HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620556Generated: October 26, 2026
Piperidinium acetate → HCID 178456939, compound
https://huagongshe.com/reaction/1620556
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidinium acetate | HCID 3014295 | — |
| Reactant | 1-{1-[2,4-Bis(trifluoromethyl)phenyl]ethyl}piperidine-4-carbaldehyde | HCID 86678736 | — |
| Reactant | HCID 178456890 | HCID 178456890 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178456939 | HCID 178456939 | 70.9% |
Reaction Steps
To a solution of 1-{1-[2,4-bis(trifluoromethyl)phenyl]ethyl}piperidine-4-carbaldehyde (1.15 g) and 4-(prop-2-yn-1-ylamino)-1,3-thiazol-2(5H)-one (1.00 g) in 2-propanol (16.3 mL) was added piperidinium acetate (0.473 g). The reaction mixture was stirred at 60° C. overnight, allowed to cool to room temperature, and diluted with ethyl acetate. The mixture 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 (NH, ethyl acetate/hexane), further purified by silica gel column chromatography (ethyl acetate/hexane), and recrystallized from ethyl acetate/hexane to give the title compound (1.13 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-d0c16fcd68274ce9ac2e8ffd528953b4 |
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| Source note | uspto-grants-2014_07 |
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