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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095884Generated: October 31, 2026

Oxalyl chloride → HCID 58158631, compound

https://huagongshe.com/reaction/2095884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantSodium BicarbonateHCID 516892—
Reactant3-methyl-1-phenyl-1H-pyrazole-5-carboxylic acidHCID 2769592—
ReactantN-[6-(4-aminophenoxy)imidazo[1,2-a]pyridin-2-yl]cyclopropanecarboxamideHCID 58158625—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventDimethylacetamideHCID 31374—
ProductHCID 58158631HCID 5815863143.2%

Reaction Steps

To a solution of 3-methyl-1-phenyl-1H-pyrazole-5-carboxylic acid (197 mg, 973 μmol) in tetrahydrofuran (2 mL) were added oxalyl chloride (80 μL, 973 μmol) and N,N-dimethylformamide under ice-cooling, and the mixture was stirred at room temperature for 1 hr. A solution of N-[6-(4-aminophenoxy)imidazo[1,2-a]pyridin-2-yl]cyclopropanecarboxamide (200 mg, 649 μmol) in N,N-dimethylacetamide (2 mL) was added to the reaction solution, and the mixture was stirred at room temperature for 2 hr. Saturated aqueous sodium hydrogen carbonate was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with 1N aqueous sodium hydroxide solution, water and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The obtained residue was recrystallized from ethanol/water to give the title compound (138 mg, 29%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445509B2
Source datasetuspto-grants-2013_05
ORD IDord-304fb8752a0e479d8afbc1f0e5797acd
Source noteuspto-grants-2013_05