HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 10873565, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Tyramine | HCID 5610 | — |
| Reactant | 4,7-Dichloroquinoline | HCID 6866 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(3-chloropropyl)piperidine hydrochloride | HCID 79624 | — |
| Solvent | Phenol | HCID 996 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10873565 | HCID 10873565 | — |
Reaction Steps
Tyramine (10 mmol), 4,7-dichloroquinoline, and catalytic amounts of potassium iodide were melted in 10 g of phenol at 150° C. for 12 hours. The residue was crystallized with hydrochloric acid from ethyl acetate/water. The product (5 mmol), 3-piperidinopropylchloride hydrochloride (5 mmol), potassium carbonate (15 mmol), and catalytic amounts of potassium iodide were refluxed in N,N-dimethylformamide for 22 hours. The solvent was evaporated and the residue purified by flash chromatography (eluent: ethyl acetate/petroleum ether/triethylamine (95/50/5)). The solvent was removed under reduced pressure. The residue was crystallized with oxalic acid from diethyl ether/ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138413B1 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-5de46443d1254e38ab08dc2641ec210a |
| Source note | uspto-grants-2006_11 |