HCID 58216647, compound → HCID 44554812, 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].Cl[C:23]1[N:28]=[C:27]2[N:29]=[N:30][N:31]([CH2:32][C:33]([CH3:36])([OH:35])[CH3:34])[C:26]2=[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[N:28]=[C:27]3[N:29]=[N:30][N:31]([CH2:32][C:33]([OH:35])([CH3:34])[CH3:36])[C:26]3=[CH:25][CH:24]=2)=[C:6]([C:7]([NH2:9])=[O:8])[CH:5]=1Participants
3
Procedure
The title compound was prepared as described in Example 1, Step 5 using 2-amino-5-[2,6-difluoro-4-(1-hydroxy-1-methylethyl)phenyl]thiophene-3-carboxamide (23 mg, 0.074 mmol) and 1-(5-chloro-1H-[1,2,3]triazolo[4,5-b]pyridin-1-yl)-2-methylpropan-2-ol (17 mg, 0.074 mmol) as starting materials.
Sources & evidence
- ORD record
- ord-03fd481295b74d4a9a8e488e5ce0d5a3
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08344144B2
Reaction notes
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