Furan-2-boronic acid → HCID 23003238, compound

HRID 396530Notes

Reaction equation

HRID 396530 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][CH:19]=[C:18](Br)[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][CH:19]=[C:18]([C:26]2[O:25][CH:29]=[CH:28][CH:27]=2)[CH:17]=1

Participants

3

Reactant 2

HCID 2734357Furan-2-boronic acidHCID 23003560Methyl[6-chloro-2-(3-bromobenzoyl)-1h-indol-3-yl]acetate

Product 1

HCID 23003238HCID 23003238, compound

Procedure

The title compound was prepared according to the procedure described in Example 207 from methyl[6-chloro-2-(3-bromobenzoyl)-1H-indol-3-yl]acetate (Example 215) and furan-2-boronic acid.

Sources & evidence

ORD record
ord-ce46f99a25724b70a6f074ce5b39d5d7
Source dataset
uspto-grants-2003_08
Patent number
US06608070B1

Reaction notes

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