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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883534Generated: November 1, 2026

4-(4-Pyridyloxy)benzenesulfonyl chloride → 5-Methyl-4-[4-(pyridin-4-yloxy)-benzenesulfonylamino]-biphenyl-3-carboxylic acid methyl ester

https://huagongshe.com/reaction/1883534

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Pyridyloxy)benzenesulfonyl chlorideHCID 2735258—
Reactant4-Amino-5-methyl-biphenyl-3-carboxylic acid methyl esterHCID 54207530—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
Product5-Methyl-4-[4-(pyridin-4-yloxy)-benzenesulfonylamino]-biphenyl-3-carboxylic acid methyl esterHCID 5445305990.3%

Reaction Steps

To a solution of 1.43 g (5.93 mmol) of the product of Example 40 in 20 mL of pyridine was added 1.98 g (6.52 mmol) 4-(pyridin-4-yloxy)-benzenesulfonyl chloride and the reaction was stirred overnight. Additional 4-(pyridin-4-yloxy)-benzenesulfonyl chloride (0.5 g, 1.6 mmol) was added twice over the next two days. The reaction was then diluted with water and extracted three times with dichloromethane. The organics were combined, washed with brine, dried over Na2SO4, concentrated in vacuo and chromatographed on silica gel using gradient elution (100% hexane to 100% ethyl acetate) to provide 5-methyl-4-[4-(pyridin-4-yloxy)-benzenesulfonylamino]-biphenyl-3-carboxylic acid methyl ester 2.54 g (90%) as a white solid. Electrospray Mass Spec: 475.2 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06762178B2
Source datasetuspto-grants-2004_07
ORD IDord-d9385a2b74e04c7daec4314f236b3d54
Source noteuspto-grants-2004_07