HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 4-Chloro-6-(1-piperazinyl)-2-pyrrolidinopyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 4,6-Dichloro-2-(pyrrolidin-1-yl)pyrimidine | HCID 19353553 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Chloro-6-(1-piperazinyl)-2-pyrrolidinopyrimidine | HCID 22414345 | — |
Reaction Steps
A solution of 2.0 g (9.17 mmoles) of 4,6-dichloro-2-pyrrolidinopyrimidine and 3.95 g (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 twice washed with 50 ml of water each, then dried and evaporated. After recrystallizing the residue from hexane, the title product is obtained in a yield of 2.25 g (91.6%), m.p. 89°-100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05510345 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-d5fb2802070e42879c1aa71a8a010a51 |
| Source note | uspto-grants-1996_04 |