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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620735Generated: November 1, 2026

Piperidinium acetate → HCID 178456914, compound

https://huagongshe.com/reaction/1620735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidinium acetateHCID 3014295—
Reactant1-[2,4-Bis(trifluoromethyl)benzyl]piperidine-4-carbaldehydeHCID 86678663—
ReactantHCID 178456890HCID 178456890—
SolventIsopropanolHCID 3776—
ProductHCID 178456914HCID 17845691458.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 1-[2,4-bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde (35.0 g) and 4-(prop-2-yn-1-ylamino)-1,3-thiazol-2(5H)-one (23.9 g) in 2-propanol (400 mL) was added piperidinium acetate (15.0 g) at room temperature. The reaction mixture was stirred at 80° C. for 4 hr and concentrated under reduced pressure. Ethyl acetate was added to the residue, and the precipitate was removed by filtration. Water and ethyl acetate were added to the filtrate, 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/hexane), and the obtained solid was washed with diisopropyl ether to give a solid. The obtained solid was recrystallized from ethyl acetate/heptane/diisopropyl ether to give the title compound (28.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-1e2d47cd8ca749938a5601a6bf0468e5
Source noteuspto-grants-2014_07