Reaktionsgleichung
[N+](C1C=C(N)C(=CC=1)C(O)=O)([O-])=O.Cl[C:15]1[C:24]2[C:19](=[CH:20][C:21]([N+:25]([O-:27])=[O:26])=[CH:22][CH:23]=2)[N:18]=[CH:17][N:16]=1.[CH3:28][C:29]1[CH:30]=[C:31]([CH:33]=[CH:34][CH:35]=1)[NH2:32]>>[CH3:28][C:29]1[CH:30]=[C:31]([CH:33]=[CH:34][CH:35]=1)[NH:32][C:15]1[C:24]2[C:19](=[CH:20][C:21]([N+:25]([O-:27])=[O:26])=[CH:22][CH:23]=2)[N:18]=[CH:17][N:16]=1Komponenten
4
Versuchsvorschrift
Using an analogous procedure to that described in the portion of Example 1 which is concerned with the preparation of starting materials, 4-nitroanthranilic acid was converted into 4-chloro-7-nitroquinazoline. Using an analogous procedure to that described in Example 1 except that the reactants were stirred together at ambient temperature for 20 minutes, 4-chloro-7-nitroquinazoline was reacted with 3-methylaniline to give 4-(3'-methylanilino)-7-nitroquinazoline.
Quellen und Nachweise
- ORD-Eintrag
- ord-6632c2b133284985913007f1719e2f9b
- Quelldatensatz
- uspto-grants-1995_10
- Patentnummer
- US05457105
Verknüpfte Notizen
Wird geladen…