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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantBoric AcidHCID 7628—
ReactantSodium HydroxideHCID 14798—
ReactantSodium 3-nitrobenzenesulfonateHCID 31389—
Reactant5-Amino-2-methylpyridineHCID 243313—
CatalystFerrous sulfate heptahydrateHCID 62662—
SolventGlycerolHCID 753—
SolventWaterHCID 962—
Product2-Methyl-1,5-naphthyridineHCID 58903355.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969349B2
Source datasetuspto-grants-2015_03
ORD IDord-e1465dcbc634410c8c42d4b0c9d07c49
Source noteuspto-grants-2015_03