4-Chloro-6,7-dimethoxyquinazoline → 4-(6-Bromo-5-fluoro-2,3-dihydro-indol-1-yl)-6,7-dimethoxy-quinazoline hydrochloride salt
Reaktionsgleichung
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][C:10]=1[Br:11])[NH:7][CH2:6][CH2:5]2.[Cl:12][C:13]1[C:22]2[C:17](=[CH:18][C:19]([O:25][CH3:26])=[C:20]([O:23][CH3:24])[CH:21]=2)[N:16]=[CH:15][N:14]=1>CC(O)C>[ClH:12].[Br:11][C:10]1[CH:9]=[C:8]2[C:4]([CH2:5][CH2:6][N:7]2[C:13]2[C:22]3[C:17](=[CH:18][C:19]([O:25][CH3:26])=[C:20]([O:23][CH3:24])[CH:21]=3)[N:16]=[CH:15][N:14]=2)=[CH:3][C:2]=1[F:1]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Utilizing a procedure analogous to that described in Example 1, this product was prepared in 68% yield from 5-fluoro-6-bromo-indoline (1.1 eq.) and 4-chloro-6,7-dimethoxy-quinazoline (1.0 eq) in i-PrOH. (M.P. 258° C. (dec); LC-MS: 404, 406 (MH+); anal. RP18-HPLC RT: 5.06 min.).