HCID 58677657, compound → [2-Chloro-4-(2,4-difluoro-phenylamino)-phenyl]-(5-ethynyl-2-methoxy-phenyl)-methanone
Reaction equation
ClC1C=C(NC2C=CC(F)=CC=2F)C=CC=1C(C1C=C(C#C)C=CC=1C)=O.[Cl:28][C:29]1[CH:34]=[C:33]([NH:35][C:36]2[CH:41]=[CH:40][C:39]([F:42])=[CH:38][C:37]=2[F:43])[CH:32]=[CH:31][C:30]=1[C:44]([C:46]1[CH:51]=[C:50]([C:52]#[C:53][Si](C)(C)C)[CH:49]=[CH:48][C:47]=1[O:58][CH3:59])=[O:45]>>[Cl:28][C:29]1[CH:34]=[C:33]([NH:35][C:36]2[CH:41]=[CH:40][C:39]([F:42])=[CH:38][C:37]=2[F:43])[CH:32]=[CH:31][C:30]=1[C:44]([C:46]1[CH:51]=[C:50]([C:52]#[CH:53])[CH:49]=[CH:48][C:47]=1[O:58][CH3:59])=[O:45]Participants
3
Procedure
The reaction was carried out similarly as described in the preparation of compound 407, using compound 426 (0.44 mmol). The crude product was used directly in the next reaction without any further purification.
Sources & evidence
- ORD record
- ord-e8907bfedf814000843bcb0063866655
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08293772B2
Reaction notes
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