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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 58526Erstellt: 23. Oktober 2026

Triethylamine → N-(2-(5-chloro-1H-indol-3-yl)ethyl)-5-(chloromethyl)isoxazole-3-carboxamide

https://huagongshe.com/de/reaction/58526

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktThionyl ChlorideHCID 24386—
Edukt5-Chloro-1H-indole-3-ethylamine monohydrochlorideHCID 2827494—
Edukt5-(Hydroxymethyl)-1,2-oxazole-3-carboxylic acidHCID 8027249—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(2-(5-chloro-1H-indol-3-yl)ethyl)-5-(chloromethyl)isoxazole-3-carboxamideHCID 6683169922%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Thionyl chloride (0.5 mL; 7.26 mmol) was added to a mixture of 5-(hydroxymethyl)isoxazole-3-carboxylic acid (0.207 g; 7.26 mmol) and stirred at 80° C. for 72 h. The solution was concentrated under reduced pressure and the crude material was dissolved in dichloromethane (5 mL) and added to a mixture of 2-(5-chloro-1H-indol-3-yl)ethanamine hydrochloride (0.370 g; 1.60 mmol) and triethylamine (0.524 mL; 3.62 mmol) in dichloromethane (5 mL). The resulting solution was stirred at room temperature for 20 min, concentrated under reduced pressure and the crude material was purified by flash chromatography on silica gel (eluent 2 to 20% ethyl acetate in dichloromethane) to afford N-(2-(5-chloro-1H-indol-3-yl)ethyl)-5-(chloromethyl)isoxazole-3-carboxamide 0.088 g (22%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434722B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-e8aeaa6de6af4bfbb528e1622eee4e5b
Quellennotizuspto-grants-2016_09