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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587393Generated: October 27, 2026

Water → Ethyl 1-(5-fluoropyridin-2-yl)piperidine-4-carboxylate

https://huagongshe.com/reaction/587393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Bromo-5-fluoropyridineHCID 2783171—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductEthyl 1-(5-fluoropyridin-2-yl)piperidine-4-carboxylateHCID 5830299430%

Reaction Steps

A mixture of 3.4 g (20 mmol) 2-bromo-5-fluoropyridine, 4.61 g (29 mmol) ethyl isonipecotate and 3.79 g (29 mmol) DIPEA in 5 mL NMP was heated for 15 min to 170° C. and 60 min to 200° C. After cooling to room temperature water was added and the mixture was extracted with ethyl acetate and heptane. The combined organic layers were washed with brine, dried with Na2SO4, filtered and evaporated to dryness. The residue was purified by column chromatography on silica eluting with a gradient formed from heptane and ethyl acetate. The product containing fractions were evaporated to yield 1.5 g (30%) of the title compound as light yellow oil. MS m/e: 253.3 [M]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226916B2
Source datasetuspto-grants-2016_01
ORD IDord-050d18afa9674a5abddf121a55194338
Source noteuspto-grants-2016_01