Ammonia → 4-Chloro-2,6-diphenyl-2H-pyrazolo[3,4-b]pyridine
反応式
[C:1]1([N:7]2[CH:15]=[C:14]3[C:9]([N:10]=[C:11]([C:17]4[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=4)[CH:12]=[C:13]3O)=[N:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.P(Cl)(Cl)([Cl:25])=O.N>>[Cl:25][C:13]1[C:14]2[C:9](=[N:8][N:7]([C:1]3[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=3)[CH:15]=2)[N:10]=[C:11]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH:12]=1参加物
4
実験手順
5.5 g. of 2,6-diphenyl-2H-pyrazolo[3,4-b]pyridin-4-ol (0.019 mol.) and 27.5 ml. of phosphorus oxychloride are refluxed with stirring for 90 minutes. The cooled mixture is poured onto crushed ice, then made alkaline with concentrated aqueous ammonia while adding ice. The collected 4-chloro-2,6-diphenyl-2H-pyrazolo[3,4-b]pyridine is washed with water and dried at 80°; m.p. 175°-177°. A sample, recrystallized from ethanol, melts at 176°-178°; yield: 5 g. (86%).
後処理
- additionThe cooled mixture is poured