Reaktionsgleichung
ClC1C=C2C(C=CC(C)=N2)=CC=1O.C[O:15][C:16]1[CH:17]=[C:18]2[C:23](=[CH:24][C:25]=1[CH3:26])[N:22]=[CH:21][CH:20]=[CH:19]2>>[CH3:26][C:25]1[CH:24]=[C:23]2[C:18]([CH:19]=[CH:20][CH:21]=[N:22]2)=[CH:17][C:16]=1[OH:15]Komponenten
3
Versuchsvorschrift
Compound 3C was prepared following the procedure used to prepare compound 1C of Example 1, except that 6-methoxy-7-methylquinoline (3B) was used instead of compound 1B. LCMS-ESI+ (m/z): 160.2 (M+H)+.
Quellen und Nachweise
- ORD-Eintrag
- ord-296b5d80b97145caa8c698ffa015ca45
- Quelldatensatz
- uspto-grants-2016_03
- Patentnummer
- US09296758B2
Verknüpfte Notizen
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