HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium ethanethioate → HCID 54244021, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Reactant | HCID 54494532 | HCID 54494532 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54244021 | HCID 54244021 | 80.4% |
Reaction Steps
A solution of (2S,4R)-1-allyloxycarbonyl-4-methane- sulfonyloxy-2-[(2-ureidoethyl)oxymethyl]pyrrolidine (1.00 g) and potassium thioacetate (0.48 g) in dimethylformamide (6 ml) was heated at 80°-85° C. for 30 minutes. The mixture was poured into ice-water (30 ml) and extracted with ethyl acetate (12 ml×3). The organic layer was washed with brine (18 ml×2), dried over magnesium sulfate and concentrated under reduced pressure to give a syrup. The syrup was subjected to a column chromatography on silica gel (50 g) and eluted with a mixture of methanol and dichloromethane (5:95 v/v) to give (2S,4S)-4-acetylthio-1-allyloxycarbonyl-2-[(2-ureidoethyl)oxymethyl]pyrrolidine (0.76 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04822787 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-161b126ed21e4cc787d9afc934619c79 |
| Source note | uspto-grants-1989_04 |