HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21114528, compound → 1-(4-Cyanophenyl)-4-(5-aminopyridin-2-yl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21114528 | HCID 21114528 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(4-Cyanophenyl)-4-(5-aminopyridin-2-yl)piperazine | HCID 21114527 | 74.6% |
Reaction Steps
10% Palladium on carbon (25 mg, 0.024 mmol) was added to a stirred suspension of 1-(4-cyanophenyl)-4-(5-nitropyridin-2-yl)-piperazine (150 mg, 0.48 mmol) in ethanol (50 ml) at ambient temperature and the reaction stirred for 6 hours under an atmosphere of hydrogen. The reaction was filtered through a pad of celite and the solvent evaporated in vacuo. Purification by flash chromatography on alumina, eluting with 0.5% methanol in dichloromethane yielded 1-(4-cyanophenyl)-4-(5-aminopyridin-2-yl)piperazine (100 mg, 74% yield):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07235559B1 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-9b005675e71c476f8db285db7a1ef8e7 |
| Source note | uspto-grants-2007_06 |