HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 1-{3-[4-[Bis(4-fluorophenyl)methylene]piperidino]propyl}-4-(2-pyrimidinyl)piperazine dihydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Bis(4-fluorophenyl)methylene)piperidine | HCID 2724436 | — |
| Reactant | 3-[4-(2-Pyrimidinyl)piperazinyl]propyl chloride | HCID 14882737 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | 1-{3-[4-[Bis(4-fluorophenyl)methylene]piperidino]propyl}-4-(2-pyrimidinyl)piperazine dihydrochloride | HCID 19915783 | — |
Reaction Steps
A mixture of 0.89 g of 1-(3-chloropropyl)-4-(2-pyrimidinyl)piperazine, 0.80 g of 4-[bis(4-fluorophenyl)methylene]piperidine and 0.51 g of potassium carbonate in 30 ml of 4-methyl-2-pentanone is brought to reflux for 48 hours in the presence of a trace of potassium iodide. The solvent is evaporated off and the residue is taken up in dichloromethane. The solution is washed with water. It is concentrated. The residue obtained is purified on a silica column using a mixture of dichloromethane and methanol (80:20 V/V) as eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05071847 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-cdf4ecfb43b6478e81a937b37aff5d71 |
| Source note | uspto-grants-1991_12 |