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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242224Generated: November 2, 2026

4-Isobutylbenzoic acid → Ethyl 5-[5-(4-isobutylphenyl)-1,2,4-oxadiazol-3-yl]pyrazine-2-carboxylate

https://huagongshe.com/reaction/2242224

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Isobutylbenzoic acidHCID 38111—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantEthyl 5-[amino(hydroxyimino)methyl]pyrazine-2-carboxylateHCID 136368376—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 5-[5-(4-isobutylphenyl)-1,2,4-oxadiazol-3-yl]pyrazine-2-carboxylateHCID 5920430227.1%

Reaction Steps

A mixture of 4-isobutylbenzoic acid (0.28 g, 1.59 mmol), 1-hydroxybenzotriazole (0.042 g, 0.31 mmol), N-[(1H-1,2,3-benzotriazol-1-yloxy)(dimethylamino)methylene]-N-methylmethanaminium tetrafluoroborate (0.51 g, 1.59 mmol), diisopropylethylamine (1.4 mL, 7.86 mmol) and dioxane (4 mL) was stirred at room temperature for 1 hour. Ethyl 5-[amino(hydroxyimino)methyl]pyrazine-2-carboxylate (0.33 g, 1.57 mmol) was added to the reaction mixture, stirred for 1.5 hours at room temperature and 6 hours at 100° C. The reaction mixture was cooled to room temperature, quenched with H2O (10 mL) and filtered. The precipitate was dissolved in EtOAc (10 mL), washed with 1N NaOH (3×10 mL) and brine (2×10 mL), dried (Na2SO4), filtered and concentrated in vacuo to yield the title compound (0.15 g, 27%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671043B2
Source datasetuspto-grants-2010_03
ORD IDord-7ac23ec1106e409ca21bba6bb7fe27f3
Source noteuspto-grants-2010_03