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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 619333Erstellt: 26. Oktober 2026

Cyanogen Bromide → 5-(Naphthalen-2-yl)-1,3,4-oxadiazol-2-amine

https://huagongshe.com/reaction/619333

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyanogen BromideHCID 10476—
Edukt2-NaphthohydrazideHCID 123485—
EduktSodium BicarbonateHCID 516892—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt5-(Naphthalen-2-yl)-1,3,4-oxadiazol-2-amineHCID 1870747620%

Reaktionsschritte

To a stirred solution of naphthalene-2-carboxylic acid hydrazide (0.6 g, 3.22 mmol, prepared as described in example 1) in dioxane (20 ml) was added a solution of sodium hydrogen carbonate (0.27 g, 3.22 mmol) in water (15 ml) and the resulting mixture was stirred for 5 min. To the reaction mixture was added cyanogen bromide (0.35 g, 3.3 mmol) and the mixture was stirred for 3 h at room temperature. The precipitate was filtered off and washed with diethyl ether (2×15 ml) and dried in vacuo at 50° C. affording 0.4 g of crude product which was suspended in absolute ethanol (15 ml) and stirred at reflux temperature for 0.5 h. The cooled suspension was filtered and the filter cake was dried in vacuo at 50° C. affording 130 mg (20%) of the title compound as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05958957
Quelldatensatzuspto-grants-1999_09
ORD IDord-74ce89f4603944c88def162dc4d10b8f
Quellennotizuspto-grants-1999_09