2-Thiopheneboronic acid → HCID 18470702, compound
Reaction equation
[C:1]([C:4]1[C:8]([CH3:9])=[C:7]([C:10]2[CH:15]=[CH:14][N:13]=[CH:12][CH:11]=2)[NH:6][C:5]=1Br)(=[O:3])[CH3:2].[S:17]1[CH:21]=[CH:20][CH:19]=[C:18]1B(O)O>>[C:1]([C:4]1[C:8]([CH3:9])=[C:7]([C:10]2[CH:15]=[CH:14][N:13]=[CH:12][CH:11]=2)[NH:6][C:5]=1[C:18]1[S:17][CH:21]=[CH:20][CH:19]=1)(=[O:3])[CH3:2]Participants
3
Procedure
The title compound was prepared from 3-acetyl-2-bromo-4-methyl-5-(4-pyridyl)-1H-pyrrole according to the procedure of Example 46 using 2-thienylboronic acid instead of 4-pyridylboronic acid in step 3.
Sources & evidence
- ORD record
- ord-900cf400aa59498397d9b127769a9001
- Source dataset
- uspto-grants-2002_07
- Patent number
- US06417202B1
Reaction notes
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