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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874385Generated: October 26, 2026

Oxalyl chloride → N-{3-[(6-aminopyridin-3-yl)oxy]phenyl}-3-methylpyridine-2-carboxamide

https://huagongshe.com/reaction/1874385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant3-Methylpicolinic acidHCID 268757—
Reactant5-(3-Aminophenoxy)pyridin-2-amineHCID 57749166—
CatalystDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventDimethylacetamideHCID 31374—
SolventSodium BicarbonateHCID 516892—
ProductN-{3-[(6-aminopyridin-3-yl)oxy]phenyl}-3-methylpyridine-2-carboxamideHCID 5774926163.2%

Reaction Steps

To a solution of 3-methylpyridine-2-carboxylic acid (1.38 g, 10.1 mmol) in tetrahydrofuran (100 mL) were added N,N-dimethylformamide (2 drops) and oxalyl chloride (1.75 mL, 20.2 mmol) at 0° C., and the mixture was stirred at room temperature for 3 hr. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in N,N-dimethylacetamide (50 mL). A solution of 5-(3-aminophenoxy)pyridin-2-amine (1.83 g, 9.09 mmol) in N,N-dimethylacetamide (5 mL) was added with stirring at room temperature, and the mixture was stirred at room temperature for 13 hr. The reaction mixture was diluted with aqueous sodium hydrogen carbonate solution and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure and washed with ethyl acetate-hexane to give the title compound (1.84 g, 57%) as a pale-brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304557B2
Source datasetuspto-grants-2012_11
ORD IDord-5f31dea26b6c470b9cce8a08a33e9808
Source noteuspto-grants-2012_11