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HRID 1874385생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1874385

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물3-Methylpicolinic acidHCID 268757—
반응물5-(3-Aminophenoxy)pyridin-2-amineHCID 57749166—
촉매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
용매DimethylacetamideHCID 31374—
용매Sodium BicarbonateHCID 516892—
생성물N-{3-[(6-aminopyridin-3-yl)oxy]phenyl}-3-methylpyridine-2-carboxamideHCID 5774926163.2%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08304557B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-5f31dea26b6c470b9cce8a08a33e9808
출처 메모uspto-grants-2012_11