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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036928Generated: November 1, 2026

Benzenesulfonyl chloride → HCID 56966000, compound

https://huagongshe.com/reaction/1036928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantHCID 67290159HCID 67290159—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 56966000HCID 56966000—

Reaction Steps

To a solution of 2-(2-aminophenyl)-4,4-dimethyl-1,2,3,4-tetrahydroquinoline-6-carbonitrile (500 mg, 1.8 mmol) in pyridine (3 mL) was added benzenesulfonyl chloride (230 μL, 1.8 mmol) 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, concentrated. The residue was purified by HPLC to give N-[2-(6-cyano-4,4-dimethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-phenyl]-benzenesulfonamide. LC/MS m/e obsd. (ESI+) [(M+H)+] 418.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546427B2
Source datasetuspto-grants-2013_10
ORD IDord-176b907987994b79b55fabef1187360c
Source noteuspto-grants-2013_10