HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730654Generated: November 2, 2026
Ammonium Hydroxide → 6-(1H-imidazol-2-yl)-1,8-Naphthyridin-2(1H)-one
https://huagongshe.com/reaction/1730654
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 6-(1H-imidazol-2-yl)-1,8-Naphthyridin-2-amine | HCID 12297941 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 6-(1H-imidazol-2-yl)-1,8-Naphthyridin-2(1H)-one | HCID 12297942 | — |
Reaction Steps
To a mixture of 2-amino-6-(2-imidazolyl)-1,8-naphthyridine (211 mg., 1 mmole) in 40% sulphuric acid (2.5 ml.) at 5° C. is added with stirring sodium nitrite (69 mg., 1 mmole). The solution is allowed to warm to room temperature and then heated at 50° C. for 4 hours. The reaction mixture then is cooled to 5° C. and more sodium nitrite (40 mg., 0.57 mmole) added to ensure reaction goes to completion. The mixture then is heated at 50° C. for two hours, cooled to room temperature, diluted with water and neutralized with ammonium hydroxide affording 140 mg. of solid. The product is purified by dissolving in dilute acetic acid (5 ml.), treating the solution with charcoal, and neutralizing the filtered solution with a few drops of ammonium hydroxide. The product (100 mg., 47%) did not melt below 350° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03993656 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-09b58e8d68ee43dea4cd7407b37e7da1 |
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| Source note | uspto-grants-1976_11 |
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