HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891566Generated: October 31, 2026
HCID 22243003, compound → HCID 22243010, compound
https://huagongshe.com/reaction/891566
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22243003 | HCID 22243003 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22243010 | HCID 22243010 | 62% |
Reaction Steps
To a solution of 1-(4-t-butyldimethylsilyloxymethyl-1,3-thiazol-2-yl)-3-methanesulfonyloxyazetidine (326.5 mg, 0.86 mmol) (obtained as described in Reference Example 12(3)) in dimethylformamide (16 ml) was added potassium thioacetate (780 mg, 5.41 mmol) at room temperature, and the reaction mixture was then stirred in an oil bath (80° C.) for 2 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 n-hexane:ethyl acetate (4:1) as the eluant to afford 3-acetylthio-1-(4-t-butyldimethylsilyloxymethyl-1,3-thiazol-2-yl)azetidine (191 mg, yield 62%) as a brown syrup.
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-9178daadcc1a4b69885bc1c8e0c39cc4 |
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| Source note | uspto-grants-2006_02 |
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