HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 4-(6-Fluoroquinolin-2-yl)piperazine-1-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Chloro-6-fluoroquinoline | HCID 15059433 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(6-Fluoroquinolin-2-yl)piperazine-1-carbaldehyde | HCID 58765325 | — |
Reaction Steps
A solution of 2-chloro-6-fluoroquinoline from Step D (0.8 g, 4.4 mmol) and piperazine (3.79 g, 44 mmol) in N,N-dimethylformamide (20 mL) is heated at 110° C. for 2 hours. The reaction is then basified with saturated aqueous sodium bicarbonate and extracted with ethyl acetate. The extracts are dried over anhydrous magnesium sulfate, filtered, and concentrated to give a tan oil. The oil is flash chromatographed on silica gel Merck-60 with a gradient of methanolic ammonia (5–10%) in ethyl acetate to provide the title compound (0.330 g) as an off-white solid, m.p. 110–111° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07153849B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-b54080606cc74598ab86691ec2f68e88 |
| Source note | uspto-grants-2006_12 |