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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891576Generated: October 30, 2026

HCID 22242804, compound → HCID 22242732, compound

https://huagongshe.com/reaction/891576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22242804HCID 22242804—
ReactantPotassium ethanethioateHCID 23670855—
SolventDimethylformamideHCID 6228—
ProductHCID 22242732HCID 2224273268%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 1-(4-carbamoyl-1,3-thiazol-2-yl)-4-methanesulfonyloxypiperidine (1.59 g, 5.21 mmol) (obtained as described in Reference Example 15(3)) in dimethylformamide (80 ml) was added potassium thioacetate (1.19 g, 10.4 mmol) at room temperature, and the reaction mixture was stirred in an oil bath (90° C.) for 2.5 hours. After checking the completion of the reaction, the reaction mixture was partitioned between ethyl acetate and saturated aqueous sodium hydrogencarbonate solution. The obtained organic layer was washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using ethyl acetate:n-hexane (10:1) as the eluant to afford 4-acetylthio-1-(4-carbamoyl-1,3-thiazol-2-yl)piperidine (1.01 g, yield 68%) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-a0b666595f614dd58474479fd47aa193
Source noteuspto-grants-2006_02