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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928505Generated: November 2, 2026

3-(tert-Butylaminosulphonyl)benzeneboronic acid → HCID 57469127, compound

https://huagongshe.com/reaction/1928505

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(tert-Butylaminosulphonyl)benzeneboronic acidHCID 44119538—
ReactantHCID 57468734HCID 57468734—
ProductHCID 57469127HCID 57469127—

Reaction Steps

N-tert-Butyl-3-{4-[4-difluoromethyl-6-(4-trifluoromethyl-phenyl)-pyrimidin-2-yl]-pyridin-2-yl}-benzenesulfonamide was prepared from 2-(2-chloro-pyridin-4-yl)-4-difluoromethyl-6-(4-trifluoromethyl-phenyl)-pyrimidine (example E.10) (0.43 g, 1.11 mmol) and commercially available 3-(tert.-butylsulfamoyl)-phenylboronic acid (0.31 g, 1.21 mmol) according to the general procedure VI. Obtained as a light brown solid (0.37 g), which was subsequently deprotected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183262B2
Source datasetuspto-grants-2012_05
ORD IDord-5990ccdaabc94fc2a37f8f6809816afb
Source noteuspto-grants-2012_05