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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542854Generated: November 2, 2026

Triethylamine → N-(6-Methoxy-4-methyl-8-quinolinyl)-2,6-dimethyl-4-morpholinehexanamide

https://huagongshe.com/reaction/542854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,6-DimethylmorpholineHCID 110862—
Reactant6-Bromo-N-(6-methoxy-4-methyl-8-quinolinyl)hexanamideHCID 612023—
SolventBenzeneHCID 241—
ProductN-(6-Methoxy-4-methyl-8-quinolinyl)-2,6-dimethyl-4-morpholinehexanamideHCID 1385336255.1%

Reaction Steps

A mixture of 5.5 g (0.015 mole) of 6-bromo-N-(6-methoxy-4-methyl-8-quinolinyl)hexanamide and 1.85 ml (0.018 mole) of 2,6-dimethylmorpholine in 90 ml of benzene was heated under reflux for 24 hr. Triethylamine (2 ml) was added and the mixture was heated under reflux for an additional 2 hr, allowed to cool, and filtered. The filtrate was washed with water, dried and concentrated. TLC(silica gel--ethyl acetate) demonstrated a mixture of the unchanged bromo compound, Rf(silica--ethyl acetate)=0.63, and the product, Rf=0.08. A solution of the residue, 1.3 ml (0.01 mole) of 2,6-dimethylmorpholine, and 1.5 ml of triethylamine in 80 ml of benzene was heated under reflux for 40 hr, allowed to cool, filtered, washed with water, dried and concentrated. The residue was chromatographed over 200 g of silica gel with 1 liter each of the following solutions of methanol in ethyl acetate: 1.5%, 2%, 3% to afford 3.7 g of crude product. Recrystallization from hexane afforded 3.3 g of the title compound, mp 87°-90°. The NMR spectrum confirmed the presence of hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04659708
Source datasetuspto-grants-1987_04
ORD IDord-861a705abb484b67992aaa5135c24890
Source noteuspto-grants-1987_04