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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490553Generated: October 30, 2026

3-Chloro-2-methylbenzenesulfonyl chloride → HCID 11704612, compound

https://huagongshe.com/reaction/490553

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-2-methylbenzenesulfonyl chlorideHCID 522734—
ReactantHCID 68730847HCID 68730847—
SolventPyridineHCID 1049—
ProductHCID 11704612HCID 1170461221%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 5-amino-1-benzyl-1,2-dihydro-indazol-3-one (0.04 g) in pyridine (1 mL) was added 3-chloro-2-methylbenzenesulfonylchoride (0.038 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 N-(1-benzyl-3-oxo-2,3-dihydro-1H-indazol-5-yl)-3-chloro-2-methyl-benzenesulfonamide (0.015 g) as a pale yellow powder. MS (ESI+): 428.4 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528158B2
Source datasetuspto-grants-2009_05
ORD IDord-e1f37606be9b48149e3741692025f0a5
Source noteuspto-grants-2009_05