HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 15135953, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 1-Bromopropane | HCID 7840 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 15020788 | HCID 15020788 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15135953 | HCID 15135953 | 38.1% |
Reaction Steps
A mixture of 2-(1-piperazinyl)-4-(4-fluorophenyl)-5,6,7,8,9,10-hexahydrocycloocta[b]pyridine (1.4 g), n-propyl bromide (0.56 g), potassium carbonate (0.68 g), potassium iodide (0.1 g) and methanol (50 ml) is refluxed for 15 hours. The reaction mixture is concentrated under reduced pressure and thereto is added water. The mixture is extracted with ethyl acetate, washed with water, dried over anhydrous sodium sulfate, and the solvent is distilled off under reduced pressure. To the residue is added a solution of maleic acid in ethanol, and the resulting maleate product is recrystallized from ethanol to give the dimaleate of the desired compound (0.6 g), m.p. 149°-152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05021421 |
| Source dataset | uspto-grants-1991_06 |
| ORD ID | ord-b9ec7d6e9db448fdb9d9ed1e4e07d7ad |
| Source note | uspto-grants-1991_06 |