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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928415Generated: November 2, 2026

3-(tert-Butylaminosulphonyl)benzeneboronic acid → HCID 57469065, compound

https://huagongshe.com/reaction/1928415

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(tert-Butylaminosulphonyl)benzeneboronic acidHCID 44119538—
ReactantHCID 57468793HCID 57468793—
ProductHCID 57469065HCID 57469065—

Reaction Steps

N-tert-Butyl-3-{1-[6-(4-fluoro-phenyl)-4-trifluoromethyl-pyrimidin-2-yl]-1H-imidazol-4-yl}-benzenesulfonamide was prepared from 4-(4-fluoro-phenyl)-2-(4-iodo-imidazol-1-yl)-6-trifluoromethyl-pyrimidine (example E.79) (0.25 g, 0.57 mmol) and commercially available 3-(tert.-butylsulfamoyl)-phenylboronic acid (0.175 g, 0.68 mmol) according to the general procedure VI. Obtained as a light yellow solid (0.52 g) which was subsequently deprotected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183262B2
Source datasetuspto-grants-2012_05
ORD IDord-21115a33111e413e8fc711d41c74bfb3
Source noteuspto-grants-2012_05