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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1595819생성일: 2026년 10월 26일

4-Chloro-6-nitroquinoline-3-carbonitrile → 4-[3-Chloro-4-(1-methyl-1H-imidazol-2-ylsulfanyl)-phenylamino]-6-nitro-quinoline-3-carbonitrile

https://huagongshe.com/reaction/1595819

반응식

참여 물질

역할이름HCID투입량
반응물4-Chloro-6-nitroquinoline-3-carbonitrileHCID 11085690—
반응물3-chloro-4-(1-methyl-1H-imidazol-2-ylsulfanyl)phenylamineHCID 11459088—
용매EthanolHCID 702—
생성물4-[3-Chloro-4-(1-methyl-1H-imidazol-2-ylsulfanyl)-phenylamino]-6-nitro-quinoline-3-carbonitrileHCID 6995729962.8%

반응 단계

A mixture of 5.00 g (21.5 mmol) 4-chloro-6-nitro-3-quinolinecarbonitrile, 250 ml ethanol, and 6.18 g (25.8 mmol) 3-chloro-4-(1-methyl-1H-imidazol-2-ylsulfanyl)-aniline (WO-9615118) was heated to reflux under N2. Removed heat at 3½ hours and made basic with a solution of saturated sodium bicarbonate. Stripped solvents and azeotroped with ethanol. Slurried residue with hexane and collected solids. Washed with water, dried in vacuo. Boiled solids in hexane to remove excess aniline, air dried. Boiled in 2 L ethyl acetate, and because of extreme insolubility, collected solids and dried in vacuo, giving 5.90 g of yellow solid: mass spectrum (electrospray m/e): M+H=437.2, 439.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06288082B1
출처 데이터셋uspto-grants-2001_09
ORD IDord-85bd16a92baa41db879e55fb4b05271d
출처 메모uspto-grants-2001_09