Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(2-Pyridyl)piperazine | HCID 94459 | — |
| Reactant | Benzenesulfinyl chloride | HCID 4190003 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70505000 | HCID 70505000 | — |
Reaction Steps
To a solution of 4.90 g of 1-(2-pyridyl)piperazine in 150 ml of dichloromethane containing 4.59 ml of triethylamine is added dropwise with stirring under nitrogen a solution of 4.82 g of benzenesulfinyl chloride in 50 ml of dichloromethane. The reaction mixture is stirred for 3 hours at room temperature, diluted with 100 ml of dichloromethane, and washed with 150 ml water and 100 ml 5% potassium carbonate. The organic layer is dried over sodium sulfate and evaporated in vacuo to give a yellow crystalline solid. Recrystallization from ethanol affords 4.14 g of 1-(2-pyridyl)piperazine-4-benzenesulfinamide as a colorless crystalline solid, mp 83°-86° (soften 81°). A second crop (1.24 g) is obtained by concentration of the mother liquors, total yield: 5.38 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04425342 |
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| Source dataset | uspto-grants-1984_01 |
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| ORD ID | ord-5e181d8ac2d640989759296c90997302 |
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| Source note | uspto-grants-1984_01 |
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