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HRID 853215作成日:2026年10月25日

Ethanol → 4-(4-Aminophenoxy)-6-cyano-7-(2-methoxyethoxy)quinoline

https://huagongshe.com/reaction/853215

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Ammonium ChlorideHCID 25517—
反応物6-Cyano-7-(2-methoxyethoxy)-4-(4-nitrophenoxy)quinolineHCID 22936341—
触媒IronHCID 23925—
溶媒WaterHCID 962—
生成物4-(4-Aminophenoxy)-6-cyano-7-(2-methoxyethoxy)quinolineHCID 2293650672.6%

反応条件

温度80 °C

反応手順

6-Cyano-7-(2-methoxyethoxy)-4-(4-nitrophenoxy)quinoline (1.8 g), iron (1.8 g) and ammonium chloride (3.6 g) were suspended in an ethanol (30 ml)—water (7 ml) mixed solvent and the suspension was heated and stirred at 80° C. for 2 hours. After completion of the reaction, the reaction mixture was filtered with celite and washed in ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate and concentrated. The obtained solid was washed with ether and dried to obtain 1.2 g of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07253286B2
出典データセットuspto-grants-2007_08
ORD IDord-42597713a7be48559677fa5733ec24dd
出典メモuspto-grants-2007_08