HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620549Generated: October 29, 2026
Piperidinium acetate → HCID 178518156, compound
https://huagongshe.com/reaction/1620549
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidinium acetate | HCID 3014295 | — |
| Reactant | 1-[2,4-Bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde | HCID 86678663 | — |
| Reactant | HCID 178518157 | HCID 178518157 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178518156 | HCID 178518156 | 43.5% |
Reaction Steps
To a solution of 1-[2,4-bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde (1.86 g) in 2-propanol (20 mL) were added 4-[(2,3-dihydroxypropyl)amino]-1,3-thiazol-2(5H)-one (1.56 g) and piperidinium acetate (0.794 g). The reaction mixture was stirred at 80° C. for 1 hr, and the solvent was evaporated under reduced pressure. Water was added to the residue, 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 (methanol/ethyl acetate) and recrystallized from ethyl acetate/heptane to give the title compound (1.22 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-7e9c7bcc6d2b4c0abae84c5da398f9b7 |
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| Source note | uspto-grants-2014_07 |
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