Reaktionsgleichung
[NH2:1][C:2]1[C:7]([C:8]([C:10]2[CH:15]=[C:14]([F:16])[CH:13]=[CH:12][C:11]=2[O:17][CH3:18])=[O:9])=[CH:6][N:5]=[C:4]([NH:19][CH:20]2[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]2)[N:3]=1.[S:26]1[CH:30]=[C:29]([S:31](Cl)(=[O:33])=[O:32])[C:28]2[CH:35]=[CH:36][CH:37]=[CH:38][C:27]1=2>>[NH2:1][C:2]1[C:7]([C:8]([C:10]2[CH:15]=[C:14]([F:16])[CH:13]=[CH:12][C:11]=2[O:17][CH3:18])=[O:9])=[CH:6][N:5]=[C:4]([NH:19][CH:20]2[CH2:21][CH2:22][N:23]([S:31]([C:29]3[C:28]4[CH:35]=[CH:36][CH:37]=[CH:38][C:27]=4[S:26][CH:30]=3)(=[O:32])=[O:33])[CH2:24][CH2:25]2)[N:3]=1Komponenten
3
Versuchsvorschrift
The title compound was prepared from [4-amino-2-(piperidin-4-ylamino)-pyrimidin-5-yl]-(5-fluoro-2-methoxy-phenyl)-methanone, Example 59, and benzo[b]thiophene-3-sulfonyl chloride (Maybridge) by the procedure described in Example 152. HR-MS (ES, m/z) calculated for C25H25FN5O4S2 [(M+H)+] 542.1327, observed 542.1331.
Quellen und Nachweise
- ORD-Eintrag
- ord-77e2380ba7b84357ba322f1cee4f54e5
- Quelldatensatz
- uspto-grants-2007_01
- Patentnummer
- US07157455B2
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