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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036933Generated: November 1, 2026

Pyridine → HCID 56966002, compound

https://huagongshe.com/reaction/1036933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantHCID 67291611HCID 67291611—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 56966002HCID 56966002—

Reaction Steps

To a solution of 2-(4,4,6-trimethyl-1,2,3,4-tetrahydroquinolin-2-yl)aniline (150 mg, 0.56 mmol) and pyridine (0.5 mL) in dichloromethane (2 mL) was added benzenesulfonyl chloride (72 μL) at ice-bath under nitrogen. After addition, the resulting mixture was stirred at room temperature for 3 h. The reaction mixture was diluted with water, and extracted with ethyl acetate. The combined organic layer was dried over anhydrous Sodium sulfate, removed the solvent under reduced pressure, the residue was purified by HPLC to give N-[2-(4,4,6-trimethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-phenyl]-benzensulfonamide LC/MS m/e obsd. (ESI+) [(M+H)+] 407.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546427B2
Source datasetuspto-grants-2013_10
ORD IDord-37da53b08962496883ee0ee70cc8face
Source noteuspto-grants-2013_10