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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 641797생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/641797

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참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Acetyl chlorideHCID 6367—
반응물Sodium HydroxideHCID 14798—
반응물4-Chloro-1H-pyrrolo[2,3-b]pyridineHCID 11389493—
용매AcetonitrileHCID 6342—
용매TetrahydrofuranHCID 8028—
생성물4-Iodo-1H-pyrrolo[2,3-b]pyridineHCID 2187741548%

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온도80 °C

반응 단계

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+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07696225B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-d05fcf96b9114b9294d3ba0d63e8a10f
출처 메모uspto-grants-2010_04