HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620732Generated: October 31, 2026
Piperidinium acetate → HCID 178448895, compound
https://huagongshe.com/reaction/1620732
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidinium acetate | HCID 3014295 | — |
| Reactant | 1-[2,4-Bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde | HCID 86678663 | — |
| Reactant | HCID 178448893 | HCID 178448893 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178448895 | HCID 178448895 | 36.3% |
Reaction Steps
To a solution of 1-[2,4-bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde (1.91 g) in 2-propanol (20 mL) were added 4-(but-3-yn-2-ylamino)-1,3-thiazol-2(5H)-one (1.42 g) and piperidinium acetate (834 mg). The reaction mixture was stirred at 75° C. for 6 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) to give the title compound (1.0 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-caaaec1c4d384ecc85b16c4a59c61e51 |
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| Source note | uspto-grants-2014_07 |
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