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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 8-Bromo-1,7-naphthyridin-6-amine | HCID 10704335 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 8-Morpholino-1,7-naphthyridin-6-amine | HCID 13924375 | 60.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04659710 |
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| Source dataset | uspto-grants-1987_04 |
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| ORD ID | ord-fb21fdfa382a4550896f83757074d6e3 |
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| Source note | uspto-grants-1987_04 |
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