HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891724Generated: October 28, 2026
Potassium ethanethioate → HCID 86590875, compound
https://huagongshe.com/reaction/891724
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Reactant | HCID 86590874 | HCID 86590874 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86590875 | HCID 86590875 | 73% |
Reaction Steps
To a solution of 3-methanesulfonyloxy-1-{4-[(3S)-1-(p-nitrobenzyloxycarbonyl)-pyrrolidin-3-ylcarbamoyl]-1,3-thiazol-2-yl}azetidine (410 mg, 0.780 mmol) (obtained as described in Reference Example 52(7)) in dimethylformamide (21 ml) was added potassium thioacetate (534 mg, 4.68 mmol) at room temperature, and the reaction mixture was stirred in an oil bath (80° C.) for 5 hours. After checking the completion of the reaction, the reaction mixture was partitioned between ethyl acetate and 10% aqueous sodium chloride solution. The organic layer was washed successively with saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The obtained residue was purified by chromatography on a silica gel column using n-hexane:ethyl acetate (1:2)→ethyl acetate as the eluant to afford 3-acetylthio-1-{4-[(3S)-1-(p-nitrobenzyloxycarbonyl)-pyrrolidin-3-ylcarbamoyl]-1,3-thiazol-2-yl}azetidine (287 mg, yield 73%) 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-0d0687e5d9534448bf861b9d7bc12138 |
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| Source note | uspto-grants-2006_02 |
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