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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504169Generated: October 25, 2026

Dichloromethane → 2-nitro-N-(2-pyridin-3-ylethyl)benzenesulfonamide

https://huagongshe.com/reaction/1504169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
Reactant2-Nitrobenzenesulfonyl chlorideHCID 15540—
Reactant2-(Pyridin-3-yl)ethan-1-amineHCID 854051—
SolventWaterHCID 962—
Product2-nitro-N-(2-pyridin-3-ylethyl)benzenesulfonamideHCID 4655653432.9%

Reaction Steps

2-Nitrobenzene sulfonyl chloride(11.64 g) was added to a dichloromethane solution (100 ml) of 3-(2-aminoethyl)pyridine(6.11 g) and triethylamine(9 ml) at 0° C. The mixture was stirred at room temperature for 2 hours. Water was added to the reaction mixture, followed by extraction with dichloromethane. The organic layer was dried with anhydrous sodium sulfate, and condensed under reduced pressure. The residue was crystallized from ethyl acetate to give the title compound(5.06 g) as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212187B2
Source datasetuspto-grants-2015_12
ORD IDord-40e95db4edd6448481d532d469a317e3
Source noteuspto-grants-2015_12