Reaktionsgleichung
[NH2:1][C:2]1[CH:3]=[C:4]([OH:9])[CH:5]=[CH:6][C:7]=1[Cl:8].[C:10](=[O:13])([O-])[O-].[Cs+].[Cs+].Cl[C:17]1[N:26]=[CH:25][C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[N:18]=1.O.CN([CH:31]=[O:32])C>>[Cl:8][C:7]1[CH:6]=[CH:5][C:4]([O:9][C:25]2[C:24]3[C:19](=[CH:20][C:21]([O:13][CH3:10])=[C:22]([O:32][CH3:31])[CH:23]=3)[N:18]=[CH:17][N:26]=2)=[CH:3][C:2]=1[NH2:1]Komponenten
Versuchsvorschrift
A solution of 3-amino-4-chlorophenol (1.00 g, 7.0 mmol) and cesium carbonate (3.38 g, 10.4 mmol) in DMF (20 mL) were heated at 80 C for 1 hr. The chloroquinazoline (1.61 g, 7.2 mmol) was added and the mixture heated for an additional hour. The mixture was poured into water (300 mL) and extracted with EtOAc twice. The combined extracts were washed with brine, dried with magnesium sulfate, filtered and concentrated. The residue was purified using silica gel chromatography eluting with EtOAc/hexane (30-70%), the main peak collected and triturated with DCM to afford 2-chloro-5-(6,7-dimethoxyquinazolin-4-yloxy)aniline. 1H NMR (300 MHz, DMSO d6) δ 3.96 (s, 6H), 5.55 (s, 2H), 6.45 (t, 1H), 6.76 (d, 1H), 7.25 (d, 1H), 7.36 (s, 1H), 7.50 (s, 1H), 8.55 (s, 1H); LC-MS (ESI) m/z 332 (M+H)+
Aufarbeitung
- temperaturethe mixture heated for an additional hour
- extractionextracted with EtOAc twice
- washThe combined extracts were washed with brine
- dry with materialdried with magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customThe residue was purified
- washeluting with EtOAc/hexane (30-70%)
- customthe main peak collected
- customtriturated with DCM
Quellen und Nachweise
- ORD-Eintrag
- ord-c8daab87a4af45feb3e9508fdf9db2dd
- Quelldatensatz
- uspto-grants-2013_12
- Patentnummer
- US08618289B2
Verknüpfte Notizen
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