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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874418Generated: November 1, 2026

Oxalyl chloride → HCID 57749231, compound

https://huagongshe.com/reaction/1874418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant1-Methyl-2-pyrrolecarboxylic acidHCID 81453—
ReactantN-[6-(3-aminophenoxy)[1,2,4]triazolo[1,5-a]pyridin-2-yl]cyclopropanecarboxamideHCID 57749117—
CatalystDimethylformamideHCID 6228—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57749231HCID 5774923141.6%

Reaction Steps

To a solution of 1-methyl-1H-pyrrole-2-carboxylic acid (121 mg, 0.970 mmol) in tetrahydrofuran (5 mL) were added oxalyl chloride (169 μL, 1.94 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-Aminophenoxy)[1,2,4]triazolo[1,5-a]pyridin-2-yl]cyclopropanecarboxamide (100 mg, 0.323 mmol) was added thereto 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 (56.0 mg, 14%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304557B2
Source datasetuspto-grants-2012_11
ORD IDord-c2100091cef247b499e46ef64c72974d
Source noteuspto-grants-2012_11