Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Chloro-6-nitroquinoline-3-carbonitrile → 4-[3-Chloro-4-(1-methyl-1H-imidazol-2-ylsulfanyl)-phenylamino]-6-nitro-quinoline-3-carbonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Chloro-6-nitroquinoline-3-carbonitrile | HCID 11085690 | — |
| 반응물 | 3-chloro-4-(1-methyl-1H-imidazol-2-ylsulfanyl)phenylamine | HCID 11459088 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 4-[3-Chloro-4-(1-methyl-1H-imidazol-2-ylsulfanyl)-phenylamino]-6-nitro-quinoline-3-carbonitrile | HCID 69957299 | 62.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06288082B1 |
| 출처 데이터셋 | uspto-grants-2001_09 |
| ORD ID | ord-85bd16a92baa41db879e55fb4b05271d |
| 출처 메모 | uspto-grants-2001_09 |