2-Fluoropyridine-3-boronic acid → HCID 11522662, compound
Reaction equation
C[O:2][C:3](=[O:19])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH2:10][O:11][C:12]2[CH:17]=[CH:16][C:15](I)=[CH:14][CH:13]=2)[CH:5]=1.[F:20][C:21]1[C:26](B(O)O)=[CH:25][CH:24]=[CH:23][N:22]=1>>[F:20][C:21]1[C:26]([C:15]2[CH:16]=[CH:17][C:12]([O:11][CH2:10][C:6]3[CH:5]=[C:4]([CH:9]=[CH:8][CH:7]=3)[C:3]([OH:2])=[O:19])=[CH:13][CH:14]=2)=[CH:25][CH:24]=[CH:23][N:22]=1Participants
3
Procedure
3-[4-(2-Fluoro-pyridin-3-yl)-phenoxymethyl]-benzoic acid was prepared using the procedure described above for the synthesis of Example 4 from 3-(4-iodo-phenoxymethyl)-benzoic acid methyl ester (of Intermediate 1) and 2-fluoropyridine-3-boronic acid (ASDI Incorporated, Newark, Del.). Mass spectrum MH+=324.
Sources & evidence
- ORD record
- ord-b288e9c5448345d9bd4f29b43bcf2bc6
- Source dataset
- uspto-grants-2009_04
- Patent number
- US07524870B2
Reaction notes
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