Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233585Generated: October 31, 2026

HCID 135961971, compound → HCID 135961967, compound

https://huagongshe.com/reaction/2233585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 135961971HCID 135961971—
ReactantHCID 178418260HCID 178418260—
SolventPyridineHCID 1049—
ProductHCID 135961967HCID 13596196710.5%

Reaction Conditions

Temperature21 °C

Reaction Steps

To a solution of 100 mg of 3-{2-bromo-4-[4-butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethoxy]-phenyl}-4H-[1,2,4]oxadiazol-5-one in 4 ml of pyridine was added 29 mg of copper cyanide. The resulting mixture was stirred under microwave heating at 21° C. for 10 minutes, then concentrated under reduced pressure. The residue was taken into ethyl acetate, washed with a pH 9 aqueous solution of ammonia, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by preparative thin layer chromatography on silica gel (dichloromethane 95/methanol 5) and precipitated from ethyl acetate/diisopropyl ether/pentane to give 9.5 mg of 5-[4-butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethoxy]-2-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzonitrile

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709509B2
Source datasetuspto-grants-2010_05
ORD IDord-ab2b963894a24ce6838395bbc86de923
Source noteuspto-grants-2010_05