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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 402511Erstellt: 26. Oktober 2026

Diisopropylethylamine → 5-(1-(6-Chloro-5-methylpyrimidin-4-yl)piperidin-4-yl)-3-isopropyl-1,2,4-oxadiazole

https://huagongshe.com/reaction/402511

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt4,6-Dichloro-5-methylpyrimidineHCID 818860—
Edukt4-(3-Isopropyl-1,2,4-oxadiazol-5-YL)piperidine hydrochlorideHCID 53400827—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-(1-(6-Chloro-5-methylpyrimidin-4-yl)piperidin-4-yl)-3-isopropyl-1,2,4-oxadiazoleHCID 8666161143%

Reaktionsbedingungen

Temperatur27 °C

Reaktionsschritte

A solution of 4-(3-isopropyl-1,2,4-oxadiazol-5-yl)piperidine hydrochloride (2.0 gm, 0.008369 moles) and diisopropylethylamine (2.78 gm, 0.0215 moles) in dichloromethane (30 ml) was added to an ice-cooled solution of 4,6-dichloro-5-methylpyrimidine (2.1 gm, 0.001295 moles) in dichloromethane (10 ml) and the reaction was stirred at 27° C. for 2 h. The reaction mixture was diluted with dichloromethane and washed with water and brine, dried over sodium sulfate and evaporated under reduced pressure. The crude was purified by flash column chromatography (silica gel, 15% ethyl acetate in hexane) to afford the title compound as a white solid (43% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08742117B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-1835680b8e5e4078a7d45ff6eb06ff2d
Quellennotizuspto-grants-2014_06