HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Azaindole → 3-(1,2,3,5,8,8a-hexahydro-7-indolizinyl)-1H-5-Azaindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Azaindole | HCID 9220 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(1,2,3,5,8,8a-hexahydro-7-indolizinyl)-1H-5-Azaindole | HCID 10130974 | 102.9% |
Reaction Steps
A mixture of 5-azaindole (0.5 g, 4.23 mmol), 1,2,3,5,6,8,8a-heptahydrohydro-7-oxo-indolizine (589 mg, 4.23 mmol) and pyrrolidine (3.0 g, 42.3 mmol) in ethanol (4 mL) were heated to reflux for 6 hrs. The reaction mixture was cooled, filtered, and the collected solid washed with ether to give 3-(1,2,3,5,8,8a-hexahydro-7-indolizinyl)-1H-5-Azaindole (0.521 g, 51.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06191141B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-feab868e0f7f4ebfb97ce1a038163ae6 |
| Source note | uspto-grants-2001_02 |