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HRID 40720作成日:2026年10月23日

Water → 1-(4-Methoxybenzyl)-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid

https://huagongshe.com/ja/reaction/40720

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物4-Methoxybenzyl bromideHCID 165021—
反応物methyl 1H-pyrrolo[2,3-b]pyridine-5-carboxylateHCID 22832049—
溶媒DimethylformamideHCID 6228—
生成物1-(4-Methoxybenzyl)-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acidHCID 5822016225.1%

反応条件

温度0 °C

反応手順

To a stirred cooled 0° C. suspension of NaH (272 mg, 6.81 mmol) in DMF (23 mL) was added 1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid methyl ester (400 mg, 2.27 mmol). After 5 min, PMBBr (548 mg, 2.72 mmol) and KI (377 mg, 2.27 mmol) were added and the reaction mixture was allowed to warm to room temperature and stirring was continued overnight. The following day, water was added to quench the remaining Nail and the aqueous mixture was washed with EtOAc, which was discarded. The aqueous phase was collected and carefully acidified (pH ˜3) before extraction with EtOAc. The combined organics were dried and evaporated to afford 1-(4-methoxy-benzyl)-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid (160 mg, 0.57 mmol, 25% yield). ES MS (M+H+)=283.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530483B2
出典データセットuspto-grants-2013_09
ORD IDord-7decd16c2ab94af9ac129939d6ac8506
出典メモuspto-grants-2013_09