4-(4-(Pyridin-3-yl)pyrimidin-2-ylamino)benzoic acid → 4-(4-(Pyridin-3-yl)pyrimidin-2-ylamino)-N-(2-aminophenyl)benzamide
Reaktionsgleichung
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[NH:8][C:9](=[O:30])[C:10]1[CH:15]=[CH:14][C:13](CNC2N=C(C3C=NC=CN=3)C=CN=2)=[CH:12][CH:11]=1.[N:31]1[CH:36]=[CH:35][CH:34]=[C:33]([C:37]2[CH:42]=[CH:41][N:40]=[C:39]([NH:43]C3C=CC(C(O)=O)=CC=3)[N:38]=2)[CH:32]=1>>[N:31]1[CH:36]=[CH:35][CH:34]=[C:33]([C:37]2[CH:42]=[CH:41][N:40]=[C:39]([NH:43][C:13]3[CH:12]=[CH:11][C:10]([C:9]([NH:8][C:3]4[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=4[NH2:1])=[O:30])=[CH:15][CH:14]=3)[N:38]=2)[CH:32]=1Komponenten
3
Versuchsvorschrift
Title compound was obtained in 54% yield according to the procedure described for the synthesis of compound 26a (scheme 6, step 4) replacing acid 25a by the acid 343. Characterization of the title compound is provided in the Table 12.
Quellen und Nachweise
- ORD-Eintrag
- ord-192d742e1ed242a5bb2c2566d7bb63df
- Quelldatensatz
- uspto-grants-2012_01
- Patentnummer
- US08088805B2
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