HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → N-(1-hexylpiperidin-4-yl)xanthene-9-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Iodohexane | HCID 12527 | — |
| Reactant | N-(piperidin-4-yl)xanthene-9-carboxamide hydrochloride | HCID 23283003 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(1-hexylpiperidin-4-yl)xanthene-9-carboxamide | HCID 11794863 | — |
Reaction Steps
60 mg of potassium carbonate and 25 ml of iodohexane were successively added to 5.0 ml of acetonitrile suspension having 50 mg of N-(piperidin-4-yl)xanthene-9-carboxamide hydrochloride, followed by reflux under heating for 4 hours. After cooled to room temperature, water was added to the reaction solution, followed by extraction with ethyl acetate and drying over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, the obtained residue was purified by preparative thin layer chromatography (Kieselgel™60F254, Art5744 produced by Merck Co.: chloroform/methanol=10/1), and 35 mg of the title compound as a white solid was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06140338 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-5d9b8530ec924490abf026fab400f5d0 |
| Source note | uspto-grants-2000_10 |