HCID 59525576, compound → HCID 25123488, compound
Reaction equation
[NH2:1][C:2]1[S:3][C:4]([C:10]2[C:15]([F:16])=[CH:14][C:13]([C:17]([OH:20])([CH3:19])[CH3:18])=[CH:12][C:11]=2[F:21])=[CH:5][C:6]=1[C:7]([NH2:9])=[O:8].Br[C:23]1[N:28]=[C:27]([CH2:29][NH:30][CH:31]([CH3:36])[C:32]([CH3:35])([OH:34])[CH3:33])[CH:26]=[CH:25][CH:24]=1>>[F:16][C:15]1[CH:14]=[C:13]([C:17]([OH:20])([CH3:18])[CH3:19])[CH:12]=[C:11]([F:21])[C:10]=1[C:4]1[S:3][C:2]([NH:1][C:23]2[CH:24]=[CH:25][CH:26]=[C:27]([CH2:29][NH:30][CH:31]([CH3:36])[C:32]([OH:34])([CH3:33])[CH3:35])[N:28]=2)=[C:6]([C:7]([NH2:9])=[O:8])[CH:5]=1Participants
3
Procedure
The title compound was prepared by using the procedure listed in Example 1 with 2-amino-5-[2,6-difluoro-4-(1-hydroxy-1-methylethyl)phenyl]thiophene-3-carboxamide (0.080 g, 0.26 mmol) and 3-{[(6-bromopyridin-2-yl)methyl]amino}-2-methylbutan-2-ol (0.070 g, 0.26 mmol) as the starting materials.
Sources & evidence
- ORD record
- ord-cd0f4c04894d496a97a300348de03606
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08367706B2
Reaction notes
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