3-Chloro-2-fluorophenylboronic Acid → 2-(3-Chloro-2-fluorophenyl)thiazole-4-carboxylic acid
Reaction equation
[F:1][C:2]1[CH:7]=[C:6](OC)[CH:5]=[C:4](F)[C:3]=1[C:11]1[S:12][CH:13]=[C:14]([C:16]([OH:18])=[O:17])[N:15]=1.[Cl:19]C1C(F)=C(B(O)O)C=CC=1>>[Cl:19][C:7]1[C:2]([F:1])=[C:3]([C:11]2[S:12][CH:13]=[C:14]([C:16]([OH:18])=[O:17])[N:15]=2)[CH:4]=[CH:5][CH:6]=1Participants
3
Procedure
Following the procedure of Intermediate 104, replacing 2,6-difluoro-4-methoxyphenylboronic acid with (3-chloro-2-fluorophenyl)boronic acid gave the title compound.
Sources & evidence
- ORD record
- ord-a63b7eb45fe84cd9ac9da2873e56a3c7
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09328106B2
Reaction notes
Loading…