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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522009Generated: November 1, 2026

tert-Butyl 4-ethynylpiperidine-1-carboxylate → HCID 90412447, compound

https://huagongshe.com/reaction/1522009

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-ethynylpiperidine-1-carboxylateHCID 15550481—
ReactantN-(4-Chloro-5-fluoro-3-iodo-2-pyridinyl)-2,2-dimethylpropanamideHCID 50986342—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
ProductHCID 90412447HCID 90412447—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of N-(4-chloro-5-fluoro-3-iodopyridin-2-yl)pivalamide (1 g, 2.80 mmol), tert-butyl 4-ethynylpiperidine-1-carboxylate (0.880 g, 4.21 mmol), copper(I) iodide (0.053 g, 0.28 mmol), and bis(triphenylphosphine)palladium(II) dichloride (0.197 g, 0.280 mmol) in 50 mL tetrahydrofuran was degassed with nitrogen. The mixture was stirred at room temperature for 48 hours and at 50° C. for 8 hours. The mixture was filtered and the filtrate was diluted with water and extracted with ethyl acetate. The organic phase was washed with brine, dried over sodium sulfate, filtered and concentrated. The residue was purified by silica-gel column chromatography eluting with 0-40% ethyl acetate in heptane to afford the title compound. MS (ESI(+)) m/e 438 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073922B2
Source datasetuspto-grants-2015_07
ORD IDord-ea94053a09f0406daa704c6c4ae74882
Source noteuspto-grants-2015_07