반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([CH2:11][C:12]#[N:13])(=[O:10])=[O:9])=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].[C:20]([C:22]1[CH:23]=[C:24]([N:28]=[C:29]=[S:30])[CH:25]=[CH:26][CH:27]=1)#[N:21].[CH3:31]I>CC(C)=O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([S:8]([C:11](=[C:29]([NH:28][C:24]2[CH:25]=[CH:26][CH:27]=[C:22]([C:20]#[N:21])[CH:23]=2)[S:30][CH3:31])[C:12]#[N:13])(=[O:9])=[O:10])=[CH:6][CH:7]=1참가 물질
실험 절차
A solution of 4-chlorophenylsulfonylacetonitrile (1.0 g, 4.64 mmol) in dry acetone (10 ml) was stirred while dry potassium carbonate (1.28 g, 9.28 mmol) and 3-cyanophenyl isothiocyanate (0.78 g, 4.87 mmol) were added. The resulting mixture was stirred at room temperature under nitrogen for 20 h. Excess of potassium carbonate was filtered off, methyl iodide (0.859 ml, 13.9 mmol) was added to the filtrate, and stirring was continued for 3 h. The mixture was evaporated and the residue was dissolved in dichloromethane and extracted with water and brine. The organic phase was dried over magnesium sulphate, filtered and evaporated to afford 1.74 g (96%) of the title compound as golden brown crystals. Mp 168-170° C. 1H NMR (200 MHz, CDCl3): δ=2.22 (s, 3H), 7.50-7.68 (m, 6H), 7.84-7.93(m, 2H), 9.89 (br s, 1H).
후처리
- additionwere added
- filtrationExcess of potassium carbonate was filtered off
- stirringstirring
- waitwas continued for 3 h
- customThe mixture was evaporated
- dissolutionthe residue was dissolved in dichloromethane
- extractionextracted with water and brine
- dry with materialThe organic phase was dried over magnesium sulphate
- filtrationfiltered
- customevaporated
출처 및 근거
- ORD 기록
- ord-402b08af9dbc43d7a51f29e05e70d838
- 출처 데이터셋
- uspto-grants-2002_03
- 특허 번호
- US06362205B1
연결된 노트
불러오는 중…