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HRID 341247Erstellt: 25. Oktober 2026

N-Iodosuccinimide → 7-Chloro-3-iodoimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/341247

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-IodosuccinimideHCID 120273—
Edukt7-Chloroimidazo(1,2-a)pyridineHCID 19695901—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt7-Chloro-3-iodoimidazo[1,2-a]pyridineHCID 5749769775,3%

Reaktionsschritte

To a solution of 7-Chloro-imidazo[1,2-a]pyridine (30.9 g, 186 mmol, 1.0 equiv) in DMF (280 ml) was added N-iodosuccinimide (43.6 g, 194 mmol, 1.05 equiv) and the resulting mixture was stirred overnight at RT. The thin brown slurry was diluted with water (840 ml), brine (280 ml) and extracted with EtOAc (560 ml). The aqueous was further extracted with EtOAc (3×280 ml). The combined organic phases were washed with water (2×280 ml), 10% w/v sodium thiosulfate (280 ml), brine (280 ml), dried (MgSO4), filtered and concentrated in vacuo to give a brown residue. The residue was triturated with ether (200 ml), filtered and the solid was washed ether (2×50 ml) and dried on the filter to give 39 g of product. MS: [M+H]+ 279

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08895745B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-ec0333197fe042abba71d365ce1829c1
Quellennotizuspto-grants-2014_11