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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387454Generated: October 31, 2026

Potassium Carbonate → HCID 178485503, compound

https://huagongshe.com/reaction/387454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloropyridine-2-carboxamideHCID 303543—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant3-[5-(4-Chloro-3-trifluoromethyl-phenylamino)-4h[1,2,4]triazol-3-yl]-phenolHCID 178515989—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 178485503HCID 178485503—

Reaction Conditions

Temperature80 °C

Reaction Steps

3-[5-(4-chloro-3-trifluoromethyl-phenylamino)-4H[1,2,4]triazol-3-yl]-phenol (100 mg, 0.282 mmol) was dissolved in 2 mL of anhydrous DMF in a 5 mL microwave vial (Personal Chemistry). Solid potassium bis(trimethylsilyl)amide (140.6 mg, 0.705 mmol) was added and the reaction mixture was stirred with heating at 80° C. for 15 min, then 4-chloro-2-pyridine-carboxamide (52.9 mg, 0.31 mmol) was added, followed by anhydrous K2CO3 (19.5 mg, 0.141 mmol). Then the vial was capped and microwaved at 250° C. for 20 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. The product was isolated as a TFA salt (25.0 rug of white solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372971B2
Source datasetuspto-grants-2013_02
ORD IDord-2fe858e6e05a4c8ea20eaf2972da8b63
Source noteuspto-grants-2013_02