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HRID 641797作成日:2026年10月26日

Sodium Iodide → 4-Iodo-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/641797

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物Acetyl chlorideHCID 6367—
反応物Sodium HydroxideHCID 14798—
反応物4-Chloro-1H-pyrrolo[2,3-b]pyridineHCID 11389493—
溶媒AcetonitrileHCID 6342—
溶媒TetrahydrofuranHCID 8028—
生成物4-Iodo-1H-pyrrolo[2,3-b]pyridineHCID 2187741548%

反応条件

温度80 °C

反応手順

To a solution of 4-Chloro-1H-pyrrolo[2,3-b]pyridine (12.9 g, 84.3 mmol) and NaI (40 g, 168 mmol) in acetonitrile (150 mL) was slowly added acetyl chloride (12.6 mL, 176 mmol). The mixture was allowed to stir at 80° C. for 4 days, and then the excess acetonitrile was removed in vacuo. 300 mL of 10% K2CO3 (aq) was added to the residue and the mixture extracted with CH2Cl2 (3×100 mL). The combined organic extracts were washed with 10% sodium bisulfite (aq) and brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give crude product (22.2 g). To a solution of this crude product in THF (150 mL) was added 1M NaOH (100 mL). The mixture was stirred at room temperature for 2 hr prior to evaporation of the solvent in vacuo, dilution with water and extraction with CH2Cl2. The extracts were washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The resulting brown solid was purified by chromatography over silica gel and recrystallized from acetonitrile to give pure 4-Iodo-1H-pyrrolo[2,3-b]pyridine (9.75 g, 48%). MS (ES+): 245 [MH+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07696225B2
出典データセットuspto-grants-2010_04
ORD IDord-d05fcf96b9114b9294d3ba0d63e8a10f
出典メモuspto-grants-2010_04