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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387472Generated: October 29, 2026

Potassium Carbonate → HCID 59135413, compound

https://huagongshe.com/reaction/387472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-BromopyrimidineHCID 78344—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 136179690HCID 136179690—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 59135413HCID 5913541359.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-(5-{[2-chloro-5-(trifluoromethyl)phenyl]amino}-1,3,4-oxadiazol-2-yl)phenol (177.85 mg, 0.5 mmol) was dissolved in 3 mL of anhydrous DMF in a 2-5 mL microwave vial (Personal Chemistry). Solid potassium bis(trimethylsilyl)amide (200.0 mg, 1.0 mmol) was added and the reaction mixture was stirred with heating at 80° C. for 10 min, then 5-bromopyrimidine (95.4 mg, 0.6 mmol) was added, followed by anhydrous K2CO3 (69.1 mg, 0.5 mmol). Then the vial was capped and microwaved at 180° C. for 40 min. Then the reaction mixture was diluted with ca. 1 mL of MeOH, filtered through 0.22 um syringe filter and purified by reverse-phase preparative HPLC in acetonitrile/water system with 0.01% TFA. Fractions, containing the product, were partitioned between ca. 50 mL of EtOAc and ca. 50 mL of saturated aqueous NaHCO3. EtOAc layer was washed with brine, dried over anhydrous Na2SO4 and filtered. Solvent was removed in vacuo to give the title product as a beige solid (129.1 mg). Yield 59.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372971B2
Source datasetuspto-grants-2013_02
ORD IDord-fded77e0af1d42dbb4b3a7cd28d4e3c2
Source noteuspto-grants-2013_02