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HRID 501271作成日:2026年10月24日

Methyl iodide → 6-Bromo-1-methyl-1H-indazole

https://huagongshe.com/ja/reaction/501271

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Sodium hydrideHCID 24758—
反応物6-Bromo-1H-indazoleHCID 17842471—
溶媒TetrahydrofuranHCID 8028—
生成物6-bromo-2-methyl-2H-indazoleHCID 2255862443%
生成物6-Bromo-1-methyl-1H-indazoleHCID 2255867551%

反応手順

To 6-bromoindazole (402A) (5.0 g, 25.4 mmol) in THF (50 mL) was added sodium hydride (95%, 672 mg, 26.6 mmol) with ice bath cooling. The mixture was stirred for 30 minutes. Methyl iodide (6.36 mL, 102 mmol) was added at room temperature. The reaction mixture was quenched with ammonium chloride solution and the layers were separated. The aqueous layer was extracted with ethyl acetate. The combined organic layer was washed with brine, dried over sodium sulfate and concentrated. Purification by column chromatography (SiO2, ethyl acetate/hexane gradient) afforded 1-methyl-6-bromoindazole (402B) (2.71 g, 51%) as a yellow oil and 2-methyl-6-bromoindazole (402C) (2.28 g, 43%) as a yellow crystalline solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07772263B2
出典データセットuspto-grants-2010_08
ORD IDord-11ee07161b1848069adbb6445ffc0db4
出典メモuspto-grants-2010_08