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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777362Generated: October 26, 2026

Potassium Carbonate → 1-{4-[5-(3-Chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-methylpiperidine-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1777362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4-methylpiperidine-4-carboxylateHCID 19361805—
Reactant5-(3-Chloro-4-isobutylphenyl)-3-(4-chloromethylphenyl)-[1,2,4]-oxadiazoleHCID 86715143—
SolventDimethylformamideHCID 6228—
Product1-{4-[5-(3-Chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-methylpiperidine-4-carboxylic acid ethyl esterHCID 70869458—

Reaction Conditions

Temperature67.5 °C

Reaction Steps

Potassium carbonate (0.29 g, 0.0021 mol) and 4-methylpiperidine-4-carboxylic acid ethyl ester (0.36 g, 0.0021 mol) are added to a solution of 5-(3-chloro-4-isobutylphenyl)-3-(4-chloromethylphenyl)-[1,2,4]-oxadiazole (0.5 g, 0.0014 mol) in N,N-dimethylformamide (10 mL). The reaction mixture is heated at 65-70° C. for 2 hours. Removal of solvent gives a crude residue which is purified by column chromatography (silica gel 230-400 mesh, toluene:ethyl acetate 4:1) to give 1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-methylpiperidine-4-carboxylic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266867B2
Source datasetuspto-grants-2016_02
ORD IDord-fc8c392f678447b8b6d3e8314edb1c0d
Source noteuspto-grants-2016_02