HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroquinoline → 1-(2-(2-Quinolinylamino)ethyl)-4-(2-methoxyphenyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroquinoline | HCID 11928 | — |
| Reactant | 1-(2-Aminoethyl)-4-(2-methoxyphenyl)piperazine | HCID 10399186 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 1-(2-(2-Quinolinylamino)ethyl)-4-(2-methoxyphenyl)piperazine | HCID 23290959 | 12.4% |
Reaction Steps
1-(2-aminoethyl)-4-(2-methoxyphenyl)piperazine (9.4 g, 40 mmol) and 2-chloroquinoline (6.5 g, 40 mmol) were heated at 160° C. for 3 h, then at 120° C. for 18 h in a sealed vessel. The resultant brown tar was taken up into dilute hydrochloric acid (300 ml), washed with dichloromethane (3×100 ml) basified with sodium hydroxide, extracted into dichloromethane (3×100 ml), dried (MgSO4) then evaporated in vacuo to give a brown oil. The oil was purified by chromatography [alumina; ethyl acetate-toluene (1:4)] to give the product (1.8 g) as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06127357 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-2e3029fcef974cf897be40ffa1ed8faf |
| Source note | uspto-grants-2000_10 |