Furan-2-boronic acid → HCID 22316925, compound
Reaction equation
[O:1]1C=C[CH:3]=[C:2]1B(O)O.[Br:9][C:10]1[CH:15]=[CH:14][C:13]([C:16]2[N:20]([C:21]3[CH:26]=[CH:25][C:24]([S:27]([CH3:30])(=[O:29])=[O:28])=[CH:23][CH:22]=3)[N:19]=[C:18]([CH2:31][OH:32])[CH:17]=2)=[CH:12][CH:11]=1>>[Br:9][C:10]1[CH:11]=[CH:12][C:13]([C:16]2[N:20]([C:21]3[CH:26]=[CH:25][C:24]([S:27]([CH3:30])(=[O:29])=[O:28])=[CH:23][CH:22]=3)[N:19]=[C:18]([C:31]([O:1][CH2:2][CH3:3])=[O:32])[CH:17]=2)=[CH:14][CH:15]=1Participants
3
Procedure
The title compound was prepared according to the procedure of Example 1 using 2-furanboronic acid instead of 2-thiophenboronic acid acid and 4-[5-[4-Bromophenyl]-3-hydroxymethy-1-[4-(methylsulfonyl)phenyl]-1H-pyrazole instead of 1-[4-(Methylsulfonyl)phenyl]-5-(4-bromophenyl)-3-trifluoromethyl-1H-pyrazole in step 2.
Sources & evidence
- ORD record
- ord-d99354d19fc74fb0acfe299956254529
- Source dataset
- uspto-grants-2003_08
- Patent number
- US06608095B2
Reaction notes
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