HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 1-pyrimidin-2-yl-1,4-diazepane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Hexahydro-1,4-diazepine | HCID 68163 | — |
| Reactant | 2-Chloropyrimidine | HCID 74404 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-pyrimidin-2-yl-1,4-diazepane | HCID 2772409 | 48% |
Reaction Steps
50 ml of acetonitrile was added to 10.0 g (0.1 mole) of homopiperazine, 2.9 g (0.025 mole) of 2-chloropyrimidine, 6.9 g (0.05 mole) of potassium carbonate and a catalytic amount of potassium iodide, and the mixture was refluxed under heating for 11 hours. The mixture was cooled to room temperature and then filtered, the filtrate obtained was concentrated under reduced pressure, and the residue was applied to silica gel column chromatography (eluent; a chloroform:methanol=8:2 mixed solution) to obtain 2.14 g of 1-(2-pyrimidyl)homopiperazine as a pale yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06034086 |
| Source dataset | uspto-grants-2000_03 |
| ORD ID | ord-dd1f95b2fd884e55b18f349aa1d75c39 |
| Source note | uspto-grants-2000_03 |