반응식
S(=O)(=O)(O)O.[O-]S(OOS([O-])(=O)=O)(=O)=O.[K+].[K+].[Br:18][C:19]1[CH2:23][CH:22]([C:24]([O:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])=[O:25])[N:21]([C:32]2[C:37]([Cl:38])=[CH:36][CH:35]=[CH:34][N:33]=2)[N:20]=1.C(#N)C>O>[Br:18][C:19]1[CH:23]=[C:22]([C:24]([O:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])=[O:25])[N:21]([C:32]2[C:37]([Cl:38])=[CH:36][CH:35]=[CH:34][N:33]=2)[N:20]=1참가 물질
실험 절차
0.5 ml of concentrated sulfuric acid and 1.4 g of potassium peroxodisulfate were added to a mixed solution comprising 1.0 g of pentyl 3-bromo-1-(3-chloropyridin-2-yl)-4,5-dihydro-1H-pyrazole-5-carboxylate and 20 ml of acetonitrile, followed by reflux with heating for 3 hours and 20 minutes. After the reaction liquid was stood to cool, the reaction liquid was slowly added to water, followed by stirring for 15 minutes. The mixed liquid was subjected to extraction with ethyl acetate, and the organic layer was washed with a saturated sodium hydrogen carbonate aqueous solution and a sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=8.5/1.5 to 8/2) to obtain 0.47 g of the oily desired product.
후처리
- temperatureby reflux
- temperaturewith heating for 3 hours and 20 minutes
- customAfter the reaction liquid
- temperatureto cool
- customthe reaction liquid
- extractionThe mixed liquid was subjected to extraction with ethyl acetate
- washthe organic layer was washed with a saturated sodium hydrogen carbonate aqueous solution
- dry with materiala sodium chloride aqueous solution and dried over anhydrous sodium sulfate
- distillationThe solvent was distilled off under reduced pressure
- customthe residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=8.5/1.5 to 8/2)
출처 및 근거
- ORD 기록
- ord-032ebdf5381f4ae0978ae90bac72ddb4
- 출처 데이터셋
- uspto-grants-2012_02
- 특허 번호
- US08115006B2
연결된 노트
불러오는 중…