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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 641797Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/641797

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktAcetyl chlorideHCID 6367—
EduktSodium HydroxideHCID 14798—
Edukt4-Chloro-1H-pyrrolo[2,3-b]pyridineHCID 11389493—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-Iodo-1H-pyrrolo[2,3-b]pyridineHCID 2187741548%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

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+].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07696225B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-d05fcf96b9114b9294d3ba0d63e8a10f
Quellennotizuspto-grants-2010_04