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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874481Generated: November 2, 2026

Oxalyl chloride → HCID 25128179, compound

https://huagongshe.com/reaction/1874481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant1-Ethyl-3-methyl-1H-pyrazole-5-carboxylic acidHCID 2743794—
ReactantN-[6-(3-amino-4-fluorophenoxy)[1,2,4]triazolo[1,5-a]pyridin-2-yl]cyclopropanecarboxamideHCID 57749270—
CatalystDimethylformamideHCID 6228—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 25128179HCID 2512817990%

Reaction Steps

To a solution of 1-ethyl-3-methyl-1H-pyrazole-5-carboxylic acid (188 mg, 1.22 mmol) in tetrahydrofuran (7 mL) were added oxalyl chloride (160 μL, 1.83 mmol) and N,N-dimethylformamide (1 drop), and the mixture was stirred at room temperature for 1 hr. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in N,N-dimethylacetamide (3 mL). N-[6-(3-Amino-4-fluorophenoxy)[1,2,4]triazolo[1,5-a]pyridin-2-yl]cyclopropanecarboxamide (200 mg, 0.611 mmol) was added with stirring under ice-cooling, and the mixture was stirred at room temperature for 15 hr. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure, and the residue was purified by column chromatography (NH silica gel, ethyl acetate) and recrystallized from ethyl acetate to give the title compound (254 mg, 90%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304557B2
Source datasetuspto-grants-2012_11
ORD IDord-2309f470562c4ac280d31ded0652dc3b
Source noteuspto-grants-2012_11