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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75991Generated: October 26, 2026

4-(2-Methylbutan-2-yl)benzene-1-sulfonyl chloride → n-(4-Chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenyl)-4-(1,1-dimethyl-propyl)-benzenesulfonamide

https://huagongshe.com/reaction/75991

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Methylbutan-2-yl)benzene-1-sulfonyl chlorideHCID 22281976—
Reactant4-Chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenylamineHCID 59428114—
SolventPyridineHCID 1049—
Productn-(4-Chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenyl)-4-(1,1-dimethyl-propyl)-benzenesulfonamideHCID 25135042—

Reaction Steps

A 4 mL scintillation vial was charged with 4-chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenylamine (100 mg, 0.363 mmol), 4-(1,1-dimethyl-propyl)-benzenesulfonyl chloride (98 g, 0.399 mmol), and pyridine (1 mL). The resultant solution was stirred 4 hours at 80° C. and then partitioned with EtOAc/1 M HCl. The organics were subsequently washed with 1 M HCl, saturated aqueous sodium bicarbonate, and brine; dried over anhydrous sodium sulfate; and removed in vacuo. The resultant residue was then purified via automated silica gel chromatography to afford the desired sulfonamide: MS (ES) M+H expected 456.2, found 456.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835468B2
Source datasetuspto-grants-2014_09
ORD IDord-675f9c9f37914158a540573c6559152c
Source noteuspto-grants-2014_09