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HRID 1817383作成日:2026年10月26日

2-Nitrophenol → Quinazoline

https://huagongshe.com/reaction/1817383

反応式

関与物質

役割名称HCID仕込み量
反応物2-NitrophenolHCID 6947—
反応物QuinazolineHCID 9210—
反応物4-ChloroquinolineHCID 69140—
反応物4-(Nitrophenoxy)quinolineHCID 21890535—
触媒HCID 178418390HCID 178418390—
触媒HCID 178502593HCID 178502593—
溶媒DimethylformamideHCID 6228—
生成物QuinazolineHCID 9210—
生成物4-(Aminophenoxy)quinolineHCID 21890324—

反応手順

Next, a 4-(aminophenoxy)quinoline derivative or a corresponding quinazoline derivative is produced by reacting nitrophenol with the 4-chloroquinoline derivative or corresponding quinazoline derivative in the presence or absence of a suitable solvent to synthesize a 4-(nitrophenoxy)quinoline derivative or a corresponding quinazoline derivative, then conducting stirring in a suitable solvent, for example, N,N-dimethyl formamide, in the presence of a catalyst, for example, palladium hydroxide-carbon or palladium-carbon, under a hydrogen atmosphere. Alternatively, the 4-(aminophenoxy)quinoline derivative or a corresponding quinazoline derivative may also be produced by reacting amino phenol with a 4-chloroquinoline derivative or a corresponding quinazoline derivative in the presence of a base, for example, sodium hydride.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07598258B2
出典データセットuspto-grants-2009_10
ORD IDord-84c2fb696c4a42c8b8fd59fb00e33e09
出典メモuspto-grants-2009_10