Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247848Generated: November 2, 2026

Methylthiouracil → 4(1H)-Pyrimidinone, 2-(((2-(dimethylamino)phenyl)methyl)thio)-6-methyl-

https://huagongshe.com/reaction/2247848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylthiouracilHCID 667493—
ReactantThiouracilHCID 1269845—
ReactantSodiumHCID 5360545—
ReactantHCID 178486212HCID 178486212—
SolventEthanolHCID 702—
SolventSodium ethoxideHCID 2723922—
Product4(1H)-Pyrimidinone, 2-(((2-(dimethylamino)phenyl)methyl)thio)-6-methyl-HCID 13574425847.7%

Reaction Steps

355 mg (2.5 mmol) of 6-methyl-2-thiouracil are dissolved in a sodium ethoxide solution prepared from 116 mg (5.05 mmol) of sodium metal and 15 ml of anhydrous ethanol. The mixture is gently warmed to dissolve the thiouracil, then 515 mg (2.5 mmol) of (2-chloromethylphenyl)-dimethylammonium chloride are added and the reaction mixture is refluxed under stirring for 1 hour. Sodium chloride is immediately precipitated from the solution. After evaporation under reduced pressure the residue is taken up in water, extracted 3 times with 20 ml of chloroform each, then the combined organic phase is washed with 20 ml of water, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The pale yellow oily residue is rubbed with an 1:1 mixture of benzene and petroleum ether to obtain 287 mg (47.7%) of the title compound as a white crystalline product, m.p.: 151°-153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05037830
Source datasetuspto-grants-1991_08
ORD IDord-baa6d9552ea542a68ccfd12b5de6b346
Source noteuspto-grants-1991_08