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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928150Generated: October 31, 2026

3-(tert-Butylaminosulphonyl)benzeneboronic acid → 3'-[4-(4-Chloro-phenyl)-6-methyl-pyrimidin-2-yl]-biphenyl-3-sulfonic acid tert-butylamide

https://huagongshe.com/reaction/1928150

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(tert-Butylaminosulphonyl)benzeneboronic acidHCID 44119538—
Reactant2-(3-Bromo-phenyl)-4-(4-chloro-phenyl)-6-methyl-pyrimidineHCID 57468761—
Product3'-[4-(4-Chloro-phenyl)-6-methyl-pyrimidin-2-yl]-biphenyl-3-sulfonic acid tert-butylamideHCID 60209426—

Reaction Steps

3′-[4-(4-Chloro-phenyl)-6-methyl-pyrimidin-2-yl]-biphenyl-3-sulfonic acid tert-butylamide was prepared from 2-(3-bromo-phenyl)-4-(4-chloro-phenyl)-6-methyl-pyrimidine (example E.44) (0.11 g, 0.3 mmol) and commercially available 3-(tert.-butylsulfamoyl)-phenylboronic acid (0.09 g, 0.35 mmol) according to the general procedure VI. Obtained as a light brown solid (0.16 g), which was subsequently deprotected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183262B2
Source datasetuspto-grants-2012_05
ORD IDord-348cb51e6cf940efb9cd2b2d41b74308
Source noteuspto-grants-2012_05