Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Tert-butyl 3-oxopyrrolidine-1-carboxylate | HCID 471360 | — |
| Reactant | Ethyl (4-formyl-1H-pyrazol-1-yl)acetate | HCID 53491200 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68766810 | HCID 68766810 | 35% |
Reaction Steps
To a solution of 1-(t-butoxycarbonyl)pyrrolidin-3-one (6.8 g) in ethanol (200 ml) were added ethyl(4-formyl-1H-pyrazol-1-yl)acetate (8.0 g) and pyrrolidine (600 μl). The resulting mixture was stirred at 80° C. for 45 minutes, cooled to room temperature, and the solvent was evaporated in vacuo. The residue was purified by chromatography on silica gel using a mixture of hexane, ethyl acetate and dichloromethane (2:1:1) as the eluent to afford the title compound as a yellow amorphous solid (4.47 g, yield: 35%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07829580B2 |
|---|
| Source dataset | uspto-grants-2010_11 |
|---|
| ORD ID | ord-e0beed6f4e304f088a5126da10ca4542 |
|---|
| Source note | uspto-grants-2010_11 |
|---|