Morpholine → 9-morpholino-8-chloro-5-methyl-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid

HRID 1583623Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1583623
F[C:2]1[CH:14]=[C:12]2[C:13]3[N:8]([CH:9]=[C:10]([C:16]([OH:18])=[O:17])[C:11]2=[O:15])[CH:7]([CH3:19])[CH2:6][CH2:5][C:4]=3[C:3]=1[Cl:20].[NH:21]1[CH2:26][CH2:25][O:24][CH2:23][CH2:22]1>CN(C)P(=O)(N(C)C)N(C)C>[O:24]1[CH2:25][CH2:26][N:21]([C:2]2[CH:14]=[C:12]3[C:13]4[N:8]([CH:9]=[C:10]([C:16]([OH:18])=[O:17])[C:11]3=[O:15])[CH:7]([CH3:19])[CH2:6][CH2:5][C:4]=4[C:3]=2[Cl:20])[CH2:22][CH2:23]1

Komponenten

4

Versuchsvorschrift

An autoclave containing a mixture of 3 g of 9-fluoro-8-chloro-5-methyl-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid, 8 g of morpholine and 30 ml of hexamethylphosphoric triamide was immersed in an oil bath at 190° C. and reaction was continued for 5 hours. After completion of reaction, the reaction mixture was cooled to precipitate crystals which then were collected by filtration. The crystals thus obtained were recrystallized from dimethylformamide to give 0.77 g of 9-morpholino-8-chloro-5-methyl-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid. m.p. 271° to 274° C., white rhombic crystals.

Aufarbeitung

  1. additionAn autoclave containing
  2. customwas immersed in an oil bath at 190° C.
  3. customreaction
  4. customAfter completion of reaction
  5. temperaturethe reaction mixture was cooled
  6. customto precipitate crystals which
  7. filtrationthen were collected by filtration
  8. customThe crystals thus obtained
  9. customwere recrystallized from dimethylformamide

Quellen und Nachweise

ORD-Eintrag
ord-67aa6c012d6540fa82cea576215366c9
Quelldatensatz
uspto-grants-1985_11
Patentnummer
US04552879

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