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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542828Generated: October 26, 2026

Triethylamine → 6-[(6-Methoxy-4-methyl-8-quinolinyl)amino]-1-hexanol

https://huagongshe.com/reaction/542828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant6-Chloro-1-hexanolHCID 74828—
Reactant6-Methoxy-4-methyl-8-quinolinamineHCID 604753—
ReactantChlorohexanolHCID 12768704—
SolventAcetoneHCID 180—
Product6-[(6-Methoxy-4-methyl-8-quinolinyl)amino]-1-hexanolHCID 1307753155.5%

Reaction Steps

To a stirred mixture of 1.9 g (0.01 mole) of 6-methoxy-4-methyl-8-quinolinamine and 1.4 g (0.01 mole) of 6-chlorohexanol at 150° was added portionwise over one hr 1.4 ml (0.01 mole) of triethylamine. The mixture was stirred for 1 hr at the same temperature, and then 0.8 g (0.0056 mole) of 1-chlorohexanol was added, followed by the portionwise addition of 0.8 (0.0056 mole) of triethylamine. The mixture was stirred for 1 hr and the procedure was repeated with 0.5 g (0.0037 mole) of 1-chlorohexanol and 0.5 ml of triethylamine. After the mixture was stirred an additional hr, the mixture was allowed to cool, diluted with acetone, filtered, and concentrated to dryness in vacuo. The residue was dissolved in dichloromethane and chromatographed over 70 g of silica gel first with 500 ml of dichloromethane and then with the following solutions of ethyl acetate in dichloromethane: 5% (500 ml), 10% (1 liter), 15% (500 ml), and finally 20% (500 ml). Fractions of the 20% eluant containing the product, Rf(silica--ethyl acetate)=0.3, were combined and concentrated to dryness in vacuo. Recrystallization from 2-propanol afforded 1.6 g (55%) of the title compound, mp 97°-99°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04659708
Source datasetuspto-grants-1987_04
ORD IDord-36d900ce57a04747b519e497255e2464
Source noteuspto-grants-1987_04