HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → (S)-7-(1-Pyrrolidinyl)-1,2,3,5,8,8a-hexahydroindolizin-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | HCID 58681494 | HCID 58681494 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Pyrrolidine | HCID 31268 | — |
| Product | (S)-7-(1-Pyrrolidinyl)-1,2,3,5,8,8a-hexahydroindolizin-5-one | HCID 58681493 | 204.1% |
Reaction Steps
(S)-1,2,3,5,6,7,8,8a-octahydroindolizin-5,7-dione (117 mg (0.76 mmol), prepared as described in 3)) was dissolved in ethanol (1.2 ml). To the solution was added pyrrolidine (128 μl, 1.53 mmol), and the resulting mixture was allowed to stand at room temperature for 5 minutes. At the end of this time, the reaction mixture was concentrated by distillation under reduced pressure to remove solvents and any excess of pyrrolidine, to give the title compound (160 mg) as a light yellow powder (yield quantitative).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091352B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-5f9f9d01fa924902888dbe11994c4910 |
| Source note | uspto-grants-2006_08 |