(2-Chloro-4-o-tolylamino-phenyl)-(2-methyl-5-nitro-phenyl)-methanone → (5-Amino-2-methyl-phenyl)-(2-chloro-4-o-tolylamino-phenyl)-methanone

HRID 2067211Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2067211
NC1C=CC(C)=C(C(C2C=CC(NC3C=CC(C(F)(F)F)=CC=3)=CC=2Cl)=O)C=1.[Cl:29][C:30]1[CH:35]=[C:34]([NH:36][C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][C:38]=2[CH3:43])[CH:33]=[CH:32][C:31]=1[C:44]([C:46]1[CH:51]=[C:50]([N+:52]([O-])=O)[CH:49]=[CH:48][C:47]=1[CH3:55])=[O:45]>>[NH2:52][C:50]1[CH:49]=[CH:48][C:47]([CH3:55])=[C:46]([C:44]([C:31]2[CH:32]=[CH:33][C:34]([NH:36][C:37]3[CH:42]=[CH:41][CH:40]=[CH:39][C:38]=3[CH3:43])=[CH:35][C:30]=2[Cl:29])=[O:45])[CH:51]=1

Komponenten

3

Versuchsvorschrift

The reaction was carried out similarly as described in the preparation of compound 415, using compound 417 (0.39 mmol). The crude product was used without any further purification.

Aufarbeitung

  1. customThe crude product was used without any further purification

Quellen und Nachweise

ORD-Eintrag
ord-cfe0f526b9254355a236ce3800219f53
Quelldatensatz
uspto-grants-2012_10
Patentnummer
US08293772B2

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