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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233572Generated: November 2, 2026

Pyridine → HCID 135508486, compound

https://huagongshe.com/reaction/2233572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl AcetateHCID 8857—
ReactantPhenyl chloroformateHCID 15891—
ReactantHCID 178432506HCID 178432506—
SolventDichloromethaneHCID 6344—
ProductHCID 135508486HCID 135508486—

Reaction Steps

138 mg of 2-Fluoro-N-hydroxy-4-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazole-5-ylmethoxy]-benzamidine were dissolved in 2 ml dichloromethane. 35 μl pyridine and 53 μl phenylchloroformate were added and the mixture stirred at room temperature for thirty minutes. The mixture was diluted by the addition of 20 ml ethyl acetate, washed with brine and dried over MgSO4. The solvent was evaporated in vacuo. The resulting residue was dissolved in 2 ml acetonitrile and 105 μl 1,8-Diazabicyclo[5.4.0]undec-7-ene was added. The mixture was stirred at room temperature for 10 minutes. The mixture was evaporated in vacuo and the resulting crude material was purified by reversed phase HPLC to obtain 70 mg 3-{2-Fluoro-4-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazole-5-ylmethoxy]-phenyl}-4H-[1,2,4]oxadiazole-5-one as an amorphous lyophilisate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709509B2
Source datasetuspto-grants-2010_05
ORD IDord-0299eeb0863e4d7eba0b4621a684514f
Source noteuspto-grants-2010_05