Reaction equation
Br[CH2:2][C:3]1[CH:7]=[C:6]([C:8]2[CH:13]=[CH:12][C:11]([C:14]([F:17])([F:16])[F:15])=[CH:10][CH:9]=2)[S:5][C:4]=1[C:18](OC)=[O:19].[CH:22]([C:25]1[N:30]=[C:29]([OH:31])[CH:28]=[C:27]([CH3:32])[N:26]=1)([CH3:24])[CH3:23]>>[CH:22]([C:25]1[N:30]=[C:29]([O:31][CH2:2][C:3]2[CH:7]=[C:6]([C:8]3[CH:9]=[CH:10][C:11]([C:14]([F:17])([F:15])[F:16])=[CH:12][CH:13]=3)[S:5][C:4]=2[CH2:18][OH:19])[CH:28]=[C:27]([CH3:32])[N:26]=1)([CH3:24])[CH3:23]Participants
3
Procedure
The title compound was prepared using methyl 3-(bromomethyl)-5-[4-(trifluoromethyl)phenyl]thiophene-2-carboxylate (intermediate 132) and 2-isopropyl-6-methyl-4-pyrimidinol.
Sources & evidence
- ORD record
- ord-af55f1b94a2548bbb8c81307374898be
- Source dataset
- uspto-grants-2006_08
- Patent number
- US07091237B2
Linked notes
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