Reaktionsgleichung
COC1C=CC(S([O:12][C:13]2[C:21]3[C:16](=[CH:17][CH:18]=[C:19]([O:22][CH3:23])[CH:20]=3)[NH:15][N:14]=2)(=O)=O)=CC=1.[H-].[Na+].[OH:26][C:27]1[CH:34]=[CH:33][C:32]([N+:35]([O-:37])=[O:36])=[CH:31][C:28]=1[CH2:29]Cl.[OH2:38].C[S:40]([CH3:42])=[O:41]>>[OH:26][C:27]1[CH:34]=[CH:33][C:32]([N+:35]([O-:37])=[O:36])=[CH:31][C:28]=1[CH2:29][N:14]1[C:13](=[O:12])[C:21]2[C:16](=[CH:17][CH:18]=[C:19]([O:22][CH3:23])[CH:20]=2)[N:15]1[S:40]([C:42]1[CH:21]=[CH:20][C:19]([O:22][CH3:23])=[CH:18][CH:17]=1)(=[O:38])=[O:41]Komponenten
6
Versuchsvorschrift
5.01 g (15 mmol) of 5-methoxy-1H-indazol-3-yl 4-methoxybenzenesulphonate are dissolved in 70 ml of DMSO and treated in portions with 1.5 g (37.5 mmol) of sodium hydride (60 percent). After stirring for 2 hours, a solution of 2.81 g (15 mmol) of 2-hydroxy-5-nitrobenzyl chloride in 25 ml of DMSO is added dropwise and the mixture is stirred at 90-100° C. for 3 hours. After cooling, 400 ml of water are added, and the mixture is stirred for 3 hours and extracted three times with 400 ml of ethyl acetate. The combined organic phases are washed with 100 ml of water, dried over sodium sulphate, distilled to dryness in vacuo and the residue is recrystallized from ethanol.
Aufarbeitung
- stirringthe mixture is stirred at 90-100° C. for 3 hours
- temperatureAfter cooling
- stirringthe mixture is stirred for 3 hours
- extractionextracted three times with 400 ml of ethyl acetate
- washThe combined organic phases are washed with 100 ml of water
- dry with materialdried over sodium sulphate
- distillationdistilled to dryness in vacuo
- customthe residue is recrystallized from ethanol
Quellen und Nachweise
- ORD-Eintrag
- ord-c071f75f633949b28c254c8a60b8ebe9
- Quelldatensatz
- uspto-grants-2001_01
- Patentnummer
- US06180637B2
Verknüpfte Notizen
Wird geladen…