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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928153Generated: November 1, 2026

3-(tert-Butylaminosulphonyl)benzeneboronic acid → HCID 57468900, compound

https://huagongshe.com/reaction/1928153

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(tert-Butylaminosulphonyl)benzeneboronic acidHCID 44119538—
ReactantHCID 57468763HCID 57468763—
ProductHCID 57468900HCID 57468900—

Reaction Steps

N-tert-Butyl-3-{4-[4-methyl-6-(4-trifluoromethyl-phenyl)-pyrimidin-2-yl]-pyridin-2-yl}-benzenesulfonamide was prepared from 2-(2-chloro-pyridin-4-yl)-4-methyl-6-(4-trifluoromethyl-phenyl)-pyrimidine (example E.46) (0.29 g, 0.83 mmol) and commercially available 3-(tert.-butylsulfamoyl)-phenylboronic acid (0.26 g, 1.0 mmol) according to the general procedure VI. Obtained as a light brown solid (0.23 g), which was subsequently deprotected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183262B2
Source datasetuspto-grants-2012_05
ORD IDord-689ed94d38884d67b9b0ec9664811cfa
Source noteuspto-grants-2012_05