1-(6-Chloropyridin-3-yl)-2,2,2-trifluoroethan-1-ol → 5-[2-Fluoro-4-(1-hydroxy-1-methylethyl)phenyl]-2-{[5-(2,2,2-trifluoro-1-hydroxyethyl)pyridin-2-yl]amino}thiophene-3-carboxamide
Reaction equation
[NH2:1][C:2]1[S:3][C:4]([C:10]2[CH:15]=[CH:14][C:13]([C:16]([OH:19])([CH3:18])[CH3:17])=[CH:12][C:11]=2[F:20])=[CH:5][C:6]=1[C:7]([NH2:9])=[O:8].Cl[C:22]1[N:27]=[CH:26][C:25]([CH:28]([OH:33])[C:29]([F:32])([F:31])[F:30])=[CH:24][CH:23]=1>>[F:20][C:11]1[CH:12]=[C:13]([C:16]([OH:19])([CH3:17])[CH3:18])[CH:14]=[CH:15][C:10]=1[C:4]1[S:3][C:2]([NH:1][C:22]2[CH:23]=[CH:24][C:25]([CH:28]([OH:33])[C:29]([F:32])([F:31])[F:30])=[CH:26][N:27]=2)=[C:6]([C:7]([NH2:9])=[O:8])[CH:5]=1Participants
3
Reactant 2
Product 1
Procedure
The title compound was prepared as described in Example 1 using 2-amino-5-[2-fluoro-4-(1-hydroxy-1-methylethyl)phenyl]thiophene-3-carboxamide (150 mg, 0.51 mmol) and 1-(6-chloropyridin-3-yl)-2,2,2-trifluoroethanol (108 mg, 0.51 mmol) as starting materials.
Sources & evidence
- ORD record
- ord-ebabc08d526541359645418a98f2ef13
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08367706B2
Reaction notes
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