Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661440Generated: November 2, 2026

Ethyl Acetate → HCID 68678952, compound

https://huagongshe.com/reaction/661440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-N-methylpicolinamideHCID 1476814—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 136179697HCID 136179697—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 68678952HCID 68678952—

Reaction Conditions

Temperature100 °C

Reaction Steps

7.23 g (19.73 mmol) of 4-(3-{[4-chloro-3-(trifluoromethyl)phenyl]amino}-1,2,4-triazin-5-yl)phenol can be dissolved in 80 mL of anhydrous DMF under argon atmosphere. 2.44 g (21.71 mmol, 1.1 equivalent) of solid potassium tert-butoxide can be added to the solution. The resulting mixture can be heated to about 100° C. and stirred at that temperature for 15 min. Then a solution of 3.7 g (21.71 mmol, 1.1 equivalent) of 4-chloro-pyridine-2-carboxylic acid methylamide in 10 mL of anhydrous DMF can be added, followed by 3.28 g (23.68 mmol, 1.2 equivalent) of anhydrous K2CO3. The reaction mixture can be heated at 140° C. for 30 hrs. The progress of the reaction can be monitored by LC/MS. Then it can be allowed to cool down to ambient temperature. The resulting mixture can be poured into 500 mL of water and 100 mL of ethyl acetate. The aqueous layer can be extracted with a number of solvents, such as ethyl acetate, methylene chloride or ether. The combined extracts can be washed 3 times with 100 mL of water, then with brine and dried over anhydrous sodium sulfate. Solvent can be removed in vacuum to yield crude 4-[4-(3-phenylamino-[1,2,4]triazin-6-yl)-phenoxy]-pyridine-2-carboxylic acid methylamide. The product can be than purified using silica gel column chromatography. Those having ordinary skill in the art can determine which solvent system can be used as an eluents in the chromatographic purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084618B2
Source datasetuspto-grants-2011_12
ORD IDord-5ddd1a473a0c494aa2db62d26b0d8d5e
Source noteuspto-grants-2011_12