5-Fluoro-2-nitrophenol → N-(3-((5-fluoro-2-((2-hydroxy-4-(2-methoxyethoxy)phenyl)amino)pyrimidin-4-yl)amino)phenyl)acrylamide
Reaction equation
[F:1][C:2]1[C:3]([NH:21][C:22]2[CH:23]=[C:24]([NH:28][C:29](=[O:32])[CH:30]=[CH2:31])[CH:25]=[CH:26][CH:27]=2)=[N:4][C:5]([NH:8][C:9]2[CH:14]=[CH:13][C:12]([O:15][CH2:16][CH2:17][O:18][CH3:19])=[C:11](O)[CH:10]=2)=[N:6][CH:7]=1.FC1C=CC([N+]([O-])=O)=C([OH:40])C=1>>[F:1][C:2]1[C:3]([NH:21][C:22]2[CH:23]=[C:24]([NH:28][C:29](=[O:32])[CH:30]=[CH2:31])[CH:25]=[CH:26][CH:27]=2)=[N:4][C:5]([NH:8][C:9]2[CH:10]=[CH:11][C:12]([O:15][CH2:16][CH2:17][O:18][CH3:19])=[CH:13][C:14]=2[OH:40])=[N:6][CH:7]=1Participants
3
Procedure
The synthesis of N-(3-((5-fluoro-2-((3-hydroxy-4-(2-methoxyethoxy)phenyl)amino)pyrimidin-4-yl)amino)phenyl)acrylamide was achieved as described above for N-(3-((5-fluoro-2-((3-hydroxy-4-(2-methoxyethoxy)phenyl)amino)pyrimidin-4-yl)amino)phenyl)acrylamide (I-13) in Example 7 using 5-fluoro-2-nitrophenol in place of 2-fluoro-5-nitrophenol in the first step.
Sources & evidence
- ORD record
- ord-471a2becb29e4a61a3af2b28f0ecd8a6
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09415049B2
Reaction notes
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