HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891569Generated: October 30, 2026
Potassium ethanethioate → 4-Acetylthio-1-(4-ethoxycarbonyl-1,3-thiazol-2-yl)piperidine
https://huagongshe.com/reaction/891569
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Reactant | 1-(4-Ethoxycarbonyl-1,3-thiazol-2-yl)4-methanesulfonyloxypiperidine | HCID 86590851 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Acetylthio-1-(4-ethoxycarbonyl-1,3-thiazol-2-yl)piperidine | HCID 22242921 | 94% |
Reaction Steps
To a solution of 1-(4-ethoxycarbonyl-1,3-thiazol-2-yl)-4-methanesulfonyloxypiperidine (76 mg, 0.23 mmol) (obtained as described in Reference Example 13(3)) in dimethylformamide (4.0 ml) was added potassium thioacetate (145 mg, 1.3 mmol) at room temperature, and the reaction mixture was then stirred in an oil bath (80° C.) for 8 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 magnesium sulfate, filtered and concentrated under reduced pressure. The obtained residue was purified by chromatography on a silica gel column using n-hexane:ethyl acetate (1:1) as the eluant to afford 4-acetylthio-1-(4-ethoxycarbonyl-1,3-thiazol-2-yl)piperidine (67 mg, yield 94%) 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-409c6842269d4bccbb06a26eb48083f7 |
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| Source note | uspto-grants-2006_02 |
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