Tert-Butylamine → HCID 178449125, 화합물
반응식
[O:1]1[CH2:20][CH:2]1[CH2:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[NH:12][CH:13]=[C:14]([C:16]([F:19])([F:18])[F:17])[N:15]=2)=[CH:7][CH:6]=1.[C:21]([NH2:25])([CH3:24])([CH3:23])[CH3:22]>>[C:21]([NH:25][CH2:20][CH:2]([OH:1])[CH2:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[NH:12][CH:13]=[C:14]([C:16]([F:19])([F:18])[F:17])[N:15]=2)=[CH:7][CH:6]=1)([CH3:24])([CH3:23])[CH3:22]참가 물질
3
실험 절차
A solution of 2-[4-(2,3-epoxypropoxy)phenyl] trifluoromethylimidazole (2.5 g.) in tert. butylamine (20 ml.) is heated 6 hours at reflux. The excess tert.butylamine is removed by distillation at atmospheric pressure over steam. The residue is triturated with nitromethane (5 ml.) and the resulting solid removed by filtration. After recrystallization from acetonitrile, (1.2 g.) of 2-[4-(3-tert. butylamino-2-hydroxypropoxy)-phenyl]-4-trifluoromethylimidazole is obtained, m.p. 185.5°-186.5° C.
후처리
- temperatureat reflux
- customThe excess tert.butylamine is removed by distillation at atmospheric pressure over steam
- customThe residue is triturated with nitromethane (5 ml.)
- customthe resulting solid removed by filtration
- custom