HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891598Generated: October 30, 2026
HCID 22242775, compound → HCID 22243034, compound
https://huagongshe.com/reaction/891598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22242775 | HCID 22242775 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22243034 | HCID 22243034 | 55.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07001897B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-7ede9ca5cd1947f7a70a2dec24601d50 |
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| Source note | uspto-grants-2006_02 |
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