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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372883Generated: October 30, 2026

1-((6-Chloronaphthalen-2-yl)sulfonyl)piperazine → 1-(6-Chloronaphthalene-2-sulfonyl)-4-(6-chloropyridazin-3-ylcarbonyl)piperazine

https://huagongshe.com/reaction/1372883

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-((6-Chloronaphthalen-2-yl)sulfonyl)piperazineHCID 11358825—
Reactant6-Chloropyridazine-3-carbonyl chlorideHCID 21781185—
SolventPyridineHCID 1049—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product1-(6-Chloronaphthalene-2-sulfonyl)-4-(6-chloropyridazin-3-ylcarbonyl)piperazineHCID 2107267476.4%

Reaction Steps

To a solution of 1-(6-chloronaphthalen-2-ylsulfonyl)-piperazine (0.450 g, 1.45 mmol) in methylene chloride (100 mL) and pyridine (0.154 mL) was added dropwise 6-chloropyridazine-3-carbonyl chloride (1.74 mmol). After the addition of the acid chloride, pyridine (0.154 mL) was added, and the reaction mixture was stirred overnight. The reaction mixture was diluted with chloroform (500 mL), washed with saturated sodium bicarbonate (200 mL), water (200 mL),and brine and dried over MgSO4. After filtration and evaporation of the solvent, trituration of the residue with ethyl acetate and filtration gave the product as a white powder (0.5 g, 76%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160878B2
Source datasetuspto-grants-2007_01
ORD IDord-c2732702d5f64975b55e9c81357befb9
Source noteuspto-grants-2007_01