戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 31149作成日:2026年10月24日

2-Aminophenol → 4-(Aminophenoxy)quinazoline

https://huagongshe.com/ja/reaction/31149

反応式

関与物質

役割名称HCID仕込み量
反応物2-AminophenolHCID 5801—
反応物QuinazolineHCID 9210—
反応物Sodium hydrideHCID 24758—
反応物4-ChloroquinolineHCID 69140—
溶媒Dimethyl SulfoxideHCID 679—
生成物4-(Aminophenoxy)quinazolineHCID 22637147—

反応手順

Alternatively, the 4-(aminophenoxy)quinoline derivative or corresponding quinazoline derivative may be produced by reacting an aminophenol derivative with the 4-chloroquinoline derivative or corresponding quinazoline derivative in a suitable solvent, for example, dimethyl sulfoxide, in the presence of a base, for example, sodium hydride. Alternatively, the 4-(aminophenoxy)quinazoline derivative may also be produced by dissolving an aminophenol derivative in an aqueous sodium hydroxide solution and subjecting the solution to a two-phase reaction with a solution of the 4-chloroquinazoline derivative in a suitable organic solvent, for example, ethyl methyl ketone, in the presence of a phase transfer catalyst, for example, tetra-n-butylammonium chloride, or in the absence of the catalyst.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425564B2
出典データセットuspto-grants-2008_09
ORD IDord-29ee2f96bcba4431ad89bde7ba652589
出典メモuspto-grants-2008_09