HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620605Generated: November 2, 2026
Piperidinium acetate → HCID 178456922, compound
https://huagongshe.com/reaction/1620605
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidinium acetate | HCID 3014295 | — |
| Reactant | 1-[2,4-Bis(trifluoromethyl)benzyl]-2-oxopiperidine-4-carbaldehyde | HCID 86678775 | — |
| Reactant | HCID 178456890 | HCID 178456890 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178456922 | HCID 178456922 | 34.6% |
Reaction Steps
To a solution of 1-[2,4-bis(trifluoromethyl)benzyl]-2-oxopiperidine-4-carbaldehyde (1.00 g) and 4-(prop-2-yn-1-ylamino)-1,3-thiazol-2(5H)-one (0.66 g) in 2-propanol (10 mL) was added piperidinium acetate (0.41 g). The reaction mixture was stirred at 80° C. for 4 hr and concentrated. Ethyl acetate was added to the residue, and the precipitate was removed. Water was added to the filtrate, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) and recrystallized from ethanol/heptane to give the title compound (0.48 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772277B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-28694367f6554fbea65e944be6c54436 |
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| Source note | uspto-grants-2014_07 |
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