반응식
[Br:1][C:2]1[CH:6]=[C:5]([C:7](=[O:11])SCC)[N:4]([C:12]2[C:17]([Cl:18])=[CH:16][CH:15]=[CH:14][N:13]=2)[N:3]=1.[NH2:19][C:20]1[CH:33]=[CH:32][C:31]([Cl:34])=[CH:30][C:21]=1[C:22]([NH:24][CH:25]([CH:27]1[CH2:29][CH2:28]1)[CH3:26])=[O:23].S([O-])([O-])(=O)=O.[Na+].[Na+].CC(C)([O-])C.[K+]>CS(C)=O.O>[Br:1][C:2]1[CH:6]=[C:5]([C:7]([NH:19][C:20]2[CH:33]=[CH:32][C:31]([Cl:34])=[CH:30][C:21]=2[C:22](=[O:23])[NH:24][CH:25]([CH:27]2[CH2:29][CH2:28]2)[CH3:26])=[O:11])[N:4]([C:12]2[C:17]([Cl:18])=[CH:16][CH:15]=[CH:14][N:13]=2)[N:3]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
0.35 g of S-ethyl 3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carbothioate and 0.24 g of 2-amino-5-chloro-N-(1-cyclopropylethyl)benzamide were dissolved in 5 ml of dimethyl sulfoxide, and 0.85 g of anhydrous sodium sulfate was added, followed by stirring for 5 minutes. 0.14 g of potassium tert-butoxide was added at room temperature, followed by stirring for 1.5 hours. The reaction liquid was added to water, followed by extraction with ethyl acetate. The organic layer was washed with a saturated 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=1/0 to 1/1) to obtain 0.24 g of the desired product.
후처리
- stirringby stirring for 1.5 hours
- customThe reaction liquid
- extractionfollowed by extraction with ethyl acetate
- washThe organic layer was washed with a saturated sodium chloride aqueous solution
- dry with materialdried 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=1/0 to 1/1)
출처 및 근거
- ORD 기록
- ord-03f86ded675b4afea7a5b6b732205db2
- 출처 데이터셋
- uspto-grants-2012_02
- 특허 번호
- US08115006B2
연결된 노트
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