HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 22414342, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 2,4-Dichloro-6-(pyrrolidin-1-yl)pyrimidine | HCID 19428524 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22414342 | HCID 22414342 | — |
Reaction Steps
A solution containing 2.0 g (9.17 mmoles) of 2,4-dichloro-6-pyrrolidinopyrimidine and 3.95 (45.9 mmoles) of piperazine in ethanol is boiled under reflux for 1 hour and then evaporated. The evaporation residue is distributed between 100 ml of chloroform and 100 ml of 1% sodium hydroxide solution. After separation the organic phase is washed twice with 50 ml of water each, then dried and evaporated. The evaporation residue is subjected to chromatography on a silica gel column. By using a 9:1 mixture of chloroform/methanol as eluent and recrystallizing the obtained product from hexane, the title compound is obtained in a yield of 1.66 g (67.6%), m.p.: 77°-92° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05510345 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-6eca85fc07104ea8b87dc92c2b5766d9 |
| Source note | uspto-grants-1996_04 |