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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189086Generated: October 30, 2026

4-Pentynoic acid → 5-(But-3-ynyl)-3-(2-methoxyphenyl)-1,2,4-oxadiazole

https://huagongshe.com/reaction/1189086

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Pentynoic acidHCID 22464—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN-Hydroxy-2-methoxy-benzamidineHCID 4652214—
Solvent1,4-DioxaneHCID 31275—
Product5-(But-3-ynyl)-3-(2-methoxyphenyl)-1,2,4-oxadiazoleHCID 8608679636.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

In a reactor tube, a mixture of N′-hydroxy-2-methoxybenzamidine (598 mg, 3.6 mmol), 4-pentynoic acid (350 mg, 3.6 mmol), HOBT (0.55 g, 3.6 mmol) and EDCI.HCl (1.03 g, 5.4 mmol) in dioxane (7.4 mL) was stirred at R.T for 3h. After this time the mixture was heated at 80° C. overnight in a reaction block. The mixture was concentrated and the crude product was purified by flash chromatography (Prepacked column 25 g with DCM as eluent) to afford 299 mg of 5-(but-3-ynyl)-3-(2-methoxyphenyl)-1,2,4-oxadiazole (36%) as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674106B2
Source datasetuspto-grants-2014_03
ORD IDord-b058cc6385f9447e8399db8ba04c4fa0
Source noteuspto-grants-2014_03