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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036885Generated: November 3, 2026

Pyridine → HCID 56966788, compound

https://huagongshe.com/reaction/1036885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
ReactantHCID 67290769HCID 67290769—
SolventDichloromethaneHCID 6344—
ProductHCID 56966788HCID 56966788—

Reaction Steps

To a stirred solution of 2-(6-chloro-4,4-dimethyl-1,2,3,4-tetrahydroquinolin-2-yl)aniline (100 mg, 0.35 mmol) in dichloromethane (5 mL) was added pyridine (0.6 mL) and 4-fluorobenzenesulfonyl chloride (68 mg, 0.35 mmol) at ice-bath. The reaction mixture was stirred at room temperature overnight. The reaction mixture was washed with water. The aqueous layer was extracted with dichloromethane. The combined organic layer was washed by brine, dried over anhydrous sodium sulfate, concentrated in vacuo. The residue was purified by HPLC to give N-[2-(6-chloro-4,4-dimethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-phenyl]-4-fluoro-benzenesulfonamide LC/MS m/e obsd. (ESI+) [(M+H)+] 445.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546427B2
Source datasetuspto-grants-2013_10
ORD IDord-7c33bd0ab9ce441a87776fd5122c0c98
Source noteuspto-grants-2013_10