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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1516194Erstellt: 26. Oktober 2026

N-Aminomorpholine → 6-(5-Methyl-3-phenyl-isoxazol-4-ylmethoxy)-N-morpholin-4-yl-nicotinamide

https://huagongshe.com/reaction/1516194

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-AminomorpholineHCID 20315—
EduktDiisopropylethylamineHCID 81531—
EduktO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Edukt6-(5-Methyl-3-phenyl-isoxazol-4-ylmethoxy)-nicotinic acidHCID 66599213—
LösungsmittelDimethylformamideHCID 6228—
Produkt6-(5-Methyl-3-phenyl-isoxazol-4-ylmethoxy)-N-morpholin-4-yl-nicotinamideHCID 4980097540%

Reaktionsschritte

To a stirred solution of 6-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-nicotinic acid (100 mg, 0.32 mmol) in DMF (5 mL) at room temperature under argon was added N-aminomorpholine (36 mg, 0.35 mmol), 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (0.114 g, 0.35 mmol) and N,N-diisopropylethylamine (208 mg, 1.6 mmol). After 15 h the reaction mixture was concentrated, diluted with water and extracted with ethyl acetate. The combined organic extracts were dried over sodium sulfate, filtered and concentrated. Purification by chromatography (silica, dichloromethane:methanol 1:0 to 97.5:2.5) afforded the title compound (50 mg, 40%) as a white solid. MS: m/e=395.1 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08227461B2
Quelldatensatzuspto-grants-2012_07
ORD IDord-61168f36e94d43deaf1feca82ad20dde
Quellennotizuspto-grants-2012_07