HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 10442842, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Phosphate | HCID 1061 | — |
| Product | HCID 10442842 | HCID 10442842 | 12% |
Reaction Steps
A solution of nicotinaldehyde (5.1 ml, 54 mmol) in methanol (60 ml) was added to a stirred solution of piperazine (14.0 g, 160 mmol) and potassium cyanide (5.4 g, 83 mmol) in water (60 ml) and 1M phosphate buffer solution (pH 7.3: 60 ml). The reaction mixture was stirred for 48 h at ambient temperature and partitioned between water (80 ml) and ethyl acetate (2×100 ml). The organics were dried over anhydrous sodium sulphate, filtered and concentrated. Chromatography (silica gel: 2% methanol in DCM) gave 4-(3-pyridylcyanomethyl)piperazine (1.3 g, 12%) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05563151 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-2bb39cd28e814303b96846ec8ca244ea |
| Source note | uspto-grants-1996_10 |