Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528343Generated: October 29, 2026

1,1'-Carbonyldiimidazole → 3-[(Z)-N-[(2-amino-1,3-thiazol-4-yl)methoxy]-C-phenylcarbonimidoyl]-4H-1,2,4-oxadiazol-5-one

https://huagongshe.com/reaction/1528343

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant(2Z)-2-[(2-amino-1,3-thiazol-4-yl)methoxyimino]-N'-hydroxy-2-phenylethanimidamideHCID 136626361—
SolventDimethylformamideHCID 6228—
Product3-[(Z)-N-[(2-amino-1,3-thiazol-4-yl)methoxy]-C-phenylcarbonimidoyl]-4H-1,2,4-oxadiazol-5-oneHCID 13662635988.5%

Reaction Steps

To a solution of (1Z,2Z)-2-{[(2-amino-1,3-thiazol-4-yl)methoxy]imino}-N′-hydroxy-2-phenylethanimidamide (3 g, 10.29 mmol, 1 eq.) in DMF (50 ml) was added CDI (1.66 g, 10.29 mmol, 1 eq.) and stirring at room temperature was allowed for 30 min before heated to 80° C. for 6 h. The reaction was quenched by addition of water and extracted with EtOAc (3×50 ml). The organics were combined, washed with aq. sat. NaCl, dried over MgSO4 and concentrated. The residue was triturated in MeCN and a white solid was isolated by filtration giving 3-[(Z)-{[(2-amino-1,3-thiazol-4-yl)methoxy]imino}(phenyl)methyl]-1,2,4-oxadiazol-5(4H)-one (2.89 g, 50% purity, 43% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090600B2
Source datasetuspto-grants-2015_07
ORD IDord-342e384051334fdaa58d71568c24bbc1
Source noteuspto-grants-2015_07