Acetic Acid → HCID 22346771, 화합물
반응식
Cl[C:2]1[N:7]=[CH:6][CH:5]=[CH:4][N:3]=1.C(O)(=O)C.[Br:12][C:13]1[CH:19]=[CH:18][C:16]([NH2:17])=[CH:15][CH:14]=1.C(=O)([O-])O.[Na+]>O1CCOCC1>[Br:12][C:13]1[CH:19]=[CH:18][C:16]([NH:17][C:2]2[N:7]=[CH:6][CH:5]=[CH:4][N:3]=2)=[CH:15][CH:14]=1참가 물질
실험 절차
Under an argon atmosphere, 2-chloropyrimidine (2.68 g) and acetic acid (1.97 ml) were added to a solution of 4-bromoaniline (4.03 g) in dioxane (200 ml), and the resulting mixture was stirred for 3 hours while heating the mixture to reflux. Saturated aqueous sodium hydrogen carbonate solution was added in small portions to the reaction solution to neutralize it, and the resulting mixture was concentrated. Ethyl acetate (500 ml) was added to the residue and the resulting mixture was stirred at room temperature for 10 minutes, followed by removing insoluble matter by filtration. The filtrate was washed with saturated aqueous sodium hydrogen carbonate solution and with saturated brine, and dried over anhydrous sodium sulfate. After removing anhydrous sodium sulfate by filtration, the filtrate was concentrated. The residue was recrystallized from ethyl acetate to obtain N-(4-bromophenyl)pyrimidin-2-amine (3.02 g).
후처리
- temperaturewhile heating the mixture
- temperatureto reflux
- concentrationthe resulting mixture was concentrated
- additionEthyl acetate (500 ml) was added to the residue
- stirringthe resulting mixture was stirred at room temperature for 10 minutes
- customby removing insoluble matter
- filtrationby filtration
- washThe filtrate was washed with saturated aqueous sodium hydrogen carbonate solution and with saturated brine
- dry with materialdried over anhydrous sodium sulfate
- customAfter removing anhydrous sodium sulfate
- filtrationby filtration
- concentrationthe filtrate was concentrated
- customThe residue was recrystallized from ethyl acetate
출처 및 근거
- ORD 기록
- ord-2c67bda640fa482a9657144649b3a8b7
- 출처 데이터셋
- uspto-grants-2011_02
- 특허 번호
- US07879837B2
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