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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891601Generated: October 29, 2026

HCID 22242713, compound → HCID 22242798, compound

https://huagongshe.com/reaction/891601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22242713HCID 22242713—
ReactantPotassium ethanethioateHCID 23670855—
SolventDimethylformamideHCID 6228—
ProductHCID 22242798HCID 2224279864%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1-(4-thiomorpholinocarbonyl-1,3-thiazol-2-yl)-3-methanesulfonyloxyazetidine (709 g, 1.95 mmol) (obtained as described in Reference Example 25(3)) in dimethylformamide (20 ml) was added potassium thioacetate (1.34 g, 11.7 mmol) at room temperature. The 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 saturated 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 ethyl acetate:n-hexane:methylene chloride (1:1:1) as the eluant to afford 3-acetylthio-1-(4-thiomorpholinocarbonyl-1,3-thiazol-2-yl)azetidine (413 mg, yield 64%) as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-08f6a6f9182d4272b25dfabcec9b5577
Source noteuspto-grants-2006_02