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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989615Generated: October 30, 2026

3-(tert-Butylaminosulphonyl)benzeneboronic acid → HCID 57469042, compound

https://huagongshe.com/reaction/1989615

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(tert-Butylaminosulphonyl)benzeneboronic acidHCID 44119538—
ReactantHCID 57468808HCID 57468808—
ProductHCID 57469042HCID 57469042—

Reaction Steps

The N-tert-butyl-3-{4-[4-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-2-yl]-pyrimidin-2-yl}-benzenesulfonamide was prepared from 2-chloro-4-[4-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-2-yl]-pyrimidine (example E.97) (0.350 g, 1.0 mmol) and commercially available 3-(tert-butylsulfamoyl)-benzeneboronic acid (0.283 g, 1.1 mmol) according to the general procedure VI. Obtained as a white solid (0.400 g, 76%). MS (ISP) 527.2 [(M+H)+]; mp 218° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642264B2
Source datasetuspto-grants-2010_01
ORD IDord-65360aad530248deb0c311e13f6685a6
Source noteuspto-grants-2010_01