HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-((6-Chloronaphthalen-2-yl)sulfonyl)piperazine → 1-(6-Chloronaphthalene-2-sulfonyl)-4-(6-chloropyridazin-3-ylcarbonyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-((6-Chloronaphthalen-2-yl)sulfonyl)piperazine | HCID 11358825 | — |
| Reactant | 6-Chloropyridazine-3-carbonyl chloride | HCID 21781185 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(6-Chloronaphthalene-2-sulfonyl)-4-(6-chloropyridazin-3-ylcarbonyl)piperazine | HCID 21072674 | 76.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07160878B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-c2732702d5f64975b55e9c81357befb9 |
| Source note | uspto-grants-2007_01 |