HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethylethylenediamine → N-[2-(dimethylamino)ethyl]-2-(5-methYl-2-thienyl)-4-quinolinamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethylethylenediamine | HCID 66053 | — |
| Reactant | N-[1-(5-Methyl-2-thienyl)ethylidene]-2-(trifluoromethyl)aniline | HCID 19087626 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-[2-(dimethylamino)ethyl]-2-(5-methYl-2-thienyl)-4-quinolinamine | HCID 19087628 | 82% |
Reaction Conditions
| Temperature | -10 °C |
|---|
Reaction Steps
A solution of N,N-dimethylethylenediamine (0.66 ml, 6.0 mmol) in ether (15 mL) was treated with a commercial solution of n-butyllithium (6.0 mmol) in hexanes at -10° C., and the resultant mixture was stirred at -10° C. for 20 minutes before treatment with a solution of ketimine 12q (0.42 g, 1.5 mmol) in ether (5 mL). The mixture was stirred at -10° C. for an additional 45 minutes, and then quenched with water (0.5 mL). The organic layer was concentrated on a rotary evaporator to give a crystalline residue. Removal of colored polymeric materials on a short silica gel column by eluting quinoline 9g with hexanes/Et3N/EtOH (7:2:1) was followed by crystallization of the purified 9g from hexanes; yield 82%, mp 103°-105° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05304554 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-634a4a160f614b9b88dec3304b3db6dc |
| Source note | uspto-grants-1994_04 |