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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529338Generated: October 30, 2026

2-Bromopyridine → Ethyl 2-(1-(pyridin-2-yl)piperidin-4-yl)acetate

https://huagongshe.com/reaction/529338

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
ReactantPotassium CarbonateHCID 11430—
ReactantPiperidin-4-yl-acetic acid ethyl ester hydrochlorideHCID 45358839—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-(1-(pyridin-2-yl)piperidin-4-yl)acetateHCID 6838534725.1%

Reaction Conditions

Temperature130 °C

Reaction Steps

To a stirred solution of ethyl 2-(piperidin-4-yl)acetate, hydrochloride (2.0 g, 9.63 mmol) in DMF (40 mL) was added K2CO3 (3.99 g, 28.9 mmol) followed by 2-bromopyridine (1.521 g, 9.63 mmol) and stirred at 130° C. for 16 h. Reaction mixture was diluted with water (200 mL) and extracted with ethyl acetate (2×100 mL). The combined organic layer was washed with water (2×100 mL), brine (100 mL) and dried over Na2SO4 filtered and concentrated under reduced pressure. The residues was purified by column chromatography using 100-200 silica gel by eluting with 20% ethyl acetate in petroleum ether to afford ethyl 2-(1-(pyridin-2-yl)piperidin-4-yl)acetate (600 mg, 19.86% yield) as color less liquid. LCMS (ES) m/e 249.20 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346840B2
Source datasetuspto-grants-2016_05
ORD IDord-ab4c7b58d21147f78f9dfaeb9a36baad
Source noteuspto-grants-2016_05