HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 4-[2,6-Bis(2-pyridinyl)-4-pyrimidinyl]piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 4-Chloro-2,6-di(2-pyridinyl)pyrimidine | HCID 2767066 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-[2,6-Bis(2-pyridinyl)-4-pyrimidinyl]piperazine | HCID 15230687 | — |
Reaction Steps
4-Chloro-2,6-bis(2-pyridinyl)pyrimidine [prepared by the method of J.A.C.S. 32, 1591 (1967), 4.2 g] piperazine (13.44 g) and ethanol (70 ml) is heated at reflux for 2 hr. The mixture is allowed to cool and the solvent is removed under reduced pressure. The residue is dissolved in chloroform (250 ml), washed with water (twice), dried over sodium sulfate and concentrated under reduced pressure to give an oil. The oil is crystallized from ether to give the title compound, mp 159-161°; MS (m/e) 318 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04996318 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-98a220d9cf1d4468af85217d0f49f0cb |
| Source note | uspto-grants-1991_02 |