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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520252Generated: October 26, 2026

Pyridine → HCID 71627023, compound

https://huagongshe.com/reaction/520252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetonitrileHCID 6342—
ReactantCyclohexanolHCID 7966—
Reactant3-[(Z)-N-[(2-amino-1,3-thiazol-4-yl)methoxy]-C-phenylcarbonimidoyl]-2-methyl-1,2,4-oxadiazol-5-oneHCID 71626945—
ProductHCID 71627023HCID 7162702377%

Reaction Steps

To a solution of 3-[(Z)-{[(2-amino-1,3-thiazol-4-yl)methoxy]imino}(phenyl)methyl]-2-methyl-1,2,4-oxadiazol-5(2H)-one (100 mg, 0.277 mmol, 1 eq.) in acetonitrile (2 ml) was added 4-fluorophenylcarbonochloridate (0.040 mL, 0.304 mmol, 1.1 eq.), followed by pyridine (0.022 mL, 0.277 mmol, 1 eq.) and stirring was allowed for 2 hours at room temperature. Cyclohexanol (0.032 mL, 0.304 mmol, 1.1 eq.) was then added and the resulting mixture was refluxed for 15 h. After concentration, the residue was purified by chromatography on silica gel to give Cyclohexyl {4-[({[(Z)-(3-methoxyphenyl)(2-methyl-5-oxo-2,5-dihydro-1,2,4-oxadiazol-3-yl)methylene]amino}oxy)methyl]-1,3-thiazol-2-yl}carbamate (110 mg, 77% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09326515B2
Source datasetuspto-grants-2016_05
ORD IDord-e0eee15586c04438aab6348bacf0f8ff
Source noteuspto-grants-2016_05