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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542714Generated: October 26, 2026

Morpholine → 8-Morpholino-1,7-naphthyridin-6-amine

https://huagongshe.com/reaction/542714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactant8-Bromo-1,7-naphthyridin-6-amineHCID 10704335—
SolventMethanolHCID 887—
Product8-Morpholino-1,7-naphthyridin-6-amineHCID 1392437560.9%

Reaction Steps

To a mixture of 800 mg of 6-amino-8-bromo-1,7-naphthyridine and 3.12 g of morpholine, 40 ml of methanol was added. The resultant mixture was refluxed for 13 hours. After the reaction, methanol was distilled off under reduced pressure and chloroform was added to the residue. After washing the chloroform solution with water, it was dried with anhydrous magnesium sulfate. Chloroform was distilled off under reduced pressure and a small amount of acetone was added to the residue to dissolve same. Hexane was then added to the residue, followed by removal of insoluble matter by filtration. The filtrate was concentrated and the residue was recrystallized from a mixed solvent of chloroform and hexane, thereby obtaining 500 mg of 6-amino-8-morpholino-1,7-naphthyridine (Compound No. 3) as yellowish crystals (yield: 60.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04659710
Source datasetuspto-grants-1987_04
ORD IDord-fb21fdfa382a4550896f83757074d6e3
Source noteuspto-grants-1987_04