Reaktionsgleichung
F[C:2](F)(F)C(O)=O.[NH2:8][C:9]1[C:14]([C:15]([C:17]2[CH:22]=[C:21]([F:23])[CH:20]=[CH:19][C:18]=2[O:24][CH3:25])=[O:16])=[CH:13]N=[C:11]([NH:26][CH:27]2[CH2:32][CH2:31][NH:30][CH2:29][CH2:28]2)[N:10]=1.[CH:33]([S:36](Cl)(=[O:38])=[O:37])([CH3:35])[CH3:34]>>[NH2:8][C:9]1[C:14]([C:15]([C:17]2[CH:22]=[C:21]([F:23])[CH:20]=[CH:19][C:18]=2[O:24][CH3:25])=[O:16])=[CH:13][CH:2]=[C:11]([NH:26][CH:27]2[CH2:32][CH2:31][N:30]([S:36]([CH:33]([CH3:35])[CH3:34])(=[O:38])=[O:37])[CH2:29][CH2:28]2)[N:10]=1Komponenten
3
Versuchsvorschrift
The title compound was prepared from [4-amino-2-(piperidin-4-ylamino)-pyrimidin-5-yl]-(5-fluoro-2-methoxy-phenyl)-methanone trifluoroacetic acid salt (Example 22) and isopropyl sulfonyl chloride (Aldrich 97%) using the procedure described in Example 24. HRMS, observed: 451.1814, Calcd for (M+H)+: 451.1810.
Quellen und Nachweise
- ORD-Eintrag
- ord-a3e226a410c248d2a8aaa06ac3cfb5b0
- Quelldatensatz
- uspto-grants-2008_09
- Patentnummer
- US07423051B2
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