2-Methoxyaniline → 3-(7-Isopropyl-pyrido[2,3-d]pyrimidin-4-ylamino)-N-(2-methoxy-phenyl)-4-(4-methoxy-phenylsulfanyl)-benzamide
Reaction equation
[CH:1]([C:4]1[CH:5]=[CH:6][C:7]2[C:12]([NH:13][C:14]3[CH:15]=[C:16]([CH:20]=[CH:21][C:22]=3[S:23][C:24]3[CH:29]=[CH:28][C:27]([O:30][CH3:31])=[CH:26][CH:25]=3)[C:17](Cl)=[O:18])=[N:11][CH:10]=[N:9][C:8]=2[N:32]=1)([CH3:3])[CH3:2].[CH3:33][O:34][C:35]1[C:36]([NH2:41])=[CH:37][CH:38]=[CH:39][CH:40]=1.NC1C=C(O)C(C)=CC=1>>[CH:1]([C:4]1[CH:5]=[CH:6][C:7]2[C:12]([NH:13][C:14]3[CH:15]=[C:16]([CH:20]=[CH:21][C:22]=3[S:23][C:24]3[CH:29]=[CH:28][C:27]([O:30][CH3:31])=[CH:26][CH:25]=3)[C:17]([NH:41][C:36]3[CH:37]=[CH:38][CH:39]=[CH:40][C:35]=3[O:34][CH3:33])=[O:18])=[N:11][CH:10]=[N:9][C:8]=2[N:32]=1)([CH3:3])[CH3:2]Participants
4
Reactant 3
Product 1
Procedure
The product from Example 137B was reacted with o-anisidine according to the procedure from Example 137C substituting o-anisidine for 5-amino-o-cresol to provide the title compound as an off white solid after silica gel chromatography (120 mg, 67%). 1H NMR (300 MHz, DMSO-D6) δ ppm: 1.34 (d, J=6.99 Hz, 6H), 3.12-3.28 (m, 1H), 3.78 (s, 3H), 3.81 (s, 3H), 6.92-7.05 (m, 4H), 7.05-7.12 (m, 1H), 7.13-7.23 (m, 1H), 7.40 (d, J=8.82 Hz, 2H), 7.64 (d, J=8.46 Hz, 1H), 7.71 (d, J=7.72 Hz, 1H), 7.81 (d, J=8.82 Hz, 1H), 7.99 (s, 1H), 8.59 (s, 1H), 8.86 (d, J=8.46 Hz, 1H), 9.44 (s, 1H), 9.44 (s, 1H); MS (APCI) m/z 553 (M+H)+.
Sources & evidence
- ORD record
- ord-de098c85285d4016bedfab002a9b24a0
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07910595B2
Reaction notes
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