Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441690Generated: November 1, 2026

Pyridine → 3-{4-[2-(Benzooxazol-2-yl-butyl-amino)-ethyl]-phenyl}-4H-[1,2,4]oxadiazol-5-one

https://huagongshe.com/reaction/1441690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenyl chloroformateHCID 15891—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 178449016HCID 178449016—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product3-{4-[2-(Benzooxazol-2-yl-butyl-amino)-ethyl]-phenyl}-4H-[1,2,4]oxadiazol-5-oneHCID 136128883—

Reaction Steps

280 mg 4-[2-(Benzooxazol-2-yl-butyl-amino)-ethyl]-N-hydroxy-benzamidine were dissolved in 5 ml dichloromethane. 78 μl pyridine and 120 μl phenylchloroformate were added and the mixture stirred at room temperature for ten minutes. The mixture was diluted by the addition of 15 ml acetonitrile and 115 μl ml 1,8-Diazabicyclo[5.4.0]undec-7-ene were 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 105 mg 3-{4-[2-(Benzooxazol-2-yl-butyl-amino)-ethyl]-phenyl}-4H-[1,2,4]oxadiazol-5-one as an amorphous lyophilisate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655679B2
Source datasetuspto-grants-2010_02
ORD IDord-f99f8cb3233c4709940f4230b9a849d3
Source noteuspto-grants-2010_02