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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891637Generated: October 30, 2026

Potassium ethanethioate → HCID 58595136, compound

https://huagongshe.com/reaction/891637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium ethanethioateHCID 23670855—
ReactantHCID 87884665HCID 87884665—
SolventDimethylformamideHCID 6228—
ProductHCID 58595136HCID 5859513663.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1-{4-[(1S)-1-(t-butyldimethylsilyloxymethyl)propylcarbamoyl]-1,3-thiazol-2-yl}-3-methanesulfonyloxyazetidine (1.02 g, 2.20 mmol) (obtained as described in Reference Example 34(5)) in dimethylformamide (50 ml) was added potassium thioacetate (1.51 mg, 13.2 mmol) at room temperature. The mixture was stirred in an oil bath (80° C.) overnight. 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 residue was purified by chromatography on a silica gel column using n-hexane:ethyl acetate (4:1→2:1) as the eluant to afford 3-acetylthio-1-{4-[(1S)-1-(t-butyldimethylsilyloxymethyl)propylcarbamoyl]-1,3-thiazol-2-yl}azetidine (618 mg, yield 63%) as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-b4538ecb07dc43c780abe3607944d53d
Source noteuspto-grants-2006_02