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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874433Generated: October 31, 2026

Oxalyl chloride → HCID 57749153, compound

https://huagongshe.com/reaction/1874433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2,2-Difluorocyclopropane-1-carboxylic acidHCID 2782823—
ReactantHCID 57749095HCID 57749095—
CatalystDimethylformamideHCID 6228—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57749153HCID 5774915327%

Reaction Steps

To a solution of 2,2-difluorocyclopropanecarboxylic acid (104 mg, 0.850 mmol) in tetrahydrofuran (1 mL) were added oxalyl chloride (74.3 μL, 0.850 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-{5-[(2-Amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)oxy]-2-fluorophenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamide (65.0 mg, 0.170 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 (silica gel, hexane/ethyl acetate=80/20→0/100) and recrystallized from ethyl acetate to give the title compound (22.0 mg, 27%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304557B2
Source datasetuspto-grants-2012_11
ORD IDord-4285335e1e3f47c1923efa6fc86bc5aa
Source noteuspto-grants-2012_11