반응식
[Br:1][C:2]1[C:3](Cl)=[N:4][CH:5]=[CH:6][CH:7]=1.[NH:9]1[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]1.Cl.Cl.N1CCNCC1>O>[Br:1][C:2]1[C:3]([N:9]2[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]2)=[N:4][CH:5]=[CH:6][CH:7]=1참가 물질
5
반응 조건
- 온도
- 190 °C
실험 절차
Add 3-bromo-2-chloro-pyridine (10.08 g, 52.4 mmol) to piperazine (45 g) and piperazine dihydrochloride (83.4 g). Heat the mixture to 190° C. with stirring for one hr. Allow the mixture to cool to about 80° C. then pour the material into water and extract 5 times with DCM. Dry the solution (sodium sulfate), filter and concentrate. Purify using silica gel chromatography, eluting with 15:85 methanol (with 2 M ammonia): DCM to give 1-(3-bromo-pyridin-2-yl)-piperazine as a white solid (8.98 g, 71%).
후처리
- temperatureAllow the mixture to cool to about 80° C.
- extractionextract 5 times with DCM
- dry with materialDry the solution (sodium sulfate)
- filtrationfilter
- concentrationconcentrate
- customPurify
- washeluting with 15:85 methanol (with 2 M ammonia)
출처 및 근거
- ORD 기록
- ord-db0422694fed4110a18c86f5a7031188
- 출처 데이터셋
- uspto-grants-2012_06
- 특허 번호
- US08202873B2
연결된 노트
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