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HRID 217592作成日:2026年10月25日

2-Methoxypyrimidine-5-boronic acid → (3-amino-2,6-difluoro-phenyl)-[5-(2-methoxy-pyrimidin-5-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-methanone

https://huagongshe.com/reaction/217592

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methoxypyrimidine-5-boronic acidHCID 2736778—
反応物HCID 58368852HCID 58368852—
触媒Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
溶媒Potassium CarbonateHCID 11430—
生成物(3-amino-2,6-difluoro-phenyl)-[5-(2-methoxy-pyrimidin-5-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-methanoneHCID 5956959943.6%

反応条件

温度160 °C

反応手順

In a microwave vial, (3-amino-2,6-difluoro-phenyl)-(5-iodo-1H-pyrrolo[2,3-b]pyridin-3-yl)-methanone (19, 1.36 g, 3.41 mmol), 2-methoxy-pyrimidine-5-boronic acid (20, 1.05 g, 6.81 mmol), and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (0.25 g, 0.34 mmol) were mixed in 22 mL of 1.00 M potassium carbonate in water and 18 mL of acetonitrile. The resulting mixture was heated at 160° C. in the microwave for 15 minutes. The resulting mixture was filtered through a thin layer of celite, and the celite bed was washed with a mixture of water and ethyl acetate. The two layers of the filtrate were separated, and the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate, filtered, and the filtrate concentrated under vacuum. The residue was purified by flash silica gel chromatography eluting with ethyl acetate and dichloromethane to provide the desired compound (21, 0.567 g). MS (ESI) [M+H+]+=382.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198273B2
出典データセットuspto-grants-2012_06
ORD IDord-0fe67580fcf141079f561e1207acb3e2
出典メモuspto-grants-2012_06