HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620697Generated: October 30, 2026
Piperidinium acetate → HCID 178504889, compound
https://huagongshe.com/reaction/1620697
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidinium acetate | HCID 3014295 | — |
| Reactant | 1-[2,4-Bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde | HCID 86678663 | — |
| Reactant | HCID 178504888 | HCID 178504888 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178504889 | HCID 178504889 | 56.4% |
Reaction Steps
To a solution of 4-{[2-(methylsulfonyl)ethyl]amino}-1,3-thiazol-2(5H)-one (1.39 g) and 1-[2,4-bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde (1.77 g) in 2-propanol (20 mL) was added piperidinium acetate (757 mg). The reaction mixture was stirred at 80° C. for 3 hr and concentrated under reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate. The extract was washed with water and 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 the obtained solid was recrystallized from ethyl acetate/heptane to give the title compound (1.6 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-4bdc68c02fa64a32a867e3e1ce04f947 |
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| Source note | uspto-grants-2014_07 |
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