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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989595Generated: October 31, 2026

3-(tert-Butylaminosulphonyl)benzeneboronic acid → N-tert-Butyl-3-[6-methyl-4-(4-trifluoromethyl-phenyl)-[2,3']bipyridinyl-5'-yl]-benzenesulfonamide

https://huagongshe.com/reaction/1989595

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(tert-Butylaminosulphonyl)benzeneboronic acidHCID 44119538—
Reactant5'-Bromo-6-methyl-4-(4-trifluoromethylphenyl)-[2,3']bipyridinylHCID 68692484—
ProductN-tert-Butyl-3-[6-methyl-4-(4-trifluoromethyl-phenyl)-[2,3']bipyridinyl-5'-yl]-benzenesulfonamideHCID 24760815—

Reaction Steps

The title compound was prepared from 5′-bromo-6-methyl-4-(4-trifluoromethylphenyl)-[2,3′]bipyridinyl (example E.24) (0.200 g, 0.5 mmol) and commercially available 3-(tert-butylsulfamoyl)-benzeneboronic acid (0.157 g, 0.6 mmol) according to the general procedure VI. Obtained as an off-white solid (0.182 g, 68%). MS (ISP) 526.3 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642264B2
Source datasetuspto-grants-2010_01
ORD IDord-4a47146d6d6444f0956cc98d2180dcd3
Source noteuspto-grants-2010_01