Furan-2-boronic acid → HCID 23003460, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:24])[CH2:4][C:5]1[C:13]2[C:8](=[CH:9][C:10]([Cl:14])=[CH:11][CH:12]=2)[NH:7][C:6]=1[C:15](=[O:23])[C:16]1[CH:21]=[CH:20][C:19](Br)=[CH:18][CH:17]=1.[O:25]1[CH:29]=[CH:28][CH:27]=[C:26]1B(O)O>>[CH3:1][O:2][C:3](=[O:24])[CH2:4][C:5]1[C:13]2[C:8](=[CH:9][C:10]([Cl:14])=[CH:11][CH:12]=2)[NH:7][C:6]=1[C:15](=[O:23])[C:16]1[CH:21]=[CH:20][C:19]([C:26]2[O:25][CH:29]=[CH:28][CH:27]=2)=[CH:18][CH:17]=1Participants
3
Procedure
The title compound was prepared according to the procedure described in Example 207 from methyl[6-chloro-2-(4-bromobenzoyl)-1H-indol-3-yl]acetate (Example 206) and furan-2-boronic acid.
Sources & evidence
- ORD record
- ord-b990949e531944ae9741be3fa84002b7
- Source dataset
- uspto-grants-2003_08
- Patent number
- US06608070B1
Reaction notes
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