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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233583Generated: October 30, 2026

Pyridine → 3-{4-[4-butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethoxy]-2-trifluoromethyl-phenyl}-4H-[1,2,4]oxadiazol-5-one

https://huagongshe.com/reaction/2233583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenyl chloroformateHCID 15891—
ReactantHCID 178441583HCID 178441583—
SolventDichloromethaneHCID 6344—
Product3-{4-[4-butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethoxy]-2-trifluoromethyl-phenyl}-4H-[1,2,4]oxadiazol-5-oneHCID 135961980—

Reaction Steps

To a solution of 89.3 mg of 4-[4-butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethoxy]-N-hydroxy-2-trifluoromethyl-benzamidine in 2 ml of anhydrous dichloromethane were added 92 μl pyridine followed by 21.6 μl phenylchloroformate dropwise. The resulting mixture was stirred at room temperature for 1 h. The solvent was removed in vacuo. To a solution of the resulting residue in 2.5 ml of acetonitrile was added 88 μl of 1,8-diazabicyclo[5.4.0]undec-7-ene. The mixture was stirred under microwave heating at 180° C. for 10 minutes (or stirred at room temperature overnight). The solvent was removed in vacuo and the crude product was purified by column chromatography on silica gel (heptane 1/ethyl acetate 1 then dichloromethane 95/methanol 5 followed by another column with dichloromethane 90/acetone 10) to give 65 mg of 3-{4-[4-butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethoxy]-2-trifluoromethyl-phenyl}-4H-[1,2,4]oxadiazol-5-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709509B2
Source datasetuspto-grants-2010_05
ORD IDord-b0835dc2feac44908f863676fff34caa
Source noteuspto-grants-2010_05