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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891778Generated: October 28, 2026

Ethyl Acetate → HCID 22242926, compound

https://huagongshe.com/reaction/891778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantHCID 22242986HCID 22242986—
ReactantPotassium ethanethioateHCID 23670855—
SolventDimethylformamideHCID 6228—
ProductHCID 22242926HCID 22242926100%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 1-[4-(benzoylaminomethyl)-1,3-thiazol-2-yl]-3-methanesulfonyloxyazetidine (739 mg, 2.01 mmol) (obtained as described in Reference Example 64(3)) in dimethylformamide (20 ml) was added potassium thioacetate (1.38 g, 12.1 mmol) at room temperature, and the mixture was stirred in an oil bath (90° C.) for 3.5 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 hexane:ethyl acetate=(1:1)→ethyl acetate as the eluant to afford 3-acetylthio-1-[4-(benzoylaminomethyl)-1,3-thiazol-2-yl]azetidine (698 mg, yield 100%) as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-6406334a35834a828793cbc9ffe17630
Source noteuspto-grants-2006_02