Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | HCID 57457970 | HCID 57457970 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57501858 | HCID 57501858 | 106.1% |
Reaction Steps
2.62 ml (31.4 mmol) of pyrrolidine were added to a solution of 2.62 g (15.7 mmol) of (8aS)-8-methyl-1,2,3,5,6,7,8,8a-octahydroindolizine-5,7-dione [obtained as described in Preparative Example 9(iii)′ above] in 30 ml of ethanol and the resulting mixture was stirred for 30 minutes at 80° C. After the reaction was completed, the solvent and excess pyrrolidine were removed from the reaction mixture by evaporation under reduced pressure to afford 3.67 g (yield: quantitative) of the title compound as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07122666B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-72c48dd123f943288a027bc69249cf54 |
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| Source note | uspto-grants-2006_10 |
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