HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 3-[1-(2-Dimethylaminoethyl)-4-piperidyl]-1,2-benzisoxazole difumarate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 2-Chloro-N,N-dimethylethylamine | HCID 7901 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Fumaric Acid | HCID 444972 | — |
| Reactant | 3-(Piperidin-4-yl)benzo[d]isoxazole | HCID 13076436 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-[1-(2-Dimethylaminoethyl)-4-piperidyl]-1,2-benzisoxazole difumarate | HCID 13076443 | 31.6% |
Reaction Steps
A suspension of 4.5 g of 3-(4-piperidyl)-1,2-benzisoxazole, 2.6 g of 2-dimethylaminoethyl chloride, 3.0 g of potassium iodide and 5.0 g of potassium carbonate in 100 ml of butanol was heated under reflux for 2 hrs, cooled to room temperature and filtered. The filtrate was washed with water and extracted with ether (3 times). The ether extracts were dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure to give an oil. The oil was dissolved in 10 ml of acetonitrile and 3.2 g of fumaric acid was added. The reaction mixture was stirred for 2 hrs, filtered and the filter cake was recrystallized three times from ethanol-ether to give 2.2 g (19.8%) of product, mp, 215°-217°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04355037 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-4891782c96f842faa3f389ab153f3d4a |
| Source note | uspto-grants-1982_10 |