Reaktionsgleichung
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](Cl)=[O:7])=[CH:4][N:3]=1.[CH3:11][C:12]([C:14]1[C:19]([NH2:20])=[CH:18][C:17]2[O:21][CH2:22][O:23][C:16]=2[CH:15]=1)=[O:13]>>[Cl:1][C:2]1[N:3]=[CH:4][C:5]([C:6]([NH:20][C:19]2[CH:18]=[C:17]3[O:21][CH2:22][O:23][C:16]3=[CH:15][C:14]=2[C:12]([CH3:11])=[O:13])=[O:7])=[CH:9][CH:10]=1Komponenten
3
Versuchsvorschrift
The title compound was prepared from 6-chloronicotinoyl chloride and 2-amino-4,5-methylenedioxyacetophenone as a light grey-yellow solid as described in Example 1. 1H NMR (CDCl3): 9.09-9.08 (m, 1H), 8.55 (s, 1H), 8.30-8.27 (m, 1H), 7.50-7.47 (m, 1H), 7.35 (s, 1H), 6.10 (s, 2H), 2.64 (s, 3H).
Quellen und Nachweise
- ORD-Eintrag
- ord-da1a5f409be0466eb2ef2b96eccfe875
- Quelldatensatz
- uspto-grants-2004_09
- Patentnummer
- US06794397B2
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