HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → Methyl 6-(piperazin-1-yl)pyridine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Methyl 6-bromopyridine-3-carboxylate | HCID 13349623 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 6-(piperazin-1-yl)pyridine-3-carboxylate | HCID 14987928 | 56% |
Reaction Steps
A mixture of 2-bromopyridine-5-carboxylic acid methyl ester (1.40 g, 6.5 mmol) and piperazine (5.59 g, 65 mmol) was dissolved in acetonitrile (50 ml) and heated at reflux temperature for 2.5 h. The reaction mixture was concentrated in vacuo, dissolved in dichloromethane (50 ml) and extracted with water (3×50 ml). The organic solution was dried (MgSO4) and evaporated in vacuo, affording 0.80 g (56%) of 2-(1-piperazinyl)-5-pyridinecarboxylic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06133268 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-2317f5255dca4a91bef9ffbdca3ae0cc |
| Source note | uspto-grants-2000_10 |