참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonia | HCID 222 | — |
| 반응물 | 4-Chloro-3-nitroquinoline | HCID 11275808 | — |
| 용매 | 1-Propanol | HCID 1031 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 3-Nitroquinolin-4-amine | HCID 280005 | — |
반응 단계
Compound 7 was prepared as described elsewhere [Van Galen, P. J. M. et. al. (1991) ibid.]. In brief, ammonia gas was passed, while stirring, through a solution of 3-nitro-4-chloroquinoline 6 (7.0 g, 30 mmol) in toluene (95 ml) and propanol (15 ml) till the product was formed. During the course of the reaction, the temperature was gradually raised till 70° C. After cooling, the solid was separated by filtration and washed successfully with toluene/2-propanol (70:30), ether and cold water until Cl− could no longer be detected. The solid was filtered off and dried at 80° C. Yield: 6.1 g (95%). Mp.: 255-257° C. 1H NMR (DMSO-d6): δ 7.50-7.66 (m, 1H, Ar); 7.81-7.92 (m, 2H, Ar); 8.59 (d, 1H, J=8.0 Hz, Ar); 9.03 (broad s, 2H, NH2); 9.18 (s, 1H, Ar)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09326978B2 |
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| 출처 데이터셋 | uspto-grants-2016_05 |
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| ORD ID | ord-9ff76148eb4d465181f0b2dfcfe1c3fb |
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| 출처 메모 | uspto-grants-2016_05 |
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