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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1962907Generated: October 25, 2026

3-(tert-Butylaminosulphonyl)benzeneboronic acid → N-tert-Butyl-3-{1-[4-(5-chloro-thiophen-2-yl)-6-trifluoromethyl-pyrimidin-2-yl]-1H-imidazol-4-yl}-benzenesulfonamide

https://huagongshe.com/reaction/1962907

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(tert-Butylaminosulphonyl)benzeneboronic acidHCID 44119538—
Reactant4-(5-Chloro-thiophen-2-yl)-2-(4-iodo-imidazol-1-yl)-6-trifluoromethyl-pyrimidineHCID 67393367—
ProductN-tert-Butyl-3-{1-[4-(5-chloro-thiophen-2-yl)-6-trifluoromethyl-pyrimidin-2-yl]-1H-imidazol-4-yl}-benzenesulfonamideHCID 67393551—

Reaction Steps

N-tert-Butyl-3-{1-[4-(5-chloro-thiophen-2-yl)-6-trifluoromethyl-pyrimidin-2-yl]-1H-imidazol-4-yl}-benzenesulfonamide was prepared from 4-(5-chloro-thiophen-2-yl)-2-(4-iodo-imidazol-1-yl)-6-trifluoromethyl-pyrimidine (example B.1) (0.46 g, 1.0 mmol) and commercially available 3-(tert.-butylsulfamoyl)-phenylboronic acid (0.28 g, 1.1 mmol) according to the general procedure III. Obtained as a light yellow solid (0.3 g) which was subsequently deprotected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415380B2
Source datasetuspto-grants-2013_04
ORD IDord-8d74063893524b59857bc1f64639e47f
Source noteuspto-grants-2013_04