4-Aminoacetanilide → 7-[3(4-Acetamidophenyl)thioureido]-3,4-dihydro-2(1H)quinolone
Reaktionsgleichung
[N:1]([C:4]1[CH:13]=[C:12]2[C:7]([CH2:8][CH2:9][C:10](=[O:14])[NH:11]2)=[CH:6][CH:5]=1)=[C:2]=[S:3].[C:15]([NH:18][C:19]1[CH:25]=[CH:24][C:22]([NH2:23])=[CH:21][CH:20]=1)(=[O:17])[CH3:16]>C1COCC1>[C:15]([NH:18][C:19]1[CH:25]=[CH:24][C:22]([NH:23][C:2](=[S:3])[NH:1][C:4]2[CH:13]=[C:12]3[C:7]([CH2:8][CH2:9][C:10](=[O:14])[NH:11]3)=[CH:6][CH:5]=2)=[CH:21][CH:20]=1)(=[O:17])[CH3:16]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution containing 0.8 g of 7-isothiocyanato-3,4-dihydro-2(1H)quinolone and 0.59 g of 4-acetamidoaniline in 10 ml of THF was stirred for 5 h at room temperature. The product was filtered, dried and used as such to the next step. Yield 0.45 g (32%).