2-Fluoro-4-methylbenzonitrile → 2-(2-Fluoro-4-methylphenyl)thiazole-4-carboxylic acid
Reaction equation
Br[C:2]1[CH:3]=[CH:4][C:5]([F:16])=[C:6]([C:8]2[S:9][CH:10]=[C:11]([C:13]([OH:15])=[O:14])[N:12]=2)[CH:7]=1.F[C:18]1C=C(C)C=CC=1C#N>>[F:16][C:5]1[CH:4]=[C:3]([CH3:18])[CH:2]=[CH:7][C:6]=1[C:8]1[S:9][CH:10]=[C:11]([C:13]([OH:15])=[O:14])[N:12]=1Participants
3
Procedure
Following the procedure of Intermediate 129, replacing 5-bromo-2-fluoro-benzonitrile with 2-fluoro-4-methylbenzonitrile gave the title compound.
Sources & evidence
- ORD record
- ord-e68348b4c62b4b2586c8f20bceef8714
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09328106B2
Reaction notes
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