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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453805Generated: November 2, 2026

Water → 4-(4-Methyl-5-(methylthio)-4H-1,2,4-triazol-3-yl)pyridine

https://huagongshe.com/reaction/1453805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
Reactant4-methyl-5-(pyridin-4-yl)-4H-1,2,4-triazole-3-thiolHCID 738547—
SolventAcetoneHCID 180—
Product4-(4-Methyl-5-(methylthio)-4H-1,2,4-triazol-3-yl)pyridineHCID 86598782%

Reaction Steps

To a mechanically stirred and cooled (9° C.) suspension of 4-methyl-5-pyridin-4-yl-2,4-dihydro-3H-1,2,4-triazole-3-thione (267 g) and methyl iodide (197.7 g) in acetone (2.6 L), was added a solution of sodium hydroxide (54 g in 600 mL of water) at such a rate (ca. 20 mL/min) as to maintain the temperature between 10 and 15° C. Another portion of water (50 mL) was then added and the temperature was allowed to come to 21 to 24° C. After another 2 h, the acetone was distilled off from the reaction mixture in vacuo (water-bath kept at 30° C.). Another portion of water (750 mL) was then added before cooling (17 to 18° C.) and collection of the formed precipitate by filtration. This solid was then washed with water (2×1 L) before drying at 100 mbar under a gentle stream of air for 3 days to yield 235 g of the title compound as a white powder. 1H NMR (DMSO-d6): 2.7 (s, 3H), 3.6 (s, 3H), 7.7 (m, 2H), 8.8 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476684B2
Source datasetuspto-grants-2009_01
ORD IDord-5b7a7d1f6ca74994983317c6f5f702d9
Source noteuspto-grants-2009_01