(6-Fluoropyridin-3-yl)boronic acid → HCID 11530019, compound
Reaction equation
C([O:3][C:4]([C:6]1[N:7]=[C:8]([CH2:11][O:12][C:13]2[CH:18]=[CH:17][C:16](I)=[CH:15][CH:14]=2)[S:9][CH:10]=1)=[O:5])C.[F:20][C:21]1[CH:26]=[CH:25][C:24](B(O)O)=[CH:23][N:22]=1>>[F:20][C:21]1[N:22]=[CH:23][C:24]([C:16]2[CH:15]=[CH:14][C:13]([O:12][CH2:11][C:8]3[S:9][CH:10]=[C:6]([C:4]([OH:3])=[O:5])[N:7]=3)=[CH:18][CH:17]=2)=[CH:25][CH:26]=1Participants
3
Procedure
2-[4-(6-Fluoro-pyridin-3-yl)-phenoxymethyl]-thiazole-4-carboxylic acid was prepared using the procedure described above for the preparation of Example 23 from 2-(4-iodo-phenoxymethyl)-thiazole-4-carboxylic acid ethyl ester (of Intermediate 2) and 2-fluoropyridine-5-boronic acid (available from Frontier Scientific, Inc., Logan, Utah). Mass spectrum MH+=331.
Sources & evidence
- ORD record
- ord-6ec6fc3e68c040c7bf6ebe6e2e6d0b90
- Source dataset
- uspto-grants-2009_04
- Patent number
- US07524870B2
Reaction notes
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