Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[CH:5]2.C=O.[CH3:13][NH:14][CH3:15].[C:16](O)(=O)C>O1CCOCC1>[CH3:13][N:14]([CH2:16][C:5]1[C:4]2[CH:3]=[C:2]([Br:1])[CH:10]=[CH:9][C:8]=2[NH:7][CH:6]=1)[CH3:15]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
This material was prepared by the method of Procedure 67B from 49.5 g. of 5-bromoindole, 20 ml. of 37% aqueous formaldehyde, 55 ml. of 25% aqueous dimethylamine, 250 ml. of acetic acid and 250 ml. of dioxane; yield 60.6 g., m.p. 154°-156° C. The structure was confirmed by examination of the NMR spectrum.
Aufarbeitung
- customThis material was prepared by the method of Procedure 67B from 49.5 g
Quellen und Nachweise
- ORD-Eintrag
- ord-b8d02287528a42eeb37d82ed1423ce24
- Quelldatensatz
- uspto-grants-1980_11
- Patentnummer
- US04234595
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