Potassium Carbonate → Ethyl 7-(4-acetonyl-1-piperazinyl)-6-fluoro-1-methyl-4-oxo-4H-(1,3)thiazeto(3,2-a)quinoline-3-carboxylate
Reaktionsgleichung
[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[N:12]1[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]1)[N:8]1[CH:18]([CH3:20])[S:19][C:7]1=[C:6]([C:21]([O:23][CH2:24][CH3:25])=[O:22])[C:5]2=[O:26].C(=O)([O-])[O-].[K+].[K+].Br[CH2:34][C:35](=[O:37])[CH3:36]>CN(C)C=O>[CH2:34]([N:15]1[CH2:16][CH2:17][N:12]([C:11]2[CH:10]=[C:9]3[C:4]([C:5](=[O:26])[C:6]([C:21]([O:23][CH2:24][CH3:25])=[O:22])=[C:7]4[S:19][CH:18]([CH3:20])[N:8]43)=[CH:3][C:2]=2[F:1])[CH2:13][CH2:14]1)[C:35]([CH3:36])=[O:37]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Ethyl 6-fluoro-1-methyl-7-(1-piperazinyl)-4-oxo-4H-(1,3)thiazeto(3,2-a)quinoline-3-carboxylate (3.8 g) was suspended in 50 ml of N,N-dimethylformamide, 1.66 g of potassium carbonate was added thereto, 1.65 g of bromoacetone was dropped in with ice cooling and stirring, and the mixture was stirred at room temperature for 20 hours. The reaction solution was poured over into ice water and the crystals separated out were collected by filtration, washed with water, dried and recrystallized from ethanol to give 3.7 g of desired compound in colorless powdery crystals, m.p. 196°-200° C. (decompn.).
Aufarbeitung
- stirringthe mixture was stirred at room temperature for 20 hours
- customthe crystals separated out
- filtrationwere collected by filtration
- washwashed with water
- customdried
- customrecrystallized from ethanol
Quellen und Nachweise
- ORD-Eintrag
- ord-462c230f94fd418fb8cc10a9dffeec41
- Quelldatensatz
- uspto-grants-1989_06
- Patentnummer
- US04843070
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