Hydrogen Bromide → 2-(3-piperidinopropyl)-4-phenyl-1(2H)-isoquinolone hydrobromide
반응식
[N:1]1([CH2:7][CH2:8][CH2:9][N:10]2[CH:19]=[C:18]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11]2=[O:26])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[BrH:27]>CC(C)=O>[BrH:27].[N:1]1([CH2:7][CH2:8][CH2:9][N:10]2[CH:19]=[C:18]([C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=3)[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11]2=[O:26])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1참가 물질
4
실험 절차
10.4 g of 2-(3-piperidinopropyl)-4-phenyl-1(2H)-isoquinolone was dissolved in 50 ml of acetone and 10 ml of a 47% aqueous solution of hydrobromic acid was added thereto and the mixture was warmed. After cooling, the precipitated crystals were filtered and recrystallized from a mixture of methanol and petroleum ether to obtain 11.6 g of 2-(3-piperidinopropyl)-4-phenyl-1(2H)-isoquinolone hydrobromide having a melting point of 300° C. as colorless needles.
후처리
- temperaturethe mixture was warmed
- temperatureAfter cooling
- filtrationthe precipitated crystals were filtered
- customrecrystallized from a mixture of methanol and petroleum ether
출처 및 근거
- ORD 기록
- ord-223778dc61644cefab979ce2233bba35
- 출처 데이터셋
- uspto-grants-1983_07
- 특허 번호
- US04393210
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