3-Fluoropyridine-4-carboxylic acid → 3-{[4-(Propan-2-yloxy)benzyl]amino}pyridine-4-carboxylic acid
Reaktionsgleichung
[CH:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]([CH2:11][NH2:12])=[CH:7][CH:6]=1)([CH3:3])[CH3:2].F[C:14]1[CH:22]=[N:21][CH:20]=[CH:19][C:15]=1[C:16]([OH:18])=[O:17]>>[CH3:2][CH:1]([O:4][C:5]1[CH:6]=[CH:7][C:8]([CH2:11][NH:12][C:19]2[CH:20]=[N:21][CH:22]=[CH:14][C:15]=2[C:16]([OH:18])=[O:17])=[CH:9][CH:10]=1)[CH3:3]Komponenten
3
Versuchsvorschrift
The title compound was prepared in 28% yield from 1-(4-isopropoxyphenyl)-methanamine and 3-fluoroisonicotinic acid according to the procedure for the preparation of Example 3. 1H NMR (400 MHz, DMSO-d6): δ 8.12 (s, 1H), 7.80 (d, 1H, J=5.0 Hz), 7.56 (d, 1H, J=5.0 Hz), 7.28 (d, 2H, J=8.0 Hz), 7.21 (d, 2H, J=8.0 Hz), 4.49 (s, 2H), 2.82-2.89 (m, 1H), 1.19 (d, 6H, J=4.5 Hz). [M+H] calc'd for C16H18N2O3, 287. found 287.
Quellen und Nachweise
- ORD-Eintrag
- ord-d14444f7b0784a0ba0c3123c71a406c4