HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891589Generated: October 30, 2026
Potassium ethanethioate → HCID 58595089, compound
https://huagongshe.com/reaction/891589
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Reactant | HCID 86590856 | HCID 86590856 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58595089 | HCID 58595089 | 90% |
Reaction Steps
To a solution of (3S)-1-(4-carbamoyl-1,3-thiazol-2-yl)-3-methanesulfonyloxypyrrolidine (1.15 g) (obtained as described in Reference Example 20(8)) in acetonitrile (35 ml) was added potassium thioacetate (1.35 g, 11.8 mmol) at room temperature, and the mixture was heated under reflux for 6 hours. After checking the completion of the reaction, the reaction mixture was partitioned between ethyl acetate and saturated aqueous sodium hydrogencarbonate solution. The organic layer was washed with 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 ethyl acetate→2% methanol in ethyl acetate as the eluant to afford (3R)-3-acetylthio-1-(4-carbamoyl-1,3-thiazol-2-yl)pyrrolidine (962 mg, yield 90%) 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-0043fd5a452249e6b2293cdcf656aa19 |
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| Source note | uspto-grants-2006_02 |
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