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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575556Generated: October 29, 2026

Methyl iodide → 2-Methyl-2,7-naphthyridin-1-one

https://huagongshe.com/reaction/575556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,2-Dihydro-2,7-naphthyridin-1-oneHCID 820151—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-Methyl-2,7-naphthyridin-1-oneHCID 8987035013.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (2.9 g, 72.5 mmol, 60% in oil) was added in portions to 2H-2,7-naphthyridin-1-one (3.5 g, 24.0 mmol) in dry DMF (50 mL) at 0° C. After stirring at 0° C. for 30 min, MeI (17.0 g, 118.7 mmol) was added and the mixture was stirred for an additional 30 min. Saturated aqueous NH4Cl (250 mL) and ethyl acetate (100 mL) were added. Extractive work up with ethyl acetate and purification by silica gel chromatography (DCM:MeOH=100:1 to 10:1) gave the title compound (0.5 g, 13.1%) as a yellow solid. 1H NMR (CDCl3, 400 MHz) δ 9.54 (1H, s), 8.64-8.62 (1H, d, J=5.6 Hz), 7.27-7.26 (1H, d, J=5.2 Hz), 7.22-7.20 (1H, d, J=5.6 Hz), 6.37-6.35 (1H, d, J=7.2 Hz), 3.54 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034900B2
Source datasetuspto-grants-2015_05
ORD IDord-44ba4e74ea6d440a98ebd64a5f54aa58
Source noteuspto-grants-2015_05