Reaktionsgleichung
[CH3:1][NH:2][C:3]1[CH:4]=[N:5][CH:6]=[CH:7][C:8]=1[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[CH3:15].[CH3:16][O:17][C:18]1[CH:26]=[CH:25][C:21]([C:22]([OH:24])=O)=[CH:20][C:19]=1[C:27]([F:30])([F:29])[F:28]>>[CH3:16][O:17][C:18]1[CH:26]=[CH:25][C:21]([C:22]([N:2]([CH3:1])[C:3]2[CH:4]=[N:5][CH:6]=[CH:7][C:8]=2[C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[CH3:15])=[O:24])=[CH:20][C:19]=1[C:27]([F:30])([F:29])[F:28]Komponenten
3
Versuchsvorschrift
The title compound was prepared in analogy to example 90, from N-methyl-4-o-tolylpyridin-3-amine (example 1, intermediate a) and 4-methoxy-3-(trifluoromethyl)benzoic acid (CAS RN 213598-09-5) after a reaction time of 88 hours. Brown solid (4%). MS (ESI): m/z=401.15 [M+H]+.
Quellen und Nachweise
- ORD-Eintrag
- ord-b8e8a74ea59244f0bea3083d3a42b187
- Quelldatensatz
- uspto-grants-2015_03
- Patentnummer
- US08987307B2
Verknüpfte Notizen
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