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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1918512Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1918512

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
PatentnummerUS08618138B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-3f31bf62192c46e889b5c6eb27cf5023
Quellennotizuspto-grants-2013_12