HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15852Generated: October 23, 2026
Cesium carbonate → 2-Methyl-5-[(3R)-3-methyl-1-piperazinyl]quinoline
https://huagongshe.com/en/reaction/15852
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 2-Methylpiperazine, (R)- | HCID 7330434 | — |
| Reactant | 2-Methylquinolin-5-yl trifluoromethanesulfonate | HCID 49851899 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Methyl-5-[(3R)-3-methyl-1-piperazinyl]quinoline | HCID 57444339 | 58% |
Reaction Steps
(2R)-2-Methylpiperazine (0.550 g; 2 eq), caesium carbonate (1.78 g; 2 eq), palladium acetate (0.123 g; 0.2 eq) and 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.513 g; 0.3 eq) were added to a solution of 2-methyl-5-quinolinyl trifluoromethanesulfonate (D1) (0.8 g; 1 eq) in toluene (30 mL) under an inert atmosphere. The reaction mixture was stirred at reflux under nitrogen for 3 hours. The reaction cooled to room temperature, quenched using saturated aqueous ammonium chloride solution (15 mL) and extracted with ethyl acetate (3×20 mL). The organic layers were combined, dried over sodium sulfate and concentrated under reduced pressure. The crude was purified by flash chromatography on silica gel, eluting with dichloromethane-methanol (95:5) affording the title compound in 58% yield (0.383 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07732600B2 |
|---|
| Source dataset | uspto-grants-2010_06 |
|---|
| ORD ID | ord-cf90e6509db44c63a078279acad2d9c7 |
|---|
| Source note | uspto-grants-2010_06 |
|---|