HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868956Generated: November 1, 2026
Sulfuric Acid → 2-Methyl-1,5-naphthyridine
https://huagongshe.com/reaction/868956
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Boric Acid | HCID 7628 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium 3-nitrobenzenesulfonate | HCID 31389 | — |
| Reactant | 5-Amino-2-methylpyridine | HCID 243313 | — |
| Catalyst | Ferrous sulfate heptahydrate | HCID 62662 | — |
| Solvent | Glycerol | HCID 753 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Methyl-1,5-naphthyridine | HCID 589033 | 55.8% |
Reaction Steps
A mixture of concentrated sulfuric acid (14 mL), boric acid (1.55 g, 39 mmol), sodium m-nitrobenzenesulfonate (11.30 g, 50 mmol), and iron sulfate heptahydrate (0.90 g, 3.23 mmol) was stirred at room temperature. Glycerol (8 mL) was added to the mixture followed by 3-amino-6-picoline (2.79 g, 25 mmol) and water (14 mL). The mixture was heated at 135° C. for 18 h. The reaction mixture was cooled to room temperature, basified using 4 N aqueous sodium hydroxide to pH 8, and extracted with EtOAc (50 mL×3). The organic extracts were combined, concentrated, and the residue was purified by column chromatography to afford 2-methyl-1,5-naphthyridine (2.01 g) as a light brown crystalline solid. MS (ESI): m/z 145 [M+H]+. See, e.g., J. Med. Chem. 2004, 47, 4494-4506.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969349B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-e1465dcbc634410c8c42d4b0c9d07c49 |
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| Source note | uspto-grants-2015_03 |
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