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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 4-methylpiperidine-4-carboxylate | HCID 19361805 | — |
| Reactant | 5-(3-Chloro-4-isobutylphenyl)-3-(4-chloromethylphenyl)-[1,2,4]-oxadiazole | HCID 86715143 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-{4-[5-(3-Chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-methylpiperidine-4-carboxylic acid ethyl ester | HCID 70869458 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266867B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-fc8c392f678447b8b6d3e8314edb1c0d |
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| Source note | uspto-grants-2016_02 |
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