Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994055Generated: October 27, 2026

3-Chloro-2-fluoro-5-(trifluoromethyl)benzoyl chloride → 3-Chloro-2-fluoro-N-{5-[4-(pyridin-3-yloxy)phenyl]-1,3,4-oxadiazol-2-yl}-5-(trifluoromethyl)-benzamide

https://huagongshe.com/reaction/1994055

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-2-fluoro-5-(trifluoromethyl)benzoyl chlorideHCID 2773782—
Reactant5-[4-(Pyridin-3-yloxy)phenyl]-1,3,4-oxadiazol-2-amine hydrobromide saltHCID 68679658—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
Product3-Chloro-2-fluoro-N-{5-[4-(pyridin-3-yloxy)phenyl]-1,3,4-oxadiazol-2-yl}-5-(trifluoromethyl)-benzamideHCID 5913541134.8%

Reaction Steps

5-[4-(Pyridin-3-yloxy)phenyl]-1,3,4-oxadiazol-2-amine hydrobromide salt (167.5 mg, 0.5 mmol) was suspended in 2 mL of anhydrous pyridine. Neat 3-chloro-2-fluoro-5-trifluoromethylbenzoyl chloride (250 uL) was added directly into the solution. The reaction mixture formed a red solution with a small amount of white precipitate. It was left to stir for 18 hours. Then it was diluted with ca. 1 mL of MeOH, filtered through 0.22 u syringe filter and purified by reverse phase preparative HPLC using acetonitrile/water mixture containing 0.01% of TFA. Fractions, containing the product, were combined and partitioned between ca. 40 mL of EtOAc and ca. 40 mL of saturated aqueous NaHCO3. The EtOAc layer was washed with brine, dried over anhydrous sodium sulfate and filtered. Solvent was removed in vacuo to give the title product as a yellow solid (83.4 mg). Yield 34.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652051B2
Source datasetuspto-grants-2010_01
ORD IDord-9a63ffe0f7ff4d99beb95c50d35c6ac5
Source noteuspto-grants-2010_01