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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524102Generated: October 30, 2026

Methyl iodide → 6-Methyl-3-methylsulfanyl-4H-[1,2,4]triazin-5-one

https://huagongshe.com/reaction/524102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
Reactant6-Aza-2-thiothymineHCID 1263666—
SolventEthanolHCID 702—
Product6-Methyl-3-methylsulfanyl-4H-[1,2,4]triazin-5-oneHCID 13541899747.9%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 6-methyl-3-thioxo-3,4-dihydro-1,2,4-triazin-5(2H)-one (4, 5.80 g, 40.6 mmol) in absolute ethanol (250 mL) was added NaOH (1.96 g, 49.1 mmol) followed by MeI (11.5 g, 81.2 mmol). The mixture was heated at 40° C. for 15 h. Most of the solvent was evaporated under reduced pressure. Water was added to the residue. The precipitated white solid was collected by filtration and washed with ethanol to give 5 (3.06 g). The aqueous phase was extracted with CH2Cl2 (80 mL×4). The combined extracts were dried over Na2SO4 and concentrated to give 3.34 g crude product. This was purified by column chromatography on silica gel, and eluted with 1:1 to 1:2 petroleum ether-ethyl acetate to provide 6-methyl-3-(methylthio)-1,2,4-triazin-5(4H)-one (5). MS: m/z, 158 (100%, M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340523B2
Source datasetuspto-grants-2016_05
ORD IDord-0ba28f1703bb427aa6a2b0d51e72aa40
Source noteuspto-grants-2016_05