반응식
[Cl:1][C:2]1[C:7]([CH2:8]Cl)=[CH:6][C:5]([CH3:10])=[CH:4][N:3]=1.[N+:11]([N:14]=[C:15]1[NH:19][CH2:18][CH2:17][NH:16]1)([O-:13])=[O:12].C(=O)([O-])[O-].[K+].[K+].[Cl-].[Cs+]>C(#N)C>[Cl:1][C:2]1[C:7]([CH2:8][N:16]2[CH2:17][CH2:18][NH:19][C:15]2=[N:14][N+:11]([O-:13])=[O:12])=[CH:6][C:5]([CH3:10])=[CH:4][N:3]=1참가 물질
실험 절차
2-chloro-3-chloromethyl-5-methylpyridine (1.3 g, 0.0076 moles) was added to a well-stirred material comprising 2-nitroimino-1, 3-diazacyclopentane (1.18 g, 0.00912 moles), potassium carbonate (1.16 g, 0.0083 moles), cesium chloride (0.04 g, 0.00024 moles) in acetonitrile (20 ml) solvent at room temperature. The reaction mixture was refluxed for 8 hours. The solvent was removed under reduced pressure and the mass diluted with water (25 ml). The mass was then extracted with methylene chloride (2×50 ml) and the layers were separated. Organic layer was dried over sodium sulphate and solvent removed under reduced pressure. The residue thus obtained was subjected to chromatographic purification on silica gel to give 1-(2-chloro-5-methyl-3-pyridylmethyl)2-nitroiminoimidazolidine in 90% yield.
후처리
- customat room temperature
- temperatureThe reaction mixture was refluxed for 8 hours
- customThe solvent was removed under reduced pressure
- additionthe mass diluted with water (25 ml)
- extractionThe mass was then extracted with methylene chloride (2×50 ml)
- customthe layers were separated
- dry with materialOrganic layer was dried over sodium sulphate and solvent
- customremoved under reduced pressure
- customThe residue thus obtained
- customwas subjected to chromatographic purification on silica gel
출처 및 근거
- ORD 기록
- ord-9e0e5b816c2f4bac938a2cceb69764b1
- 출처 데이터셋
- uspto-grants-2003_05
- 특허 번호
- US06566528B1
연결된 노트
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