Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278240Generated: October 31, 2026

2-Aminopyridine → Tert-butyl 4-(imidazo[1,2-a]pyridin-3-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/278240

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
Reactanttert-Butyl 4-(1-bromo-2-oxoethyl)piperidine-1-carboxylateHCID 21912701—
SolventEthanolHCID 702—
ProductTert-butyl 4-(imidazo[1,2-a]pyridin-3-yl)piperidine-1-carboxylateHCID 2191273635.4%

Reaction Steps

To a solution of 1.15 g of 1-(t-butoxycarbonyl)-4-(1-bromo-2-oxoethyl)piperidine (from Procedure 23, Step C) in 15 mL ethanol was added 388 mg of 2-aminopyridine. After refluxing for 18 h, the solvent was evaporated. The mixture was partitioned between ethyl acetate and saturated sodium bicarbonate solution. Aqueous layer was extracted with ethyl acetate (3×). The combined organic phase was washed with brine, dried over magnesium sulfate and concentrated. The residue was purified by flash chromatography with 50% ethyl acetate in hexanes, followed by 100% ethyl acetate to give 401 mg of the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358979B1
Source datasetuspto-grants-2002_03
ORD IDord-9f6650a385004edf8c82a06d73f99809
Source noteuspto-grants-2002_03