Dimethylamine → HCID 20379981, 화합물
반응식
F[C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:32])[CH2:9][CH2:10][CH2:11][N:12]2[CH2:17][CH2:16][CH:15]([C:18]([OH:31])([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)[C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH2:14][CH2:13]2)=[CH:4][CH:3]=1.[CH3:33][NH:34][CH3:35]>CS(C)=O>[CH3:33][N:34]([CH3:35])[C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:32])[CH2:9][CH2:10][CH2:11][N:12]2[CH2:17][CH2:16][CH:15]([C:18]([OH:31])([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)[C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH2:14][CH2:13]2)=[CH:4][CH:3]=1참가 물질
4
실험 절차
Through a solution of 18 g (0.041 mole) of 4'-fluoro-4-[4-(α-hydroxy-α-phenylbenzyl)piperidino]butyrophenone in 150 ml of dimethylsulfoxide (DMSO) was vigorously bubbled dimethylamine for 6 hours at 100°C. Most of the DMSO was removed at reduced pressure and a temperature of 120°C. The remaining mixture was poured into water and sodium carbonate to which was added a small amount of methanol. The resulting solid was filtered and dissolved in warm methanol and isopropyl alcohol, treated with charcoal filtered, and cooled. The solid which formed upon cooling was filtered off and recrystallized from acetone-heptane to give the desired product, M.P. 148°-150°C.
후처리
- customfor 6 hours
- customat 100°C
- customMost of the DMSO was removed at reduced pressure
- customa temperature of 120°C
- additionThe remaining mixture was poured into water and sodium carbonate to which
- additionwas added a small amount of methanol
- filtrationThe resulting solid was filtered
- dissolutiondissolved in warm methanol
- additionisopropyl alcohol, treated with charcoal
- filtrationfiltered
- temperaturecooled
- customThe solid which formed
- temperatureupon cooling
- filtrationwas filtered off
- customrecrystallized from acetone-heptane
출처 및 근거
- ORD 기록
- ord-267a52e876d9415a907a57d373f19522
- 출처 데이터셋
- uspto-grants-1976_06
- 특허 번호
- US03965257
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