HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462716Generated: October 30, 2026
Water → 5-Methyl-2-oxo-1,2-dihydro-1,6-naphthyridine-3-carboxylic acid
https://huagongshe.com/reaction/462716
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 5-methyl-2-oxo-1H-1,6-naphthyridine-3-carbonitrile | HCID 5713068 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-Methyl-2-oxo-1,2-dihydro-1,6-naphthyridine-3-carboxylic acid | HCID 13232052 | — |
Reaction Steps
E-6. 1,2-Dihydro-5-methyl-2-oxo-1,6-naphthyridine-3-carboxylic acid--A mixture containing 63 g of 1,2-dihydro-5-methyl-2-oxo-1,6-naphthyridine-3-carbonitrile, 100 ml of concentrated sulphuric acid and 100 ml of water was heated on a steam bath for 16 hours, after which time tlc analyses (20% methanol in ether) indicated the presence of a considerable amount of starting material. Therefore, the reaction mixture was heated in a oil bath at 135°-140° C. for 8 hours, cooled to room temperature and poured on ice (1 l. beaker, 1/3 filled). The resulting aqueous mixture was neutralized by adding aqueous ammonium hydroxide until slightly basic and was then reacidified by adding acetic acid. The resulting solid was collected, washed successively with water and methanol, and dried at 100° C. to yield 54.8 g of 1,2-dihydro-5-methyl-2-oxo-1,6-naphthyridine-3-carboxylic acid, m.p. 255°-257° C. with decomposition. Another 7.2 g of the product, m.p. 252° -255° C. was obtained from the mother liquor.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04517190 |
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| Source dataset | uspto-grants-1985_05 |
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| ORD ID | ord-5846d8dde2564718af43c6ebd0fc4564 |
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| Source note | uspto-grants-1985_05 |
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