Reaktionsgleichung
Cl[S:2]([C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][CH:13]=1)[NH:10][C:9](=[O:14])[CH2:8]2)(=[O:4])=[O:3].[CH3:15][NH:16][CH3:17]>CO>[CH3:15][N:16]([CH3:17])[S:2]([C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][CH:13]=1)[NH:10][C:9](=[O:14])[CH2:8]2)(=[O:4])=[O:3]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A suspension of 2.3 g of 5-chlorosulfonyl-2-oxindole in 10 mL of 2M dimethylamine in methanol was stirred at room temperature for 4 hours at which time a white solid was present. The precipitate was collected by vacuum filtration, washed with 5 mL of 1N sodium hydroxide and 5 mL of 1N hydrochloric acid and dried under vacuum at 40° C. overnight to give 1.9 g (79 % yield) of 5-dimethylaminosulfonyl-2-oxindole.
Aufarbeitung
- filtrationThe precipitate was collected by vacuum filtration
- washwashed with 5 mL of 1N sodium hydroxide and 5 mL of 1N hydrochloric acid
- customdried under vacuum at 40° C. overnight
Quellen und Nachweise
- ORD-Eintrag
- ord-7bcb2d7ac49545c89c9ba19bf5d8cc73
- Quelldatensatz
- uspto-grants-2004_03
- Patentnummer
- US06706709B2
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