HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-(12-Tosyloxydodecyl)-6-(4-ethyl-1-piperazinyl)pyridine-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | N-(12-hydroxydodecyl)-6-(4-ethyl-1-piperazinyl)pyridine-3-carboxamide | HCID 15462624 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(12-Tosyloxydodecyl)-6-(4-ethyl-1-piperazinyl)pyridine-3-carboxamide | HCID 15462633 | 76.2% |
Reaction Steps
To a suspension of 210 mg of N-(12-hydroxydodecyl)-6-(4-ethyl-1-piperazinyl)pyridine-3-carboxamide in 10 ml of methylene chloride were added 0.03 ml of pyridine, 115 mg of tosyl chloride and a catalytic amount of 4-dimethylaminopyridine and the mixture was stirred at room temperature for one hour. The reaction solution was washed with water and a saturated aqueous solution of sodium chloride and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue thus obtained was chromatographed over a silica gel column to afford 219 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06046201 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-4f7a1027276546e9818b5c44e911e1fe |
| Source note | uspto-grants-2000_04 |