2,2-trifluoroethyl)piperazine-1-amine (4.72 g, 25.8 mmol) in ethanol (43 mL), ethyl 2-ethoxy-4-oxo-4,5-dihydrofuran-3-carboxylate (4.70 g, 23.5 mmol) which similarly prepared according to the procedure described in the Example 74, Third step was added at ambient temperature. The mixture was stirred for 2 h. The precipitate was collected by filtration, washed with diethyl ether and hexane then dried to afford ethyl 4-oxo-2-{[4-(2,2,2-trifluoroethyl)piperazinyl]amino}-4,5-dihydrofuran-3-carboxylate as solid (5.64 g, y. 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08742113B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-4d39176845a5446dbc3da72c37974a13 |
| Source note | uspto-grants-2014_06 |