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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891826Generated: October 30, 2026

Potassium ethanethioate → HCID 86590892, compound

https://huagongshe.com/reaction/891826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium ethanethioateHCID 23670855—
ReactantHCID 86590891HCID 86590891—
SolventDimethylformamideHCID 6228—
ProductHCID 86590892HCID 8659089254.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 3-methanesulfonyloxy-1-{4-[(3R)-1-(p-nitrobenzyloxycarbonyl)-pyrrolidin-3-ylcarbamoyl]-1,3-oxazol-2-yl}azetidine (540 mg, 1.06 mmol) (obtained as described in Reference Example 77(3)) in dimethylformamide (27 ml) was added potassium thioacetate (726 mg, 6.36 mmol) at room temperature, and the mixture was stirred in an oil bath (80° C.) for 9 hours. After checking the completion of the reaction, the mixture was partitioned between ethyl acetate and 10% aqueous sodium chloride solution. The organic layer was washed 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 (1:6)→ethyl acetate as the eluant to afford 3-acetylthio-1-{4-[(3R)-1-(p-nitrobenzyloxycarbonyl)-pyrrolidin-3-ylcarbamoyl]-1,3-oxazol-2-yl}azetidine (281 mg, yield 54%) as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-4fad693c1bb140f58d012c5af7276579
Source noteuspto-grants-2006_02