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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712203Generated: October 29, 2026

Hexane → Ethyl 1-(5-bromo-3-pyridyl)-4-methyl-piperidine-4-carboxylate

https://huagongshe.com/reaction/712203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantCesium carbonateHCID 10796—
Reactant3,5-DibromopyridineHCID 69369—
Reactant4-Methylpiperidine-4-carboxylic acid hydrochlorideHCID 51000379—
SolventDimethyl SulfoxideHCID 679—
ProductEthyl 1-(5-bromo-3-pyridyl)-4-methyl-piperidine-4-carboxylateHCID 6697715214%

Reaction Steps

To a solution of 4-methylpiperidine-4-carboxylate hydrochloride (3.6 g, 21.10 mmol) in DMSO (5 mL) was added Cs2CO3 (1.63 g, 5 mmol) at rt. The resulting mixture was stirred at rt for 10 min followed by addition of 3,5-dibromopyridine (1.0 g, 4.20 mmol). The reaction was heated up to 150° C. for 48 h. After completion (by TLC), the reaction mixture was poured into 100 mL of ice-cold water and extracted with EtOAc (3×100 mL). The combined organics were washed with brine, dried over anhydrous Na2SO4, filtered and evaporated under reduced pressure. The crude residue was purified over 100-200 M silica-gel by using 20.0% EtOAc:hexane to obtain a viscous liquid product (0.2 g, 14% yield). MS: 327.08 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181234B2
Source datasetuspto-grants-2015_11
ORD IDord-8a8e40439d944a59bf726a063be720fb
Source noteuspto-grants-2015_11