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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891598Generated: October 30, 2026

HCID 22242775, compound → HCID 22243034, compound

https://huagongshe.com/reaction/891598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22242775HCID 22242775—
ReactantPotassium ethanethioateHCID 23670855—
SolventDimethylformamideHCID 6228—
ProductHCID 22243034HCID 2224303455.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1-(4-cyano-1,3-oxazol-2-yl)-3-methanesulfonyloxyazetidine (309 mg, 1.27 mmol) (obtained as described in Reference Example 23(3)) in dimethylformamide (15 ml) was added potassium thioacetate (0.87 g, 7.62 mmol) at room temperature. 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 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 hexane:ethyl acetate (2:1) as the eluant to afford 3-acetylthio-1-(4-cyano-1,3-oxazol-2-yl)azetidine (157 mg, yield 55%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-7ede9ca5cd1947f7a70a2dec24601d50
Source noteuspto-grants-2006_02