Water → 2-[3-(2,6-Dichlorophenyl)sulfonyl-2,5-dimethylindol-1-yl]acetic acid
Reaktionsgleichung
ClC1C=C(C(OO)=[O:9])C=CC=1.[Cl:12][C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([Cl:19])[C:14]=1[S:20][C:21]1[C:29]2[C:24](=[CH:25][CH:26]=[C:27]([CH3:30])[CH:28]=2)[N:23]([CH2:31][C:32]([OH:34])=[O:33])[C:22]=1[CH3:35].S([O-])([O-])(=O)=S.[Na+].[Na+].[OH2:43]>C(#N)C>[Cl:12][C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([Cl:19])[C:14]=1[S:20]([C:21]1[C:29]2[C:24](=[CH:25][CH:26]=[C:27]([CH3:30])[CH:28]=2)[N:23]([CH2:31][C:32]([OH:34])=[O:33])[C:22]=1[CH3:35])(=[O:9])=[O:43]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
3-Chlorobenzenecarboperoxoic acid (0.34 g) was added to a solution of the product from example 24 step a) (0.18 g) in acetonitrile (5 ml) and water (0.5 ml). The reaction was stirred for 1 h, 1M aqueous sodium thiosulphate (2 ml) added and stirred for a further 15 min. The mixture was filtered, purified by reverse phase HPLC and evaporated in vacuo to yield the title compound as a white solid (40 mg).
Aufarbeitung
- stirringstirred for a further 15 min
- filtrationThe mixture was filtered
- custompurified by reverse phase HPLC
- customevaporated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-fb0869ec06584809b2853a9589c32c5f
- Quelldatensatz
- uspto-grants-2010_05
- Patentnummer
- US07723373B2
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