반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([N:10]2[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]2)=[CH:6][CH:5]=1)([O-:3])=[O:2].C(=O)([O-])[O-].[K+].[K+].I[CH:23]1[CH2:27][CH2:26][CH2:25][CH2:24]1.C1OCCOCCOCCOCCOCCOC1>C(#N)C>[CH:23]1([N:13]2[CH2:14][CH2:15][N:10]([C:7]3[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:9][CH:8]=3)[CH2:11][CH2:12]2)[CH2:27][CH2:26][CH2:25][CH2:24]1참가 물질
6
실험 절차
A mixture of 1-(4-nitrophenyl)piperazine (12 g, 57.9 mmol) (Acros Organics), powdered potassium carbonate (5.4 g, 39 mmol), iodocyclopentane (7 mL, 60.8 mmol) (Aldrich) and a catalytic amount of 18-crown-6 in acetonitrile (90 mL) was heated at reflux overnight. The mixture was filtered, and the filter cake was washed with acetonitrile. The solvent was evaporated from the combined filtrates and the residue was partitioned between water and ethyl acetate. The layers were separated and the aqueous layer was extracted twice with ethyl acetate. The combined organic layers were dried (Na2SO4), filtered, evaporated to a yellow solid and dried under vacuum to give 1-cyclopentyl-4-(4-nitrophenyl)piperazine) (6.6 g, 41%.)
후처리
- temperatureat reflux overnight
- filtrationThe mixture was filtered
- washthe filter cake was washed with acetonitrile
- customThe solvent was evaporated from the combined filtrates
- customthe residue was partitioned between water and ethyl acetate
- customThe layers were separated
- extractionthe aqueous layer was extracted twice with ethyl acetate
- dry with materialThe combined organic layers were dried (Na2SO4)
- filtrationfiltered
- customevaporated to a yellow solid
- customdried under vacuum
출처 및 근거
- ORD 기록
- ord-e01217a216ad48d18573a7662bc91efb
- 출처 데이터셋
- uspto-grants-2006_08
- 특허 번호
- US07094896B2
연결된 노트
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