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HRID 79270作成日:2026年10月24日

Isopropanol → 1-((6-methylpyridin-2-yl)methyl)-4-nitro-3-vinyl-1H-indazole

https://huagongshe.com/ja/reaction/79270

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropanolHCID 3776—
反応物TriethylamineHCID 8471—
反応物Potassium vinyltrifluoroborateHCID 23679353—
反応物3-iodo-1-((6-methylpyridin-2-yl)methyl)-4-nitro-1H-indazoleHCID 67259762—
溶媒TetrahydrofuranHCID 8028—
生成物1-((6-methylpyridin-2-yl)methyl)-4-nitro-3-vinyl-1H-indazoleHCID 6725970387.4%

反応条件

温度95 °C

反応手順

To a reaction vial was added 3-iodo-1-((6-methylpyridin-2-yl)methyl)-4-nitro-1H-indazole (216 mg, 0.548 mmol) and potassium trifluoro(vinyl)borate (156 mg, 1.64 mmol). Isopropanol (2 mL) and tetrahydrofuran (0.5 mL) were added. Argon was bubbled through the mixture for 20 minutes. Triethylamine (229 μL, 1.64 mmol) and 1,1′-bis(diphenylphosphino)ferrocene-palladium(II)dichloride dichloromethane complex (44.8 mg, 0.0548 mmol) were added. The vial was sealed and the mixture was heated at 90-100° C. for 3 hours. The mixture was allowed to cool and filtered through glass fiber filter paper, washing with ethyl acetate. The solution was concentrated under reduced pressure. The residue was dissolved in chloroform (30 mL) and washed with water (10 mL). The solution was dried over magnesium sulfate, filtered and concentrated under reduced pressure to give 1-((6-methylpyridin-2-yl)methyl)-4-nitro-3-vinyl-1H-indazole as an oil (141 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841455B2
出典データセットuspto-grants-2014_09
ORD IDord-d095b51903c94877b397a4f239969812
出典メモuspto-grants-2014_09