3-Fluoro-4-(methoxycarbonyl)benzeneboronic acid → HCID 71060843, compound
Reaction equation
[NH2:1][C:2]1[N:16]=[CH:15][C:14](Br)=[CH:13][C:3]=1[C:4]([NH:6][C:7]1[CH:12]=[CH:11][N:10]=[CH:9][CH:8]=1)=[O:5].[F:18][C:19]1[CH:20]=[C:21](B(O)O)[CH:22]=[CH:23][C:24]=1[C:25]([O:27][CH3:28])=[O:26]>>[CH3:28][O:27][C:25](=[O:26])[C:24]1[CH:23]=[CH:22][C:21]([C:14]2[CH:15]=[N:16][C:2]([NH2:1])=[C:3]([C:4](=[O:5])[NH:6][C:7]3[CH:12]=[CH:11][N:10]=[CH:9][CH:8]=3)[CH:13]=2)=[CH:20][C:19]=1[F:18]Participants
3
Procedure
Reaction of 2-amino-5-bromo-N-pyridin-4-yl-nicotinamide with 3-fluoro-4-methoxycarbonyl-phenylboronic acid gives “A80”; method 1: HPLC/MS: 1.48 min, [M+H]=367;
Workup
- customgives “A80”
- custom1.48 min, [M+H]=367
Sources & evidence
- ORD record
- ord-0959eafbce404ef580654f2268ac1a1e
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09273029B2
Reaction notes
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