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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891724Generated: October 28, 2026

Potassium ethanethioate → HCID 86590875, compound

https://huagongshe.com/reaction/891724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium ethanethioateHCID 23670855—
ReactantHCID 86590874HCID 86590874—
SolventDimethylformamideHCID 6228—
ProductHCID 86590875HCID 8659087573%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 3-methanesulfonyloxy-1-{4-[(3S)-1-(p-nitrobenzyloxycarbonyl)-pyrrolidin-3-ylcarbamoyl]-1,3-thiazol-2-yl}azetidine (410 mg, 0.780 mmol) (obtained as described in Reference Example 52(7)) in dimethylformamide (21 ml) was added potassium thioacetate (534 mg, 4.68 mmol) at room temperature, and the reaction mixture was stirred in an oil bath (80° C.) for 5 hours. 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 obtained residue was purified by chromatography on a silica gel column using n-hexane:ethyl acetate (1:2)→ethyl acetate as the eluant to afford 3-acetylthio-1-{4-[(3S)-1-(p-nitrobenzyloxycarbonyl)-pyrrolidin-3-ylcarbamoyl]-1,3-thiazol-2-yl}azetidine (287 mg, yield 73%) as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-0d0687e5d9534448bf861b9d7bc12138
Source noteuspto-grants-2006_02