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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1691607Erstellt: 26. Oktober 2026

Ammonia → 5-Fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxamide

https://huagongshe.com/reaction/1691607

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktThionyl ChlorideHCID 24386—
Edukt5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxylic acidHCID 57431513—
LösungsmittelTolueneHCID 1140—
Produkt5-Fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxamideHCID 6684569629,1%

Reaktionsschritte

A suspension, stirred at 20° C., of 2 g (6.96 mmol) of 5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxylic acid, prepared according to the protocol described in step 1.1, in 80 ml of dry toluene is admixed with 5.08 ml (69.62 mmol) of thionyl chloride. The reaction mixture is stirred at reflux for 2 hours and then concentrated under reduced pressure. The resulting product is taken up in 10 ml of dichloromethane and this solution is poured dropwise into a solution of 9.12 ml (69.62 mmol) of 30% aqueous ammonia. The reaction mixture is stirred at 20° C. for 14 hours. After this time a solid is recovered by filtration and triturated in 50 ml of diisopropyl ether. Filtration and drying under reduced pressure give 0.58 g of expected product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08153796B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-fa6bd15c00ac4b898eb0f8846c2add89
Quellennotizuspto-grants-2012_04