HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Piperidin-1-yl)aniline → n-[4-(1-Piperidinyl)phenyl]benzo[g]quinolin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Piperidin-1-yl)aniline | HCID 413501 | — |
| Reactant | 4-Chlorobenzo[g]quinoline | HCID 12407978 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | n-[4-(1-Piperidinyl)phenyl]benzo[g]quinolin-4-amine | HCID 2832014 | 85% |
Reaction Steps
4-Chlorobenzo[g]quinoline (7b) (50 mg, 0.23 mmol), 4-(1-piperidino) aniline (50 mg, 1.2 equivalents), bis(1,5-cyclooctadiene)nickel(O) (Ni(COD)2 1.5 mg, 0.02 equivalents), 1,1′-bis(diphenylphosphino)ferrocene (DPPF, 5 mg, 0.04 equivalents) and sodium t-butoxide (31 mg, 1.4 equiv) in 2.5 mL of dry toluene were refluxed under a 5 nitrogen atmosphere until observed complete by TLC. The mixture was concentrated in vacuo and purified by flash chromatography (gradient: 50:50:2 to 60:40:2 hexane: EtOAc:Et3N) to provide 69 mg of clean N-[4-(1-piperidinyl)phenyl]benzo[g]quinolin-4-amine (8), 85% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06274596B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-b35d11d2e2b7495894e00c5ac057f4eb |
| Source note | uspto-grants-2001_08 |