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HRID 57856作成日:2026年10月27日

6-Chloro-1-(6-fluoropyridin-2-yl)-1H-pyrazolo[4,3-c]pyridine → 6-(6-Ethylpyrazin-2-yl)-1-(6-fluoro-2-pyridyl)pyrazolo[4,3-c]pyridine

https://huagongshe.com/reaction/57856

反応式

関与物質

役割名称HCID仕込み量
反応物6-Chloro-1-(6-fluoropyridin-2-yl)-1H-pyrazolo[4,3-c]pyridineHCID 86280243—
反応物(6-Ethylpyrazin-2-yl)-trimethyl-stannaneHCID 86707055—
触媒HCID 178418397HCID 178418397—
溶媒DimethylacetamideHCID 31374—
生成物6-(6-Ethylpyrazin-2-yl)-1-(6-fluoro-2-pyridyl)pyrazolo[4,3-c]pyridineHCID 8670705441.3%

反応条件

温度150 °C

反応手順

To a solution of 6-chloro-1-(6-fluoro-2-pyridyl)pyrazolo[4,3-c]pyridine (85 mg; 0.34 mmol) and tetrakis(triphenylphosphine)palladium (40 mg, 0.034 mmol) in N,N-dimethylacetamide; 2.0 mL was added (6-ethylpyrazin-2-yl)-trimethyl-stannane (185 mg, 0.684 mmol). The reaction was purged with N2 for 5 min then heated at 150° C. for 45 min in biotage microwave. The reaction mixture was filtered through celite and concentrated. The crude product was diluted with EtOAc then washed with water. The organic layers was dried with sodium sulfate, filtered, and concentrated in vacuum. The crude product was purified by flash chromatography (EtOAc/Heptane eluted at 50% EtOAc) to give 6-(6-ethylpyrazin-2-yl)-1-(6-fluoro-2-pyridyl)pyrazolo[4,3-c]pyridine (45 mg) in 41% yield. MS (ESI) m/z: 321.2

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434725B2
出典データセットuspto-grants-2016_09
ORD IDord-e906e0df7413481c9589cdf8d984c21b
出典メモuspto-grants-2016_09