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HRID 1107886作成日:2026年10月27日

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

https://huagongshe.com/reaction/1107886

反応式

関与物質

役割名称HCID仕込み量
反応物Cyanogen BromideHCID 10476—
反応物2-NaphthohydrazideHCID 123485—
反応物Sodium BicarbonateHCID 516892—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物5-(Naphthalen-2-yl)-1,3,4-oxadiazol-2-amineHCID 1870747620%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06063800
出典データセットuspto-grants-2000_05
ORD IDord-0c05ee54ecef44baa159e5456f9e3a1c
出典メモuspto-grants-2000_05