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HRID 18185Erstellt: 24. Oktober 2026

Ethanol → 4-(3-Benzyl-2-carbamoyl-5-methyl-benzofuran-7-yl)-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/de/reaction/18185

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktSodium;3-oxidodioxaborirane;tetrahydrateHCID 23693097—
Edukt4-(3-Benzyl-2-cyano-5-methyl-benzofuran-7-yl)-piperazine-1-carboxylic acid tert-butyl esterHCID 59344912—
LösungsmittelWaterHCID 962—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt4-(3-Benzyl-2-carbamoyl-5-methyl-benzofuran-7-yl)-piperazine-1-carboxylic acid tert-butyl esterHCID 5934490480%

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

4-(3-Benzyl-2-cyano-5-methyl-benzofuran-7-yl)-piperazine-1-carboxylic acid tert-butyl ester (0.302 gm, 0.7 mmol), sodium perborate tetrahydrate (0.43 gm, 2.8 mmol), ethanol (8 ml) and water (8 ml) were combined in a vial and heated in a microwave reactor to 130° C. for 10 minutes. The reaction mixture was cooled to room temperature, diluted with brine and water and extracted three times with ethyl acetate. The solution was dried over magnesium sulfate and purified by column chromatography (methanol/dichloromethane gradient) to give 4-(3-benzyl-2-carbamoyl-5-methyl-benzofuran-7-yl)-piperazine-1-carboxylic acid tert-butyl ester (0.25 gm, 80% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741326B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-6e1cd638c39c4f80be55e1ba89a7d870
Quellennotizuspto-grants-2010_06