1-Bromo-2-propanol → 5-(2-Fluoro-4-iodophenylamino)-3-(2-hydroxypropyl)-8-methylpyrido[2,3-d]pyrimidine-4,7(3H,8H)-dione
Reaktionsgleichung
[OH:1][C@H:2]([CH2:26]O)[CH2:3][N:4]1[C:9](=[O:10])[C:8]2[C:11]([NH:17][C:18]3[CH:23]=[CH:22][C:21]([I:24])=[CH:20][C:19]=3[F:25])=[CH:12][C:13](=[O:16])[N:14]([CH3:15])[C:7]=2[N:6]=[CH:5]1.NC1C=CC(NC2C3C(=O)NC=NC=3N(C)C(=O)C=2)=C(F)C=1.BrCC(O)C>>[F:25][C:19]1[CH:20]=[C:21]([I:24])[CH:22]=[CH:23][C:18]=1[NH:17][C:11]1[C:8]2[C:9](=[O:10])[N:4]([CH2:3][CH:2]([OH:1])[CH3:26])[CH:5]=[N:6][C:7]=2[N:14]([CH3:15])[C:13](=[O:16])[CH:12]=1Komponenten
4
Edukt 3
Produkt 1
Versuchsvorschrift
The title compound was prepared following the same procedure for the synthesis of Compound 5G using compound 5F and 1-bromopropan-2-ol as starting material. 1H NMR (400 MHz, CDCl3) δ 8.17 (s, 1H) 7.52 (m, 2H) 7.24 (t, J=8.84 Hz, 1H) 5.81 (s, 1H) 4.39 (m, 1H) 4.25 (m, 1H) 3.57 (m, 4H), 1.35 (d, J=6.32 Hz, 3H). [M+H] calc'd for C17H16FIN4O3, 471. found, 471.
Quellen und Nachweise
- ORD-Eintrag
- ord-417a12b92aeb4113bac712ed8eef42cf
- Quelldatensatz
- uspto-grants-2013_06
- Patentnummer
- US08470837B2
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