HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891826Generated: October 30, 2026
Potassium ethanethioate → HCID 86590892, compound
https://huagongshe.com/reaction/891826
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Reactant | HCID 86590891 | HCID 86590891 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86590892 | HCID 86590892 | 54.2% |
Reaction Steps
To a solution of 3-methanesulfonyloxy-1-{4-[(3R)-1-(p-nitrobenzyloxycarbonyl)-pyrrolidin-3-ylcarbamoyl]-1,3-oxazol-2-yl}azetidine (540 mg, 1.06 mmol) (obtained as described in Reference Example 77(3)) in dimethylformamide (27 ml) was added potassium thioacetate (726 mg, 6.36 mmol) at room temperature, and the mixture was stirred in an oil bath (80° C.) for 9 hours. After checking the completion of the reaction, the mixture was partitioned between ethyl acetate and 10% aqueous sodium chloride solution. The organic layer was washed with saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using n-hexane:ethyl acetate (1:6)→ethyl acetate as the eluant to afford 3-acetylthio-1-{4-[(3R)-1-(p-nitrobenzyloxycarbonyl)-pyrrolidin-3-ylcarbamoyl]-1,3-oxazol-2-yl}azetidine (281 mg, yield 54%) as a pale brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07001897B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-4fad693c1bb140f58d012c5af7276579 |
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| Source note | uspto-grants-2006_02 |
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