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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12160Generated: October 30, 2026

(2-{[4-(2-([(tert-butyl)amino]sulfonyl}phenyl)phenyl]carbonylamino}-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamide → N-(5-chloro(2-pyridyl))(5-chloro-2-([4-(2-sulfamoylphenyl)-phenyl]carbonylamino}phenyl)-carboxamide

https://huagongshe.com/reaction/12160

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-{[4-(2-([(tert-butyl)amino]sulfonyl}phenyl)phenyl]carbonylamino}-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamideHCID 131723193—
SolventTrifluoroacetic acidHCID 6422—
ProductN-(5-chloro(2-pyridyl))(5-chloro-2-([4-(2-sulfamoylphenyl)-phenyl]carbonylamino}phenyl)-carboxamideHCID 2259629725%

Reaction Steps

The mixture of the compound of (2-{[4-(2-{[(tert-butyl)amino]sulfonyl}phenyl)phenyl]carbonylamino}-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamide example 12 (0.5 mmol) in trifluoroacetic acid (5 ml) was stirred at r.t. for 5 hrs. After the evaporation of solvent, the crude residue was purified by RP-HPLC to give N-(5-chloro(2-pyridyl))(5-chloro-2-{[4-(2-sulfamoylphenyl)-phenyl]carbonylamino}phenyl)-carboxamide as a white powder (68 mg, 25%). MS found for C25H18Cl2N4O4S

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727981B2
Source datasetuspto-grants-2010_06
ORD IDord-51b3463d197f4d3383bc60335e37cfca
Source noteuspto-grants-2010_06