Reaktionsgleichung
[NH2:1][C:2]1[CH:18]=[CH:17][C:16]([N+:19]([O-:21])=[O:20])=[CH:15][C:3]=1[C:4]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([F:13])=[CH:9][C:8]=1[CH3:14])=[O:5].[F:22][CH2:23][C:24](Cl)=[O:25]>N1C=CC=CC=1>[F:22][CH2:23][C:24]([NH:1][C:2]1[CH:18]=[CH:17][C:16]([N+:19]([O-:21])=[O:20])=[CH:15][C:3]=1[C:4]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([F:13])=[CH:9][C:8]=1[CH3:14])=[O:5])=[O:25]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
3.9 g of N-(2-amino-5-nitrobenzoyl)-2-methyl-4-fluoroaniline, 1.6 g of pyridine and 1.96 g of fluoroacetyl chloride are treated in the same manner as described in Example 1-(1), whereby 4.0 g of N-(2-fluoroacetamido-5-nitrobenzoyl)-2-methyl-4-fluoroaniline are obtained as colorless needles.
Quellen und Nachweise
- ORD-Eintrag
- ord-f34f851317ce42428e32186aebcd1f37
- Quelldatensatz
- uspto-grants-1987_12
- Patentnummer
- US04714702
Verknüpfte Notizen
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