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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387463Generated: October 29, 2026

Potassium Carbonate → 4-[4-(5-{[4-Chloro-3-(trifluoromethyl)phenyl]amino}-1,3,4-oxadiazol-2-yl)phenoxy]-n-methylpyridine-2-carboxamide trifluoroacetate salt

https://huagongshe.com/reaction/387463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloropyridine-2-carboxamideHCID 303543—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant4-(5-{[4-Chloro-3-(trifluoromethyl)-phenyl]amino}-1,3,4-oxadiazol-2-yl)phenolHCID 136179692—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
Product4-[4-(5-{[4-Chloro-3-(trifluoromethyl)phenyl]amino}-1,3,4-oxadiazol-2-yl)phenoxy]-n-methylpyridine-2-carboxamide trifluoroacetate saltHCID 8660428979.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-(5-{[4-chloro-3-(trifluoromethyl)-phenyl]amino}-1,3,4-oxadiazol-2-yl)phenol (100 mg, 0.281 mmol) was dissolved in ca. 2 mL of anhydrous DMF under argon. Solid potassium bis(trimethylsilyl)amide (140.2 mg, 0.702 mmol) was added and the resulting yellow solution was heated at 80° C. for 15 min. Then solid K2CO3 (19.4 mg, 0.140 mmol) was added, followed by 4-chloro-2-pyridine-carboxamide (52.7 mg, 0.309 mmol). The reaction mixture was microwaved at 200 C for 15 min. Then it was diluted with 1 mL of MeOH, filtered through 0.22 um syringe filter and purified by preparative reverse-phase chromatography using acetonitrile/water gradient with 0.1% TFA. The major peak having the mass of the product was collected; solvent was removed in vacuo to give the title product as a white solid (67.5 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372971B2
Source datasetuspto-grants-2013_02
ORD IDord-4fa5f00951e746c1a1d3770831999eb8
Source noteuspto-grants-2013_02