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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266406Generated: November 2, 2026

Sodium hydride → 5-[1-(3-Bromo-phenyl)-1H-imidazol-4-yl]-3-methyl-[1,2,4]oxadiazole

https://huagongshe.com/reaction/2266406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-(3-Bromo-phenyl)-1H-imidazole-4-carboxylic acid ethyl esterHCID 16128754—
ReactantHCID 178465666HCID 178465666—
SolventTetrahydrofuranHCID 8028—
Product5-[1-(3-Bromo-phenyl)-1H-imidazol-4-yl]-3-methyl-[1,2,4]oxadiazoleHCID 1612850635%

Reaction Steps

To a suspension of NaH (1.30 g, 32.64 mmol, 60% in mineral oil) in THF (15 mL) under nitrogen atmosphere was added N-hydroxy-acetamidine (2.62 g, 35.4 mmol) and stirred for 1 h at room temperature. The bromo ester 3 (8 g, 27.2 mmol) in THF (2 mL) was added and refluxed for 12 h. The reaction mixture was quenched by adding brine, extracted with ethylacetate (100 mL) and dried over anhydrous Na2SO4. The organic layer was concentrated under reduced pressure and purified by flash chromatography using 25% ethylacetate in hexane as mobile phase to furnish 4 (2.8 g, 35%) as pale yellow solid, mp=200.1-202.4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858649B2
Source datasetuspto-grants-2010_12
ORD IDord-7d095b7ed0d04e27ae4723f3d4a3b101
Source noteuspto-grants-2010_12