HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → HCID 14986606, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzhydrylpiperazine | HCID 70048 | — |
| Reactant | HCID 14986591 | HCID 14986591 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 14986606 | HCID 14986606 | — |
Reaction Steps
Under reflux for 4 hours is placed a mixture of 6.3 g (25 mmoles) of diphenylmethyl piperazine, 6.87 g (25 mmoles) of 1-(4-bromobutyl)-4-ethyloxycarbonylpyrazole, 5.17 g (37.5 moles) of potassium carbonate and 5.06 g (33.7 mmoles) of sodium iodide in 100 ml of methyl ethyl ketone. It is cooled, filtered and the filtrate evaporated to dryness. The residue is taken up again with chloroform and water, the organic phase is dried with Na2SO4, it is filtered and evaporated under vacuum. The resulting product is purified on a chromatographic silica column (eluant: chloroform-methanol 95:5) and in this way 7.4 g of 1-[4-(4-Diphenylmethyl-1-piperazinyl)butyl]-4-ethyloxycarbonylpyrazole is obtained, with a melting point 70°-74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05166205 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-46c75c5b820a4dad9b3a1c37754b7441 |
| Source note | uspto-grants-1992_11 |