Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620498Generated: October 25, 2026

tert-Butyl 4-formylpiperidine-1-carboxylate → HCID 178456946, compound

https://huagongshe.com/reaction/1620498

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
ReactantPiperidinium acetateHCID 3014295—
ReactantHCID 178456890HCID 178456890—
SolventIsopropanolHCID 3776—
ProductHCID 178456946HCID 17845694676.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of tert-butyl 4-formylpiperidine-1-carboxylate (11.2 g) in 2-propanol (230 mL) were added 4-(prop-2-yn-1-ylamino)-1,3-thiazol-2(5H)-one (16.3 g) and piperidinium acetate (3.90 g). The reaction mixture was stirred at 60° C. overnight, and the solvent was evaporated under reduced pressure. Ethyl acetate was added to the residue, the precipitate was removed, and the filtrate was 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 (14.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-2d1f4c70c0e44e019a253e196f4f8a92
Source noteuspto-grants-2014_07