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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1817383생성일: 2026년 10월 26일

2-Nitrophenol → Quinazoline

https://huagongshe.com/reaction/1817383

반응식

참여 물질

역할이름HCID투입량
반응물2-NitrophenolHCID 6947—
반응물QuinazolineHCID 9210—
반응물4-ChloroquinolineHCID 69140—
반응물4-(Nitrophenoxy)quinolineHCID 21890535—
촉매HCID 178418390HCID 178418390—
촉매HCID 178502593HCID 178502593—
용매DimethylformamideHCID 6228—
생성물QuinazolineHCID 9210—
생성물4-(Aminophenoxy)quinolineHCID 21890324—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07598258B2
출처 데이터셋uspto-grants-2009_10
ORD IDord-84c2fb696c4a42c8b8fd59fb00e33e09
출처 메모uspto-grants-2009_10