Reaktionsgleichung
[NH:1]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:4](=O)[C:2]1=[O:3].O=CC(Cl)(Cl)Cl.[Cl-].[OH:19][NH3+:20].Cl.NC1C=CC=CC=1>>[CH:8]1[CH:7]=[CH:6][C:11]([NH:1][C:2](/[CH:4]=[N:20]/[OH:19])=[O:3])=[CH:10][CH:9]=1Komponenten
6
Versuchsvorschrift
The isatin derivative (9) can be synthesized, for example, as shown in the following reaction scheme. That is, an aqueous solution obtained by adding chloral and hydroxylammonium chloride to hydrochloride of an aniline derivative (10) as a starting material is reacted for 0.5 to 2 hours with heating at 70° to 110° C. to give an isonitrosoacetanilide derivative, and this product is cyclized with concentrated sulfuric acid and hydrolyzed to give an isatin derivative (9). ##STR10## wherein R1A to R1D are as defined above.
Aufarbeitung
- customas shown in the following reaction scheme
- customan aqueous solution obtained
- customis reacted for 0.5 to 2 hours
- temperaturewith heating at 70° to 110° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-e75f94cdfd09486eb81e090e8b1e9b65
- Quelldatensatz
- uspto-grants-1997_04
- Patentnummer
- US05616441
Verknüpfte Notizen
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