HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluorophenyl isocyanate → 6-Chloro-4-[4-(4-fluorophenylaminocarbonyl)piperazin-1-yl]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluorophenyl isocyanate | HCID 70955 | — |
| Reactant | 6-Chloro-4-(piperazin-1-yl)quinoline | HCID 11470651 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Chloro-4-[4-(4-fluorophenylaminocarbonyl)piperazin-1-yl]quinoline | HCID 21101736 | — |
Reaction Steps
6-Chloro-4-(piperazin-1-yl)quinoline (0.25 g, 1.0 mmol), 4-fluorophenyl isocyanate (170 μL, 1.5 mmol), and DMAP (2 mg) in THF (10 mL) are reacted according to method C yielding the product as a colorless solid after column chromatography with hexane-EtOAc. 1H NMR ([D]6-DMSO), δ 3.17 (m, 4H), 3.75 (m, 4H), 7.08 (t, 2H), 7.10 (d, 1H), 7.46 (dd, 2H), 7.72 (dd, 1H), 7.98 (d, 1H), 8.01 (d, 1H), 8.68 (br. s, 1H), 8.72 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07220856B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-02797a29beb744f98af12ba6c8cd9b69 |
| Source note | uspto-grants-2007_05 |