HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2S,4R)-1-Benzyloxycarbonyl-2-(3-ethoxycarbonyl-2-oxopropyl)-4-methoxypyrrolidine → (2r,8As)-2-phenyl-1,2,3,5,6,7,8,8a-octahydroindolizin-7-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2S,4R)-1-Benzyloxycarbonyl-2-(3-ethoxycarbonyl-2-oxopropyl)-4-methoxypyrrolidine | HCID 57501855 | — |
| Reactant | (2s,4r)-1-Benzyloxycarbonyl-2-(3-ethoxycarbonyl-2-oxopropyl)-4-phenylpyrrolidine | HCID 57501856 | — |
| Product | (2r,8As)-2-phenyl-1,2,3,5,6,7,8,8a-octahydroindolizin-7-one | HCID 57457955 | 27% |
Reaction Steps
In a similar manner to that described in Preparative Example 1(iii)′ above, a reaction was conducted, using (2S,4R)-1-benzyloxycarbonyl-2-(3-ethoxycarbonyl-2-oxopropyl)-4-phenylpyrrolidine [obtained as described in Preparative Example 6(iv)′ above] instead of (2S,4R)-1-benzyloxycarbonyl-2-(3-ethoxycarbonyl-2-oxopropyl)-4-methoxypyrrolidine, to give the title compound as a pale yellow oil (yield: 27%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07122666B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-64d68903b31d4c3e9ce3bbf89b9773b2 |
| Source note | uspto-grants-2006_10 |