Reaktionsgleichung
[NH2:1][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[CH:4][C:3]=1[C:12]1[N:17]=[CH:16][N:15]=[C:14]([O:18][C:19]2[C:24]3[N:25]=[C:26]([NH:28][C:29](=[O:31])[CH3:30])[S:27][C:23]=3[CH:22]=[CH:21][CH:20]=2)[CH:13]=1.[CH3:32][C:33]([O:36][C:37]([N:39]1[CH2:44][CH2:43][CH:42]([CH:45]=O)[CH2:41][CH2:40]1)=[O:38])([CH3:35])[CH3:34]>>[C:33]([O:36][C:37]([N:39]1[CH2:44][CH2:43][CH:42]([CH2:45][NH:1][C:2]2[CH:7]=[C:6]([C:8]([F:11])([F:9])[F:10])[CH:5]=[CH:4][C:3]=2[C:12]2[CH:13]=[C:14]([O:18][C:19]3[C:24]4[N:25]=[C:26]([NH:28][C:29](=[O:31])[CH3:30])[S:27][C:23]=4[CH:22]=[CH:21][CH:20]=3)[N:15]=[CH:16][N:17]=2)[CH2:41][CH2:40]1)=[O:38])([CH3:35])([CH3:32])[CH3:34]Komponenten
3
Edukt 2
Produkt 1
Versuchsvorschrift
The title compound was prepared from N-{4-[6-(2-amino-4-trifluoromethyl-phenyl)-pyrimidin-4-yloxy]-benzothiazol-2-yl}-acetamide (Example 151) and N-Boc-4-piperidinylcarboxaldehyde according the procedure described in Example 159. MS(ESI, pos. ion) m/z: 643 (M+1).
Quellen und Nachweise
- ORD-Eintrag
- ord-ff5aaa95da364177a2839aa5230f0e80
- Quelldatensatz
- uspto-grants-2006_12
- Patentnummer
- US07144888B2
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