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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620784Generated: October 31, 2026

Piperidinium acetate → HCID 178484589, compound

https://huagongshe.com/reaction/1620784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidinium acetateHCID 3014295—
Reactant1-[2,4-Bis(trifluoromethyl)benzyl]piperidine-4-carbaldehydeHCID 86678663—
ReactantHCID 178484587HCID 178484587—
SolventEthanolHCID 702—
ProductHCID 178484589HCID 17848458938%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1-[2,4-bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde (5.57 g) and N2-[2-oxo-2,5-dihydro-1,3-thiazol-4-yl]-N,N-dimethyl-D-serinamide (5.70 g) in ethanol (80 mL) was added piperidinium acetate (2.39 g). The reaction mixture was stirred at 80° C. overnight, 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 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) and silica gel column chromatography (methanol/ethyl acetate), and the obtained solid was washed with diisopropyl ether to give a solid. The obtained solid was recrystallized from ethyl acetate/heptane to give the title compound (3.45 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-e8f9561478ed42e0a5a8bdb063a3ee90
Source noteuspto-grants-2014_07