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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40720생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물4-Methoxybenzyl bromideHCID 165021—
반응물methyl 1H-pyrrolo[2,3-b]pyridine-5-carboxylateHCID 22832049—
용매DimethylformamideHCID 6228—
생성물1-(4-Methoxybenzyl)-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acidHCID 5822016225.1%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530483B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-7decd16c2ab94af9ac129939d6ac8506
출처 메모uspto-grants-2013_09