HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 1-(Thiazol-2-yl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromothiazole | HCID 76430 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ammonia | HCID 222 | 28% |
| Product | 1-(Thiazol-2-yl)piperazine | HCID 911806 | 140.3% |
Reaction Steps
In 50 ml of acetonitrile was dissolved 5.0 g (0.0305 mole) of 2-bromothiazole, and 13.3 g (0.153 mole) of piperazine, 8.4 g (0.061 mole) of potassium carbonate and a catalytic amount of potassium iodide were added thereto. The mixture was refluxed by heating for 5 hours. The mixture was cooled to room temperature and then filtered. The filtrate was concentrated under reduced pressure, and the residue was applied to silica gel column chromatography (the eluent used was a mixture of chloroform: methanol : 28% aqueous ammonia = 40 : 9 : 1) to obtain 3.62 g of 1-(2-thiazolyl)piperazine as colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05519016 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-a2e35d4bbafe4ea5a1558451a6aebd19 |
| Source note | uspto-grants-1996_05 |