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HRID 269481作成日:2026年10月25日

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

https://huagongshe.com/reaction/269481

反応式

関与物質

役割名称HCID仕込み量
反応物2-Pyridineacetic acid, hydrochloride (1:1)HCID 85317—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物methyl 1H-pyrrolo[2,3-b]pyridine-3-carboxylateHCID 21110084—
溶媒TetrahydrofuranHCID 8028—
生成物2-Pyridin-2-yl-1-(1H-pyrrolo[2,3-b]pyridin-3-yl)-ethanoneHCID 59832245—

反応条件

温度-78 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07446199B2
出典データセットuspto-grants-2008_11
ORD IDord-ebe10ceb71664519a80050fdc239dbbd
出典メモuspto-grants-2008_11