반응식
[Cl:1][C:2]1[CH:3]=[C:4]([N:9]2[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]2)[CH:5]=[CH:6][C:7]=1[Cl:8].Cl[CH2:16][CH2:17][CH2:18][CH2:19][C:20]#[N:21].C(=O)([O-])[O-].[Na+].[Na+]>CC(C)CC(=O)C.[I-].[K+]>[Cl:1][C:2]1[CH:3]=[C:4]([N:9]2[CH2:14][CH2:13][N:12]([CH2:16][CH2:17][CH2:18][CH2:19][C:20]#[N:21])[CH2:11][CH2:10]2)[CH:5]=[CH:6][C:7]=1[Cl:8]참가 물질
6
실험 절차
A mixture of 1-(3,4-dichlorophenyl)piperazine (0.1 mol), 5-chloropentanenitrile (0.13 mol), sodium carbonate (10 g) and potassium iodide (0.1 g) in 4-methyl-2-pentanone (280 ml) was stirred and refluxed for 10 hours. The reaction mixture was cooled, filtered and the filtrate was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH 95/5). The pure fractions were collected and the solvent was evaporated, yielding 22.5 g (72%) of 4-(3,4-dichlorophenyl)-1-piperazinepentanenitrile (interm. 2).
후처리
- temperaturerefluxed for 10 hours
- temperatureThe reaction mixture was cooled
- filtrationfiltered
- customthe filtrate was evaporated
- customThe residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH 95/5)
- customThe pure fractions were collected
- customthe solvent was evaporated
출처 및 근거
- ORD 기록
- ord-4a5bdc30be874aee83bdc8629aaa3da8
- 출처 데이터셋
- uspto-grants-2001_05
- 특허 번호
- US06224849B1
연결된 노트
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