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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490559Generated: October 31, 2026

3-Chlorobenzenesulphonyl chloride → HCID 11524825, compound

https://huagongshe.com/reaction/490559

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chlorobenzenesulphonyl chlorideHCID 17909—
ReactantHCID 68833576HCID 68833576—
SolventPyridineHCID 1049—
ProductHCID 11524825HCID 1152482551.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 5-amino-1-(4-fluoro-benzyl)-1,2-dihydro-indazol-3-one (0.100 g) in pyridine (1 mL) was added 3-chlorobenzenesulfonylchoride (0.082 g) in one go. The solution was stirred at 60° C. for 24 hours. The pyridine was then removed in vacuo and the residue was dissolved in EtOAc/water and separated. The aqueous phase was extracted a further two times with EtOAc and the combined organic phases were washed with brine and dried over sodium sulfate. The drying agent was removed by filtration and the volatiles were removed in vacuo to afford a crude residue. The crude material was purified via flash column chromatography eluting with EtOAc/nHeptane/1% AcOH) to afford the desired 3-chloro-N-[1-(4-fluoro-benzyl)-3-oxo-2,3-dihydro-1H-indazol-5-yl]-benzenesulfonamide (0.087 g) as a brown solid. MS (ESI+): 432.4 [M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528158B2
Source datasetuspto-grants-2009_05
ORD IDord-e21b954b15c2446795a73a2586d134c1
Source noteuspto-grants-2009_05