4'-Fluoro(1,1'-biphenyl)-2-amine → HCID 44250945, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:9]([NH2:14])=[CH:10][CH:11]=[CH:12][CH:13]=2)=[CH:4][CH:3]=1.[Cl:15][C:16]1[CH:21]=[CH:20][C:19]([NH:22][C:23](=[O:30])[CH2:24][O:25][CH2:26][C:27](O)=[O:28])=[C:18]([C:31]([O:33]C)=[O:32])[CH:17]=1>>[Cl:15][C:16]1[CH:21]=[CH:20][C:19]([NH:22][C:23](=[O:30])[CH2:24][O:25][CH2:26][C:27]([NH:14][C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[C:5]2[CH:4]=[CH:3][C:2]([F:1])=[CH:7][CH:6]=2)=[O:28])=[C:18]([CH:17]=1)[C:31]([OH:33])=[O:32]Participants
3
Procedure
Using the same method as in Example 1-(ii), 4′-fluoro-(1,1′-biphenyl)-2-amine was reacted with the (2-([4-chloro-2-(methoxycarbonyl)phenyl]amino)-2-oxoethoxy)acetic acid obtained in Example 1-(i) to give 5-chloro-2-[((2-[(4′-fluorobiphenyl-2-yl)amino]-2-oxoethoxy)acetyl)amino]benzoic acid.methyl ester (yield: 60%).
Sources & evidence
- ORD record
- ord-198056166d5c448c975b58692e9f8137
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08415479B2
Reaction notes
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