4-Aminobenzonitrile → HCID 46191049, Verbindung

HRID 523863Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 523863
[C:1]([C:3]1[CH:9]=[CH:8][C:6]([NH2:7])=[CH:5][CH:4]=1)#[N:2].Cl[C:11]1[C:16]([N+:17]([O-:19])=[O:18])=[CH:15][CH:14]=[C:13](Cl)[N:12]=1.[CH3:21][C:22]1[CH:27]=[C:26]([CH2:28][CH:29]=[CH2:30])[CH:25]=[C:24]([CH3:31])[C:23]=1[OH:32]>>[CH3:21][C:22]1[CH:27]=[C:26]([CH2:28][CH:29]=[CH2:30])[CH:25]=[C:24]([CH3:31])[C:23]=1[O:32][C:13]1[N:12]=[C:11]([NH:7][C:6]2[CH:8]=[CH:9][C:3]([C:1]#[N:2])=[CH:4][CH:5]=2)[C:16]([N+:17]([O-:19])=[O:18])=[CH:15][CH:14]=1

Komponenten

4

Versuchsvorschrift

4-cyano aniline was coupled with 2,6-dichloro-3-nitropyridine by Method B in Preparation Example 1 to prepare 6-chloro-N2-(4′-cyanobenzene)-3-nitropyridine (intermediate II-1), which was coupled with 2,6-dimethyl-4-allylphenol by Method B in Preparation 2 to get Compound 15.

Quellen und Nachweise

ORD-Eintrag
ord-44444958a5c54493bdfb60346ad67858
Quelldatensatz
uspto-grants-2016_05
Patentnummer
US09340492B2

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