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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium ethanethioateHCID 23670855—
Reactant1-(4-Ethoxycarbonyl-1,3-thiazol-2-yl)4-methanesulfonyloxypiperidineHCID 86590851—
SolventDimethylformamideHCID 6228—
Product4-Acetylthio-1-(4-ethoxycarbonyl-1,3-thiazol-2-yl)piperidineHCID 2224292194%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-409c6842269d4bccbb06a26eb48083f7
Source noteuspto-grants-2006_02