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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350755Generated: November 1, 2026

Tetrahydrofuran → HCID 21088583, compound

https://huagongshe.com/reaction/350755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 21088584HCID 21088584—
SolventWaterHCID 962—
ProductHCID 21088583HCID 2108858328%

Reaction Steps

To a mixture of 3-{3-[2-(1H-benzoimidazol-1-yl)-4-(4-chlorophenyl)-5-oxazolyl]propanoyl}thiazolidine (25 mg) and tetrahydrofuran (10 mL) was added m-chloroperbenzoic acid (14.4 mg) with stirring under ice-cooling, and the mixture was stirred overnight at room temperature. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium hydrogen carbonate and then with saturated brine, dried (MgSO4) and concentrated. The residue was introduced into preparative HPLC and purified to give 3-{3-[2-(1H-benzoimidazol-1-yl)-4-(4-chlorophenyl)-5-oxazolyl]propanoyl}thiazolidine-1-oxide (7.3 mg, yield 28%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183276B2
Source datasetuspto-grants-2007_02
ORD IDord-8ffef582733145bda6fc92c2d4f1c07e
Source noteuspto-grants-2007_02