HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171708Generated: November 2, 2026
HCID 23138739, compound → HCID 74020258, compound
https://huagongshe.com/reaction/1171708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 23138739 | HCID 23138739 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 74020258 | HCID 74020258 | 97.7% |
Reaction Steps
Potassium thioacetate (5.91 g) was added to a solution of 5-((acetylsulfanyl){1-[2-(ethoxycarbonyl)ethyl]-1H-pyrazol-3-yl}methyl)-1-(triphenylmethyl)-1,2,3,6-tetrahydropyridine (3.00 g), in dimethyl sulfoxide (30 ml). The mixture was stirred at 80° C. for 4 hours. After cooling to room temperature, the mixture was diluted with ethyl acetate, and washed successively with water and a saturated aqueous sodium chloride solution. After the extract was dried over anhydrous sodium sulfate, it was concentrated under reduced pressure, and the residue was purified by silica gel chromatography using ethyl acetate and hexane (1:9 to 2:3) as eluents to afford a crude product of 4-(acetylsulfanyl)-3-({1-[2-(ethoxycarbonyl)ethyl]-1H-pyrazol-3-yl}methylidene)-1-(triphenylmethyl)piperidine (2.93 g) as a mixture of geometric isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07829580B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-1ec091a3395a40d6ba4c4b65b56f22a8 |
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| Source note | uspto-grants-2010_11 |
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