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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368601Generated: October 29, 2026

Pyridine → Methyl 3-(5-phenyl-1,3,4-oxadiazol-2-yl)propanoate

https://huagongshe.com/reaction/2368601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
ReactantMethyl 4-(2-benzoylhydrazino)-4-oxobutanoateHCID 569517—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-(5-phenyl-1,3,4-oxadiazol-2-yl)propanoateHCID 5760026272%

Reaction Steps

Thionyl chloride (0.34 mL, 4.7 mmol) was added to the mixture of methyl 4-(2-benzoylhydrazino)-4-oxobutanoate (900 mg, 4 mmol), Pyridine (0.87 mL, 0.011 mol) in tetrahydrofuran (20 mL) at room temperature. After stirring for 3 hours, the reaction mixture was concentrated. The residue was mixed with toluene (20 mL) and refluxed overnight. The reaction was diluted with water and extracted with ethyl acetate three times. The combined organic layers were dried with sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by flash column chromatography to yield the desired product (600 mg, 72%). LCMS calculated for C12H13N2O3 (M+H): 233.1. Found: 233.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703783B2
Source datasetuspto-grants-2014_04
ORD IDord-ad01e629fba249618104007c37f20423
Source noteuspto-grants-2014_04