HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620595Generated: October 31, 2026
1-[2,4-Bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde → HCID 178459113, compound
https://huagongshe.com/reaction/1620595
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-[2,4-Bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde | HCID 86678663 | — |
| Reactant | HCID 178459112 | HCID 178459112 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Piperidinium acetate | HCID 3014295 | — |
| Product | HCID 178459113 | HCID 178459113 | 85.8% |
Reaction Steps
To a solution of 1-[2,4-bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde (400 mg) in 2-propanol (10 mL) were added a solution of 4-[(4-hydroxy-4-methylpent-2-yn-1-yl)amino]-1,3-thiazol-2(5H)-one (365 mg) in 2-propanol (5 mL) and piperidinium acetate (175 mg). The reaction mixture was stirred at 60° C. overnight and concentrated. 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 (540 mg).
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-779a654f344e4a8198131c5e890bf18e |
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| Source note | uspto-grants-2014_07 |
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