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HRID 269481생성일: 2026년 10월 24일

2-Pyridineacetic acid, hydrochloride (1:1) → 2-Pyridin-2-yl-1-(1H-pyrrolo[2,3-b]pyridin-3-yl)-ethanone

https://huagongshe.com/ko/reaction/269481

반응식

참여 물질

역할이름HCID투입량
반응물2-Pyridineacetic acid, hydrochloride (1:1)HCID 85317—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물methyl 1H-pyrrolo[2,3-b]pyridine-3-carboxylateHCID 21110084—
용매TetrahydrofuranHCID 8028—
생성물2-Pyridin-2-yl-1-(1H-pyrrolo[2,3-b]pyridin-3-yl)-ethanoneHCID 59832245—

반응 조건

온도-78 °C

반응 단계

To a solution of 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid methyl ester (200 mg, 1.13 mmol) and 2-pyridinyl-acetic acid hydrochloride (440 mg, 2.53 mmol) in anhydrous THF (10 mL) was added LiHMDS (1.0 M in THF, 10 mL, 10.0 mmol) at −78° C. The solution was stirred at −78° C. for 30 min and was allowed to warm up to RT. After stirring at RT for another 30 min, the reaction mixture was heated under reflux for 14 h. The solvent was then evaporated, the residue was taken up to ethyl acetate (50 mL), and washed with aq. NaHCO3. The organic layer was dried over MgSO4, filtered, and evaporated. The residue was used directly for the next reaction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07446199B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-ebe10ceb71664519a80050fdc239dbbd
출처 메모uspto-grants-2008_11