Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2178582생성일: 2026년 10월 24일
Methoxyisopropylamine → 7-(3,5-Dimethylisoxazol-4-yl)-6-methoxy-N-(1-methoxypropan-2-yl)-3-nitroquinolin-4-amine
https://huagongshe.com/ko/reaction/2178582
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Methoxyisopropylamine | HCID 123458 | — |
| 반응물 | 4-(4-Chloro-6-methoxy-3-nitroquinolin-7-yl)-3,5-dimethylisoxazole | HCID 57465580 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 7-(3,5-Dimethylisoxazol-4-yl)-6-methoxy-N-(1-methoxypropan-2-yl)-3-nitroquinolin-4-amine | HCID 70980504 | 111.5% |
반응 단계
To a solution of 4-(4-chloro-6-methoxy-3-nitroquinolin-7-yl)-3,5-dimethylisoxazole (Manchester Organics) (20 g, 59.9 mmol) in 1,4-dioxane (200 ml) was added 1-methoxypropan-2-amine (31.6 ml, 300 mmol) and the reaction mixture heated at 70° C. for 1.5 h. The solvent was removed under reduced pressure and the resulting solid partitioned between ethyl acetate (3×750 ml) and water (750 ml). The organic layers were combined, dried (hydrophobic frit) and evaporated under reduced pressure to give 7-(3,5-dimethylisoxazol-4-yl)-6-methoxy-N-(1-methoxypropan-2-yl)-3-nitroq uinolin-4-amine (25.8 g), which was used without further purification in the subsequent step.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09067936B2 |
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| 출처 데이터셋 | uspto-grants-2015_06 |
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| ORD ID | ord-aecf6af5387a40b59c6c8c01234ba708 |
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| 출처 메모 | uspto-grants-2015_06 |
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