Diethyl Ether → 6-Bromo-N-[(4-chlorophenyl)methyl]-8-fluoro-3-quinolinecarboxamide

反応式

[Br:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[C:4]([F:9])[CH:3]=1.C1(=O)OC(O[C:17]([CH2:21]C)([CH2:19]C)[CH3:18])OC(=O)C1.[Cl:25][C:26]1[CH:33]=[CH:32][C:29]([CH2:30][NH2:31])=[CH:28][CH:27]=1.C([O:36]CC)C>>[Br:1][C:2]1[CH:8]=[C:7]2[C:5](=[C:4]([F:9])[CH:3]=1)[N:6]=[CH:18][C:17]([C:21]([NH:31][CH2:30][C:29]1[CH:32]=[CH:33][C:26]([Cl:25])=[CH:27][CH:28]=1)=[O:36])=[CH:19]2

参加物

反応物 4

HCID 3283Diethyl Ether

HCID 660364-Chlorobenzylamine

HCID 1230504-Bromo-2-fluoroaniline

HCID 131717023Diethylethoxymethylene malonate

生成物 1

HCID 104306946-Bromo-N-[(4-chlorophenyl)methyl]-8-fluoro-3-quinolinecarboxamide

反応条件

温度: 130 °C

実験手順

A mixture of 9.50 g of 4-bromo-2-fluoroaniline and 10.81 g diethylethoxymethylene malonate is heated to 130° C. in a flask equipped with a Dean-Stark trap to collect formed ethanol. The mixture is then cooled to 75° C. and diluted with hexanes. The resulting solid is collected and dried. The solid is then dissolved in 60 mL diphenyl ether and heated to 250° C. for 2 h in a flask equipped with a Dean-Stark trap to collect the ethanol. The solution is allowed to cool to room temperature and the resulting solid is collected, washed with hexanes and dried to yield 8.69 g. This material (0.49 g) and 5 mL of 4-chlorobenzylamine are heated at 180° C. for 1 h. The reaction is cooled and poured into 80 mL diethyl ether. The resulting solid is filtered and recrystallized from ethyl acetate/hexanes to give the title compound as an off-white solid (0.35 g).