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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421091Generated: October 25, 2026

Benzenecarboximidic acid, ethyl ester, hydrochloride (1:1) → 2-(5-Methyl-3-phenyl-isoxazol-4-yl)-5-phenyl-[1,3,4]oxadiazole

https://huagongshe.com/reaction/2421091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenecarboximidic acid, ethyl ester, hydrochloride (1:1)HCID 79249—
Reactant5-Methyl-3-phenyl-4-isoxazolecarbohydrazideHCID 727924—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
Solvent1,4-DioxaneHCID 31275—
Product2-(5-Methyl-3-phenyl-isoxazol-4-yl)-5-phenyl-[1,3,4]oxadiazoleHCID 1672253258.4%

Reaction Conditions

Temperature180 °C

Reaction Steps

To a solution of ethyl benzimidate hydrochloride (376 mg; 2.03 mmol) in ethanol (4 mL) was added at 0° C. sodium ethoxide (2.72 M in ethanol, 355 L, 0.99 mmol) and stirred for 15 min. The suspension was filtered off and 5-methyl-3-phenyl-isoxazole-4-carboxylic acid hydrazide (200 mg, 0.92 mmol) was added and stirred for 90 h at 70° C. The reaction mixture was suspended in dioxane (4 mL) and heated in the microwave for 30 min at 180° C. Concentration and then purification by chromatography (SiO2, heptane:ethyl acetate=95:5 to 60:40) afforded the title compound (163 mg, 29%) as a white solid. MS: m/e=304.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956074B2
Source datasetuspto-grants-2011_06
ORD IDord-fe6219d3faba43e1aab7b2a71187a38f
Source noteuspto-grants-2011_06