Phenylboronic Acid → HCID 86607715, compound

HRID 1752902Notes

Reaction equation

HRID 1752902 reaction equation
Br[C:2]1[CH:3]=[C:4]([S:12]([NH2:15])(=[O:14])=[O:13])[CH:5]=[C:6]([CH:10]=[O:11])[C:7]=1[O:8][CH3:9].[C:16]1(B(O)O)[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>>[CH:10]([C:6]1[CH:5]=[C:4]([S:12]([NH2:15])(=[O:14])=[O:13])[CH:3]=[C:2]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[C:7]=1[O:8][CH3:9])=[O:11]

Participants

3

Reactant 2

HCID 66827Phenylboronic AcidHCID 866076983-Bromo-5-formyl-4-methoxy-benzenesulfonamide

Product 1

HCID 86607715HCID 86607715, compound

Procedure

Proceeding as in Reference 19, but substituting 3-bromo-5-formyl-4-methoxy-benzenesulfonamide and benzene boronic acid, gave 5-formyl-6-methoxy-biphenyl-3-sulfonic acid amide.

Sources & evidence

ORD record
ord-c500096ccf004f21902dbd249f2e29ef
Source dataset
uspto-grants-2015_10
Patent number
US09162986B2

Reaction notes

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