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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464253Generated: October 26, 2026

N,N-Dimethylethylenediamine → N-[2-(dimethylamino)ethyl]-2-(5-methYl-2-thienyl)-4-quinolinamine

https://huagongshe.com/reaction/1464253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylethylenediamineHCID 66053—
ReactantN-[1-(5-Methyl-2-thienyl)ethylidene]-2-(trifluoromethyl)anilineHCID 19087626—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductN-[2-(dimethylamino)ethyl]-2-(5-methYl-2-thienyl)-4-quinolinamineHCID 1908762882%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05304554
Source datasetuspto-grants-1994_04
ORD IDord-634a4a160f614b9b88dec3304b3db6dc
Source noteuspto-grants-1994_04