2-Chloro-5-fluoro-4-iodopyridine → 3-(4-Bromo-phenyl)-1-(2-chloro-5-fluoro-pyridin-4-yl)-3-o-tolyl-propan-1-one
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[CH3:22])[CH2:9][C:10](N(OC)C)=[O:11])=[CH:4][CH:3]=1.[Cl:23][C:24]1[CH:29]=[C:28](I)[C:27]([F:31])=[CH:26][N:25]=1>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[CH3:22])[CH2:9][C:10]([C:28]2[C:27]([F:31])=[CH:26][N:25]=[C:24]([Cl:23])[CH:29]=2)=[O:11])=[CH:6][CH:7]=1Participants
3
Procedure
In analogy to example 74, step 5, from 3-(4-bromo-phenyl)-N-methoxy-N-methyl-3-o-tolyl-propionamide (example 74, step 4) and 2-chloro-5-fluoro-4-iodopyridine (CAS RN: [659731-48-3]) was prepared the title compound as a white solid, MS (ESI−): m/z=430.0013 ([M−H]−, 1Br).
Sources & evidence
- ORD record
- ord-89598e34b1ca497ebdb916558f0c3c74
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08765730B2
Reaction notes
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