HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2S,4S)-4-Acetylthio-1-allyloxycarbonyl-2-carboxypyrrolidine → (2S,4S)-4-acetylthio-1-allyloxycarbonyl-2-(6-allyloxy-3-(E-2-allyloxycarbonyl-1-ethenyl)phenylcarbamoyl)pyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2S,4S)-4-Acetylthio-1-allyloxycarbonyl-2-carboxypyrrolidine | HCID 15299255 | — |
| Reactant | Allyl 4-allyloxy-3-aminocinnamate | HCID 54090444 | — |
| Reactant | Allyl 3-aminocinnamate | HCID 54165426 | — |
| Product | (2S,4S)-4-acetylthio-1-allyloxycarbonyl-2-(6-allyloxy-3-(E-2-allyloxycarbonyl-1-ethenyl)phenylcarbamoyl)pyrrolidine | HCID 86749573 | — |
Reaction Steps
Allyl 4-allyloxy-3-aminocinnamate was condensed with (2S,4S)-4-acetylthio-1-allyloxycarbonyl-2-carboxypyrrolidine by the method described in example 1 for allyl 3-aminocinnamate to give (2S,4S)-4-acetylthio-1-allyloxycarbonyl-2-(6-allyloxy-3-(E-2-allyloxycarbonyl-1-ethenyl)phenylcarbamoyl)pyrrolidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05527791 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-1eea76a397184006aa501dbfecfceb1a |
| Source note | uspto-grants-1996_06 |