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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715853Generated: November 2, 2026

Pyridine → 1-(5-Chloro-2-methoxy-benzenesulfonyl)-7-nitro-1,2,3,4-tetrahydro-quinoline

https://huagongshe.com/reaction/1715853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant7-Nitro-1,2,3,4-tetrahydroquinolineHCID 252513—
Reactant5-Chloro-2-methoxybenzene-1-sulfonyl chlorideHCID 2734272—
SolventDichloromethaneHCID 6344—
Product1-(5-Chloro-2-methoxy-benzenesulfonyl)-7-nitro-1,2,3,4-tetrahydro-quinolineHCID 68432739—

Reaction Steps

A solution of 5-chloro-2-methoxybenzenesulfonyl chloride (2.75 g, 11.20 mmol) in dichloromethane (0.15 L) was treated with pyridine (14.59 mL, 181.26 mmol) and a solution of 7-nitro-1,2,3,4-tetrahydro-quinoline (1.90 g, 10.66 mmol) in dichloromethane (6.00 mL). The mixture was stirred at room temperature for 120 hours, then the volatiles were evaporated. The residue was redissolved in dichloromethane and washed with water. The organic phase was dried over magnesium sulphate and evaporated. The residue was purified by flash chromatography (dichloromethane/methanol gradient) to yield 1-(5-chloro-2-methoxy-benzenesulfonyl)-7-nitro-1,2,3,4-tetrahydro-quinoline as an orange solid, 3.46 g (85%), MS (ISP): m/e=383.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799933B2
Source datasetuspto-grants-2010_09
ORD IDord-a3110554556d4e5f9b67e93e6b6e9ad9
Source noteuspto-grants-2010_09