Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20074Generated: October 25, 2026

4-Bromopyridine → Ethyl 4-(pyridin-4-ylamino)piperidine-1-carboxylate

https://huagongshe.com/reaction/20074

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromopyridineHCID 14268—
ReactantEthyl 4-amino-1-piperidinecarboxylateHCID 100867—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductEthyl 4-(pyridin-4-ylamino)piperidine-1-carboxylateHCID 2229322341.1%

Reaction Steps

A solution of ethyl 4-aminopiperidine-1-carboxylate (2.20 g, 12.7 mmol), 4-bromopyridine (3.47 g, 17.8 mmol), sodium t-butoxide (4.54 g, 47.2 mmol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.398 g, 0.639 mmol) and palladium acetate (0.143 g, 0.639 mmol) in toluene (40 mL) was heated at 60° C. overnight. The reaction was cooled and partitioned between ethyl acetate and water. The aqueous layer was washed 3 times with methylene chloride, and the combined organic layers dried over sodium sulfate. The crude product was purified by chromatography (silica gel, 0 to 10% {5% ammonium hydroxide in methanol}in methylene chloride gradient elution), which gave the title compound (1.3 g, 41% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745427B2
Source datasetuspto-grants-2010_06
ORD IDord-101a650b45d542b081d56e34c403fdfc
Source noteuspto-grants-2010_06