Ethyl Acetate → 3-Benzoyl-4-(2-methoxyphenylamino)-8-methoxyquinoline

HRID 1382325Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1382325
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]=1

Komponenten

5

Versuchsvorschrift

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°.

Aufarbeitung

  1. temperaturewas heated
  2. customThe solvent was evaporated
  3. dissolutionthe residue was dissolved in dichloromethane
  4. washwashed with dilute hydrochloric acid, sodium hydrogen carbonate solution, water and brine
  5. customThe organic solution was dried
  6. customevaporated to an oil which
  7. customwas chromatographed (silica gel, 1% methanol in dichloromethane)
  8. customto give an oil which

Quellen und Nachweise

ORD-Eintrag
ord-5f51b2bab7174239a6d55b6bda0fd751
Quelldatensatz
uspto-grants-1989_02
Patentnummer
US04806550

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