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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643902Generated: October 31, 2026

Benzenesulfonyl chloride → N-(1-Benzenesulfonyl-6-bromo-1,2,3,4-tetrahydroquinolin-3-yl)-benzenesulfonamide

https://huagongshe.com/reaction/1643902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantN-(6-Bromo-1,2,3,4-tetrahydroquinolin-3-yl)-benzenesulfonamideHCID 18177113—
SolventPyridineHCID 1049—
ProductN-(1-Benzenesulfonyl-6-bromo-1,2,3,4-tetrahydroquinolin-3-yl)-benzenesulfonamideHCID 5977814593%

Reaction Steps

To a solution of compound 87A (98 mg, 0.299 mmol) in pyridine (3 mL) was added benzenesulfonyl chloride (0.042 mL, 0.33 mmol). The mixture was stirred at RT overnight, then concentrated. The residue was chromatographed (10 g silica gel) eluting with EtOAc (0-60%) in hexane to give the title compound (140 mg, 93%) as a white foam. HPLC: 99% at 7.06 min (retention time) (Conditions: Zorbax SB C18 (4.6×75 mm); Eluted with 0% to 100% B, 8 min gradient. (A=90% H2O−10% MeOH−0.1% H3PO4 and B=10% H2O−90% MeOH−0.1% H3PO4); Flow rate at 2.5 mL/min. UV detection at 220 nm). MS (ES): m/z 529 [M+Na]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119808B2
Source datasetuspto-grants-2012_02
ORD IDord-5530bb27f8f643df927ca663963f44f9
Source noteuspto-grants-2012_02