Ethyl Acetate → 3-Benzoyl-4-(2-methoxyphenylamino)-8-methoxyquinoline
반응식
C(C1C=NC2C(C=1Cl)=CC=CC=2OC)(=O)C1C=CC=CC=1.[C:22]([C:30]1[CH:31]=[N:32][C:33]2[C:38]([C:39]=1[NH:40][C:41]1[CH:46]=[CH:45][CH:44]=[CH:43][C:42]=1[O:47][CH3:48])=[CH:37][CH:36]=[CH:35][C:34]=2[O:49][CH3:50])(=[O:29])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1.C(OCC)(=O)C>O1CCOCC1.COC1C(N)=CC=CC=1>[C:22]([C:30]1[CH:31]=[N:32][C:33]2[C:38]([C:39]=1[NH:40][C:41]1[CH:46]=[CH:45][CH:44]=[CH:43][C:42]=1[O:47][CH3:48])=[CH:37][CH:36]=[CH:35][C:34]=2[O:49][CH3:50])(=[O:29])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1참가 물질
5
실험 절차
Preparation of 3-benzoyl-4-(2-methoxyphenylamino)-8-methoxyquinoline 3-Benzoyl-4-chloro-8-methoxyquinoline (2.8 g, 0.0094 mol) was heated under reflux in a mixture of 1,4-dioxan (50 ml) and o-anisidine (7 ml) for 1 hour. The solvent was evaporated and the residue was dissolved in dichloromethane, and washed with dilute hydrochloric acid, sodium hydrogen carbonate solution, water and brine. The organic solution was dried and evaporated to an oil which was chromatographed (silica gel, 1% methanol in dichloromethane) to give an oil which afforded yellow crystals of 3-benzoyl-4-(2-methoxyphenylamino)-8-methoxyquinoline (2.2 g, 61%) from ethyl acetate, m.p. 200°-202°.
후처리
- temperaturewas heated
- customThe solvent was evaporated
- dissolutionthe residue was dissolved in dichloromethane
- washwashed with dilute hydrochloric acid, sodium hydrogen carbonate solution, water and brine
- customThe organic solution was dried
- customevaporated to an oil which
- customwas chromatographed (silica gel, 1% methanol in dichloromethane)
- customto give an oil which
출처 및 근거
- ORD 기록
- ord-5f51b2bab7174239a6d55b6bda0fd751
- 출처 데이터셋
- uspto-grants-1989_02
- 특허 번호
- US04806550
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