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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036879Generated: October 31, 2026

Pyridine → HCID 56966718, compound

https://huagongshe.com/reaction/1036879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3-Fluorobenzenesulfonyl ChlorideHCID 2734258—
ReactantHCID 67290769HCID 67290769—
SolventDichloromethaneHCID 6344—
ProductHCID 56966718HCID 56966718—

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 3-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]-3-fluoro-benzenesulfonamide. LC/MS m/e obsd. (ESI−) [(M−H)−] 443.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546427B2
Source datasetuspto-grants-2013_10
ORD IDord-5d181c61d8504a75ab33edfd1aef85fa
Source noteuspto-grants-2013_10