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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791855Generated: November 4, 2026

Benzenesulfonyl chloride → HCID 22033525, compound

https://huagongshe.com/reaction/1791855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantAmino-3-[2-(4-cyanophenyl)ethoxy]-2-methylbenzeneHCID 22033540—
SolventPyridineHCID 1049—
ProductHCID 22033525HCID 2203352572%

Reaction Steps

Benzenesulfonyl chloride (0.24 mL; 1.9 mmol) was added to a stirred solution of amino-3-[2-(4-cyanophenyl)ethoxy]-2-methylbenzene (0.42 g ; 1.7 mmol; from step (iii) above) in dry pyridine (20 mL) under nitrogen. The reaction was left overnight at room temperature. After evaporation of the solvent the residue was partitioned between 10% aqueous HCl and EtOAc. The organic layer was washed with brine, dried (MgSO4) and the solvent removed in vacuo. Purification by flash chromatography afforded 0.47 g (72%) of the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074820B2
Source datasetuspto-grants-2006_07
ORD IDord-e7aa3513f10e42e6a97b30503cbcad8b
Source noteuspto-grants-2006_07