N-bromobutanimide → 4-Bromo-1-hydroxyisoquinoline
반응식
[Br:1][C:2]1[C:11]2[C:6](=[CH:7][C:8](S(Cl)(=O)=O)=[CH:9][CH:10]=2)[C:5](Cl)=[N:4][CH:3]=1.C1([OH:27])C2C(=CC=CC=2)C=CN=1.BrN1C(=O)CCC1=O>CC#N>[Br:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5](=[O:27])[NH:4][CH:3]=1참가 물질
5
실험 절차
4-Bromo-1-chloro-7-isoquinolinesulphonyl chloride ##STR198## A suspension of isoquinolinol (10 g, 68.9 mmol) in MeCN (250 ml) at 50° C., was treated with N-bromosuccinimide (12.6 g, 70.8 mmol) whereupon almost complete solution occurred before a thick white precipitate was formed. After heating under reflux for 3 h, the reaction mixture was cooled in ice and the solid filtered, washed with MeCN, and dried to afford 4-bromo-1-(2H)-isoquinolone (7.6 g, 34.0 mmol).
후처리
- customwas formed
- temperatureAfter heating
- temperatureunder reflux for 3 h
- temperaturethe reaction mixture was cooled in ice
- filtrationthe solid filtered
- washwashed with MeCN
- customdried
출처 및 근거
- ORD 기록
- ord-b0f146c8ff934f41aee8bfff8e9c916c
- 출처 데이터셋
- uspto-grants-2000_07
- 특허 번호
- US06093731
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