(5-Fluoropyridin-3-yl)boronic acid → HCID 68410003, compound
Reaction equation
[C:1]([O:5][C:6](=[O:28])[NH:7][CH:8]([C:20]1[CH:25]=[CH:24][C:23]([Cl:26])=[C:22]([Cl:27])[CH:21]=1)[C:9]([C:11]1[CH:16]=[CH:15][C:14](Br)=[C:13]([O:18][CH3:19])[CH:12]=1)=[O:10])([CH3:4])([CH3:3])[CH3:2].[F:29][C:30]1[CH:31]=[C:32](B(O)O)[CH:33]=[N:34][CH:35]=1>>[C:1]([O:5][C:6](=[O:28])[NH:7][CH:8]([C:20]1[CH:25]=[CH:24][C:23]([Cl:26])=[C:22]([Cl:27])[CH:21]=1)[C:9]([C:11]1[CH:16]=[CH:15][C:14]([C:32]2[CH:33]=[N:34][CH:35]=[C:30]([F:29])[CH:31]=2)=[C:13]([O:18][CH3:19])[CH:12]=1)=[O:10])([CH3:4])([CH3:3])[CH3:2]Participants
3
Procedure
The title compound was prepared from rac-[2-(4-bromo-3-methoxy-phenyl)-1-(3,4-dichloro-phenyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester and 5-fluoropyridine-3-boronic acid in analogy to Example 1b): MS (ISN): 503.0 (M−H)− and 429.01 ((M-tBuOH)−H)−.
Sources & evidence
- ORD record
- ord-0701e393674b4e649b2df3043991854b
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08367838B2
Reaction notes
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