HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620689Generated: November 1, 2026
Piperidinium acetate → HCID 178484552, compound
https://huagongshe.com/reaction/1620689
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidinium acetate | HCID 3014295 | — |
| Reactant | 1-[2,4-Bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde | HCID 86678663 | — |
| Reactant | HCID 178484550 | HCID 178484550 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178484552 | HCID 178484552 | 43.3% |
Reaction Steps
To a solution of 1-[2,4-bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde (520 mg) and N,N-dimethyl-N3-(2-oxo-2,5-dihydro-1,3-thiazol-4-yl)-β-alaninamide (330 mg) in 2-propanol (60 mL) was added piperidinium acetate (223 mg). The reaction mixture was stirred at 80° C. for 4 hr and concentrated. 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 (ethyl acetate/methanol). The obtained solid was recrystallized from ethyl acetate/heptane to give the title compound (356 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08772277B2 |
|---|
| Source dataset | uspto-grants-2014_07 |
|---|
| ORD ID | ord-f3d08d24b7d1481eb59bc07bdeae7e92 |
|---|
| Source note | uspto-grants-2014_07 |
|---|