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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,6-Dimethylmorpholine | HCID 110862 | — |
| Reactant | 6-Bromo-N-(6-methoxy-4-methyl-8-quinolinyl)hexanamide | HCID 612023 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-(6-Methoxy-4-methyl-8-quinolinyl)-2,6-dimethyl-4-morpholinehexanamide | HCID 13853362 | 55.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04659708 |
|---|
| Source dataset | uspto-grants-1987_04 |
|---|
| ORD ID | ord-861a705abb484b67992aaa5135c24890 |
|---|
| Source note | uspto-grants-1987_04 |
|---|