4-Chloro-2-pyridinecarbonitrile → 4-Amino-3-(trifluoromethyl)phenoxyl pyridine-2-carbonitrile
Reaktionsgleichung
NC1C=C(C=CC=1)O[C:6]1[CH:11]=[CH:10][N:9]=[C:8]([C:12]([NH2:14])=O)[CH:7]=1.[NH2:18][C:19]1[CH:24]=[CH:23][C:22]([OH:25])=[CH:21][C:20]=1[C:26]([F:29])([F:28])[F:27].ClC1C=CN=C(C#N)C=1>>[NH2:18][C:19]1[CH:24]=[CH:23][C:22]([O:25][C:7]2[C:8]([C:12]#[N:14])=[N:9][CH:10]=[CH:11][CH:6]=2)=[CH:21][C:20]=1[C:26]([F:27])([F:28])[F:29]Komponenten
4
Versuchsvorschrift
This material is prepared by a method analogous to that described for preparation of 2C, starting from 4-amino-3-(trifluoromethyl)phenol and 4-chloro-2-cyanopyridine.
Aufarbeitung
- customThis material is prepared by a method analogous to
Quellen und Nachweise
- ORD-Eintrag
- ord-a38d4f9ee7694621b9181727e1cd2ac1
- Quelldatensatz
- uspto-grants-2009_09
- Patentnummer
- US07582645B2
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