[2-Chloro-4-(2,4-difluoro-phenylamino)-phenyl]-(5-iodo-2-methyl-phenyl)-methanone → [2-Chloro-4-(4-fluoro-phenylamino)-phenyl]-(5-iodo-2-methyl-phenyl)-methanone
Reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([NH:8][C:9]2[CH:14]=[CH:13][C:12]([F:15])=[CH:11][C:10]=2F)[CH:5]=[CH:4][C:3]=1[C:17]([C:19]1[CH:24]=[C:23]([I:25])[CH:22]=[CH:21][C:20]=1[CH3:26])=[O:18].NC1C=CC(C)=C(C(C2C=CC(NC3C=CC(F)=CC=3)=CC=2Cl)=O)C=1>>[Cl:1][C:2]1[CH:7]=[C:6]([NH:8][C:9]2[CH:10]=[CH:11][C:12]([F:15])=[CH:13][CH:14]=2)[CH:5]=[CH:4][C:3]=1[C:17]([C:19]1[CH:24]=[C:23]([I:25])[CH:22]=[CH:21][C:20]=1[CH3:26])=[O:18]Participants
3
Procedure
The reaction was carried out similarly as described in the preparation of compound 405, using compound 429 (8.46 mmol). The crude product was purified by flash chromatography using EtOAc/petroleum ether (40-60) 2:8 followed by 3:7 as the eluent to afford the title compound as solid.
Workup
- customThe crude product was purified by flash chromatography
Sources & evidence
- ORD record
- ord-4621356e2f864caf9e7fbce6c832f793
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08293772B2
Reaction notes
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