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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5449Erstellt: 24. Oktober 2026

Triethylamine → 5-(Phthalimidomethylthio)imidazo[1,2-a]pyridine

https://huagongshe.com/de/reaction/5449

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1H-Isoindole-1,3(2H)-dione, 2-(bromomethyl)-HCID 79244—
EduktHCID 178418687HCID 178418687—
LösungsmittelEthanolHCID 702—
Produkt5-(Phthalimidomethylthio)imidazo[1,2-a]pyridineHCID 2336286469,4%

Reaktionsschritte

To a suspension of 5-mercaptoimidazo[1,2-a]pyridine (3.00 g, 20 mmoles) and N-bromomethylphthalimide (5.28 g, 22 mmoles) in ethanol (200 ml) was added triethylamine (4.2 ml, 30 mmoles) and the mixture was stirred at room temperature for 1 hour. After the solvent was distilled off, chloroform was added to the residue, which was washed with water, dried over anhydrous magnesium sulfate and the solvent was distilled off. Then, the residue was purified by column chromatography (eluent: ethyl acetate) to obtain 4.29 g of the desired product (69.4%, pale yellow crystals).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05244908
Quelldatensatzuspto-grants-1993_09
ORD IDord-831db6ca9bbd41e0aaa035a1763a8ec1
Quellennotizuspto-grants-1993_09