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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247855Generated: November 3, 2026

Water → 2-[(3,5-dimethyl-4-methoxypyridin-2-yl)methyl]thio-6-methyl-4(3H)-pyrimidinone

https://huagongshe.com/reaction/2247855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
ReactantMethylthiouracilHCID 667493—
Reactant2-(Chloromethyl)-4-methoxy-3,5-dimethylpyridin-1-ium chlorideHCID 45925697—
SolventEthanolHCID 702—
Product2-[(3,5-dimethyl-4-methoxypyridin-2-yl)methyl]thio-6-methyl-4(3H)-pyrimidinoneHCID 13555918536%

Reaction Steps

After dissolving 0.22 g (4.0 mmol) of potassium hydroxide in the mixture of 15 ml of ethanol and 3 ml of water, first 0.28 g (2.0 mmol) of 6-methyl-2-thiouracil, then a solution of 0.44 g (2.0 mmol) of 2-chloromethyl-3,5-dimethyl-4-methoxypyridinium chloride (m.p.: 127°-128° C.) in 15 ml of ethanol are added. The reaction mixture is stirred at room temperature for 20 hours, then ethanol is evaporated under reduced pressure, 10 ml of water are added to the residue and the product is extracted 3 times with 5 ml of chloroform each. The combined organic phase is washed with water, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The residue is recrystallized from 2-propanol to obtain 0.21 g (36%) of the title compound as a white crystalline product, m.p.: 231°-233° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05037830
Source datasetuspto-grants-1991_08
ORD IDord-48b8c66ff79d4cc18b4b20a622b10b48
Source noteuspto-grants-1991_08