HuagongsheHuagongshe Chemistry Print Report · For research reference only
4,7-Dichloroquinoline → HCID 11670888, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4,7-Dichloroquinoline | HCID 6866 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Bis(3-aminopropyl)piperazine | HCID 81629 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11670888 | HCID 11670888 | — |
Reaction Steps
A solution of 4,7-dichloroquinoline (1.58 g, 8.0 mmol) and 1,4-bis(3-aminopropyl)piperazine (0.33 mL, 1.6 mmol) in DMF (5 mL) is refluxed (160° C.) for 18 h in the presence of K2CO3 (1.77 g, 12.8 mmol). After evaporation, the media is diluted with HCl 1M, and washed with ethyl acetate. Aqueous layer is alcalinised with NaHCO3, extracted with CH2Cl2, and dried over MgSO4. Crude compound is purified by precipitation in ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09044478B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-27e29f203d3d4ae099ebd97919962b4e |
| Source note | uspto-grants-2015_06 |