반응식
Cl[S:2]([C:5]1[CH:14]=[C:13]2[C:8]([C:9]([Cl:16])=[CH:10][N:11]=[C:12]2[Cl:15])=[CH:7][CH:6]=1)(=[O:4])=[O:3].[NH3:17]>>[Cl:15][C:12]1[C:13]2[C:8](=[CH:7][CH:6]=[C:5]([S:2](=[O:4])(=[O:3])[NH2:17])[CH:14]=2)[C:9]([Cl:16])=[CH:10][N:11]=1참가 물질
3
실험 절차
7-chlorosulphonyl-1,4-dichloroisoquinoline (110 mg, 0.37 mmol) was dissolved in a solution of saturated methanolic ammonia (NH3) (10 mL) and the solution stirred at room temperature for 1.5 hours. The solvents were evaporated in vacuo and the residue was azeotroped with CH2Cl2 and then partitioned between EtOAc and water. The organic phase was washed with brine, dried (MgSO4) and evaporated in vacuo to give 1,4-dichloro-7-sulphamoylisoquinoline (98 mg, 0.35 mmol) as a white solid.
후처리
- customThe solvents were evaporated in vacuo
- customthe residue was azeotroped with CH2Cl2
- custompartitioned between EtOAc and water
- washThe organic phase was washed with brine
- dry with materialdried (MgSO4)
- customevaporated in vacuo
출처 및 근거
- ORD 기록
- ord-2cafeccf2f0a4c2499c528193bf31747
- 출처 데이터셋
- uspto-grants-2001_06
- 특허 번호
- US06248738B1
연결된 노트
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