(4-Aminophenoxy)benzene → 3-Hydroxy-4,6-dimethoxy-4'-phenoxypicolinanilide

HRID 350644

Reaktionsgleichung

Reaktionsgleichung von HRID 350644
C(OC1C(C(O)=O)=NC=CC=1OC)C1C=CC=CC=1.C([O:27][C:28]1[C:29]([C:38]([OH:40])=O)=[N:30][C:31]([O:36][CH3:37])=[CH:32][C:33]=1[O:34][CH3:35])C1C=CC=CC=1.CO[C:43]1[CH:56]=[CH:55][C:46]([O:47][C:48]2[CH:54]=[CH:53][C:51]([NH2:52])=[CH:50][CH:49]=2)=[CH:45][CH:44]=1.O(C1C=CC(N)=CC=1)C1C=CC=CC=1>>[OH:27][C:28]1[C:29]([C:38]([NH:52][C:51]2[CH:50]=[CH:49][C:48]([O:47][C:46]3[CH:55]=[CH:56][CH:43]=[CH:44][CH:45]=3)=[CH:54][CH:53]=2)=[O:40])=[N:30][C:31]([O:36][CH3:37])=[CH:32][C:33]=1[O:34][CH3:35]

Komponenten

5

Edukt 4

HCID 8764(4-Aminophenoxy)benzeneHCID 1014024-(4-Methoxyphenoxy)anilineHCID 177986653-Benzyloxy-4,6-dimethoxypicolinic acidHCID 199602893-Benzyloxy-4-methoxypicolinic acid

Produkt 1

HCID 210888473-Hydroxy-4,6-dimethoxy-4'-phenoxypicolinanilide

Versuchsvorschrift

The procedure of Example 29 was repeated, except that 3-benzyloxy-4-methoxypicolinic acid was changed to 3-benzyloxy-4,6-dimethoxypicolinic acid and 4-(4′-methoxyphenoxy)aniline was changed to 4-phenoxyaniline. Thus, the title compound was prepared.

Quellen und Nachweise

ORD-Eintrag
ord-deb09f7442ed4a409214d7dd60d84981
Quelldatensatz
uspto-grants-2007_02
Patentnummer
US07183278B1

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