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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82707Generated: October 25, 2026

1,1'-Carbonyldiimidazole → 3-(4-amino-1,2,5-oxadiazol-3-yl)-4-(3-chlorophenyl)-1,2,4-oxadiazol-5(4H)-one

https://huagongshe.com/reaction/82707

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 178509308HCID 178509308—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product3-(4-amino-1,2,5-oxadiazol-3-yl)-4-(3-chlorophenyl)-1,2,4-oxadiazol-5(4H)-oneHCID 5855826795.4%

Reaction Steps

A solution of 4-amino-N-(3-chlorophenyl)-N′-hydroxy-1,2,5-oxadiazole-3-carboximidamide (540 mg, 2.1 mmol) and N,N-carbonyldiimidazole (380 mg, 2.3 mmol) in tetrahydrofuran (10 mL) was heated at 80° C. for 1 h. The reaction mixture was diluted with ethyl acetate (150 mL) and washed with 0.1 N HCl (3×75 mL) and brine (75 mL). The organic layer was dried with sodium sulfate, filtered, and concentrated to give the desired product (560 mg, 94%) as a white solid which was used without further purification. LCMS for C10H7ClN5O3 (M+H)+: m/z=279.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846726B2
Source datasetuspto-grants-2014_09
ORD IDord-898fbf3238ab48bb8f3eff4f829d9947
Source noteuspto-grants-2014_09